IE62095B1 - Pharmaceutical formulations for parenteral use - Google Patents

Abstract

PURPOSE: To obtain the subject composition reduced in problems accompanied by precipitation of a medicine at the injection site and/or the lungs or other organs after parenteral administration by combining a medicine which is lipophilic and unstable in water with a specific cyclodextrin derivative. CONSTITUTION: This composition is obtained by dissolving a medicine which is insoluble or sparingly soluble in water and/or unstable in water into an aqueous parenteral solution containing 20-50% hydroxypropyl, hydroxyethyl, glycosyl, maltosyl or maltotriosyl derivative of β- or γ-cyclodextrin, and reduced in inclination which gathers in lung or other organs by precipitation at injection site or its vicinity and/or the lungs or other organs. The medicine includes antineoplastic medicine, sedative, tranquilizer, anticonvulsant, antidepressant, hypnotic, muscle relaxant and antispasmodic.

Description

PHARMACEUTICAL FORMULATIONS FOR PARENTERAL USE FIELD OF THE INVENTION: The present invention relates to aqueous parenteral solutions of drugs which are insoluble or only sparingly soluble in water and/or which are unstable in water, combined with selected cyclodextrins. The solutions provide a means for alleviating problems associated with drug precipitation at the injection site and/or in the lungs or other organs following parenteral administration.

BACKGROUND OF THE INVENTION: Cyclodextrins are cyclic oligosaccharides. The most common cyclodextrins are α-cyclodextriη , which is composed of a ring of six glucose residues, β-cyclodextrin, which is composed of a ring of seven glucose residues, and γ-cyclodextrin, which is composed of a ring of eight glucose units. The inside cavity of a cyclodextrin is lipophilic, while the outside of the cyclodextrin is hydrophilic: this combination of properties has led to widespread study of the natural cyclodextrins, particularly in connection with pharmaceuticals, and many inclusion complexes have been reported. β-Cyclodextrin has been of special interest because of its cavity size, but its relatively low aqueous solubility has limited its use in the pharmaceutical field. -2Attempts to modify the properties of the natural cyclodextrins have resulted in the development of heptakis (2,6-di-0-methyl)-β-cyclodextrin, heptakis (2,3,6-tri-0-methyl )-β-cyclodextri n, hydroxypropyi - β5 cyclodextrin, β-cyclodextrin-epichiorohydrin polymer and others. For a comprehensive review of cyclodextrlns and their use in pharmaceutical research, see Pitha et al, in Controlled Drug Delivery, ed. S.O. Bruck, Vol. I, CRC Press, Boca Raton, Florida, pp. 12510 148 (1983). For an even more recent overview, see Uekama et al, in CRC Critical Reviews in Therapeutic Drug Carrier Systems, Vol. 3 (1), 1-40 (1987); Uekama, i n Topics in Pharmaceutical Sciences 1987, eds. D.D. Breimer and P. Speiser, Elsevier Science Publishers B.V. (Biomedical Division), 1987, 181-194; and Pagington, Chemistry in Britain, May 1987, pp. 455458.

Inclusion complexes of α-, β- or γ-cyclodextrin or their mixtures with a variety of drugs have been de20 scribed by numerous parties and various advantages have been attributed to the complexes. These descriptions include the following: INVENTOR U.S. PATENT NO. ACTIVE . INGREDIENT USE ADVANTAGE Noda et al 4,024.223 menthol A/or methyl salicylate antiphlogistic, analgesic reduced unpleasant odor. Increased wet packing effect Szejtll et al 4,228.160 Indomethacln anti-inflammatory, protective during pregnancy reduced ulcerative effect HayasM et al 4,232,009 •-halo-PGI? analogs hypotensive, uterine contraction stimulating, blood platelet aggregation Inhibiting Increased stability Matsumoto et al 4,351,846 3-hydroxy- and 3-oxo- prostaglandln analogs uterine contraction stimulating Increased stability Yamahlra et al 4,352,793 bencyclane fumarate anticonvulsant, vasodilative Increased stability at strong acid pH, faster gastric enptylng, higher blood concentrations less Irritation, Improved hemolytic activity 11 pari 4,383,992 steroids— corticosteroids, androgens, anabolic steroids, estrogens, progestagens hormonal Improved water solubility. Increase* therapeutic response 1n eye Nlcolau 4,407,795 p-hexadecylam1nobenzolc antiatherosclerotic enhanced b1oava1lab111ty ac1d sodium salt INVENTOR N.S. MOENT NO. ACTIVE INGREDIENT USE ADVANTAGE Tuttle1 4,424,209 3,4-dlIsobutyryl oxy-N-[3-(4Isobutyryloxyphenyl)-1methyl-npropyl]-Bphenethylamine cardiac contractility agent Tuttle 4,425,336 3,4-dihydroxyN-[3-(4-hydroxyphenyl)-1methyl-npropylj-ephenethylamine cardiac contractility agent capable of oral administration Wagu et al 4,438,106 EPA and OHA (fatty acids) deodorized, storage stable Masuda et al2 4,474.811 2-(2-fluoro-4blphenylyl)propionic acid or salt anti- inf 1 ammatory ophthalmic reduced eye Irritation, higher concentrations, no side effects, highly soluble, long stability, excellent pharmacological effects Shlnoda et al 4,478,995 acid addition salt of (2*benzyloxycarbonyl )phenyl trans-4-guan1dlnomethyl eyelohexanecarboxylate anti-ulcer excellent water solubility, good absorption In digestive tract, gotod anti-ulcer activity Hayashl et al 4,479,944 PGI? analog for treatment of stabilization against artereoscl erosls, decomposition cardiac failure or thrombosis INVENTOR U.S. PATENT NO. ACTIVE INGREDIENT USE ADVANTAGE Hayashl et al 4.479.966 6,9-methanoPGIZ analogs for hypertension, cerebral thrombosis and the like , Increased stability Harada et al 4,497.803 lankacidingroup antibiotic antibiotic for swine dysentery enhanced water solubility and stability. Increased rate and amount of absorption Masuda 4,499,085 prostaglandin analog treating anoxia of brain cells Szejtli et al 4,518,588 phendlllne, 1.e. N-(l-phenylethyl)-3,3dlphenyl propyl amine or Its hydrochloride coronary dilator calcium antagonist improved water solubility, accelerated and Increased in vivo resorption & dissolution at pH/ temperature of gastric acid Szejtli et al 4,524,068 piperonyl butoxide synerglzes pesticidal effect easily handled crystalline solid; of known Insect1- improved water solucides and fungi- biHty, Increased cides absorption & velocity of penetration through biological membranes Jones 4,555,504 a cardiac glycoside cardiac effect high aqueous solubility, apparently better bloavallablllty Uekama et aP 4,565,807 plrprofen anti-inflam- matory, analgesic, antipyretic Improved stability to oxidation, freedom from bitter taste, less 1rr1ta- ting -6non-volatile potder vs. relative oil INVENTOR U.S.

PATENT NO ACTIVE INGREDIENT USE ADVANTAGE Ueda et al 4,575,548 2-nltroxymethyl- for vascular 6-chloropyridlne disorders Ohwakl et al* 4,598,070 trlpamlde anti-hypertensive improved solubility Ch1es1 et al 4,603,123 piroxicam, i.e. ant1-1nf1am4-hydroxy-2- matory, analgesic methy1-N-2- pyr1dy1-2H-l,2- benzoth1az1ne-3- carboxaralde-1,1- dloxide Hasegawa et al 4,608.366 mobenzoxamlne. antlemetlc, 1.e. l-[2-(4- antispasmodic methoxybenzhy- dry!oxy)ethyl]- 4-[3-(4-fluoro- benzoylIpropyl]- plperazlne storage stability, better absorption through digestive tract Hlral et al2 4,659,696 polypeptide Improving drug absorption by nonoral and noninjection routes Szejtll et al 4,623,641 PGI^ methyl anti-ulcer ester Improved storage stability Nlnger et al 4.663,316 unsaturated antibiotic, phosphorus- ant 1funga1, containing antitumor antibiotics. Including phosphotrlenin enhanced stability against oxidation -7U.S. ACTIVE INVENTOR PATENT NO. INGREDIENT USE ADVANTAGE Fukazawa et al 4.675,395 hinokltlol bactericidal, bacteriostatic improved water solubility, less odor 1 Tuttle also describes use of 2,6-dl-O-methyl-e-cyclodextrln and 2,3,6-tri-Omethyl-e-cyclodextrin to form the Inclusion complex.

This may not be an Inclusion complex, but simply a physical mixture.

This 1s a mixture and/or an Inclusion compound. 4 The Inventors also mention prior known solubility Improvements of cyclodextrin inclusions of barbituric acid derivatives, mefenamlc acid, indomethacin and chloramphenicol.

The inventors refer to this as an “occlusion compound. -8Inclusion complexes of 2,6-di-0-methyl-Scyclodextrin with dibenzo[bd]pyran derivatives and salts having analgesic, antemetic and narcosispotentiating activities have been described in Nogradi et al U.S. Patent No. 4,599,327; increased water solubility and thus improved biological activity have been claimed for the complexes. A review of the pharmaceutical applications of such methylated cyclodextrins has been published by Uekama, Pharm. Int., March 1985, 61-65; see also Pitha, Journal of Inclusion Phenomena 2_, 477-485 ( 1984).

Cyclodextrin polymer has been reported by Fenyvesi et al, Chem. Pharm. Bull. 32 (2), 665-669 (1984) to improve the dissolution of furosemide. Improvements in the dissolution and absorption of phenytoin using a water-soluble β-cyclodextrin epichlorohydrin polymer have been described by Uekama et al , International Journal of Pharmaceutics, 23, 35-42 (1985).

Hydroxypropyl-β-cyclodextrin (HPCO) and its preparation by propylene oxide addition to βcyclodextrin were described in Gramera et al United States Patent No. 3,459,731 nearly 20 years ago.

Gramera et al also described the analogous preparation of hydroxyethyl-β-cyclodextrin by ethylene oxide reaction with β-cyclodextrin. Much more recently, Pitha and co-workers have described the improved preparation of this cyclodextrin derivative and its effects on the dissolution of various drug molecules. Pitha United States Patent No. 4,596,795, dated June 24, 1986, describes inclusion complexes of sex hormones, particularly testosterone, progesterone, and estradiol, with specific cyclodextrins, preferably hydroxypropyl-9v β-cyclodextrin and poly-B-cyclodextriη . The complexes enable the sex hormones to be successfully delivered to the systemic circulation via the sublingual or buccal route; the effectiveness of this delivery is believed to be due to the high dissolution power of hydrophilic derivatives of cyclodextrins , the non-aggregated structure of their complexes with steroids, and their low toxicity and irritancy of mouth tissue. Success with other cyclodextrins , including poly-y-cyclodextrin and hydroxypropyi-γ-cyclodextrin , have also been noted in the Pitha patent. See also Pitha et al, J. Pharm. Sci. , Vol. 74, No. 9, September 1985 , 987-990, concerning the same and related studies. Pitha et al also describe in the J. Pharm. Sci. article the storage stability of tablets containing a testosteronehydroxypropyl -β-cyclodextrin complex and the lack of toxicity of the cyclodextrin itself, as well as the importance of the amorphous nature of the cyclodextrin derivatives and their complexes with drugs in improving dissolution properties.

The improved, optimized preparation and purification of hydroxypropyi-β-cyclodextrin has been recently described by Pitha et al, International Journal of Pharmaceutics, 29, 73-82 (1986). In the same publication, the authors have described increased water solubility for 32 drugs in concentrated (40 to 50%) aqueous solutions of hydroxypropyi-β-cyclodextrin; improved solubilization of acetamidophen, apomorphine, butylated hydroxytoluene, chlorthalidone, cholecalci30 ferol, dexamethasone, dicumarol, digoxin, diphenylhydantoin, estradiol, estriol, ethiny1estradiol-3methyl ether, ethisterone, furosemide, hydroflumethiazide, indomethacin, iproniazid phosphate, 17-10methyltestosterone, nitroglycerin, norethindrone, ouabain, oxprenolol, progesterone, retinal, retinoic acid (all trans and salt forms), retinol, spironolactone, sulpiride, testosterone and theophylline was noted. The authors indicated this to be an extension of their earlier work with hydroxypropyl - β-cyclodextrin, which was previously found effective for oral administration of the sex hormones to humans. Their later work reported in Pitha et al, International Journal of Pharmaceutics, 29, 73-82 (1986), has also been very recently described in Pitha United States Patent No. 4,727,064, dated February 23, 1988. That patent claims a composition containing an amorphous complex of cyclodextrin and a drug, and a method of producing a stabilizing amorphous complex of a drug and a mixture of cyclodextrins comprising (1) dissolving an intrinsically amorphous mixture of cyclodextrin derivatives which are water soluble and capable of forming inclusion complexes with drugs in water; and (2) solubilizing lipophilic drugs into aqueous media to form a solution and form a solubilized drug/cyclodextrin complex.

Uekama et al, CRC Critical Reviews in Therapeutic Drug Carrier Systems, Vol. 3 (1), pp. 1-40 (1987), have described the characteristics of various cycl odextrins, including hydroxypropyl-β-cyclodextrin . The authors have presented data showing improved solubilization in water in the presence of 15 mg/mL of HPCD for the drugs carmofur, diazepam, digitoxin, digoxin, flurbiprofen, indomethacin, isosorbide dinitrate, phenytoin, prednisolone, progesterone and testosterone. In a discussion of the metabolism and toxicity of cyclodextrins, Uekama -11et al have indicated that cyclodextrins at sufficiently high concentrations cause hemolysis, and that the methylated cyclodextrins have higher hemolytic activity than the natural cyclodextrins. Hydroxypropyl - 65 cyclodextrin is said to cause hemolysis beginning at 4.5 mM. The authors have further indicated that parenteral administration of large doses of cyclodextrins should be avoided, but that γ-cyclodextrin and hydroxypropyl -β-cyclodextrin seem to be useful in drug solubilization for injections and liquid preparations used for mucous membranes.

JANSSEN PHARMACEUTICA N.V.’s International Patent Application No. PCT/EP84/00417, published under International Publication No. W085/02767 on July 4, 1985, has described pharmaceutical compositions comprising inclusion compounds of drugs, which are unstable or only sparingly soluble in water, with partially etherified β-cyclodextrin derivatives having hydroxyalkyl and optionally additional alkyl groups. Among the cyclodextrin derivatives contemplated is hydroxypropyl -β-cycl odextri η , while the drugs include nonsteroidal anti-rheumatic agents, steroids, cardiac glycosides and derivatives of benzodiazepine, benzimidazole, piperidine, piperazine, imidazole and triazole. Preferred drugs include etomidate, ketoconazole, tubulazole, itraconazole, levocabastine and flunarizine. The pharmaceutical compositions of the invention include oral, parenteral and topical formulations, with 4 to lflt solutions of cyclodextrin derivatives being utilized to solubilize various drugs. Improved solubilities of indomethacin, digitoxin, progesterone, dexamethasone, hydrocortisone and -12diazepam using 10% HPCD are shown, and an injectable formulation of diazepam in 7% HPCD is specifically described. The relatively low cyclodextrin concentrations used reflect a desire to avoid or minimize the hemolytic effects observed at higher cyclodextrin concentrations .

Carpenter et al, The Journal of Pediatrics, 111, 507-512 (October 1987) describe intravenous infusion of 2-hydroxypropy1 -β-cyclodextriη, prepared as a 5% solution in water, to treat severe hypervitaminosis A. It was found that, during infusion, circulating retinyl esters increased transiently, while total vitamin A excreted in the urine was enhanced after infusion.

Thus, intravenous infusion of 51 HPCD was found to decrease in vivo levels of the vitamin, presumably by complexing with the vitamin and removing some of the excess from the body.

The inclusion characteristics of yet other derivatized cyclodextrins have also been described in the literature. Studies of branched cyclodextrins which are glucosyl and maltosyl derivatives of α-, β- and γ-cyclodextrin and their inclusion complexes with drugs have recently been reported. Uekama, in Topics in Pharmaceutical Sciences 1987 , eds. D. D. Breimer and P. Speiser, Elsevier Science Publishers Β. V. (Biomedical Division), 1987, 181-194, has described the effects on bio-pharmaceutical properties of maltosyl and glucosyl cyclodextrin derivatives, including enhanced drug absorption. Koizumi et al, Chem. Pharm. Bull. 35 (8), 3413-3418 (1987), have reported on inclusion complexes of poorly water-soluble drugs with glucosyl cyclodextrins, namely 6-0-a-D-13glucosyl-α-CD (G^-a-CD), 6-0-a-D-glucosyl-β-CD (G|0-CD) and 6D-di-O-a-D-gl ucosyl-β-CD (ZG^e-CD). Okada et al, Chem. Pharm. Bull., 36 (6), 2176-2185 (1988), have reported on the inclusion complexes of poorly water-soluble drugs with maltosyl cyclodextrins, namely 6-0-a-maltosyl-α-CD (G2-a-CD), 6-0-a-maltosyl ¢-CD (G2-8-CD), 6-0-a-maltosyl-γ-CD (G2-y-CD), 6-0a-mal totriosyl -a-CD (Gg-a-CD), 6-0-a-maltotriosyl-βCD (G^-e-CD) and 6-0-a-maltotriosyl-γ-CD (Gg-y-CD).

The delivery of drugs to the brain is often seriously limited by transport and metabolism factors and, more specifically, by the functional barrier of the endothelial brain capillary wall, i.e. the bloodbrain barrier or BBB. Site-specific delivery and sustained delivery of drugs to the brain are even more difficult.

A dihydropyridine * pyridinium salt redox system has recently been successfully applied to delivery to the brain of a number of drugs. Generally speaking, according to this system, a dihydropyridine derivative of a biologically active compound is synthesized, which derivative can enter the CNS through the blood-brain barrier following its systemic administration. Subsequent oxidation of the dihydropyridine species to the corresponding pyridinium salt leads to delivery of the drug to the brain.

Three main approaches have been published thus far for delivering drugs to the brain using this redox system. The first approach involves derivation of -14selected drugs which contain a pyridinium nucleus as an integral structural component. This approach was first applied to delivering to the brain N-methylpyridinium2-carbaldoxime chloride (2-PAM), the active nucleus of which constitutes a quaternary pyridinium salt, by way of the dihydropyridine latentiated prodrug form thereof. Thus, a hydrophilic compound (2-PAM) was made lipoidal (i.e. lipophilic) by making its dihydropyridine form (Pro-2-PAM) to enable its penetration through lipoidal barriers. This simple prodrug approach allowed the compound to get into the brain as well as other organs, but this manipulation did not and could not result in any brain specificity. On the contrary, such approach was delimited to relatively small mole15 cule quaternary pyridinium ring-containing drug species and did not provide the overall ideal result of brainspecific, sustained release of the desired drug, with concomitant rapid elimination from the general circulation, enhanced drug efficacy and decreased toxi20 city. No trapping in the brain of the 2-PAM formed in situ resulted, and obviously no brain-specific, sustained delivery occurred as any consequence thereof: the 2-PAM was eliminated as fast from the brain as it was from the general circulation and other organs.

Compare U.S. Patents Nos. 3,929,813 and 3,962,447; Bodor et al, J. Pharm. Sci , 67, No. 5, 685 ( 1978). See also Bodor, Novel Approaches for the Design of Membrane Transport Properties of Drugs, in Design of Biopharmaceutical Properties Through Prodrugs and Analogs, Roche, E.B. (ed.), APhA Academy of Pharmaceutical Sciences, Washington, D.C., 98-135 (1976). Subsequent extension of this first approach to -15delivering a much larger quaternary salt, berberine, to the brain via its dihydropyridine prodrug form was, however, found to provide site-specific sustained delivery to the brain of that anticancer agent. See Bodor et al, Sci ence, Vol. 214, December 18, 1981, pp. 1370-1372.

The second approach for delivering drugs to the brain using the redox system involves the use of a pyridinium carrier chemically linked to a biologically active compound. Bodor et al, Science, Vol. 214, December 18, 1981, pp. 1370-1372, outline a scheme for this specific and sustained delivery of drug species to the brain, as depicted in the following Scheme I: -16i ENZYMATIC -(O-OCl* CLEAVAGE IN circulatory system (Ol ♦ (QClj* ‘3 Elimination SCHEME 1: BBB, SLOOP-SNA IN BARRIER. -17According to the scheme in Science, a drug [D] is coupled to a quaternary carrier [QC]+ and the [D-QC]+ which results is then reduced chemically to the lipoidal dihydro form [D-DHC]. After administration of [D-OHC] in vivo, it is rapidly distributed throughout the body, including the brain. The dihydro form [DDHC] is then in situ oxidized (rate constant, kj) (by the NAD * NADH system) to the ideally inactive original [D-QC]+ quaternary salt which, because of its ionic, hydrophilic character, should be rapidly eliminated from the general circulation of the body, while the blood-brain barrier should prevent its elimination from the brain (kg>>k2; kj^ky). Enzymatic cleavage of the [D-QC]+ that is locked in the brain effects a sustained delivery of the drug species [D], followed by its normal elimination (kg), metabolism. A properly selected carrier [QC] + will also be rapidly eliminated from the brain (kg^kg). Because of the facile elimination of [D-QC]+ from the general circulation, only minor amounts of drug are released in the body [kg>>k4); [D] will be released primarily in the brain (k4>k;>). The overall result ideally will be a brainspecific sustained release of the target drug species. Specifically, Bodor et al worked with phenyl25 ethylamine as the drug model. That compound was coupled to nicotinic acid, then quaternized to give compounds of the formula -18whlch were subsequently reduced by sodium dithionite to the corresponding compounds of the formula I R Testing of the N-methyl derivative in vivo supported the criteria set forth in Scheme I. Bodor et al speculated that various types of drugs might possibly be delivered using the depicted or analogous carrier systems and indicated that use of N-methylnicotinic acid esters and amides and their pyridine ringsubstituted derivatives was being studied for delivery of amino- or hydroxyl-containing drugs, including small peptides, to the brain. No other possible specific carriers were disclosed. Other reports of this work with the redox carrier system have appeared in The Friday Evening Post, August 14, 1981, Health Center Communications, University of Florida, Gainesville, Florida; Chemical A Engineering News, December 21, 1981, pp. 24-25; and Science News, January 2, 1982, Vol. 121, No. 1, page 7. More recently, the redox carrier system has been substantially extended in terms of possible carriers and drugs to be delivered. See International Patent Application No. PCT/US83/00725, filed May 12, 1983 and published November 24, 1983 under International Publication No. W083/03968. Also see Bodor et al, Pharmacology and Therapeutics, Vol. 19, No. 3, pp. 337-386 (1983); and Bodor United States Patent No. 4,540,564, Issued September 10, 1985. -19The third approach for delivering drugs to the brain using the redox system provides derivatives of centrally acting amines in which a primary, secondary or tertiary amine function has been replaced with a dihydropyridine/pyridinium salt redox system. These brain-specific analogs of centrally acting amines have been recently described in International Patent Application No. PCT/US85/OO236, filed February 15, 1985 and published September 12, 1985 under International Publi10 cation No. W085/03937. The dihydropyridine analogs are character!zed by the structural formula 0.0 wherein D is secondary or the formula the residue of a centrally tertiary amine, and - o acting primary, is a radical of wherein the dotted line in formula (a) indicates the presence of a double bond in either the 4 or 5 position of the dihydropyridine ring; the dotted line in formula (b) indicates the presence of a double bond 1n either the 2 or 3 position of the d1hydroquinol1ne ring system; m is zero or one; n is zero, one or two; p is -20zero, one or two, provided that when p is one or two, each R in formula (b) can be located on either of the two fused rings; q is zero, one, or two, provided that when q is one or two, each R in formula (c) can be located on either of the two fused rings; and each R is independently selected from the group consisting of halo, Cj-Cy alkyl, Cj-Cy alkoxy, Cg-Cg alkoxycarbonyl, C^-Cg alkanoyloxy, Cj-Cy haloalkyl, Cj-Cy alkylthio, Cj-Cy alkylsulfinyl, Cj-Cy a 1kylsulfonyl, -CH»N0R'” wherein R'' ' is H or Cj-Cy alkyl, and -CONR'R’’ wherein R' and R'', which can be the same or different, are each H or Cj-Cy alkyl. These dihydropyridine analogs act as a delivery system for the corresponding biologically active quaternary compounds in vivo. Due to its lipophilic nature, the d1hydropyridine analog will distribute throughout the body and has easy access to the brain through the blood-brain barrier. Oxidation in vivo will then provide the quaternary form, which will be locked preferentially in the brain. In con20 tradistinet 1 on to the drug-carrier entities described in Bodor U.S. Patent No. 4,540,564 and related publications, however, there is no readily metabolical 1y cleavable bond between drug and quaternary portions, and the active species delivered is not the original drug from which the dihydro analog was derived, but rather is the quaternary analog itself.

Each of the major dihydropyridine * pyridinium redox systems for brain-targeted drug delivery thus has Its own unique characteristics but also has properties in common with the other approaches. Common to the various approaches 1s Introduction of a dihydropyridine-type nucleus into the drug molecule, which renders -21the dihydropyridine-containing drug derivative substantially more lipophilic than the parent drug from which it is derived. The increased 1ipophi1icity enables the derivative to readily penetrate biological membranes, including the blood-brain barrier. Also common to the various approaches is the fact that the redox nature of the dlhydropyridine-type moiety means that the lipophilic dihydropyridine form is oxidizable in vivo to the hydrophilic, ionic pyridinium salt form, thus locking in the brain either the active drug or the quaternary precursor, depending on which approach is employed .

The dihydropyridine * pyridinium salt redox carrier and analog systems have achieved remarkable success in targeting drugs to the brain in laboratory tests. This success is, of course, due in part to the highly lipophilic nature of the dihydropyridinecontaining derivatives, which allows brain penetration. At the same time, the increased 1ipophi1icity makes it practically impossible to formulate aqueous solutions of these derivatives for injection; moreover, even when the d1hydropyridines are dissolved in organic solvents such as dimethylsulfoxide, they have a propensity for precipitating out of solution upon injection, particularly at higher concentrations, and especially at the injection site or in the lungs.

Indeed, even in the absence of noticeable crystallization, it has been found that the redox derivatives frequently display not only the desired concentration 1n the brain but undesired lung concentrations as well, so that while the brain to blood ratios are at appropriate high levels, the initial lung to brain -22levels are high as well. Still further, the dihydropyridine-containing derivatives suffer from stability problems, since even in the dry state they are very sensitive to oxidation as well as to water addition.

These problems, which must be overcome so that the dihydropyridine * pyridinium salt redox systems can be fully commercialized, have been addressed by applicant's copending Irish Application No. 3717/88, filed December 13, 1988 and are also addressed by the present application. In particular, the present application addresses the problems related to unfavorable concent ration/precipi tation of the dihydropyridine ♦ pyridinium salt redox systems at or near the injection site and/or in the lungs, following parenteral administration, as well as similar problems encountered with other drugs which are insoluble,, sparingly soluble and/or unstable in water.

SUMMARY AND OBJECTS OF THE INVENTION: One object of the present invention is to provide imoroved aqueous parenteral solutions of drugs which are insoluble, sparingly soluble and/or unstable in water.

Another object of the present invention is to provide a method for the preparation of a composition for decreasing the tendency of lipophilic and/or waterinstable drugs to precipitate at or near the injection site and/or in the lungs following parenteral drug administration.

Yet another object of the present invention is to provide improved aqueous parenteral solutions containing the reduced, di hydropyridine form of a -23dihydropyridine * pyridinium salt redox system for braintargeted drug delivery.

Still another object of the present invention is to provide a method for decreasing the tendency of the reduced, dihydropyridine form of a dihydropyridine ♦ pyridinium salt redox system for brain-targeted drug delivery to precipitate at or near the injection site and/or in the lungs following parenteral administration.

The foregoing objects are achieved by means of 10 aqueous parenteral solutions of drugs which are insoluble, sparingly soluble and/or unstable in water, said solutions comprising from about 20 to about 50% of a hydroxypropyl, hydroxyethyl, glucosyl, maltosyl or maltotriosyl derivative of β- or γ-cyclodextrin. The invention provides a novel method for decreasing the tendency of lipophilic and/or water-unstable drugs to precipitate at or near the injection site and/or in the lungs or other organs following parenteral drug administration, said method comprising formulating said drug in an aqueous solution adapted for parenteral administration containing from about 20% to about 50% of a hydroxypropyl, hydroxyethyl, glucosyl, maltosyl or maltotriosyl derivative of β- or γ-cyclodextrin. In one aspect of the invention, the drug is the reduced, biooxidizable, blood-brain barrier penetrating lipoidal form of a d1hydropyridine * pyridinium salt redox system for brain-targeted drug delivery.

BRIEF DESCRIPTION OF THE DRAWINGS: Other objects and advantages of the present invention will be apparent from the following detailed description and accompanying drawings, in which: -24FIG. 1 is a pair of semi-1ogarithmic plots, the first comparing the concentrations of an estradiol-CDS, 176-[(l-methyl-l,4-dihydro-3-pyridinyl)carbonyloxy]estra-l ,3,5(10)-trien-3-ol, hereafter referred to as Eg-CDS, in lung tissue in ug per gram dose following systemic administration to rats of either 15 mg/kg EgCDS in dimethylsulfoxide (0) or 5 mg/kg Eg-CDS inclusion complex with hydroxypropyl - β-cyclodextriη (Δ) in water, corrected for dose, and the second comparing the lung concentrations of the quaternary cation, 176[(1-methyl-3-pyridinium)carbonyloxy]estra-l,3,5(I0)trien-3-ol, hereafter referred to as EgO* or Quat, following the same E2-COS administration; and FIG. 2 is a bar graph illustrating, at selected time points, the concentrations of the quaternary cation, Ε^0+ or Quat, in the brain in ng per gram dose, following systemic administration to rats of either 15 mg/kg E2-CDS in dimethylsulfoxide (□) or 5 mg/kg E2-COS inclusion complex with hydroxypropyl-β-cyclodextrin () in water, corrected for dose.

DETAILED DESCRIPTION OF THE INVENTION; The term lipophilic is used herein to describe drugs which are lipid-soluble and hydrophobic, i.e. which are insoluble or sparingly soluble in water.

The expression parenteral as used herein refers to routes of administration other than through the gastrointestinal tract or lungs, and to formulations for use in administering drugs by such routes. Thus, parenteral as used herein includes, for example, intramuscular, subcutaneous, intra-articular (i.e. into -25the joint, which in turn includes intra-synovial, i.e. into the synovial fluid) and, especially, intravenous routes and formulations. The words parenteral and injectable are used interchangeably herein.

Numerous drugs suffer from problems associated with their lack of water solubility and/or lack of stability in water. These lipophilic and/or waterlabile drugs cannot be practically formulated as aqueous parenteral solutions. Consequently, the drugs are either unavailable for injection at the present time, or they are available for injectable use only in combination with undesirable organic vehicles.

Injection of such vehicles is undesirable because of the systemic and local toxicity which can result. Some of the organic solvents commonly used as vehicles include dimethylacetamide (DMA), dimethylsul foxide (DMSO), propylene glycol(PG), benzyl alcohol and ethanol. Examples of the toxicity associated with these solvents include central nervous system depression, nystagmus, lymphocytosis, liver and kidney damage, blood disorders, jaundice, weight loss, anemia, convulsions, hallucinations, mutagenic effects, cyanosis, hypotension, bronchial spasms, cardiac standstill and death.

Moreover, parenteral administration of lipophilic or water-labile drugs in organic vehicles can result in precipitation of the drug at and/or near the injection site and/or in the lungs or other organs, which in turn leads to increased toxicity. Precipitation of drugs in the lungs, for example, has led to severe respiratory distress and even death in laboratory animals. On the -26other hand, when lack of a suitable solvent results in the fact that the drug is only available as an oral formulation, then bioavailability becomes a concern since drugs are frequently less bioavailable from oral delivery forms than they are from parenteral, especially intravenous, forms.

Among the lipophilic and/or water-labile drugs which are contemplated for use in aqueous parenteral formulations in accord with the present invention, there can be mentioned antineoplastics (anticancer/ antitumor agents), sedatives, anti-inflammatory steroids, tranquilizers, anticonvulsants, antivirals, vitamins/nutritional factors, emetics, anticoagulants, cardiotonics (including cardiac glycosides), diuretics, non-steroidal anti-inflammatory agents (NSAID's), androgens, estrogens, vasodilators, antidepressants, hypnotics, antifungals, progestins, anti protozoals , anesthetics, vasoconstrictors, hypoglycemics, antibacterial s/anti bi oti cs , platelet inhibitors, muscle relaxants, antiemetics, radiodiagnostics, antispasmodics, antiarrhythmics, carbonic anhydrase inhibitors, narcotic antagonists, narcotic agonists, mixed narcotic agonists-antagonists, pharmacologically active proteins such as peptide hormones, enzymes, antibodies and other biologically produced substances, antiParkinsonism/dopamineric agents and drugs for treating Alzheimer's disease.

Specific drugs contemplated for parenteral formulation with hydroxypropyl-β-cyclodextrin in accord with the present invention Include antineoplastics such as chlorambucil, lomustine, melphalan, methotrexate, -27hexamethylmelamine, teniposide, etoposide, semustine (methyl CCNU) , fazarabine (Ara-AC), mercaptopurine, tubulazole, carmofur, carmustine, amsacrine, bruceantin, diaziquone, didemnin B, echinomycin and PCNU; anti-inflammatory steroids such as dexamethasone hydrocortisone and prednisolone; estrogens such as 176 estradiol, 17α-ethynylestradiol, ethynylestradiol 3methyl ether and estriol; progestins such as norethindrone, norethindrone acetate, norgestrel, ethisterone, medroxyprogesterone acetate and progesterone; anticonvulsants such as phenytoin (diphenylhydantoin); barbiturates such as pentobarbital, phenobarbital and secobarbital, variously useful as hypnotics, anticonvulsants and sedatives; antivirals such as vidarabine; vitamins/nutritional factors such as retinol (vitamin A), vitamin A-acetate, cholecalciferol and retinal, as well as other fat-soluble vitamins such as the Ε, Π and K vitamins; emetics such as apomorphine; diuretics such as chlorthalidone, furosemide and spironolactone; anticoagulants such as dicumarol; cardiotonics such as digoxin and digitoxin; non-steroidal anti-inflammatory agents such as indomethaciη, piroxicam and flurbiprofen; androgens such as 17-methyltestosterone and testosterone; steroidal hypnotlcs/anesthetics such as alfaxalone; antidepressants such as sulpiride; antibiotics such as ampicillin and penicillin G; coronary vasodilators such as nitroglycerin and flunarizine; hypnotics such as etomidate; carbonic anhydrase inhibitors such as acetazolamide; antifungals such as ketoconazole, Itraconazole, metronidazole benzoate and miconazole; anti protozoals such as f1ubendazole; anesthetics such -28as lidocaine; hypoglycemics such as acetohexamide; ant1-emet1cs such as dimenhydrlnate; antibacterials such as co-trimoxazole; dopaminergic agents such as LOOPA; anti-Alzheimer's agents such as THA; benzodiazepines, for example chiordiazepoxide, diazepam, medazepam, oxazepam and lorazepam, variously useful as sedatives, hypnotics, anticonvulsants, tranquilizers and muscle relaxants; and prostaglandins, for example PGE's such as PGE| (alprostadl1), a vasodilator, and PGI2 (prostacyclin or epoprostenol), a platelet inhibitor.

In one particularly preferred embodiment of the present invention, the drug contemplated for use in the instant parenteral formulations is an antineoplastic. Antineoplastics such as chlorambucil, lomustine, melphalan, hexamethyImelamine, methotrexate, semustine, teniposide, etoposide and fazarabine are particularly preferred.

In another preferred embodiment of the invention, the drug contemplated for use in the instant parenteral formulations is the steroidal anesthetic/hypnotic, alfaxalone .

In yet another preferred embodiment of the invention, the drug contemplated for use in the instant parenteral formulations is the reduced, di hydropyridine form of a dihydropyridine ♦ pyridinium salt redox system for brain-targeted drug delivery.

With respect to the redox system for braintargeted drug delivery, the following definitions are applicable: -29The term lipoidal is intended to designate a redox moiety which 1s 11p1d-soluble or lipophilic.

The terms redox carrier system and redox analog system are Intended to designate two different approaches to targeting drugs to the brain using a d1hydropyrid1 ne * pyridinium salt system; compounds representing either of these approaches are contemplated for use with a selected cyclodextrin in accord with the present invention.

The redox carrier system provides for braintargeted drug delivery by means of carrier-drugs, which in their reduced form, which is the form intended for administration, can be represented by the formula [D-DHC] wherein [0] is a centrally acting drug species and [DHC] is the reduced, biooxidizable, blood-brain barrier penetrating, lipoidal form of a dihydropyridine * pyridinium salt redox carrier. In their oxidized form, which is the form locked in the brain from which the active drug is ultimately released, the carrier-drugs can be represented by the formula [D-QC]+ Xwherein X“ is the anion of a non-toxic pharmaceutically acceptable acid, [D] is a centrally acting drug species and [QC]+ is the hydrophilic, ionic pyridinium salt form of a dihydropyridine * pyridinium salt redox carrier. The redox carrier approach is discussed -30hereinabove in the section entitled BACKGROUND OF THE INVENTION; historically, the carrier system 1s the second type of redox system developed for delivering drugs to the brain.

Various aspects of the redox carrier system have been described in detail in Bodor United States Patent No. 4,479,932, issued October 30, 1984; Bodor United States Patent No. 4,540,564, issued September 10, 1985; Bodor et al United States Patent No. 4,617,298, issued October 14, 1986; and UNIVERSITY OF FLORIDA'S International Application No. PCT/US83/00725 , published under International Publication No. W083/03968 on November 24, 1983.

The redox analog system provides for braintargeted drug delivery by means of new compounds containing a dihydropyridine * pyridinium salt portion which, unlike the redox carrier, is not readily metabolically cleavable from the original drug molecule.

One redox analog approach, which provides derivatives of centrally acting amines in which a primary, secondary or tertiary amine function has been replaced with a dihydropyridine + pyridinium salt redox system, is discussed hereinabove in the section entitled BACKGROUND OF THE INVENTION; historically, this analog system is the third type of redox system developed for delivering drugs to the brain. Various aspects of this analog system are described 1n detail in UNIVERSITY OF FLORIDA'S International Application No. PCT/US85/00236, published under International Publication No.

W085/03937 on September 12, 1985. r.. -31Another redox analog approach provides novel amino acids and peptides containing them which comprise a dihydropyridine ί pyridinium salt portion, the redox system being appended directly or via an alkylene bridge to the carbon atom adjacent to the carboxyl carbon. These amino acids and peptides are described in detail in UNIVERSITY OF FLORIDA'S copending Irish Patent Application No. 763/88, filed March 15, 1988. Briefly, the novel redox amino acids in the reduced form have the structural formula wherein Z is either a direct bond or Cj-Cg alkylene and can be attached to the heterocyclic ring via a ring carbon atom or via the ring nitrogen atom; Ry is Cy-C7 alkyl, C^-Cy haloalkyl or Cy-C|2 aralkyl when Z is attached to a ring carbon atom; Rj is a direct bond when Z is attached to the ring nitrogen atom; R2 and Rg, which can be the same or different, are selected from the group consisting of hydrogen, halo, cyano, Cj20 C7 alkyl, Cj-Cy alkoxy, C2-Cg alkoxycarbonyl, C2-Cg alkanoyloxy, Cj-Cy haloalkyl, C^-Cy alkylthio, Cj-Cy alkylsulfiny1 , Cj-Cy alkylsulfonyl , -CH = NOR'1' wherein r.. -32R* ' ' is hydrogen or Cj-Cy alkyl, and -CONR'R'1 wherein R' and R'' , which can be the same or different, are each hydrogen or Cj-Cy alkyl; or one of R2 and R3 together with the adjacent ring carbon atom forms a benzene ring fused to the heterocyclic ring, which benzene ring may optionally bear one or two substituents, which can be the same or different, selected from the group consisting of hydroxy, protected hydroxy, halo, cyano, Cj-Cy alkyl, Cj-Cy alkoxy, alkoxycarbonyl, C£-Cg alkanoyloxy, C^-Cy haloalkyl, CjCy alkylthio, Cj-Cy a 1ky1su1finy1, Cj-Cy alkylsulfonyl, -CHaNOR''' wherein R*’' is hydrogen or Cj-Cy alkyl, and -CONR'R'' wherein R' and R’’, which can be the same or different, are each hydrogen or Cj-C7 alkyl; R4 is hydrogen or a carboxyl protective group; Rg is hydrogen or an amino protective group; and the dotted lines indicate that the compound contains a 1,4- or 1,6dihydropyridine , a 1,4- or 1,2-dihydroquinol ine, or a 1,2-dihydroisoquinoline ring system.

The new dihydropyridine amino acid analogs depicted above and the corresponding oxidized forms are useful in the preparation of novel redox peptides of the partial formulas: (reduced for·) £ -33«nd (oxidized for·) the new peptide analogs of partial structure (A) act as a delivery system for the corresponding quaternary salts of partial structure (B) in vivo; the quaternary derivatives, which also are chemical intermediates to the dihydro compounds, are pharmacologically active or convertible in vivo to pharmacologically active peptides, and are characterized by site-specific and sustained delivery to the brain when administered via the corresponding dihydropyridine form. Methods for the preparation of these analog amino acids and peptides utilize methods known in the art for introduction of the dihydropyridine * pyridinium salt moiety or a precursor thereof, e.g. from the aforementioned International Publications Nos. W083/03968 and W085/03937, appropriately combined with well-known methods for peptide synthesis. Ultimately, the quaternary forms of the amino acids and peptides are subjected to reduction to afford the corresponding dihydropyridines, according to the methods of the Bodor -34U.S. patents and above-mentioned published PCT appli cations .

In a preferred aspect of the present invention, the redox system selected for use with a hydroxypropyl, hydroxyethyl, glucosyl, maltosyl or maltotriosyl derivative of β- or γ-cyclodextrin in accord with the present invention is a redox carrier system. The drug and carrier portions of the redox carrier system are described in more detail below and of course in the various carrier patents and patent applications identified above. Selection of appropriate drugs and carrier moieties need not be limited to specific drugs and specific carriers disclosed in the aforementioned patents and applications or in the present application, just so long as the selected drug and carrier meet the general requirements of the drug/carrier system as described in the aforenoted documents.

The term drug as used herein means any substance intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease or in the enhancement of desirable physical or mental development and conditions in man or animal.

By centrally acting drug species, active agent or compound as utilized herein, there is of course intended any drug species or the like, a significant (usually, principal) pharmacological activity of which is CNS and a result of direct action in the brain.

Exemplary such centrally acting drug species are the CNS-am1nes and other nervous system agents, whether sympathetic or parasympathetic, e.g., phenylethy1 amine (a stimulant), dopamine (a neurotransmitter and -35dopaminergic agent used, e.g., in the treatment of Parkinsonism or hyperprolact 1nemia), tyramine (a stimulant), L-OOPA (a dopamine precursor used, for example, in the treatment of Parkinsonism); muscle relaxants, tranquilizers and antidepressants, e.g., benzodiazeplne tranqui1izers such as diazepam and oxazepam and phenothiazine tranquilizers such as carphenazine, fluphenazine and the like; mild and strong analgesics and narcotics; sedatives and hypnotics; narcotic antagonists; vascular agents; stimulants; anesthetics; small peptides, such as the di-, tri-, tetra and pentapeptides, and other small 220 amino acid unit containing peptides, e.g. the enkephalins (for example, Tyr-Gly-Gly-Phe-Leu), which, besides being analgesics, i ni 11 ate epileptic activity in the brain at doses that are about tenfold lower than for effecting analgesic activity; growth-promoting substances; antiepi 1eptic and anticonvulsant drugs generally, including hydantoins such as phenytoin and ethotoin, barbiturates such as phenobarbital; hormones, such as the steroid hormones, e.g., estradiol, testosterone, 17 o-ethynyl testosterone (ethisterone), and the like (recent studies on histological mapping of hormone-sensitive and specific steroid binding cells in the brain have underscored the importance of the steroid action in the brain on sexual behavior); amphetamine-like drugs; anticancer and antiParklnsonism agents; anti-hypertensives, agents to enhance learning capacity and the memory processes, Including treatment of dementias, such as Alzheimer's disease, such as 9-amino-1,2,3,4-tetrahydroacridine; antibacterials; centrally acting hypotensive agents; -36centrally acting prostaglandins, such as PGD£; diagnostic agents, such as radiopharmaceuticals; monoamine oxidase (MAO) inhibitor drugs; CNS or brain important/essential amino acids, such as tryptophan (which is an antidepressant as well as a nutrient); and any like centrally acting compounds. For the purposes of this invention, dopa or L-DOPA is not classified as an amino acid but rather as a CNS amine and dopaminergic agent used, e.g. in the treatment of Parki nsoni sm.

Other illustrative ultimate species of centrally acting drug entities are: amphetamine, dextroamphetamine, 1evamphetamine , aletamine, cypenamine, fencamfamin, fenozolone, zylofuramine, methamphetamine, phenmetrazine and phentermine, which are sympathomimetic amines/cerebral stimulants and appetite suppressants; etryptamine, a cerebral stimulant; codeine, oxycodone, pentazocine, anileridine, hydromorphone, morphine and oxymorphone, which are narcotic analgesics; desipramine, nortriptyline, octriptyline, maprotiline, oplpramol and protriptyline, which are cerebral stimulants/tricylic antidepressants of the dibenzazepine type used, e.g., in endogenous depressions; clonidine and methyldopa, which are sympatholytic agents used, e.g., in hypertension; biperiden, cycrimine and procyclidine, which are centrally acting anticholinergics; tranylcypromine, a sympathomimetic cerebral stimulant/MAO inhibitor and antidepressant; acetophenazine, carphenazine, fluphenazine, perphenazine and p1peracetazlne, which are phenoth1 azine-type tranquilizers; benzoctamine, a sedative/muscle relaxant which structurally is an -37analogue of the phenothiazine tranqui1izers; chlordiazepoxide, clorazepate, nitrazepam and temazepam, which are benzodiazepine-type tranquilizers; noracymethadol , a narcotic analgesic of the methadone type; piminodine, a narcotic analgesic of the meperidine type; tracazolate, a sedative/hypotensive; prizidilol a centrally acting hypotensive; sulpiride, an antidepressant/psychotropic; haloperidol and clopenthixol which are tranqui 1 izers; norepinephrine, a sympatheti stimulant/adrenergic agent; nalorphine and naloxone, narcotic antagonists; hydralazine, a hypotensive; ethotoin, phenobarbital and aminoglutethimide, anticonvulsants; epinephrine, an adrenergic agent; ethamivan, a medullary stimulant; bemegride, a barbiturate antagonist; amiphenazole, a stimulant; iopydol, iodopyracet, iodouppurate (o-iodohippuric acid), iodamide and lopanoic acid, which are radiodiagnostics; ephedrine, pseudoephedrine, oxymetazoline and phenylephrine, which are sympathomimetic amines and decongestants; estradiol, estrone and estriol, the natural estrogens; amoxicillin, oxacillin, carbenici 11iη , benzylpenicillin, phenoxymethylpenici 11in, methicillin, nafcillin, ticarcillin bacampici 111 η , epicillin, hetacillin, pivampaci11iη , the methoxymethyl ester of hetacillin, and ampicillin which are penicillin-type antibiotics; amobarbital, a sedative; trihexyphenidyl, a centrally acting anticholinergic; hydroxyzine, a tranquilizer; chlorte tracycllne, demeclocycline, minocycline, doxycycline, oxytetracycl1ne, tetracycline and methacycline, which are tetracycline-type antibiotics; flurazepam, bromazepam, demoxepam and lorazepam, benzodiazepine -38tranquilizers; phenytoin, an anticonvulsant; glutethimide, a mild hypnotic/sedative; clindamycin, lincomycin, nalidixic acid, oxolinic acid and phenazopyridine, antibacterials/antibiotics; bethanidine and guanethidine, hypotensives/sympatholytics; captopril, a hypotensive; methyprylon, a mild hypnotic; amedalin, bupropion, cartazolate, daledalin, difluanine, fluoxetine and nisoxetine, which are cerebral stimulants; propranolol, a β-blocker antihypertensive; cloxacillin and di cl oxaci 11iη , penicillin-type antibacterials; butalbital, a barbiturate sedative; GABA, γ-vinyl GABA, γ-acetylenic GABA, neurotransmitters for possible use in epilepsy; valproic acid and its metabolites such as 5-hydroxy-2-n-propylpentanoic acid, 4-hydroxy-2-npropylpentanoic acid, 3-hydroxy-2-n-propy1 pentanoic acid, for use as anticonvulsants; valpromide, a valproic acid derivative for use as an anticonvulsant; apomorphine, a narcotic depressant/emetic which has been used in the treatment of photosensitive epilepsy; pholcodine, a narcotic antitussive; methotrexate, mitoxantrone , podophy11otoxin derivatives (etopside, teniposlde), doxorubicin, daunamycin and cyclophosphamide, anti-cancer/antitumor agents; methylphenidate, a stimulant; thiopental, an anesthetic; ethinyl estradiol and mestranol, estrogens; meptazinol, cyclazocine, phenazocine, profadol , metopon, drocode and myfadol, which are narcotic analgesics; buprenorphine, nalbuphine, butorphanol, 1eval1 orphan, naltrexone, nalmefene, alazocine, oxllorphan and nalmexone, which are narcotic antagonists or agonist-antagonists; norgestrel and norethindrone, progestins; cephalothin, cephalexin, -39cefazolin, cefoxitin, moxalactam, ceforanide, cefroxadine and cephapirin, cephalosporin antibiotics; atenolol, nadolol, timolol and metoprolol, βblockers/hypotensives; ACTH (corticotropin), a hormone which stimulates glucocorticoid production; LHRH, a neurotransmitter which stimulates secretion of the pituitary hormones, LH and FSH, and has been used to induce ovulation as well as for fertility control/ contraception; sulfadiazine and other sulfonamide antibiotics; ribavirin and acyclovir, antiviral agents; chlorambucil and melphalan, nitrogen mustard-type anticancer/ant1tumor agents; methotrexate and aminopterin, which are folic acid antagonist-type anticancer/antitumor agents; platinum coordination complexes, i.e. cisplatin analogue-type anticancer/antitumor agents; dactinomycin and mitomycin C, used in cancer chemotherapy; thioguanine, a purine/pyrimidine antagonist used in cancer treatment; vincristine and vinblastine, anticancer alkaloids; hydroxyurea and DON, anticancer urea derivatives; FSH, HCG and HCS, pituitary and nonpituitary gonadotropins, used, for example, in certain reproductive disorders; N,N‘-bis(di chioracety1)-1,8octamethylenediamine (fertilysin) , an agent for male fertility inhibition; levorphanol, a narcotic anal25 gesic; benzestrol and di ethylsti1bestrol , synthetic estrogens; ethyl β-carboline-3-carboxylate, a benzodiazepine antagonist; furosemide, a diuretic/antihypertensive; dipyridamole and nifedipine, coronary vasodilators; and progabide, a GABA-agonist and prodrug of GABA. Yet other ultimate species Include non-steroidal antiinflammatory agents/non-narcotic analgesics, e.g. propionic acid derivatives, acetic acid derivatives, -40fenamic acid derivatives and bi phenyl carboxylic acid derivatives. Specific NSAID's/non-narcotic analgesics contemplated for combination with the redox carrier include ibuprofen, naproxen, flurbiprofen, zomepirac, sulindac, indomethaciη , fenbufen, fenoprofen, indoproxen, ketoprofen, fluprofen, bucloxic acid, tolmetin, alclofenac, fenclozic acid, ibufenac, flufenisal, pirprofen, flufenamic acid, mefenamic acid, clonixeril, clonixin, meclofenamic acid, flunixin, diclofenac, carprofen, etodolac, fendosal , prodolic acid, sermetacin, indoxole, tetrydamine, diflunisal, naproxol , piroxicam, metazamide, flutiazin and tesicam.

Preferred classes of centrally acting drugs for combination with the redox carrier are the central neurotransmitters, steroids, anticancer and antitumor agents, antiviral agents, tranquilizers, memory enhancers, hypotensives, sedatives, antipsychotics and cerebral stimulants (especially tricyclic antidepressants). Among the neurotransmitters, there can be mentioned amino acids, such as GABA, GABA derivatives and other omega-amino acids, as well as glycine, glutamic acid, tyrosine, aspartic acid and other natural amino acids; catecholamines, such as dopamine, norepinephrine and epinephrine; serotonin, histamine and tryptamine; and peptides such as neurotensin, luteinizing hormone-releasing hormone (LHRH), somatostatin, enkephalins such as met5enkephalin and 1eu^-enkephaliη, endorphins such as γ-·., a- and 0-endorphins, oxytocin M and vasopressin. Synthetic and semi-synthet1c analogues, e.g. analogues of LHRH in which one or more amino acid(s) has/have been eliminated and/or replaced with one or more -41different amino acid(s), and which may be agonists or antagonists, are also contemplated, e.g. the primary and secondary amine LHRH analogues disclosed in United States Patents No. 4,377,574, 3,917,825, 4,034,082 and 4,338,305. Among the steroids, there can be mentioned anti-inflammatory adrenal cortical steroids such as hydrocortisone, betamethasone, cortisone, dexamethasone, flumethasone, fluprednisol one , meprednisone, methyl prednisolone, prednisolone, prednisone, triamcinolone, cortodoxone, fludrocortisone, f1urandrenolone acetonide (flurandrenollde), paramethasone and the like; male sex hormones (androgens), such as testosterone and its close analogues, e.g. methyl testosterone (1715 methyl testosterone); and female sex hormones, both estrogens and progestins, e.g. progestins such as norgestrel, norethindrone, norethynodrel, ethisterone, dimethisterone, al1y1estrenol, cingestol, ethynerone, lynestrenol, norgesterone, norvinisterone, ethynodiol, oxogestone and tigestol, and estrogens such as ethinyl estradiol, mestranol, estradiol, estriol, estrone and quinestrol and the like. Among the anticancer and antitumor agents, there can be mentioned Ara-AC, pentostatin (2'-deoxycoformycin), Ara-C (cytarabine), 3-deazaguanine, dihydro-5-azacytidine, tiazofurin, sangivamycin, Ara-A (vitarabine) , 6-MMPR, PCNU, FENU, HENU and other nitrosoureas, spiromustine, bisbenzlmldazole, L-alanosine (6-diazo-5-oxo-Lnorleucine), DON, L-ICRF, trimethyl TMM, 5-methyl30 tetrahydrohomofol 1c acid, glyoxyllc acid sulfonylhydrazone, OACH, SR-2555, SR-2508, desmethylmi sonidazole, mitoxantrone, menogarol, aclacinomycin A, -42phyl1anthoside, bactobolin, aphidocolin, homoharringtonine, 1evonantradol , acivicin, streptozotociη, hydroxyurea, chlorambucil, cyclophosphamide, uracil mustard, melphalan, 5-FU (5-fluorouracil), 5-FUDR (f1oxuridine), vincristine, vinblastine, cytosine arabinoside, 6-mercaptopurine, thioguanine, 5azacytidine, methotrexate, adriamycin (doxorubicin), daunomycin (daunorubicin), largomycine polypeptide, aminopterin, dactinomycin, mitomycin C, and podophyl1otoxin derivatives, such as etoposide (VP-16) and teniposide. Among the antiviral agents, there can be mentioned ribavirin; acyclovir (ACV); amantadine (also of possible value as an anti-Parkinsonism agent); di aryl ami dines such as 5-amidi no-2-(5-amidino-2-benzofuranyl)indole and 41,6-diimidazolino-2-phenylbenzo(b)thiophene; 2-aminooxazoles such as 2-guanidino-4,5di-n-propyloxazole and 2-guanidi no-4,5-diphenyloxazole; benzimidazole analogues such as the syn and anti isomers of 6[[(hydroxyimino)phenyljmethyl]-1-[(1methylethyl )sulfonyl]-l±-benzimi dazol-2-ami ne; bridgehead C-nucl eosides such as 5,7-dimethyl-2ribofuranosyl-s-triazole(l,5-a)pyrimidine: glycosides such as 2-deoxy-J)-gl ucose, glucosamine, 2-deoxy-2f 1 uoro-J^-mannose and 6-ami no-6-deoxy-JT-gl ucose; phenyl glucoside derivatives such as pheny1-6-chloro-6-deoxy0-_D_-g 1 ucopyranoside; (S)-9-( 2,3-dihydroxypropyl )adenine; tiazofurin; selenazofurin; 3-deazauridine; 3deazaguanosine; DHPG; 6-azauridine; idoxuridine; tr1flur1d1ne (trifluorothymldine); BDVU (bisdihydroxyvinyl uri d1 ne); zidovudine (AZT); dideoxycytidine; and 5,6-d1 chi oro-1- $-0_-r1 bofu ra nosy 1 benzimidazole. Among the anti-cancer/antitumor and antiviral agents, those -43of the nucleoside type (i.e. a purine or pyrimidine base-type structure bearing a singly or multiply hydroxylated substituent) are of particular interest. This group includes such compounds as Ara-AC, pentostatin, Ara-C, dihydro-5-azacytidine, tiazofurin, sangivamyciη , Ara-A, 6-MMPR, desmethylmisonidazole, 5FUDR, cytosine arabinoside, 5-azacytidine, ribavirin, acyclovir, (S)-9-(2,3-dihydroxypropy1)adenine, 6a zauri dine, 5,6-dichloro-l- 0-D_- ri bof uranosyl benzimidazole, 5,7-di methyl -2- ri bof uranosyl - striazole(1,5-a)pyrimidine, zidovudine (AZT), dideoxycyt1 dine, dideoxyadenosine , di deoxyinosine and DHPG. Among the tranquilizers, there can be mentioned benzodiazepine tranquilizers, such as diazepam, oxazepam, lorazepam, chiordiazepoxide, flurazepam, bromazepam, chiorazepate, nitrazepam and temazepam; hydantoin-type tranqui1izers/anticonvulsants such as phenytoin, ethotoin, mephenytoin; phenothiazine-type tranquilizers such as acetophenazine, carphenazine, fluphenazine , perphenazine and piperacetazine; and others. Among the hypotensives, there can be mentioned clonidine, methyldopa, bethanidine, debrisoquin, hydralazine, and guanethidine and its analogues. Among the sedatives, tranquilizers and antipsychotics, there can be mentioned the many specific compounds of this type disclosed above, especially the phenothiazines and benzodiazepines and their analogues. Among the cerebral stimulants, there also can be mentioned the many specific compounds set forth hereinabove, particularly the sympathomimetic amine-type cerebral stimulants and the tricyclic antidepressants, -44especially preferred tricyclics being the dibenzazepines and their analogues.

Also illustrative of the centrally acting drug species contemplated for combination with the redox carrier are centrally active metabolites of centrally acting drugs. Such metabolites are typified by hydroxylated metabolites of tricyclic antidepressants, such as the E- and Z-isomers of 10-hydroxynortriptyI1ne, 2-hydroxyimipramine, 2-hydroxydesipramine and 8hydroxychloripramine; hydroxy-1ated metabolites of phenothiazine tranquilizers, e.g. 7-hydroxychlorpromazine; and desmethyl metabolites of N-methyl benzodiazepine tranquilizers, e.g. desmethyldiazepam. Other CNS active metabolites for use herein will be apparent to those skilled in the art, e.g. SL 75102, which is an active metabolite of progabide, a GABA agonist, and hydroxy-CCNU, which is an active metabolite of CCNU, an anti-cancer nitrosourea. Typically, these CNS active metabolites have been identified as such in the scientific literature but have not been administered as drugs themselves. [n many cases, the active metabolites are believed to be comparable in CNS activity to their parent drugs; frequently, however, the metabolites have not been administered per se because they are not themselves able to penetrate the blood-brain barrier.

As indicated hereinabove, diagnostic agents, including radiopharmaceuticals, are encompassed by the expression “centrally acting drug or the like as used herein. Any diagnostic agent which can be derivatized to afford a redox carrier system which will penetrate -4510 the BBB and concentrate in the brain in its quaternary form and can be detected therein is included. The diagnostic may be cold and be detected by X-ray (e.g. radiopaque agents) or other means such as mass spectrophotometry, NMR or other non-invasive techniques (e.g. when the compound includes stable isotopes such as C13, N15, 018, S33 and S34). The diagnostic alternatively may be hot, i.e. radiolabelled, such as with radioactive iodine (I 123, I 125, I 131) and detected/imaged by radiation detect!on/imaging means. Typical cold diagnostics for derivation herein include o-iodohippuric acid, iothalamic acid, iopydol , iodamide and iopanoic acid. Typical radiolabelled diagnostics include diohippuric acid (I 125, I 131), diotyrosine (I 125, I 131), o-iodohippuric acid (I 131), iothalamic acid (I 125, I 131), thyroxine (I 125, I 131), iotyrosine (I 131) and iodometaraminol (I 123), which has the structural formula In the case of diagnostics, unlike the case of drugs which are for the treatment of disease, the locked in quaternary form will be the form that is imaged or otherwise detected, not the original diagnostic itself. Moreover, any of the centrally acting drugs which are intended for the treatment or prevention of medical disorders but which can be radiolabelled, e.g. with a radioisotope such as iodine, or labelled with a -46stable isotope, can thus be converted to a diagnostic for incorporation into the redox carrier system.

It will be apparent from the known structures of the many drug species exemplified above, that in many cases the selected drug will possess more than one reactive functional group, and, in particular, that the drug may contain hydroxyl or carboxyl or amino or other functional groups in addition to the groups to which the carrier will be linked, and that these additional groups will at times benefit from being protected during synthesis and/or during administration. The nature of such protection is described in more detail in the various patents and patent applications referred to herein. Obviously, such protected drug species are encompassed by the definition of drug set forth hereinabove.

It too will be appreciated that by d1hydropyridine carrier or [DHC], there is intended any nontoxic carrier moiety comprising, containing or including the dihydropyridine nucleus, whether or not a part of any larger basic nucleus, and whether substituted or unsubstituted, the only criterion therefor being capacity for BBB penetration and in vivo oxidation thereof to the corresponding quaternary pyridinium salt carrier [QC]+. As aforesaid, the ionic pyridinium salt drug/carrier prodrug entity [D-QC]+ which results from such in vivo oxidation is prevented from efflux from the brain, while elimination from the general circulation 1s accelerated. Subsequently, the covalent or equivalent bond coupling the drug species [D] to the quaternary carrier [QC] + is metabol1ca11y -47cleaved, which results in sustained delivery of the drug Cnl in the brain and facile elimination of the carrier moiety [QC]+. Such covalent or equivalent bond between the drug and the quaternary carrier can be a simple direct chemical bond, e.g., an amide, an ester, or any other like bond, or same can even be comprised of a linking group or function, e.g., a thiazolldine bridge or a peptide linkage, typically necessitated when the drug species is not susceptible to direct chemical coupling to either the dihydropyridine carrier or the quaternary carrier. Nonetheless, the bond in the formulae [D-QC]+ and [D-DHC] is intended to be, and is hereby defined as inclusive of all such alternatives. And the cleavage of the [D-QC]+ prodrug to sustainedly deliver the drug species [D] in the brain with concomitant facile elimination of the carrier moiety [QC] + is characteristically enzymatic cleavage, e.g., by esterase, amidase, cholinesterase, hydrolytic enzyme, or peptidase.

The expression non-toxic pharmaceutically acceptable salts as used herein generally includes the nontoxic salts of the reduced, dihydropyridine forms of the redox carrier or redox analog systems, formed with nontoxic, pharmaceutically acceptable inorganic or organic acids HX. For example, the salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, fumaric, methanesulfonic, tolu-48enesulfonic and the like. The expression anion of a non-toxic pharmaceutically acceptable acid as used herein, e.g. in connection with the oxidized, pyridinium salt forms of the redox carrier or redox analog systems, is intended to include anions of such inorganic or organic acids HX.

In the discussion to follow, the expression at least one reactive functional group selected from the group consisting of amino, hydroxyl, mercapto, carboxyl, amide and imide or portions of that expression are used. The functional groups designated in that expression have the following meanings: The word amino means a primary or secondary amino function, i.e. -NHg or -NHR. The secondary amino function is also represented herein as -NH-, particularly since the exact identity of the R portion of -NHR is immaterial, R being a part of the drug residue 0 itself which is left unchanged by conversion of the drug to the redox carrier system.

The word hydroxyl means an -OH function. The word carboxyl means a -COOH function. The word mercapto means an -SH function. The word amide means a carbamoyl (-CONH2) or substituted carbamoyl (-CONHR) or a sulfamoyl (-SOzNHg) or substituted sulfamoyl (-SO2NHR) functional group.

The -CONHR and -SO2NHR groups may also be represented herein as -CONH- and -SO2NH-, respectively, since the Identity of R is Immaterial, R being a part of the drug residue 0 Itself which is left unchanged by conversion of the drug to the redox carrier system. -49The word imide means a functional group having the structure ;nh ‘0 that is, the structure which characterizes imides (i.e. compounds having a succinimide-type or phthalimide-type structure).

Many different dihydropyridine * pyridinium salt redox carrier moieties are illustrated in the carrier patents and applications referred to hereinabove. The following is a list of representative major classes of dihydros and the corresponding quaternaries, but is not meant to be exhaustive; (1) For linkage to a drug having at least one hydroxyl or mercapto or primary or secondary amino functional grouping, replacing a hydrogen atom from at least one of said functional groupings with one of the following [DHC] groupings: -51wherein the dotted line in formulas (a'), (b‘) and (c*) Indicates the presence of a double bond in either the 4 or 5 position of the d1hydropyridine ring; the dotted line in formulas (d'), (e') and (f‘) indicates the presence of a double bond in either the 2 or 3 position of the d1hydroquinoline ring; R| is Cj-Cy alkyl, Cj-Cy haloalkyl or Cy-CjQ aralkyl; Rj is Cj to C3 alkylene; X 1s -CONR'R'1, wherein R' and R*', which can be the same or different, are each H or Cj-Cy alkyl, or X is -CH=NOR''' wherein R''' is H or Cj-Cy alkyl; the carbonyl-containing groupings in formulas (a1) and (c‘) and the X substituent in formula (b*) can each be attached at the 2, 3 or 4 position of the dihydropyridine ring; the carbonyl-containing groupings in formulas (d‘) and (f*) and the X substituent in formula (e‘) can each be attached at the 2, 3 or 4 position of the dihydroquinoline ring; and the carbonyl-containing groupings in formulas (g1) and (j') and the X substituent in formula (h1) can each be attached at the 1, 3 or 4 position of the dihydroisoquinoline ring. (2) For linkage to a drug having at least one carboxyl functional grouping, replacing a hydrogen atom from at least one of said carboxyl groupings with one of the following [DHC] groupings: (a) When there are one or more -COOH groups to be derivatized: (iv) (<χ·) (*1') wherein the dotted line in formulas (i ' ), (ii ') and (iii') indicates the presence of a double bond in either the 4 or 5 position of the dihydropyridine ring; the dotted line in formulas (iv*) , (ν') and (vi') indicates the presence of a double bond in either the 2 or 3 position of the di hydroqui noline ring; Z' is Cy-Cg straight or branched alkylene, preferably Cj-Cg straight or branched alkylene; Q is -0- or -NH-; Rj is cl’c7 alkyl. cl“c7 haloalkyl or C7-Cj0 aralkyl; Rg is Cj-Cg alkylene; X is -CONR'R'' wherein R' and R'' , which can be the same or different, are each H or Cj-C7 -53alkyl, or X is -CH«NOR''' wherein R*'' is H or C|-Cy alkyl; the X substituent in formula (ii * ) and the carbonyl-containing grouping in formulas (i') and (Iii') can each be attached at the 2, 3 or 4 position of the dihydropyridine ring; the X substituent in formula (ν') and the carbonyl-containing groupings in formulas (iv') and (vi') can each be attached at the 2, 3 or 4 position of the dihydroquinoline ring; and the X substituent in formula (viii') and the carbonyl10 containing groupings in formulas (vii1) and (ix1) can each be attached at the 1, 3 or 4 position of the dihydroquinoline ring; (b) Alternatively, when there is only one -COOH group to be derivatized: -54wherein the dotted line in formula (xii') indicates the presence of a double bond in either the 4 or 5 position of the dihydropyridine ring; the dotted line in formula (xiii') indicates the presence of a double bond in either the 2 or 3 position of the dihydroquinoline Z “ > · ring; ( } is the skeleton of a sugar molecule; nlv is a positive integer equal to the total number of -OH functions in the sugar molecule from which said skeleton is derived; nv 1s a positive integer one less than the total number of -OH functions in the sugar molecule from which said skeleton is derived; each A in each of structures (xii1), (xiii1) and (xiv‘) can independently be hydroxy or O', 0' being the residue of a centrally acting drug containing one reactive carboxyl functional group, said residue being characterized by the absence of a hydrogen atom from said carboxyl functional group in said drug; and each R4 in each of structures (x*) and (xi ') can independently be hydroxy, or 0', -55wherein the dotted line is defined as with structures (xii ') and (xiii ' ) ; 0' is defined as with structures (xii’) , (xiii*) and (xiv'); R^ is C^-Cy alkyl, Cj-C7 haloalkyl or C7-Cjq aralkyl; and the depicted carbonyl groupings can be attached at the 2, 3 or 4 position of the pyridinium or quinolinium ring or at the 1, 3 or 4 position of the isoquinol1nium ring; with the proviso that at least one RA in each of structures (x‘) and (xi’) is wherein Rj, the dotted lines and the position of the carbonyl-containing groupings are defined as above; and with the further proviso that when more than one of the radicals in a given compound are the aforesaid -56carbonyl-containing groupings, then all such carbonylcontaining groupings in said compound are identical. (3) For linkage to a drug having at least one -NH- functional group which is part of an amide or imide structure or at least one low pKa primary or secondary amine functional group, replacing a hydrogen atom from at least one of said functional groupings with one of the following [DHC] groupings: Ococh -, R ι R1 (k ·) (o’) (p·) wherein R is hydrogen, Cy-Cy alkyl, C-y-Cg cycloalkyl, Cy-Cy haloalkyl, furyl , phenyl, or phenyl substituted by one or more halo, lower alkyl, lower alkoxy, carba5 moyl, lower alkoxycarbony1 , lower alkanoyloxy, lower haloalkyl, mono(lower alkyl)carbamoyl, di(lower alkyl)carbamoyl , lower alkylthio, lower alkylsulfinyl or lower alkylsulfonyl; the dotted line in formulas (k*), (1') and (m‘) indicates the presence of a double bond in either the 4 or 5 position of the dihydropyridine ring; the dotted line 1n formulas (n‘), (o') and (p1) Indicates the presence of a double bond 1n either the 2 or 3 position of the dihydroquinoline ring; Ry is -58C^-Cy alkyl, Cj-C7 haloalkyl or C7-C^q aralkyl; Rg is C| to Cg alkylene; X is -CONR'R'', wherein R' and R'', which can be the same or different, are each H or Cj-C7 alkyl, or X is -CHsNOR*'' wherein R’ ' ' is H or C-^-Cy alkyl; the carbonyl-containing groupings in formulas (k*) and (m‘) and the X substituent in formula (!') can each be attached at the 2, 3 or 4 position of the dihydropyridine ring; the carbonyl-containing groupings in formulas (n') and (p1) and the X substituent in formula (o') can each be attached at the 2, 3 or 4 position of the dihydroquinoline ring; and the carbonyl-containing groupings in formulas (q’) and (s') and the X substituent in formula (r*) can each be attached at the 1, 3 or 4 position of the dihydroisoquinoline ring.

Drugs containing secondary or tertiary hydroxyl functional groups can be linked to any of the [DHC] groupings (k') through (s') above in which the -CHOR portion is derived from an aldehyde RCH20 capable of reacting with said drug to form the correspond!ng hemiacetal, e.g. chloral, acetaldehyde, formaldehyde or benzaldehyde .

The following are especially preferred reduced, dihydropyridine forms of di hydropyridine * pyridinium salt redox carrier systems, also termed chemical delivery systems or CDS, for brain-targeted drug delivery which are contemplated for use in parenteral formulations with the selected cyclodextrin in accord with the present invention: Structure Chemical Name 1-methyl-3- |)N-(i-[3,«-bls(plvalyloxy)phenylJethyl )carbamoyl ||-l ,4-d1hydropyr1dtne I-methyl-3-(N-([ i-[3,4-b1a(I sobutyryIoxy)pheny1]ethy1]] )carbamoyt-t,4-dlhydropyrldlne V H I II » '<,7[’χζγ W<W(« -Τ' j .AJ* i N-|a-[3,4-bl$(ptvalylOxylpheny1]ethyl )amtnocarbonytoxymethyt 1,4dlhydro-l-methyl-3-pyrldlnecarboxylate Abbreviated Name Synthes1» Pharmacological Use dopamlne-COSt or DA-CDS U.S. Patent No. 4,540,58«, Example 23 dopaminergic agent (anti-hyperprolactinemia, antl-Parklnsonlsm) dopamlne-COS? Example 4 herelnbelow as dopamlne-COS) dopamlne-CDSj Example US herelnbelow as dopam1ne-CDS| β Structure Chemical Name 17e-[(l,4-dthydro-l-«ethyl-3pyrtdtnylcarbonyl)oxy]androat-4en-3-one ne-jtO’-Cirbimoyl-r.d·dt hydropyridt nyl)acetylloxy)androat-4-en*3-one x SJ-dtphenyl-a-Cd'-Mthyl.!*,** dlhydropyrtdtn-3'-y1)carbony1oxy methyl]-2,4-lmtdazo1tdtnedtone Abbreviated Name Syntheats Pharmacological Use teatoaterone-CDS, or T-COSj U.S. Patent No. 4,439.932, Example 3« androgenic agent teatoaterone-CDS. or T-COS2 Bodor et at, J. Pharm. Set. ΤΤ5Ϊ7Κ25ΠΚΤ9-35 ea teatoaterone-COS| phenytoln-CDSj Example 8 hereinbelow antlconvulaant agent Structure Chemical Name 3-1 (3' -carbamoyl -l',4'-dlhydropyrtdtn-l'-yDacetyloxymethyl]S,S-d1pheny1-2,4-1«1dazoltdtnedtone Abbreviated Name Synthetti Pharmacological Ute phenytoln-COSj Example IS hereinbelow at phanytotn-COS| 3-[3,-(3--cirb«i»oyl-i,,.4,-d} l-methy1-3-N-[3-(benzyloxycarbonyllpropyl Icarbamoyl -1,4dlhydropyrtdlne phenytoln-CDSj Example IS hereinbelow at phenytoln-CDSj GABA-COSj Anderton et at, anttconvultint, Ptychopharmacology UWj ·Μ·ϊ57-ΊίΓ anxiolytic agent Structure Chewicel Hawe Cm. ί i CMKCNjl/θ 1-«ethyl-3-|N-[(3*-cyclohexy)carbonyl) propyl ] )carba«oyl -1,4dlhydropyrldlne C. a ^IKN^jOCCN CNICMjCNjCNjI^ l-«ethyl-3-[2’-(2*-propy1)pentanoyloxylethylcarbaxtoyl1,4-dihydropyridine θ' '•w —CNICNjCN^Nj), l-«ethyl-3-[2*-(2*-propyl)pentanoy)oxy]ethoxycarbony!-l,4 dlhydropyrldlne Abbreviated Naaw Synthesis Pharmacological Use GABA-COS; Exaaple 20 hereinbelow ts 6ABA-C0St valproic actd-COSj Exaaple 61 hereinbelow anticonvulsant agent valproic acld-COSj Exaaple 65 hereinbelow at valproic acid-COS| CM.

Structure Chemical Mime 1-(2‘-(2-propyl{pentanoyloxy] ethyl -3-carboxamlde-l ,4dlhydropyrldtne I I ί«κ««Λ 0 »ί-Ό-Αι«,>, 1-methyl-3-lH-[(l'-ethoxycarbonyl )-2 -(4*-ptv(loyloxyphenyl)ethyl](carbamoyl-1,4dthydropyrldlne CH, e o II II ^^^omcicoc^·, J («,-θ-αΐΗΐκρ, 1-methyl-3-lM-[(1'-ethoxycarbonyl )-2 -(4-1sobutyryloxy phenyl)ethyl)(carbamoyl-1,4di hydropyri <11 ne Abbreviated Name Synthesis Pharmacological Use valproic ac1d-Cns3 Exanple 24 hereinbelow as valproic acid-CO! tyrotlne-COSj Example 29 hereinbelow neurotransmitter amino add tyrosIne-COSj Example 30 hereinbelow as tyroslne-CDS| CH, Structure Chemical Kama Abbreviated name Synthesis Pharmacological Ute ([(l,4-d1hydro-l-m6thyl-3pyridinyl)carbony1]oxylmethyl [21-(2a.Sa,e«)]-3.3*d1aMthy17-oxo-6-[(2,6-d1«ethoxy)benzaa1do]-4-th Example 43 hereinbelow antibiotic, antibacterial agent (e.g. for brain abscesses and neurosyphllls) C/rx COM! -nV: CH, Λ“·* 0 · Ho (((1,4-d1hydro-l-«ethyl-3pyrldl nyl )carbony1 ]oxylmethyl [2S-(2e.Sa,6a)]-3,3-dtaethy16-1$-«ethyl-3-phenyl*4-1soxazole carboxamide)-?-oxo-4-tht a-1azab1cyclo(3.2.0]heptane-2carboxylate oxeclllin-COS Example 44 hereinbelow I cn antibiotic, antibacterial agent (e.g. for brain abscesses, neurosyphllls) CM.

Structure Chemical Heme W £ \/£M’ f~' \jZ\w, Ho [f(1.4-dlhydro-1-methyl-3pyrldinyl )carbonyl ]oxyImethyl [2S.-(2e,Se,et)]-3,3 CM, [[(1.4-dthydro-l-methyl-3pyrldlnyl)carbonyt]oxyImethyl [2S-(2o,So,60)1-6-(3-(2chTorophenyl)-S-methy1-4lsoxazolecarboxamidoj-3,3dlmethyt-7-oxo-4-thta-lazab1cyc1o[3.2.0]heptane-2carboxylate Abbreviated Name Synthes la Pharmacological Use benzylpeniei111n-COS Example 49 hereinbelow antibiotic, antibacterial agent (e.g. for brain abscesses, neurosyphllls) cl ooc 111 in-COS Example 4S hereinbelow antibiotic, antibacterial agent (e.g. for bratn abscesses, neurosyphllls) cn cn I ►x Structure Chemical Name ci r* (Ό f[(l,4-dlhydro-,-methy,-3pyrldtny,(carbony,loxy]methy, t2S-(2o.S«,6i)1-6-(3-(2.6dI cKloropheny1)-S-methy1-4lsoxazolectrboxim,do]-3,3dlmethy,-7-oxo-4-th1a-l> aieblcyclo[3.2.0lheptane-2carboxylate [)N-[3-(10.U-d1hydro-5Hdlbenz[b,f jatepln-S-ylVTpropyl N-methy,ami no(carbonyloxy]methyl 1,4-dlhydro-l-methyl-3pyridlnecarboxy,ate Abbreviated Name Synthesis Pharmacological Use dlctoxactlHn-COS Example 46 hereinbelow antibiotic, antibacterial agent (e.g., for brain abscesses, neurosyphilis) des,pram,ne-COSj Example S6 hereinbelow antidepressant 1 σι I f Structure Chemical Name [1-jN-[3-(10,ll-d1hydro-5Hdtbenz[b,f]azeptn-S-yl)]prbpylN-methylamino(carbonyloxylethyl l,4-d1hydro-l-methyl-3-pyr1dtne carboxyl ate l-methyl-3-{(2-<9-guany1methoxy)ethoxylcarbonyl|-l,4-d1hydropyr1di Abbreviated Name Synthesis Pharmacological Use destpramlne-CDS; Example S3 hereinbelow antidepressant acyclovIr-COS Example 103 antiviral, anti-herpetic or ACV-CDS hereinbelow agent (e.g. for herpes simplex encephalitis) ι cn -~4 ι I.

Chemical Name Abbreviated Name Synthesis Pharmacological Use 3' -(1,4-dihydro-l-methy1-3pyridinylcerbony1)-S*-pivaloyl trtftuorothymtdlne tri fiuorothymtdtneCOS or 1FT-COS Example 107 hereinbelow antiviral, anti-herpetic agent « 3* -azido-3'-deoxy-5'-(1-methyl-1,4di hydro-3-pyridinyl)carbonyl]thymidine zidovudine-COS or AZT-COS Example 110 hereinbelow antiviral agent (e.g., for human immunodeficiency virus (AtOSH H-(2-ch1oroethyl)-N‘-(4-(1,4-dlhydro1-methyl-3-pyrtdlnecarbonyloxyUyclohexyl]-N-nltrosourea hydroxy-CCNU-COS or OH-CCNU-COS Raghavan at al, Anti-Canter Drug Beslgn (»B7T?T anticancer, antitumor agent -68CICNjCM, CICHjCHj Structure Chew!cel Heme 1-methyl-3-[(N-l2-[4-(|4-[b,s(2chloroethyl)J ami no(phenyl)butanoy1oxylethy, (lcarbamoyl1-1,4d,hydropyridine 1-methyl-3-H-[2-(3-lndo,y,Jethyl] carbamoyl-1,4-d,hydropyrtdlne 9-fluoro-1,i,17-dlhydroxy-liemet hy, -21-([(1-methy,-1,4-d,hydro pyrtd,n-3-y,jcarbonyl]oxy |pregna1,4-dlene-3,20-dlone Abbreviated Name Synthes1« Pharmacological Use chlorambuell-COS) Example 78 ant,cancer, herelnbelow antitumor agent tryptamlne-COS Bodor et al. Drug Design and 6ellvery (19&6). ΤΓΚΤίβΑ neurotransmitter, neuromodulator (potentiates or antagonizes serotonin) dexsmethasone-CDS Example 118 herelnbelow antiinflammatory agent o VO I o h Chemical Heme Structure *,U-d1hydroxy-2t- ([ (1-methyl 1,4-dlhydropyr1d1n-3-yi Icarbonyl]oxy ,pregn-4-ene-3,20-d1 one 3-hydroxy-l7(- ,[l-methyl -1,4dthydropyrIdin-3-yI)carbony1]oxy,19- nor-lla-pregna-l,3,5(10)-trlen20- yne Πβ- |[(l-methyl-l ,4-dlhydropyrldln1-ylIcarbonyl]oxy,-19-norpregn-4-en 20-yn-3-one bbrevtated Name Synthesis Pharmacological Use hydrocort1sone-COS Example 121 hereinbelow antllnflammitory agent ethinyl Example ¢9 estrogen- estradlol-COS hereinbelow at estradlol-COS norethIndrone-COS Brewster et al. Pharmaceutical Research ,1588), 2(5), J7B-2B5 progestin (e.g. for use In threatened abortion, endometriosis, other menstrual disorders, and at a contraceptive component) -70Structure Chemical Name Abbreviated Name JSC? 3-hydroxy-17e-[(l-methyl-l.4dlhydropyrldln-3-yl)carbony1)oxyestra-1,3,S(10)-trtene 17p- {[(1-methyl-1.4-dlhydropyrldln 3-ylJcarbonyljoxy |pregn-4-en-20-yn 3-one cscn 13-ethy1-17»-|t(l-methy1-l,4dlhydropyrldln-3-ylJcarbonyl]oxy,18,19-d1norpregn-4-ene-20-yn-3-one estradlol-COS or Ej-COS ethtsterone-COS norgestrel-COS Synthesis Pharmacological Use U.S. Patent No. 4.617.298, Example 11 estrogen (e.g. for control of menopausal symptoms, for menstrual disorders such as dysmenorrhea, as a contraceptive component, for weight control, for prostate cancer, for male sexual dysfunction) Brewster et al. Pharmaceutical Research (1986). ΤβΤΓ278-2β5 progestln- as norethlndrone-COS Brewster et al, Pharmaceutical ISsiircR 719K) 3,5,/ 278-285 progestlnas norethlndrone-COS o Chemical Heme Structure 3-[(l-methyl-l,4-d1hydro-3pyr1d1ny1)carbony1oxy]estra 1,3,5(10)-tr1en-17-one 178-((1-methyl-1,4-d1hydro-3pyrldinyl)carbony1oxy]estra1,3,5{10)-tr1en-3-o1 3-methyl ether 3,17 B-b Abbreviated Name Synthesis Pharmacological Use estrone-COS U.S. Patent No. 4,(17,298, Example 3 estrogenas estradiol-COS estradiol 3methyl ether-CDS U.S. Patent No. 4,617,298. Example 6 estrogenas estradiol-COS estradiol bls-COS Example 72 hereinbelow estrogenas estradiol-CDS -72» ♦ Chemical Name 3-(phenylcarbony1oxy)-170- ([(1methyl-1,4-dthydropyrldln-3-y1)carbonyl]oxy |estra-l ,3,5(10)-trlene Π0- |[(l-methyl-l .4-dlhydropyrldln3-yl)carbonyljoxy)-19-norpregn-5(10) en-20-yn-3-one 3-methoxy-17e- ([l-methyl-l ,4di hydropyridln-3-yl)carbonylloxy|19 nor-|7e-pregna-l,3.5(10)-tr1en20-yne Abbreviated Name estradiol benzoate-CDS norethynodrel-COS mestranol-COS Synthesis Pharmacological Use Example 75 hereinbelow estrogenas estradiol-COS from norethynodrel , analogously to methods of Brewster et al, Pharmaceutical Research (19β5). 3(5). £76-285; also U.S. Patent No. 4,540.564 progestinas norethlndrona-COS ι co I from mestranol, analogously to methods of Brewster et al. Pharmaceutical ResearcinnW7TT5T. 276-265; also U.S. Patent No. 4,617,298 estrogenan estradiol-COS Λ Structure Chemical Name l-methyl-3-[N-(2-(l-(p-chlorobenzoyl)-S-methoxy-2-methy1-3indolyl{acetoxy lethyl)carbamoy1)1,4-dlhydropyrldlne Abbreviated Name Synthesis Pharmacological Use indomethacin-CDS Example 97 hereinbelow antiinflammatory agent OCHj l-methyl-3-|h-[2-(6-methoxy-amethyI-2-naphthalenylacetoxylethyl) carbamoyl-1,4-dihydropyrldlne £'«z“z CICHjCH£ l-methy1-3-(N-(4-(4-(4-([bls(2chloroethyI)]amtno)phenyl)butanoy1 oxy]cyc,ohexyl{carbamoyl 1-1.4dlhydropyrldlne naproxen-CDS Example 96 hereinbelow anttlnflaimxatory agent 4* 1 chlorambucil-CDSj Example 82 hereinbelow as ch1oraiRbucil-COS| Ί Structure Chemical Name Abbreviated Name Synthesis Pharmacological Die 1-methyl-l-[(H-(2-[4-( |4-[b1s(2chloroethyl)jamlno{phenyl)butanoyl oxylpropyl,{carbamoyl1-1,4-dlhydro pyridine chlorambucil-COS) Example 85 hereinbelow as chlorambucil-CDS) CICNjCMj CICMjCMj l-methy1-3-[(N-|2-pheny1-2-(|4-[bts(2- chlorambucil-COS* chioroethyl)]am1no{phenyl)butanoyloxy ] |ethyl{carbamoyl1-1,4-dlhydropyrldlne Example 90 hereinbelow at chlorambucil-COS) I VI Ol I 1-methyl-3-[Ν-(11-(4-(4-|[b1s(2chloroethyl)]amf no{pheny1)but anoyloxylcyclohexylImethyl)carbamoyl]1,4-dlhydropyrldlne chlorambucil-COS) Example 101 hereinbelow as chlorambucil-COS) h Structure Chemical Nine N-(2-fluoroethyl)-N'-[2-(l,4dlhydro-l-methyl-3-pyrldlnecarbony1oxy)ethyl]-N-n1trosourea N-(2-chloroethyl)-N'-[2-( 1.4dthydro-l-methyl-3-pyrldtnecarbony1oxy)ethyl]-Nnltrosourea 3-(1,4-dlhydro-1-methy1-3pyrldlnylcarbonyloxymethyl)-5fluorourael, Abbreviated Name Synthesis Pharmacological Ute FENU-COS Example 127 hereinbelow anticancer, antitumor agent HENU-COS Example 124 hereinbelow anticancer, antitumor agent S-FU-CDS, Example 13S hereinbelow anticancer, antitumor agent Λ Structure Chemical Name l-(l,4-d1hydro-l-methyl-3pyrldlnecarbonyloxyJmethyl 5-fluorouracl, Abbreviated Name Synthes,* Pharmacological use S-FU-COS? Example 133 herelnbelow anticancer, antitumor agent -77-78The cyclodextrins contemplated for use herein are hydroxypropyl, hydroxyethyl, glucosyl, maltosyl and maltotriosyl derivatives of β-cyclodextrin and the corresponding derivatives of γ-cycl odextrin . The» hydroxyalkyl groupings may contain one or more hydroxyl groups, e.g. hydroxypropyl, di hydroxypropyl and the like. The glucosyl, maltosyl and maltotriosyl derivatives may contain one or more sugar residues, e.g. glucosyl or diglucosyl, maltosyl or dimaltosyl. Various mixtures of the cyclodextrin derivatives may be used as well, e.g. a mixture of maltosyl and dimaltosyl derivatives. Specific cyclodextrin derivatives for use herein include hydroxypropyl-β-cyclodextrin (HPCD or HPBCD), hydroxyethyl-β-cyclodextrin (HEBCD), hydroxypropyl-γ-cyclodextrin (HPGCD), hydroxyethyl-γcyclodextrin (HEGCD), dihydroxypropyl-β-cyclodextrin (2HPBCD), glucosyl-β-cyclodextrin (Gj-B-CD or G^BCD), diglucosyl-β-cyclodextrin (2Gj-B-CD or 2GJBCD), maltosyl-B-cyclodextrin (G2-B-CD or G2BCD), maltosyl-γcyclodextrin (G2-y-CD or G2GCD), maltotriosyl-βcyclodextrin (G-j-B-CD or G^BCD), maltotriosyl-γcyclodextrin (G^-y-CD or G^GCD) and dimaltosyl-βcyclodextrin (2G2-p-CD or 2G2BCD), and mixtures thereof such as maltosyl-B-cyclodextrin/dimaltosyl-Bcyclodextri n.

Hydroxypropyl-β-cyclodextrin for use in the methods of the present invention is commercially available. Alternatively, it may be prepared by known methods, especially by use of the optimized procedure of Pitha et al, International Journal of Pharmaceutics, 29, 73-82 (1986). The following is a typical procedure using the Pitha et al method: -7931 g of sodium hydroxide were dissolved in 250 mL of water. Then, 100 g of β-cyclodextrin were added and the solvent was warmed to effect solution. The flask was cooled and 50 mL of propylene oxide were added.

The flask was fitted with a dry ice/acetone condenser during the addition. The solution was allowed to come to room temperature and was stirred for 72 hours. The solution was then neutralized with concentrated hydrochloric acid and diluted with water. The solvent was removed in vacuo, leaving a syrup which was taken up in ethanol. After stirring for 30 minutes at room temperature, the sodium chloride produced was removed by filtration. The filter cake was washed with ethanol and the combined ethanol layers were reduced in vacuo. The residue was dissolved in water and dialyzed in cellulose acetate (#7, 38 mm 4.6 mL/cm, molecular weight cut off = 1000, Fisher Scientific). After 5 hours at 0°C, the solution was removed from the dialysis tubing and freeze-dried. The resulting solid was suspended in acetone and stirred overnight. The filtered solid was resuspended in acetone and stirred for 24 hours. The solid was collected by filtration and dissolved in 200 mL of water and then lyophilized. 75 grams of purified hydroxypropyl-β-cyclodextrin were obtained. The degree of substitution was calculated by NMR and by comparison with an authentic sample.

In forming a complex with Eg-CDS, a 50% solution (w/w) of 2-hydroxypropyl-β-cyclodextrin (HPCD) was made in distilled water. An excess of E2-COS was added and the solution then was purged with helium. The resulting suspension was then sonicated for 30 minutes, filtered through a glass filter (ASTM 10-15M, Pyrex No. -8036060) and freeze-dried overnight. Best results were obtained by hard-freezing the aqueous solution of the E2-CDS/HPCD complex for at least 10 hours before lyophilization. The degree of complex formation was determined by dissolving a small amount of the dry complex in methanol and then analyzing by high pressure liquid chromatography (HPLC). The degree of complexation was found to vary between 20-40 mg/g and the solubility of the complex was determined to be 2.2xl04 mg/L.

The P1tha et al method for preparation of HPCO by condensation of propylene oxide with β-cyclodextrin in alkaline aqueous solution unfortunately suffers from disadvantages, particularly in purification of the product. After completion of the condensation, the reaction mixture is neutralized with hydrochloric acid, water is evaporated under vacuum and the syrupy residue is dissolved in ethanol to precipitate sodium chloride, the main by-product of the reaction. After filtration, ethanol 1s evaporated under vacuum and the residue 1s dissolved 1n water and dialyzed to remove the remaining sodium chloride and polymerization products of propylene oxide. During dialysis, part of the hydroxypropyl-β-cyclodextrin goes through the membrane and is lost. The dialysate is then freeze-dried, twice stirred in acetone and washed to remove the remaining polymerization products. Finally, hydroxypropy1 -βcyclodextrin is freeze-dried again. The second freezedrying is necessary because the product after washing with acetone is not homogeneous. -81To overcome these difficulties with the Pitha et al process, a new method has been developed by Maciej Smulkowski of the University of Florida, Gainesville, Florida for the synthesis of HPCD. This new method involves removal of sodium hydroxide from the reaction mixture by an ion exchange resin (H ); as a result, several time-consuming steps of Pitha et al's purification can be avoided. Moreover, the amount of sodium hydroxide used by Pitha et al (7 equivalents for one of β-cyclodextrin) can be decreased to 2 equivalents of sodium hydroxide per cyclodextrin molecule, and still produce a product with the appropriate NMR and optical rotation.

According to the new method, β-cyclodextrin is first condensed with propylene oxide in alkaline solution, sodium hydroxide is removed on an ion exchange column (Dowex 50W-X8, H+ form), the eluate is evaporated under vacuum to one-half of the original volume, the remaining solution is freeze-dried, the resulting white solid is washed with acetone and freeze-dried again, then subjected to grinding and sieving. Possible modifications of this method Include: (1) use of the ionic exchange resin for neutralization in the reaction flask, with filtration of the resin and washing on the filter funnel; (2) use of calcium, magnesium, lithium or potassium hydroxide to dissolve the cyclodextrin; (3) removal of hydroxides after the reaction by saturating the reaction mixture with carbon dioxide or neutralization with sulfuric acid in place of the ion exchange resin; (4) use of even less sodium hydroxide (between 1 and 2 equivalents); and (5) elimination of the second freezed ry i n g. -82The following 1s a typical procedure using the new, improved method: g of β-cyclodextrin was dissolved in a solution of 3.53 g of sodium hydroxide in 75 mL of water and treated with 29 mL of propylene oxide at 0°C. The reaction mixture was maintained for 5 hours at that temperature, then was kept at room temperature for 42 hours. At the end of that time, the reaction mixture was passed through the Oowex 50W-X8 column (H+ form), the column was washed with water and the eluate was evaporated under vacuum to a volume of 100 mL, then freeze-dried. The resulting white solid was washed with acetone to give 51 g of HPCD, with the same degree of substitution (4.7) and NMR as the HPCD prepared by the Pitha et al method. Residue on ignition was 0.0%. Optical rotation also was identical to that of the Pitha et al product.

Condensation of 25 g of β-cyclodextrin using 7.71 g of sodium hydroxide gave similar results.

A further improvement in the new, improved HPCD synthesis utilizes activated carbon for purification of the solution prior to the last freeze-drying. Thus, when the aqueous solution from the Dowex 50 ionic exchange column was treated with activated carbon, most of the polymerization products were removed without loss of HPCD, and the filtrate after only one washing with ethyl acetate was ready for final freeze-drying.

In this way, only one freeze-drying was required. Crystallization of the final product instead of freezedrying is also possible, at least on a small scale.

The product from the modified new process (using activated carbon) appears to be superior to that of the -83original new process and the Pitha et al process.

First, the product is snow white and produces a colorless aqueous solution, whereas solutions of the earlier products were yellow. Secondly, the product is not oily, which may be due to removal of more highly substituted, less soluble, oily cyclodextrins.

HPCD can be prepared in varying degrees of substitution, such as 5 or 7. Typically, the foregoing procedure is used to produce HPCD (ASOS 7). The mass spectra for the isomeric misture of HPCD centers around degrees of substitution. This spectra is obtained by softly ionizing the sample using fast atom bombardment. The generated spectra is similar to those previously reported (obtained by Cal 1fornium-252 plasma desorption) in both the symmetry of the isomeric distribution and the numerical spread of the isomers formed .

Hydroxyethyl-β-cyclodextrin (HEBCD) can be prepared analogously to HPCD, utilizing the improved procedure detailed above but substituting an equivalent quantity of ethylene oxide for the propylene oxide there employed.

The synthesis of 2-hydroxypropyl-γ-cyclodextrin (HPGCD) similarly uses the same basic procedure as for HPCD, substituting γ-cyclodextrin for the β-cyclodextrin starting material. However, because γ-cyclodextrin contains eight glucose residues compared to seven for β-cyclodextrin, the amount of propylene oxide used can be reduced in order to lower the degree of substitution. Use of 0.75 mole of propylene oxide per 0.077 mole of γ-cyclodextrin (~ 20% excess considering OH groups) affords HPGCD with a degree of substitu-84tion of 8, while use of 0.56 mole of propylene oxide (~ 10% less than equivalent) gives a degree of substitution of about 7.

Hydroxyethyl-γ-cyclodextrin (HEGCD) can be prepared similarly to HPGCD as described in the preceding paragraph, simply using an equivalent quantity of ethylene oxide in place of the propylene oxide.

Thus, the hydroxyalkyl cyclodextrins intended for use herein can be prepared by procedures described by Pitha et al or variations thereof. Obtained by these procedures, the cyclodextrins are intrinsically amorphous mixtures. The importance of the amorphous nature of the cyclodextrins is described by Pitha et al , J. Pharm. Sci ., Vol. 74, No. 9, September 1985 , 987-990. The advantages of the amorphous nature of these materials are more pronounced at higher concentrations of cyclodextrin.

The other cyclodextrins intended for use in the present invention, i.e. the glucosyl, maltosyl and maltotriosyl derivatives of 0- and γ-cyclodextriη, are branched cyclodextrins which are highly soluble in water as compared to the parent cyclodextrins . These branched cyclodextrins can be produced by microbiological processes from the parent cyclodextrins .

Glucosyl-8-cyclodextrins can be obtained from the mother liquor of a large-scale β-cyclodextrin synthesis with Bacillus ohbensis cyclomaltodextrin glucanotransferase; see Koizumi et al, Chem. Pharm. Bull ., 35 (8), 3413-3418 ( 1987) and reference cited therein. Maltosyl and maltotriosyl 8- and γcyclodextrins can be prepared from the parent cyclodextrin and maltose or maltotriose through the reverse action of Pseudomonas isoamylase or K1ebsiel 1 a -85aerogenes pullulanase, while glucosyl-γ-cyclodextrin can be prepared by enzymatic hydrolysis of maltosyl-γcyclodextrin; see Okada et al , Chem. Pharm. Bull., 36 (6), 2176-2135 (1988) and references cited therein.

The preparation of maltosyl-β-cyclodextrin by reacting maltose with β-cyclodextrin in the presence of pullulanase is also described in Japanese Kokai 61287902, published December 18, 1986, and Japanese Kokai 61-197602, published September 1, 1986. A mixture of maltosyl-6-cyclodextrin and various dimaltosyl-βcyclodextrins may be conveniently employed, e.g. ISOELEAT™ of Ensuiko Sugar Co., Ltd., Yokohama, Japan.

The development of a carrier-mediated dihydropyrldlne * pyridinium salt redox system (which, in the d1hydropyridine form, is also termed a chemical delivery system or CDS) has resulted in the enhanced and/or sustained delivery of a variety of drugs to the central nervous system. While the physiochemical properties of the CDS are optimized for brain-uptake and retention, they are often incompatible with aqueous formulations. A salient example is E?-CDS, a CDS based on estradiol. This dihydronicotinate passes the B8B and is oxidized to the correspond!ng quaternary salt, £20*. The sustained levels of E2Q+ produced then slowly release estradiol, which exerts profound central estrogenic effects. These effects include LHsuppression in ovarlectomlzed rats and a reversible suppression of cyclicity in intact female rats and are exerted for prolonged periods. The E2-CDS is highly lipophilic and only poorly water soluble (0.2 ug/mL). This requires that E2-C0S be administered in watermiscible organic solvents such as dimethylsulfoxide (DMSO) or dimethyl acetamide (DMA). While this -86procedure is not inappropriate for laboratory animal studies, it is clearly inadequate for human use for reasons enumerated hereinabove. The development of aqueous formulation of Eg-COS was therefore Investigated. Criteria for this formulation include that it have minimal toxicity, that it be equivalent with Eg-CDS in DMSO or DMA in delivering EgQ* to the brain and that the technology developed be applicable to other dihydropyridine * pyridinium salt redox systems.

EXPERIMENTAL SECTION Materials: 3-Hydroxy-17β-[(1-methyl-1,4-dihydropyridin-3-yljcarbonyl]oxyestra-l,3,5(10)-triene (E2-CDS), l-methyl-3-{{N-{e-[3,4-bis(pivalyloxy)phenyl]ethyl }carbonyl } }-l ,4-dihydropyridine (DA-CDS), 17β-[(1,4di hydro-1-methy1-3-pyridinylearbonyl)oxy]androst-4-en3-one (T-CDSj), l-methyl-3-N-[3-(benzyloxycarbonyl)propyllcarbamoyl-1,4-dihydropyridine (GABA-CDSj), 1methyl-3-{[2-(9-guanyl methoxy) ethoxy]carbonyl }-l ,4di hydropyri d i ne (ACV-CDS) and 17β-{[(1-methyl-1,4di hydro pyridi n-3-yl jcarbonyl ]oxy}-19-norpregn-4-en-20yn-3-one (N-CDS) were synthesized according to published procedures. 2-Hydroxypropy1 -β-cyclodextrin (statistical degree of substitution = 5.1 or 7) (HPCD) was prepared according to the method of Pitha et al. Other cyclodextrins (α,β or γ) were obtained from Aldrich Chemical Co. and other steroids (estradiol, estradiol 17-valerate, estriol, estrone, estradiol 3methyl ether and testosterone 17-propionate), were purchased from Sigma Chemical Co. All prepared compounds were fully characterized by spectroscopic and microcombustion analysis (Atlantic Microlabs) prior to -87study. Mass spectroscopic studies were performed on a Kratos MS80RFA double-focusing Instrument fitted with a fast atom gun. Cyclodextrin mixtures were analyzed by fast atom bombardment of the samples prepared in a glycerol matrix. Degrees of substitution were determined from the isomeric mass distribution. Nuclear magnetic resonance spectra were obtained on a Varian EM360 60 MHz spectrometer. Values were recorded relative to an internal standard [3-(trimethylsilyl)propionic 2,2,3,3-d4 acid, sodium salt, DOS] and all samples were run in D20. The degree of substitution was calculated by comparing the integrated area attributed to the anomeric hydrogen compared to that of the hydroxypropyl functionality.

Effect of Solubilizing Agents: An excess of E2-CDS was sonicated with an aqueous solution of the appropriate solubilizing agent for 30 minutes. The suspension was then centrifuged, filtered through 0.45 um polyvinylidene difluoride (M1llex-HV4, Millipore®) membranes and analyzed by HPLC. For studies with 2-hydroxypropy1 -Scyclodextrin, an excess of E2-CDS was added to different concentrations (% w/v) of HPCD and the solubility (mg/mL) was determined spectroscopically (UV = 360 nm, ε » 6487 1n methanol). An estimation of the bulk equilibrium constant was obtained by correlating the mi 11 imol ari ty of E2-COS solubilized and the mi 11imolarity of the cyclodextrin added. This latter value was calculated using the average molecular weight of the isomeric mixture determined by mass spectroscopy. The solubilizing effect of a 50% w/w solution of HPCD was also examined for a series of steroids and -88dihydropyridines (COS). These studies were carried out in a similar manner to those previously described.

Preparation of Solid Complexes: An excess of Eg-CDS or other CDS was added to a 50% w/w solution of HPCD. The suspension was sonicated for 30 minutes, filtered through 0.45 pm PVOF membranes and freeze-dried. The degree of incorporation was determined either spectrophotometrically or by HPLC. In some cases, the effect of solubilizing agents on the degree of incorporation was examined. This involved adding small amounts of polyoxyethylene 20 cetyl ether (Brij), polyoxyethylene sorbitan monooleate (Tween 80) or ethanol to the aqueous solution prior to lyophilization.

Analytical Methodology: In determining concentrations spectrophotometrically, a Cary 219 (Varian) or an HP 8451A Diode Array (Hewlett Packard) spectrophotometer was used. Standard curves were prepared in methanol and gave correlation coefficients greater than 0.999. For the CDS, the wavelength monitored was 360 nm while for estrogen 220 nm was used.

The HPLC system consisted of either an Autochrom M500 pump fitted with a Rheodyne Injector or a PerkinElmer Series 4 pump, a Kratos Spectroflow 757 variable wavelength detector and either a Beckman recorder or an LCI-100 integrator (Perkin-Elmer). Separation was achieved on an Analytical Sciences, Inc. (ASI) 10 pm particle size, C18 reversed phase 30 cm x 3.9 mm i.d. analytical column. The flow rate was 1 mL/min, the compounds were detected at 360 nm and 1n all determinations the temperature was ambient. A mobile phase containing 82:1:1:16 (acetonitrile: tetrahydrofuran: -89acetlc acid: Η?0) eluted the Eg-CDS at 4.4 min, the DACOS at 4.4 min, the T-CDSj at 6.8 min and the N-COS at .2 min. For the GABA-CDSp a mobile phase consisting of 50:1:1:48 of the same components was required. The retention time was 5.2 min. Other compounds were assayed spectrophotometrically.

Animal Studies: Conscious, restrained Sprague-Dawley rats (female, BW = 200 g) were given either 15 mg/kg Eg-CDS in DMSO or 5 mg/kg of E^-CDS complex in HPCD (Eg-CDS-HPCD) in water by intravenous injection (tail vein). At various times after the administration, animals were sacrificed and trunk blood and organs collected. The organs were then weighed, homogenized 1n water and deproteinized with cold acetonitrile. The organ homogenates were centrifuged and the supernatant analyzed for EgO* anc* E2-CDS using a precolumn enrichment technique, the details of which are given herei nbelow.

RESULTS AND DISCUSSION As discussed hereinabove, cyclodextrins have been used to Increase the water solubility of a number of drugs, including steroids. These cyclic oligomers contain various numbers of a-l,4-11nked glucose units. The number of these units (0 = six, β = seven, γ = eight) determine the size of a cone-like cavity which is amenable to inclusion by many drugs. The stability of the complex formed depends on the fit of the drug into the cyclodextrin and the cyclodextrin concentration. Unfortunately, the cyclodextrin best suited for complexation with steroids, i.e. β-cyclodextrin, is poorly water-soluble. This property is -90derlved from the high degree of hydrogen bonding which occurs 1n the crystal lattice. To add to the problem, β-cyclodextrin is known to cause nephrosis in rats, a toxicity which results, at least partially, from its poor water solubility. In any case, little change in the aqueous solubility of Eg-CDS was observed when it was equilibrated with various solutions of either α, β or γ-cyclodextrin. As illustrated in Table I, concentrations of α-cyclodextrin up to 50 mm increased the aqueous solubility of E£-CDS only 25-fold while β and γ-cyclodextrin increase the solubility of the CDS 135 and 110-fold respectively. The relationship between the aqueous solubility of E2-CDS and the concentration of the unsubstituted cyclodextrins was I not linear, a situation which is also observed in the case of the parent steroid. In any case, the limited water solubility and the relatively poor complexation provided by α-, β- or γ-cyclodextrin are unsuitable for pharmaceutical exploitation. The toxicity of β-cyclo20 dextrin underscores this assessment. Ί-91TABLE I EFFECT OF VARIOUS CYCLOOEXTRINS ON THE WATER SOLUBILITY OF Eg-COS Cyclodextri n Cone. Range Maximum Solubi1i ty Cone, of Cyclodextrin at Max. Solubility n (mM or tw/v) (mg/ml) (mM or %w/v) None - 0.0002 - - Alpha ( a) 5-50 mM 0.005 50 mM 7 10 Beta (B) 5-15 mM 0.027 10 mM 5 Gamma (γ) 5-50 mM 0.022 10 mM 5 HPCD (7 ASDS) 0.78-62.5 %w/v 30.19 62.5 %w/v 9 15 HPCD (5.1 ASDS) 1-62.5 %w/V 35.12 62.5 %w/v 5 Several efforts have been made to increase the aqueous solubility and, therefore, usefulness of cyclodextrins. Various methylated derivatives have been described but, in general, the acute toxicity of the modified compound is greater than that of the parent. Recently, an amorphous cyclodextrin composition was obtained by hydroxypropylation of β-cyclodextrin. The product, 2-hydroxypropyl-Β-cyclodextrin (HPCD), is a mixture of isomers which can be characterized by the average statistical degree of substitution (ASDS).

Either NMR or mass spectroscopy can be used to determine this value. These highly water soluble mixtures were shown by Pitha et al to dramatically increase the solubility of a number of compounds including gonadal steroids. In addition, preliminary toxicity studies -92have shown few, if any, harmful effects after either oral or intravenous administration.

HPCD (ASDS 5.1 or 7) was prepared according to the method of Pitha et al. The mass spectra for the isomeric mixture of HPCD centered around 7 degrees of substitution. This spectra was obtained by softly ionizing the sample using fast atom bombardment. The generated spectra was similar to those previously reported (obtained by Californium-252 plasma desorption) in both the symmetry of the isomeric distribution and the numerical spread of the isomers formed. In the cited example, as in the 5.1 ASDS case, no underivatized (toxic) β-cyclodextrin was detected.

In applying this HPCD composition to E2-C0S, HPCD with low ASDS's was selected. As the degree of substitution increases, not only does the complexing propensity of the cyclodextrin decrease, presumably due to steric interactions, but the surface activity of the complex increases. This is undesirable since, iri general, as the surface activity increases, so does the tendency of the material to cause hemolysis. Both the .1 and 7 ASDS HPCD had a profound effect on the solubility of E2-CDS. In the 7 ASDS case, a linear increase (r = 0.995) in the solubility of E2-CDS was evident as the concentration of HPCD was increased. At 62.5% v/v, 30.2 mg/mL could be solubilized. In the 5.1 ASDS material, 35 mg/ml of E2-CDS could be solubilized at 62.5% w/v. The lower ASDS material gave a 15% increase in incorporation. These data reflect an Increase 1n solubility of five orders of magnitude (150,000-fold) over the solubility of E2-CDS in water -93(Table I). Plotting the data obtained from the 7 ASOS study as mi 11imolarity of Eg-CDS solubilized versus the mi 11imol arity of HPCD added (based on the average molecular weight of the mixture) gave a line with a slope of 0.2. This is an estimation of the bulk stability of the cyclodextrin complex and compares reasonably with other systems.

These solutions could be freeze-dried giving a solid complex. A 50% w/w solution of HPCD gave a solid containing 37 mg Ez-CDS/gm complex. The complex was stable as a dry powder and could be easily reconstituted with water. In these manipulations, it was Important to maintain the HPCD component greater than 20% w/v. Below this level, precipitation would occur. Several attempts were made to increase the degree of incorporation of the complex by adding various agents such as Brij (0.7% w/w), Tween 80 (0.8% w/w) or ethanol (10% v/v). While the addition of Brij increased the degree of incorporation to 189 mg/g, the complex was not stable, falling to 42 mg/g in 12 days. The other agents had only modest effects. The upper limit for a stable complex, therefore, appeared to be approximately 40 mg/g under these circumstances.

Since an inclusion complex is formed between EgCOS and the various components of the cyclodextrin mixture, it is possible that some portion of the E2-COS would not rapidly dissociate, thus lowering the biologically available concentration of E2-COS. To investigate this possibility, the ability of the HPCD (5.1 ASOS) formulation of E2-COS (E2-CDS-HPCD) to deliver E2Q+ to the brain was measured and compared with the -94delivery of EgQ+ when Eg-CDS was administered in DMSO. Brain concentrations of EgQ* were measured after systemic administration of either 15 mg/kg Eg-CDS in DMSO or 5 mg/kg Eg-CDS in aqueous HPCO. When the difference in dose is accounted for, i.e. the data is presented as % dose/g, no significant difference exists between brain levels of EgQ* after Eg-CDS administration in DMSO or Eg-CDS-HPCD in an aqueous media, although the latter produce data which are strikingly more consistent and less variable. Interestingly, the levels of EgQ* in the lung are lower after Eg-CDS-HPCD administration. One explanation for this is that when Eg-CDS is given in a water miscible solvent such as DMSO, there may be some tendency for the highly water insoluble Eg-CDS to precipitate.

After a bolus i.v. injection, the aqueous, ionic environment of the lung may provide a suitable site for this precipitation. The lower levels obtained in the lung after Eg-CDS-HPCD administrations reflect not only the higher water solubility of the complex but may also indicate something of its in vivo dissociation constant. Quite surprisingly, this dissociation appears to be fast enough so not as to alter the distribution of Eg-CDS in the CNS, but slow enough to allow pulmonary transit (or transit from other organs such as the liver) without significant precipitation.

In addition, the values for various organ concentrations are far less variable after Eg-CDS-HPCD administration, which may be explained by the higher water solubility of the complex and its lower tendency to precipitate. Ongoing pharmacological studies -95corroborate the effectiveness of the Eg-COS-HPCO formulation in brain-selective delivery.

The effect of a 50X w/w solution of HPCO on the solubility of a number of steroids and other COS is given in Table II.

TABLE II SOLUBILITY OF VARIOUS STEROIDS AMD VARIOUS DRUG CHEMICAL DELIVERY SYSTEMS IN A 50¾ W/W SOLUTION OF 2HYDROXYPROPYL-8-CYCLODEXTRIN (ASPS 5.1) AND THE AMOUNT OF DRUG INCORPORATED IN THE FREEZE-DRIED COMPLEX Drug Solubility (mg/mL) in 50¾ w/w HPCD Amount of Drug in Dry Complex (ing/g) e2-cos Estradi ol Estri ol Estrone 9.52 Estradiol 3-Methyl Ether Estradiol 17-Valerate 13.8 23.5 Testosterone r Amount of Drug in Dry Complex (mg/9) 65.6 -96Drug Testosterone 5 17-Propionate Solubility (mg/ml) in 50% w/w HPCD Testosterone-COS (T-CDSj) 17.1 29 Norethi ndrone 68 - Norethindrone-CDS (N-COS) 0.35 0 GABA-CDSj 93 160 OA-CDS 16 27 ACV-COS 14.9 25 Thus, E2-COS and several other CDS were success15 fully solubilized with HPCD, although this is not universal; norethindrone-CDS, for example, was not readily solubilized. The best solubilization of E2-COS occurred in an aqueous solution of HPCD, ASDS 5.1 or 7. These complexes could be freeze-dried and were stable. They were easily reconstituted in water so long as the cyclodextrin component was at least 20% w/v. This formulation was equivalent with E2-CDS administered in DMSO in delivering E2-Q+ to the brain of rats. In addition, the formulation significantly reduced the lung concentrations of E2Q+. Data available at present indicates this excipient is less -97toxi c, easily compressed into tablets, rapidly dissolved and readily and reproducibly synthesized.

Eg-COS and several other CDS have also been successfully complexed with other cyclodextrin derivatives as defined herein. The other cyclodextrin/CDS complexes have the improved characteristics as noted before for the HPCD complexes.

In one example of the formulation of a solid complex, an excess of a representative CDS, Ej-CDS, was added to a 40% aqueous solution of a mixture of maltosyl-B-cyclodextrin (71%) and various dimaltosyl-Bcyclodextrins (29%) obtained from Ensuiko Sugar Co., Ltd., Lot No. 88190, and mixed for several hours. The suspension was then filtered and freeze-dried, and the amount of complexed drug was determined analytically by UV spectraphotometry. The amount of incorporation was determined to be 81.88 mg/g. The comparable figure for HPCD is approximately 36.2.

In further testing, maximum concentrations of selected CDS in varying concentrations of selected cyclodextrins were determined. The concentration of Eg-CDS (mg/mL) was as follows: Cyclodextri n HPCD HEBCD HPGCD % 6.73 3.09 40% 11.9 6.07 4.0 The concentration (mg/g) of the norethindrone-CDS was 7.13 in 40% HPCD and 15.9 in 40% HPGCD. -98As noted above, use of a representative di!-ydropyridine redox system drug, i.e. Eg-CDS, complexed with a representative cyclodextrin derivative, HPCD, led to lower initial lung concentrations (and thus increased initial brain to lung concentrations) of the quaternary form as compared to administration of the redox system drug in DMSO. In studies of another representative redox system drug, namely a testosterone-CDS, T-COS|, similar observations were made, as detailed below.

EXPERIMENTAL SECTION Materials: 2-Hydroxypropyl-β-cyclodextrin (HPCO, degree of substitution 5.1) was prepared and purified according to the method of Pitha et al. The cyclodex15 trin inclusion complexes were prepared by equilibrating an excess of either testosterone propionate or T-COSj with a 50% w/v aqueous solution of 2-hydroxypropyl-6cyclodextrin. The solution was degassed and the suspension was sonicated for 30 minutes, after which it was filtered and the filtrate was lyophilized. The dried filtrate contained 65.6 mg testosterone propionate or 29.6 mg T-COSj per gram of cyclodextrin complex. Compounds were analyzed for decomposition by thin-layer chromatography and ultraviolet absorption. -99Anlmals: Male Sprague-Dawley rats, weighing 250-275 g, were purchased from Charles River Breeding Laboratories (Wilmington, MA) and were housed in an animal room which was light (14 hours; lights on at 0500 hours) and temperature (23 ± 1° C) controlled. To elevate serum luteinizing hormone (LH) and to reduce the source of endogenous testosterone, animals were bilaterally orchidectomized via a mid-ventral incision under light ether anesthesia. All experiments were initiated 2 IQ weeks after orchidectomy.

Experiment 1: On day 15 after orchidectomy, rats were ether-anesthetized and the right external jugular vein exposed. Animals were then administered one of the following: testosterone-chemical delivery system (T15 COSj or T-CDSg)* testosterone (Steraloids Inc., Wilton, NH) or the vehicle, dimethyl sulfoxide (DMSO; Fisher Scientific, Fair Lawn, NJ). The testosterone-chemical delivery systems were given at doses equimolar to testosterone (25 mg/kg) so that T-CDS| was administered 2q at 35.5 mg/kg and rats received T-COSg at a dose of 45.1 mg/kg. DMSO was injected at a volume of 1 mL/kg. All compounds were administered by infusion over a 2 minute period. One milliliter of blood was withdrawn from the external jugular vein immediately before giving the drugs (1000 hours) and blood was sampled by cardiac puncture after 6, 12, 24 hours and on days 4 and 7. The sera were separated by centrifugation at 500 x g for 20 min at 4°C and stored at -20°C. 3q Experiment 2: Two weeks after orchidectomy, rats were administered either T-CDSj, testosterone propionate -100(TP; Steraloids Inc.) or DMSO by means of intravenous infusion Into the right external jugular vein in an effort to more effectively enhance the brain delivery of testosterone. It has been shown that slow infusion Improves brain delivery of drugs attached to the chemical-del i very systems. TP was selecsted for comparison since it, like both of the T-CDS compounds, has an ester grouping (propionate) attached at carbon-17 (Cjy). Gonadally-intact animals received the drug vehicle only. Two Harvard Apparatus reciprocal infusion/withdrawal pumps (model 944) were used so that 4 animals could be simultaneously infused. Rate of infusion was 15 pL/min and animals were infused for 17 to 25 minutes. TP was given at 25 mg/kg and T-CDS was infused at a dose equimolar to TP (29.7 mg T-CDS| per kg body weight). The drug vehicle, DMSO, was administered at a dose of 1 mL/kg. One mL of blood was removed from the external jugular vein prior to drug infusion and from the sub-orbital sinus at 1, 3, 5, and 7 days. The sera were separated and stored as previously described.

Experiment 3: Orchidectomized rats were administered either testosterone-chemical delivery system (T-CI)Sj) 1n HPCD (T-CDS|-HPCD), testosterone propionate in cyclodextrin (TP-HPCD) or the vehicle, cycl odextr ii n (HPCD), via a single tail vein injection. T-CDS^-HPCD (11.9 mg/kg) was given so that animals received T-CDSj at a dose equimolar to TP-HPCD (10 mg TP/kg body weight). Control rats received 25% HPCD (w/v) at 3.0 mL/kg. Blood was removed by cardiac puncture on days 0, 1, 3, 5 and 7, and separated and stored as previously described. zT. -101To evaluate peripheral effects of the drugs, the right seminal vesicle, vas deferens and ventral prostate gland were removed, cleaned, expressed of fluid and weighed to 0.1 mg. Data are reported as mg per 100 g body weight.

Radiolwunoassay of LH: Serum LH concentrations were determined 1n duplicate with a radioimmunoassay kit (reference preparation LH-RP-2) provided through the Pituitary Hormone Distribution Program of the NIADDK.

The intra- and interassay coefficients of variation were 2.9 and 15.6, respectively.

Radlolwunoassay of Testosterone: Serum testosterone concentrations were determined in duplicate with a Coat-A-Count radioimmunoassay kit (Diagnostic Products; Los Angeles, CA).

Statistical treatment: The significance of difference among mean values for LH and peripheral tissues was determined by analysis of variance (ANOVA) and StudentNewman-Keuls (SNK) tests. The level of significance - for both tests was 0.05.

RESULTS AND DISCUSSION In Experiments 1 and 2, in which DMSO served as the drug vehicle, indications of drug insolubility upon injection were observed, i.e. respiratory distress accompanied by lesioning of the lungs, regardless of the rate of injection or infusion. In an effort to increase water solubility of the steroids, T-CnSj and TP were solubilized in a HPCD in Experiment 3. The improvement in solubility for the T-CDS^ suggests that -102a lower dose (10 mg/kg vs. 25 mg/kg) could be administered with, presumably, a diminished risk of toxicity to the animal. A 2.5-fold decrease 1n T-CDSj dosage resulted 1n a similar suppression of serum LH levels observed 1n the previous two experiments. An injection of T-CDSj-HPCD resulted in a 50t decrease 1n serum LH by 24 hours and this suppression was observed through 3 days. Suppression of LH occurred in animals treated with TP-HPCD at day 1 only.

Mild stimulation of the seminal vesicles by TCDSj-HPCD and of the ventral prostate gland by T-CDSjHPCD and TP-HPCD was observed at 7 days postinjection. As observed previously, the extent of stimulation by T-CDSj-HPCD or TP-HPCD was minor relative to tissue weights observed in control (gonadally-intact) rats.

A 5.5-fold increase in serum testosterone was observed 1 day after rats were administered T-CDSj-HPCD and serum testosterone remained elevated at day 3.. However, testosterone levels returned to pre-injection levels 5 days after injection. At no time did TP-HPCD or HPCD induce an increase in serum testosterone.

These experiments offer support for the improved delivery of testosterone to the brain when the representative redox carrier drug, T-CDSj , is complexed to the representative cyclodextrin, HPCD. The data show an equivalent suppression of LH by complexing T-COSj to HPCD and lowering the effective single dose of T-CDSj by 2.5-fold. This finding implies that the di hydropyridine form of T-CDS^ remains in solution in an aqueous medium (e.g. blood) for a longer time, thereby permitting improved passage of the drug through -103 the blood-brain barrier. Earlier studies revealed that, when administered in a DMSO vehicle, T-CDSj probably precipitated in the blood (and lungs), causing respiratory distress and/or death in rats.

No respiratory distress or animal loss occurred when T-CDSj was complexed with HPCD.

To quantitate the improvement provided by the representative cyclodextrin, HPCD, in lowering initial lung concentrations of redox carrier compounds compared to brain concentrations, another series of experiments was undertaken investigating the HPCD complex of E2-CDS. These studies, which are detailed below, utilize a reversed-phase-high-performance liquid chromatographic method for the analysis of Eg-COS and its oxidized quaternary metabolite E2-Quat in biological fluids or tissues. The assay utilizes a precolumn enrichment technique and detects plasma levels down to 10 ng/mL Eg-Quat and 20 ng/mL Eg-CDS. Sample preparation is rapid and simple. Samples are homogenized with acetonitrile, centrifuged, and the supernatant is directly injected into the HPLCsystem. A water-delivering pump injects the sample on a pre-column where the drug is concentrated.

Mobile phase backflushes the retained compound onto the analytical column. At the same time, another sample can be injected onto a second pre-column. This alternating pre-column sample enrichment technique allows the injection of large volumes up to 1800 pL. -104EXPERIMEHTAL SECTION Materi als: E^-CDS, Eg-Quat and Eg-CDS-HPCD were synthesized as described previously. Steroids (estradiol and ethinyl estradiol) were obtained from Sigma Chemical Co. HPLC grade acetonitrile and distilled, deionized water were used for the preparation of mobile phases. All other reagents used were of analytical grade.

Instrumentation: The HPLC system consisted of a LDC/Milton Roy Constametric III high-pressure pump, a LDC/M1lton Roy variable wavelength UV detector, a Perkin Elmer ISS-100 automatic injector equipped with a 2000 uL loop and a OuPont Zorbax ODS column, 15 cm x 4.6 mm I.D. (6 um particle size). Vydac guard columns (5 cm x 3.2 mm I.D.), dry-packed with OuPont Zorbax ODS material, were used. Chromatograms were recorded on a Hewlett-Packard Model 3390A computing integrator at a chart speed of 0.2 cm/min. In addition, in the precolumn enrichment system, an enrichment injector (Rheodyne Model 7067-005) with two high pressure switching valves, pneumatically turned by a tandem actuator (Rheodyne Model 7163), was inserted between the autoinjector and the analytical column. Switching of the valves was controlled via the autoinjector.

This system also contained a Bodine Electric Co. RR/035 HPLC Solvent Pump for flushing the samples onto the enrichment columns.

Methods: Assay Conditions: direct on-line HPLC Chromatographic conditions for the analysis of E2 zC.. -105COS, Eg-Ouat and estradiol were developed. The optimal wavelength for all compounds was 224 nm, but Eg-CDS can also be detected at 360 nm due to the dihydropyridine structure. Although the absorptivity at this wave5 length 1s only about half as high as it 1s at 224 nm, 360 nm was chosen as the analytical wavelength for EgCOS because of the increased selectivity. Different analytical columns were tested and mobile phases for a reversed phase chromatography of all three compounds IQ were varied widely with respect to the ratio of aqueous and organic phase as well as buffer concentration and pH. No isocratic system could be found that would detect all three compounds within a reasonable retention time and with satisfying compactness and separa15 tion of peaks. Therefore, two different systems were used for analysis.

Eg-Quat and Eg: The optimal mobile phase was found to consist of acetonitri1e/water 40:60 containing 0.03 M/L sodium salt of octanesulfonic acid and 0.003 M/L tetrabutylammonium phosphate. The pH was adjusted to pH 5-5.5. The flow rate was 1.5 mL/minute and the peaks were recorded at 224 nm.

Eg-COS: The mobile phase used for Eg-COS analysis was acetonitri 1e/water 70:30 at a flow rate of 1.5 mL/minute. Absorbance was monitored at 360 nm.

Analysis of Eg, Eg-COS and Eg-Quat by pre-column enrichment technique: The loss of sensitivity resulting from the dilution step in the procedure optimal for pre30 treatment of biological samples (see sample preparation without extraction) could be compensated for by -106developlng an HPLC system that allows injection of large volumes. A suitable HPLC-method which has been described in the literature [Roth et al, J. Chromatogr. 222: 13-22 ( 1981)] 1s based on alternating pre-column sample enrichment. The procedure used herein was as follows: The sample containing the drug is injected with a first pump A, delivering pure water, onto one of two pre-columns, which are alternatingly connected with the injection system by two pneumatically driven valves. Provided a certain 1ipophi1icity, the drug is retained and concentrated on the pre-column, while accompanying water soluble co-products like proteins are being washed out as long as water is pumped through the pre-column. This allows the direct injection of body fluids. After a certain enrichment time (6 and 8 minutes), simultaneous rotation of the two valves is induced, causing pre-column 1, where the injected drug has been absorbed, to be switched to the solvent stream of the second pump, 8. Also, at this point, the recording integrator is started. Pump B delivers the mobile phase, necessary for separation and chromatography, and backflushes the sample from precolumn 1 onto the analytical column. Parallel to this process, pre-column 2 is switched to the water stream of pump A so that a sample can be injected and enriched while the previous one is being eluted (alternating mode). Volumes up to 1800 uL can be injected due to the concentration effect of the enrichment phase.

Chromatographic conditions: This system was applicable to the quantification of E?* E^-CDS and EgQuat. The mobile phase for Eg-CDS was: Acetonitrile/water 80:20 at a flow rate of 1.8 mL/minute. -107Optlmal peak shape and retention time for Eg and EgQuat were obtained with pump B delivering a mixture of acetonitr1le/water 42:58 which contained 0.025 M/L sodium salt of 1-octanesulfonlc acid and 0.003 M/L tetrabutylammonium phosphate. The pH was adjusted to pH 5, and the flow rate was 1.5 mL/minute.

Standard solutions and stability Sample stock solutions of Eg-CDS, Eg-Quat, Eg and ethinyl-Eg containing each 50 ug/mL were prepared in acetonitrile. All solutions were stored at 6°C. For Eg-CDS, the stock solution was prepared freshly every 2 weeks. All other solutions were stable over a period of at least six months. Spiked plasma samples containing all four compounds were frozen at -20°C and analyzed repeatedly at different time intervals. No loss of drug was found under these storage conditions during two months.

Dihydropyridine derivatives like Eg-CDS are known to be easily oxidized and very labile in acidic solutions. The stability of Eg-CDS was investigated under different conditions at room temperature. These studies were performed by diluting the Eg-CDS stock solution 1:2 with different solvents or solutions at different pH values and monitoring eventual peak height loss for 24 hours by use of a modification of the direct on-line HPLC method described above: If water in the Eg-CDS mobile phase is replaced by 0.05 M phosphate buffer at pH 7 and if the detection wavelength is set to 224 nm, Eg-Quat can be detected simultaneously at 6.33 min. However, the peak is relatively broad. These conditions were used to determine the degree of Eg-CDS oxidation under the tested conditions. -108Sample preparation Extraction of Eg-Quat and Eg: Various extraction procedures from plasma were investigated under different conditions and with several solvents and solvent mixtures. Estrone could be used as an internal standard, but is known to be a potential metabolite of estradiol. Therefore, 17-8-ethinyl estradiol was chosen as internal standard. Its peak did not interfere with Eg, Eg-Quat or estrone. Without addition of an anion reagent, Eg-Quat could not be extracted from aqueous solutions. Optimal results were obtained after a single-step extraction of the drugs with potassium iodide as an ion-pairing reagent to facilitate quaternary salt extraction. The method applied was as follows: 200 pL of a saturated potassium iodide solution were added to 1 mL of spiked plasma. After vortexing for a few seconds, 10 mL of a mixture of chloroform/ethyl acetate 9:1 was added. The tubes were shaken for 10 minutes and then centrifuged for 10 minutes at 2000 rpm. The upper aqueous phase was discarded and the organic layer transferred to a clean tube to achieve complete separation from proteins and traces of aqueous phase. The organic layer was evaporated to dryness under nitrogen at 40°C and reconstituted 1n 150 uL of mobile phase. 40 pL were injected into the HPLC system. Appropriate blanks were prepared accordingly.

Extraction of Eg-CDS: Plasma and water containing Eg-CDS were repeatedly extracted with different organic solvents like chloroform, hexane, toluene, benzene and ethyl acetate. It was impossible to extract Eg-CDS -109reproducibly from aqueous phases, since the compound was shown to deteriorate unreproducibly during evaporation, even at room temperature and in the presence of oxygen-free nitrogen. Therefore, the compound had to be analyzed from biological fluids without an extraction procedure.

Preparation of plasma and tissues for analysis of Eg-CDS and Eg-Quat without extraction: Using the HPLC technique with pre-column enrichment described above, drugs can be detected from directly injected plasma without sample preparation. However, when large volumes are injected, in order to obtain maximum sensitivity, it is desirable to remove proteins to a large extent prior to Injection in order to prevent frequent pre-column packing. The procedure of deproteinization was chosen to be applicable for subsequent analysis of both Eg-CDS and Eg-Quat so that only one preparation step had to be performed.

Acidic precipitating agents, which remove proteins when only small volumes are added to biological fluids, could not be used because they Induce degradative loss of Eg-CDS. Neutral or slightly basic aqueous reagents used efficiently for deproteinizatlon like ZnS04/NaOH, CuSO^/NagSO^ or saturated (NH^JgSO^ would be more ideal to be injected onto the enrichment columns than organic solvents. But all of these reagents were shown to absorb the water-insoluble Eg-CDS on the precipitate. Thus, the method of choice to avoid instability problems and at the same time keep all compounds in solution was deproteinization with acetonitrile. -110To obtain these results, the following sample preparation procedures were used for plasma and tissues: Plasma: 0.6 mL plasma was added to 1.2 mL acetonitrile. The mixture was vortexed for 5 seconds and allowed to stand for 10 minutes at room temperature, vortexed again and centrifuged for 10 minutes at 2000 rpm. 1000-1500 yL of the supernatant was injected into the pre-column enrichment system. Tissue (e.g. brain): 1 mL of water was added to one rat brain and the organ was thoroughly meshed. After sonication for 2 minutes and centrifugation at 2000 rpm for 10 minutes, the supernatant (1000-1500 yL) was injected into the enrichment system.

Animal Studies: In a first experiment, 15 mg/kg Eg-COS dissolved in dimethylsulfoxide (DMSO) were administered intravenously to conscious, restrained male Sprague-Dawley rats weighing 190-300 g each. Animals were sacrificed in groups of 4 at 5, 15 and 30 minutes and at 1, 2, 4, 8, 24 and 48 hours after drug injection. Trunk blood was collected into heparinized tubes and plasma obtained and immediately frozen at -20°C until analysis. Organs were dissected and placed on dry ice within 2 minutes of death and stored at -20°C for later analysis by the HPLC method described above.

In a second experiment, the same procedure as above was followed, except that 5 mg/kg of Eg-COS were administered as a complex with hydroxypropyl-β-cyclodextrin (HPCO) in water. The 5 mg/kg dose of Eg-COS was delivered in 1 mL of aqueous solution containing -111approximately 20% w/v HPCO (prepared by dissolving a freeze-dried complex containing 3.5 mg E2-CDS Per 9ram in aqueous 20% HPCO, the freeze-dried complex having been prepared from a 50% solution of E2-CDS in HPCD having 5.1 degrees of substitution).

Results and Discussion The results are depicted in FIG. 1 and FIG. 2.

FIG. 1 consists of a pair of semi-1ogarithmic plots comparing the concentrations in lung tissue in ug per g dose (Cg/D) of E2-CDS in the first graph and of E2-Quat in the second, corrected for dose. It can be seen from FIG. 1 that when E2-COS was administered in DMSO, initial lung concentrations (i.e. concentrations within the first hour after drug injection) of both E2-CDS and E2-Quat were significantly (more than ten-fold) higher than the initial lung concentrations observed when E2CDS was administered as a complex with HPCD in water. The corresponding levels of E2-Quat in brain tissue, also corrected for dose, are given in FIG. 2 in the form of a bar graph depicting the brain levels in ng per g dose (CB/0) at selected time points. It can be seen that the brain levels after 1 hour are not significantly different for administration as HPCD complex in water as compared to administration in DMSO. Clearly, then, the carrier-drug can be administered as a complex with a selected cyciodextrin as defined herein, such as HPCD, in water and still achieve the brain levels needed to produce the desired biological effect, while avoiding the high initial lung concentrations responsible for respiratory distress and dysnia. -112Complexation with 2-hydroxypropy1 -β-cyclodextrin (HPCD) or other selected cyclodextrin derivative as defined herein has been found to be particularly advantageous in that it stabilizes the dihydropyridine redox systems. A direct comparison of stabilities in aqueous solution is, of course, not possible because of the low solubility of the dihydropyridine redox system drugs in water; for example, the solubility of E2-CDS in water is only 0.0002 mg/mL. The E2-CDS-HPCD complex contains about 40 mg of E2-CDS/g and easily gives aqueous solutions containing 5 mg E2-CDS/mL at 20% w/v cyclodextrin. Thus, complexation affords a 25,000-fold ‘increase in aqueous solubility of E2-CDS. The halflife of E2-CDS in such a solution at room temperature in the dark is about 12.5 days (rate: 0.0554 ± 0.0047d^).

Since the dihydropyridine redox system drugs are especially prone to oxidative degradation, a study was undertaken to quantitate the effect of a cyclodextrin derivative intended for use herein, e.g. HPCD, ori the rate of oxidation of these drugs. A representative carrier-drug, E2-CDS, was selected for this study.

The rate of ferricyanide-mediated oxidation of E2CDS was determined using a previously published method (0kamoto et al, J. Chem. Soc. Chem. Comm., 1977, 181). In this procedure, 27.5 uL of a 5 x 10^ M solution of E2-CDS in acetonitrile was added to 2.75 mL of a solution containing 1 χ IO4 M Fe(CN)g“4, 0.06 M K+, 0.001 M Fe(CN)g~3. All solutions were made using water which had been boiled for 30 minutes and cooled while a stream of pyrogal1ol-scrubbed nitrogen passed -113through it. The E2-CDS was introduced via a syringe to the solution which was maintained at 37°C in a thermostated cell holder and contained in an anaerobic screwtop cuvette. The cuvette had a Teflon-lined septum through which the compound was injected. For a given concentration of ferricyanide ions (6 x 10^ to 8 x 103 M), the rate of disappearance of the E2-CDS was determined. This was done by calculating the decrease in the absorbance band at 360 nm (± 10 nm) subtracted from base line absorbance (500 ± 10 nm). A plot of the In [Abs] versus time gave a slope for the pseudo-first-order rate constant. This was done at several different ferricyanide ion concentrations. The obtained first-order rate constants were then plotted as a function of ferricyanide ion concentration generating a slope from which the second order rate constant (kg s1 M-^) was obtained. In examining the effect of 2-hydroxypropyl-Β-cyclodextrin on the rate of E2-CDS oxidation, solutions containing the HPCD as well as those ions present in the first phase of the experiment were prepared. The second order constant was derived for each cyclodextrin concentration and a plot developed. The results show that the cyclodextrin dramatically slowed the rate of oxidation. There appears to be a saturation effect in that after 2% w/v, not much change in rate is evident. The second order rate of oxidation is inhibited by 42% at 0.5% w/v cyclodextrin, 60% at 1.0% w/v, 81% at 2% cyclodextrin and at 5-20% a value of approximately 90% reduction in the rate was obtained.

From the foregoing, it is apparent that formulation with a representative cyclodextrin derivative as -114defined herein has overcome problems associated with administration of the reduced lipoidal form of dihydropyridine + pyridinium salt redox carrier systems for brain-targeted drug delivery. In particular, it has been found that administration of aqueous parenteral carrier-drug formulations comprising from about 20 to about 50% w/w or w/v of the selected cyclodextrin, preferably hydroxypropyl-β-cyclodextriη , surprisingly changes the distribution of the drug and avoids the lung precipitation problems associated with organic solvents, leading to decreased toxicity. The advantageous time element, which could not have been predicted, is such that there is sufficient time after injection but before separation of the drug from the cyclodextrin to prevent aggregation of the drug molecules (i.e. precipitation of drug aggregates) in the lungs and other organs such as the liver, and yet the time is short enough to allow timely break-up of the drug/cyclodextriη, affording facile distribution of the drug molecules so as to achieve the desired pharmacological effect. Other 1ipophi1ic/hydrophic and/or water-labile drugs which have heretofor been formulated for parenteral administration only in organic solvents, and/or which have simply been unavailable in parenteral form, share to various extents the same sort of problems encountered with the redox carrier system and benefit from the same improved distribution and advantageous time element discussed above. Drugs which are particularly useful in the parenteral compositions and methods of the present invention are those which are relatively insoluble in water but whose water solubility can be substantially improved by formulation with -11520 to 50% of the selected cyclodextrin, e.g. HPCO, in water. These characteristics can be determined by simple experiments of the type described below for representative drugs.

Apparatus UV spectra were recorded on a Cary 210 double-beam spectrophotometer (Varian, Palo Alto, CA). High pressure liquid chromatography was performed on a component system consisting of Micromeritics 728 autosampler, Beckman 112 solvent delivery module, Waters Lambda-Max Model 481 LC spectrophotometer, and Fisher Recordall series 5000 recorder. The samples were sonicated in a Fisher Bransonic ultrasonic cleaner and equilibrated in a MGW Lauda constant temperature water bath.

Solubility Studies Phase-solubility experiments were conducted by adding excess amounts of the drug to be tested to aqueous solutions containing various amounts of 2hydroxypropyl-6-cyclodextrin and sonicating the mixture for one hour. After equilibration in a 25+l°C water bath in the dark for at least 48 hours, aliquots of the mixtures were filtered through 0.45 ym membrane filters, diluted and the drug concentrations measured by reversed-phase HPLC methods.

For comparison, the solubilities of the drugs in water were also determined. -116HPLC Methods Chiordi azepoxide Wavelength: 245 nm Column: Waters uBondapak CN, 3.9 mm (i.d.) x 30 cm 5 Mobile phase: acetonitrile, acetic acid, water (60:1:39) containing 0.1% 1-hexasulfonic acid, sodium salt Flow rate: 2.00 mL/min. Retention time: 4.0 min.

Dexamethasone 10 Wavelength: 263 nm Column: ASI C18, 10 um, 3.9 mm (i.d.) x 30 cm Mobile phase: acetonitrile, water (55:45) Flow rate: 1.00 ml/min. Retention time: 3.6 min.

Di azepam Wavelength: 241 nm Column: Waters uBondapak CN, 3.9 mm (i.d.) x 30 cm Mobile phase: acetonitrile, water (6:4) Flow rate: 2.00 ml/min. Retention time: 3.2 min.

B-Estradi ol 20 Wavelength: 280 nm Column: ASI C18, 10 um, 3.9 mm (i.d.) x 30 cm Mobile phase: acetonitrile, water (55:45) Flow rate: 2.00 ml/min. Retention time: 4.4 min. -11717α-Ethynylestradiol Wavelength: 248 nm Column: Fisher Resolvex C18, 4.6 mm (i.d.) x 25 cm Mobile phase: acetonitrile, water (6:4) Flow rate: 1.50 mL/min. Retention time: 4.4 min.

Ethynylestradiol 3-methyl ether Wavelength: 248 nm Column: Fisher Resolvex C18, 4.6 mm (i.d.) x 25 cm Mobile phase: acetonitrile, water (7:3) Flow rate: 2.00 mL/min. Retention time: 6.0 min.

Medazepam Wavelength: 253 nm Column: Waters yBondapak CN, 3.9 mm (i.d.) x 30 cm Mobile phase: acetonitrile, acetic acid, water (60:1:39) containing 0.1% 1-hexanesulfonic acid, sodium salt Flow rate: 2.00 ml/min. Retention time: 2.8 min.

Methotrexate Wavelength: 308 nm Column: Fisher Resolvex C18, 4.6 mm (i.d.) x 25 cm Mobile phase: methanol, acetic acid, water (50:1:49) containing 0.1%' 1-octanesulfonic acid, sodium salt Flow rate: 2.00 mL/min. Retention time: 3.5 min.

Norethi ndrone Wavelength: 240 nm Column: Fisher Resolvex C18, 4.6 mm (i.d.) x 25 cm Mobile phase: acetonitrile, water (6:4) Flow rate: 1.50 mL/min. Retention time: 3.6 min. -118Norethindrone acetate Wavelength: 240 nm Column: Fisher Resolvex C18, 4.6 mm (i.d.) x 25 Mobile phase: acetonitrile, water (7:3) Flow rate: 2.00 ml/min. Retention time: 5.0 0(-)-Norgestrel Wavelength: 241 nm Column: Fisher Resolvex C18, 4.6 mm (i.d.) x 25 Mobile phase: acetonitrile, water (7:3) Flow rate: 2.00 mL/min. Retention time: 3.4 Oxazepam Wavelength: 230 nm Column: Waters yBondapak CN, 3.9 mm (i.d.) x 30 Mobile phase: acetonitrile, water (35:65) Flow rate: 2.00 mL/min. Retention time: 2.6 Phenytoi n Wavelength: 258 nm Column: Fisher Resolvex C18, 4.6 mm (i.d.) x 25 Mobile phase: acetonitrile, water (55:45) Flow rate: 2.00 mL/min. Retention time: 1.6 al1-trans-Reti nol Wavelength: 325 nm Column: Waters yBondapak C18, 10 ym, 3.9 mm (i.< cm Mobile phase: acetonitrile, water (55:45) Flow rate: 1.00 ml/min. Retention time: 5.8 cm min. cm min. cm mi n. cm min. .) x mi n. -119Results TABLE Ill Solubilization of Drugs by 2-Hydroxypropyl-S-Cyclodextrin in Aqueous Solution at 25±1°C.

Drug3 Solubility in water (mg/mL) Solubility in HPCD - Water Solution Cone, of Solubility HPCO (mg/mL) Increase in Solubility (HPCD/water) Chlordiazepoxide 0.01b 50% w/w 147.8 -15,000 Dexamethasone 0.008 50% w/w 44.3 -5,500 Diazepam 0.05b 50% w/w 7.4 -150 17 8-Estradiol 0.004b 50% w/w 40.5 -10,000 17 a-Ethynyl- estradiol 0.008 50% w/w 68.2 -8,500 Ethynylestradiol 3-methyl ether 0.001 50% w/w 13.3 -13,000 Medazepam (pH 7.5) 0.01 50% w/w 8.3 -850 Methotrexate (pH 7.6) 0.045 50% w/w 10.0 -200 Norethindrone 0.005 50% w/w 19.0 -4,000 Norethindrone acetate 0.0002 50% w/w 19.5 -97,500 D(-)-Norgestrel 0.002 50% w/w 4.9 -2,500 Oxazepam 0.03 50% w/w 4.2 -150 Phenytoin 0.02 50% w/w 9.3 -450 All-trans- Retinol 0.001 50% w/w 4.6 -4,600 a) pH of the 2HPCD solution given when monitored b) Literature values' -120TABLE IV Solubilization of Drugs by 25% w/v Aqueous Hydroxypropyl -β-Cyclodextrin at 25tl^cT Drug Solubility (mg/mL) Dexamethasone 24.18 17 β-Estradi ol 19.13 17 a-Ethynylestradiol 17 a-Ethynylestradiol 34.47 3-methyl ether 7.13 10 Norethi ndrone 9.13 Norethindrone acetate 9.41 D(-)-Norgestrel 2.19 Apparatus UV spectra were taken on a Perkin-Elmer 550 SE double-beam spectrophotometer. The high pressure liquid chromatography was performed on a component system consisting of Rheodyne 7125 injector, LKB 2150 HPLC pump, LKB 2138 Lichrosorb RP18 10 mm column (4x250 mm), LKB 2138 uvicord 5 detector and Omniscribe recorder. The samples were sonicated in a Kerry Ultrasonic bath and equilibrated in Tecam TE-7 Tempette constant temperature water bath.

Solubility Studies Phase-solubility experiments were conducted by adding excess amounts of the drug to be tested to aqueous solutions containing various amounts of 2hydroxypropyl-β-cyclodextrin (HPCD) and sonicating the mixtures for up to four hours. After equilibration in -121a 30.0±0.2°C water bath in the dark for up to 72 hours, aliquots of the mixtures were filtered through 0.45 Mm membrane filters, diluted and the drug concentration determined by HPLC or UV methods. The sonication and equilibration time was kept at a minimum because of the instability of the drugs.

HPLC Methods Chiorambuci1 Wavelength: 245 nm Mobile phase: acetonitrile, acetic acid, water (45:1:54) Flow rate: 2.00 mL/min.

Retention time: 4.4 min.

Lomusti ne Wavelength: 254 nm Mobile phase: methanol, water (7:3) Flow rate: 2.00 mL/min.

Retention time: 3.6 min.

Melphalan Wavelength: 254 nm Mobile phase: Methanol, acetic acid, water (60:1:39) + 0.19% 1-pentanesulfonic acid, sodium salt.

Flow rate: 2.00 mL/min.

Retention time: 3.6 min. -122Results Chiorambuci1 The preliminary experiment indicated that the solubility was about 30 mg/g in 50% w/w HPCD/HgO solution (sonication for 30 min. followed by equilibration at 30° for 4 hours). The drug is almost insoluble in water and the p.o. dose is about 100 mg/kg/day. Further experiments were done and the results are shown in TABLE V. Significant degradation occurred during the experiments (3.5 days).

Lomusti ne The initial experiment indicated that the solubility was about 12 mg/g in 50% w/w HPCD/HgO solution. The results of the follow-up experiments are shown in TABLE VI. Some degradation occurred.

Melphalan The initial experiment indicated that the solubility was about 21.9 mg/g in 50% w/w HPCD/HgO solution (sonication for one hour followed by equilibration at 30° for 4 hours). The results of the follow-up experiments are shown in TABLE VII. Some degradation occurred. -123TABLE V Solubility of chlorambucil in aqueous solutions of 2hydroxypropy!-6-cyclodextrln (HPCD) at 30.0±0.2ο0. % w/v HPCD Solubi1ity (1) (mg/mL) (2) 0 0.01 0.41 1 0.74 0.55 2 1.48 0.84 3 2.37 0.68 4 3.22 1.50 5 1.46 1.80 7 2.71 3.76 10 4.96 5.20 15 6.36 7.60 20 8.49 13.09 25 8.85 18.40 (1) Sonication for 45 min. followed by equilibration at 30° for 3 hours. (2) Sonication for 4 hours followed by equilibration at 30° for 3.5 days. -124TABLE VI Solubility of lomustine in aqueous HPCD solutions at 30+0.2eC. % w/w HPCO Solubility (mg/mL)* 0 0.18 1 0.38 5 1.68 10 3.33 15 6.26 20 8.44 25 8.9 *) The figures shown are average numbers from up to four experiments. Solubi11ty of melphal TABLE VII an in aqueous HPCO solutions at 30.0±0.2°C. % w/v HPCD Solubility (mg/mL)* 0 1.26 1 4.16 2 4.3 3 6.24 4 7.14 5 7.2 7 10.5 10 13.37 15 17.64 20 24.75 25 31.36 *) The figures shown are average values of several experiments . -125TABLE VIII Chiorambuci1 Lomustine Melphalan p.o. dose, *) 0.1-0.2 mg/kg** 130 mg/m^*** 2-35 mg** i.v. dose, *) - - - solubility in water (mg/g) 0.41 0.18 1.26 solubility in 25% w/v HPCD (mg/g) 18.40 8.9 31.36 solubility in 20% w/v HPCD (mg/g) 13.09 8.44 24.75 increase: water/25% HPCD 44.88 49.44 24.89 *) From the Icelandic drug manual. **) Daily dose.

***) Every 6 weeks.

Solubility Studies Phase-solubility experiments were conducted by adding excess amounts of alfaxalone to phosphate buffer solutions containing 20% w/v of selected cyclodextrins and sonicating the mixtures for at least one hour.

(The phosphate buffer solution was prepared by dissolving 1.183 g KH2PO4 and 4.320 g NazHPO^ in water and diluting to 1 liter.) The mixtures were filtered through .45 um Millipore syringe filters and diluted and the drug concentrations were measured by reversed phase HPLC methods. Alfaxalone itself is virtually insoluble in water. -126HPLC Methods for Alfaxalone Wavelength: 294 nm Mobile phase: methanol:water (65:35) Flow rate: 1.5 mL/min.

Retention tiem: ~ 14 min.

The results of these studies are summarized in TABLE IX below.

TABLE IX IQ Solubilization of Alfaxalone by 20% w/v Solutions of Selected Cyclodextrins at Room Temperature Cyclodextrin Solubility (mg/mL) maltosyl-8-cyclodextrin mixture 20.02 hydroxypropyl-γ-cyclodextrin 18.41 hydroxypropyl-γ-cyclodextrin 15.11 hydroxypropyl-8-cyclodextrin 22.83 hydroxypropyl-B-cyclodextrin 24.42 The following Examples illustrate the preparation of preferred reduced, dihydropyridine * pyridinium salt redox carrier systems for brain-targeted drug delivery which are contemplated for use in accord with the present invention and which have not been specifically described in publications to date. -127EXAMPLE 1 Preparation of N-Nicotinoyldopamine: To a pyridine solution containing 11.7 g (0.05 mol) dopamine hydrobromide and 6.15 g (0.05 mol) nicotinic acid at 0°C were added 10.3 g (0.05 mol) dicyclohexylcarbodiimide (OCC). The reaction mixture was stirred at room temperature for 24 hours and the formed dicyclohexylurea was removed by filtration. The pyridine was removed in vacuo and the residue was crystallized from water at 0°C. The product was isolated by filtration and dried over phosphorous pentoxide. Recrystallization from isopropanol gave 9.0 g (0.035 mol), 70% N-nicotinoyl dop amine, m.p. 159162°C; aqueous solution of the compound gave a green color with Fe+3 and reduced AgNOg; IR (KBr) 3300, 2960, 1725, 1630, 1590, 1520, 1430, 1290, 1190, 1115, 720 and 710 cm-1; NMR (dg-OMSO) 6 9.25-6.25 (m, 7H), 3.3 (m, 2H) and 2.65 (m, 2H) ppm. Anal. (C^H^N^Og) C, Η, N.

EXAMPLE 2 Preparation of 1-Methyl-3-fN-[8-(3,4-dihydroxyphenyl)ethyl] }carbamoy1pyridinium iodide: To a solution of 2 g (7.7 mmol) of N-πicotinoy1 dopamine in 40 mL of dry methanol were added 2.5 g (17.6 mmol) of methyl iodide. The reaction mixture was refluxed with stirring for 6 hours. Methyl iodide (1.5 g, 1.05 mmol) was added and refluxing was continued overnight. Methanol was removed and ethyl acetate was added, affording yellowish crystals of the desired product. Yield 2.4 g (77%), m.p. 173-174°C. -128EXAMPLE 3 Preparation of 1-Methyl-3-|N-C[g-E3,4-bis(isobutyryl oxy)phenyl jethyljj )carbamoylpyridi nium tri f1uoroacetate: To an ice-cold solution of the product of Example 2 (3 g, 7.5 mmol) in 30 mL of trifluoroacetic acid, isobutyryl chloride (2.4 g, 22.5 mmol) was added slowly, with stirring. Stirring was continued overnight at room temperature. Trifluoroacetic acid was evaporated under vacuum and the residue was crystallized from ethyl etherrhexane (3:1). Yield 1.2 g (30.4%), m.p. 87-91°C.

EXAMPLE 4 Preparation of l-Methyl-3-{N-EEg-E3,4-bis(isobutyry1oxy)pheny1jethyl]]}carbamoy1-1,4-dihydropyridine: A solution of 0.55 g (1 mmol) of 1-methy1-3-(ΝΕΕ β-[3,4-bi s(isobutyryloxy)phenyljethylj] }carbamoylpyridinium trifluoroacetate in 50 mL of deaerated water containing 10 mL of methanol was extracted three times with 30 mL portions of ether. To the resultant aqueous solution were added NaHCOj (0.25 g, 3 mmol) and 50 mL of ethyl ether and the mixture was kept under nitrogen. To this ice-cold mixture was added sodium dithionite (0.52 g, 3 mmol) and the mixture was stirred vigorously for 30 minutes. The ether layer was separated and the aqueous layer was extracted twice with ether. The combined ether extracts were washed with water and dried over sodium sulfate. Ether was removed under vacuum, leaving an oily product. NMR analysis confirmed that the product had the structural formula: CHj EXAMPLE 5 Preparation of 5,5-0iphenyl-3-hydroxymethyl-2,4imidazolidi nedi one : Phenytoin (5 g, 0.02 mol) was suspended in 180 mL of water; 20 mL of formaldehyde (37% solution) and 0.25 g K2C03 were added and the mixture was stirred at 2530*C for 24 hours. The white solid which formed was removed by filtration and washed repeatedly with a 3% solution of formaldehyde, then air-dried for 3 to 4 hours and over P20g in a vacuum dessicator. Yield 9193%, m.p. 185-189°C. Anal. calc, for C16H14N203: C, 68.07; H, 5.00; N, 9.93. Found: C, 67.97; H, 5.05; N, 9.93. The product had the formula: -130EXAMPLE 6 Preparation of 5,5-Diphenyl-3-((31-pyridyl)carbonyloxymethyl3-2,4-imidazolIdinedione: The product of Example 5 (3.00 g, 0.011 mol) was 5 dissolved in 150 mL of dry pyridine, then nicotinic anhydride (4.25 g, 0.019 mol) was added. The resultant solution was stirred at room temperature (25-30°C), under dry conditions, for 40 hours. The solution was poured into 2.5 L of water and the resultant white solid was removed by filtration, washed well with water and dried over PgOg in a vacuum dessicator. 95t yield, m.p. 178-182°C. Anal calc, for CggHj^NgO^: C, 68,21; H, 4.42; N, 10.85. Found: C, 68.12; H, 4.43; N, 10.83. The product had the formula: 8 15 fl © · EXAMPLE 7 Preparation of 5,5-Diphenyl- 3 -C(1’-methyl-3'-pyri- di n i um)carbonyloxymethyl3-2,4-imi dazolidinedione iodide; The product of Example 6 (0.5 g, 0.0013 mol) was dissolved in 50 mL of acetonitrile, then 0.3 mL of methyl Iodide was added and the reaction mixture was maintained at room temperature for 6 days. The solvent -131was removed by vacuum distillation and ethyl ether was added to the residue. The ether solution was refrigerated for 2 hours, then the yellow, hygroscopic crystals which formed were dried over PgOg in a vacuum dessicator, giving the desired product in 85X yield.

UV and H^NMR spectra confirmed that the product had the st ructure: Repeating the above procedure in nitromethane at a 50-70°C bath temperature using excess methyl iodide, added gradually, for 5 to 6 hours, afforded the same product in nearly quantitative yield.

EXAMPLE 8 Preparation of 5,5-Diphenyl-3-[(1'-methyl-1',4'15 di hydropyri di n-31-yl) carbonyloxymethyl]-2,4imidazolidinedione: The quaternary salt obtained in Example 7 (0.4 g, 0.0008 mol) was dissolved in 40 mL of water, 3 mL of methanol and 15 mL of ethyl acetate. The reaction mixture was cooled to 0 to 5°C and deaerated, then sodium bicarbonate (0.39 g, 0.0046 mol) and sodium dithlonlte (0.54 g, 0.0032 mol) were added. The mixture was stirred under nitrogen at 0-5°C for 35 minutes. The organic layer was removed and the aqueous -1321 ayer was extracted twice with 15 mL portions of ethyl acetate and the organic solutions were extracted with 10 mL of cold deaerated water. After drying over Na2S0^, the solvent was removed by vacuum distillation and the oily yellow solid was crystallized by addition of ether. Yield 70%. UV and H^NMR analyses confirmed that the product had the formula: Preparation of 3-Bromoacetyloxymethyl-5,5-diphenyl-2,4imidazolidi nedione: ,5-Di phenyl-3-hydroxymethyl-2,4-imidazolidinedione (2 g, 0.0071 mol) was dissolved in bromoacetylchloride (15 g, 8 mL, 0.096 mol) by heating in an oil bath (70-80°C bath temperature) for about 15 minutes, until the formation of HCI ceased. The mixture was cooled and 30 mL of ethyl ether were added. White crystals formed. The mixture was cooled to 0eC, then the crystals were removed by filtration and dried over P205. Yield: 2.15 g (75%), m.p. 179-183°C. Anal, calc, for C18H15N204Br: C, 53.61, H, 3.75; N, 6.95; Br, 19.82. Found: C, 53.60; H, 3.79; N, 6.92; Br, 19.90. The product had the formula: Preparation of 3-(3'-Bromopropionyl)oxymethyl-5,5diphenyl-2,4-imidazolidinedione: ,5-Oiphenyl-3-hydroxymethyl-2,4-imidazol idi nedione (5 g, 0.018 mol) was reacted according to the procedure of Example 9 with 3-bromopropionyl chloride (6.8 g, 0.04 mol, 4 mL) using a bath temperature of 100°C. A white crystalline product was obtained in 65% yield (4.9 g), m.p. 133-134’C. Anal. calc, for C19H17N2°4Br: C* 54·69'. Η, 4·Π; N, 6.72; Br, 19.15. Found: C, 54.79; H, 4.12; N, 6.69; Br, 19.25. The product had the formula: EXAMPLE 11 Preparation of 3-(2'-ΒΓοπορΓορΐοηγ1)oxymethy1-5,5d1phenyl-2,4-1mldazol1 di nedione: ,5-01 phenyl-3-hydroxymethyl-2,4-1m1dazol1d1nedione (2 g, 0.0071 mol) was dissolved in 2-bromoproΓ -134i pionyl chloride (8.5 g, 5 mL, 0.05 mol) by heating for 30 minutes on a 100-110°C oil bath. The reaction mixture was cooled, 20 mL of ethyl ether were added, and the resultant solution was extracted with aqueous potassium carbonate, dried and then crystallized. The product was obtained as a solid white substance (1 g, 34%), m.p. 112-115’C. Anal. calc, for C19H17N204Br: C, 54.69; H, 4.11; N, 6.72; Br, 19.15. Found: C, 54.77; H, 4.15; N, 6.69; Br, 19.25. The product had the formula: EXAMPLE 12 Preparation of 3-(3'-Carbamoyl-11-pyridinium)acetyloxymethy1-5,5-diphenyl-2,4-imidazolidinedione bromide : The product of Example 9 (2.02 g, 0.005 mol) dissolved in 15 mL of nitromethane was mixed with nicotinamide (0.61 g, 0.005 mol). The solution was stirred on a 90-100°C temperature oil bath for 2 hours. The mixture was cooled to 60-70°C and the white crystals which had formed were removed by filtration and washed with nitromethane. Yield 61% (1.65 g), m.p. 193-197eC (dec). Anal. calc, for C^H^N^OgBr: C, 54.87; H, 4.03; N, 10.67; Br, 15.21. Found: C, 54.70; H, 4.05; N, 10.64; Br, 15.25. The product had the formula: EXAMPLE 13 Preparation of 3-C3'-(3ll-Carbamoy1-ll,-pyridinium)propi onyloxymethyl]-5,5-dipheny1-2,4-imidazolidinedione bromide: The product of Example 10 (2.09 g, 0.005 mol) was dissolved in 15 mL acetonitrile, then nicotinamide (0.61 g, 0.005 mol) was added. The solution was refluxed for 6 days, then the solvent was removed. To the gum-like residue, 30 mL of ethyl ether was added and the mixture was stirred for 2 hours. The white substance which formed was removed by filtration and washed with ether. Yield 78% (2.1 g); m.p. 98-100°C (dec.); UV and H^NMR as expected. The product had the formula: -136EXAMPLE 14 Preparation of 3-[2'-(3'*-Carbamoyl-l'l-pyridiniuM)propionyloxymethyl]-5,5-diphenyl - 2,4-imidazolidi nedione bromide : The product of Example 11 (0.69 g, 0.00165 mol) was dissolved in 8 mL of acetonitrile, then nicotinamide (0.2 g, 0.00165 mol) was added and the solution was refluxed for 22 hours. The solvent was removed from the resultant brown noncrystalline substance at 50°C, then ethyl ether (15 mL) was added and the mixture was stirred for 2 hours. The light brown substance was removed by filtration and washed with ether. Yield 56% (0.5 g), m.p. 158°C (dec.). The product had the formula: EXAMPLE 15 Preparation of 3-[(3'-Carbamoyl-1',41-dihydropyridin11-yl) acetyloxymethyl]-5,5-dipheny1-2,4-imidazolidinedione : The product of Example 12 (0.52 g, 0.001 mol) was dissolved in a mixture of 60 mL of water and 30 ml. of ethyl acetate. The mixture was cooled at 5°C and deaerated, then sodium bicarbonate (0.5 g, 0.006 mol) and sodium dithlonite (0.7 g, 0.004 mol) were added and the resultant mixture was stirred, with deaeration and -137cooling, for 30 minutes. The layers were separated and the aqueous layer was extracted with 30 mL of ethyl acetate. The organic solution was extracted with 20 mL of cooled, deaerated water. After drying over sodium sulfate, the solvent was removed. Yield 55% (0.25 g) of yellow crystals, melting at 155-160°C (dec.). The product reduced alcoholic silver nitrate solution and had the formula: EXAMPLE 16 Preparation of 3-[31 -(310 11 * * * 15-Carbamoyl-11',411-dihydropyri di n-l1 1-yl)propi onyloxymethyl]-5,5-dipheny1-2,4imi dazolidi nedi one : Substitution of the product of Example 13 in the general procedure of Example 15 and substantial repetition of the sodium dithionite reduction there detailed afforded the desired product in 85% yield. The product melted at 100°C (dec.) and had the formula: ONH. -138The product of Example 14 can be similarly reduced· to the corresponding dihydro derivative, melting at 105°C (dec.).

EXAMPLE 17 Preparation of 4-Aminobutanoic acid cyclohexy! ester hydrochloride : GABA (8 g, 77.6 mmol) was suspended in 100 ml. (0.96 mol) of cyclohexanol. Thionyl chloride (40 mL) was added dropwise to the mixture at 0°C. The mixture was then refluxed for 4 hours, cooled and crystallized from ethyl ether. The white crystals obtained in this manner were filtered and dried. NMR analysis confirmed the identity of the product.

EXAMPLE 18 Preparation of 3-{N-[(31-Cyclohexyloxycarbonyl) propyl]}carbamoylpyridi ne: Nicotinic acid (2.2 g, 18 mmol) was suspended in 50 ml of dry pyridine. Dicyclohexylcarhodiimide (3.68 g, 17.9 mmol) was dissolved in the solution, with stir20 ring. 4-Aminobutanoic acid cyclohexyl ester hydrochloride (4 g, 18 mmol) was added and the mixture was stirred for 48 hours. Precipitated dicyclohexylurea was removed by filtration and the filtrate was evaporated to dryness. The residue was washed with 25 mL of ice cold water and extracted into ethyl acetate. The layers were separated and the organic layer was evaporated to dryness. NMR analysis confirmed the structure of the product. -139EXAMPLE 19 Preparation of 1-Methyl-3-{N*-[(3'-Cyclohexyloxycarbonyl ) propyl] }carb amoylpyridinium iodide: The product of Example 18 (1.74 g, 6 mmol) was dissolved in a minimum amount of acetone and the resulting white precipitate was filtered. Methyl iodide (1.5 mL, 24 mmol) was added in one portion to the solution, with stirring, at 0°C. The mixture was allowed to gently reflux overnight. Filtration of a white precipitate and evaporation of the yellow filtrate produced a reddish oil, which was dissolved in acetone, filtered and evaporated to dryness. Anal, calc, for C22H2303N2I: C, 47.26; H, 5.79; N, 6.48; I, 29.38. Found: C, 47.03; H, 5.85; N, 6.44; I, 29.26.

EXAMPLE 20 Preparation of 1-Methyl-3-{N-[(31-cyclohexy!carbonyl )propyl]}carbamoyl-1,4-dihydropyridine: The product of Example 19 (0.11 g, 0.26 mmol) was dissolved in 25 mL of ice cold deaerated water. NaHC03 (0.09 g, 4-fold excess) was added, followed by Na2S204 (0.14 g, 3-fold excess). Ethyl acetate (25 mL) was added and the mixture was stirred under nitrogen for 30 minutes. The organic layer was extracted and dried to give an orange oil that reduced methanolic silver nitrate immediately. NMR analysis confirmed that the product had the structure: IHCH2CH2CH2 -140EXAMPLE 21 Preparation of Valproic acid chloride (2-Propylpentanoyl chloride): To 4.32 g (30 mmol) of valproic acid in an ice 5 bath, thionyl chloride (3.60 g, 30 mmol) was slowly added, with stirring. The neat mixture was allowed to come to room temperature and then heated in a water bath at 50®C for 30 minutes. 50 mL portions of dry benzene were twice added and removed under reduced pressure. The resultant product was used in subsequent reactions without further purification.

EXAMPLE 22 Preparation of Valproic acid 2-iodoethyl ester (2‘Iodoethyl 2-propylpentanoate): To the product of Example 21 (4.87 g, 30 mmol), 2iodoethanol (5.16 g, 30 mmol) was added with stirring and cooling in an ice bath. The neat mixture was then heated to 100°C in a water bath for 10 minutes, then removed from the heat and stirred for an additional 10 minutes. The reaction mixture was then dissolved in 50 mL of ether, washed with water (1 x 30 mL), 5% NaOH (2 x 30 mL), and again with water (2 x 30 mL). The ether layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. A light yellow liquid product was obtained in 67% yield from valproic acid (6.0 g). Silver nitrate gave a bright yellow precipitate. NMR analysis confirmed the identity of the product. -141EXAMPLE 23 Preparation of l-[2‘-(2'1-Propyl)pentanoyloxyjethyl-3carbamoylpyridinium iodide: The product of Example 22 (3.28 g, 11 mmol) and 50 5 ml of dimethylformamide were added to nicotinamide (1.22 g, 10 mmol). The mixture was heated to reflux for 3 hours, then was cooled. Removal of solvent under reduced pressure afforded a brown oily residue, which was stirred with ether (60 mL) for 30 minutes, giving a yellow powder. The ether was decanted and a fresh portion of ether (50 mL) was added. The crude product was vacuum filtered under Ng, then was recrystal 1ized from isopropanol/ether to give 3.5 g of the desired product (84% yield), m.p. lll-112eC. The product had the formula: EXAMPLE 24 Preparation of l-[21 -(211-Propyl)pentanoyloxyjethyl-3carbamoy1-1,4-dihydropyridine: To 50 mL of ice-cold degassed deionized water, the product of Example 23 (420 mg, 1 mmol) was added. To that solution, NaHCOg (366 mg, 4 mmol) and NagSgO4 (696 mg, 4 mmol) were added, with stirring. Nitrogen gas was bubbled through the solution for 30 minutes. The aqueous solution was then extracted with ether (6 x 25 -142mL) until the ether layer was no longer yellow. The combined ether extracts were washed with water (1 x 50 mL) and dried over MgS04. The ether layer was decanted from the drying agent and the solvent was removed under reduced pressure. To the oily residue, ether was added and then removed (10 x 5 mL) on a vacuum pump. A foam was formed, which returned to an oil upon exposure to the atmosphere. Structure was confirmed by NMR analysis.

EXAMPLE 25 Preparation of N-Nicotinoyltyrosine ethyl ester: Nicotinic acid (12.3 g, 0.1 mol) was dissolved in dry pyridine (300 mL). The solution was cooled and dicyclohexylcarbodiimide (20.6 g, 0.1 mol) was added.

After dissolution, tyrosine ethyl ester hydrochloride (24.6 g, 0.1 mol) was added and the solution was stirred overnight. The precipitated dicyclohexylurea (DCU) was removed by filtration. Additional OCU was removed by triturating the oil with hot water. The product was purified with acetone. Calculated for C17H18N2°4* 1/2H20: c« 63·16'» H> 5·88’· N» 8.66.

Found: C, 63.10; H, 5.96; N, 8.59. The product can also be named N-[1-ethoxycarbonyl-2-(41-hydroxyphenyl )ethyl]nicoti namide. 25 EXAMPLE 26 Preparation of N-C(1-Methyl-3-pyridinium)carbonyl]tyrosine ethyl ester Iodide: N-N1cot1noyltyrosine ethyl ester (20 g, 0.06 mol) was dissolved in 200 mL of acetone. A two molar excess -143of methyl Iodine (25.6 g, 0.18 mol) was added and the mixture was refluxed for 6 hours. The solvent was removed under reduced pressure to yield the desired product as a solid form. NMR analysis confirmed the identity of the product, which had the structural formula : and can also be named 1-methyl-3-{N-[(1'-ethoxycarbonyl )-2'-(4''-hydroxyphenyl)ethyl Jcarbamoyl 10 pyridinium iodide.

EXAMPLE 27 Preparation of 1-Methyl-3-fN-C(11-ethoxycarbonyl )-2 1 (4*1-pivaloyloxyphenyl)ethyl]fcarbamoylpyridini um tri f1uoroacetate: The product of Example 26 (6 g, 0.013 mol) was dissolved in 50 mL of cold trif1uoroacetic acid at 0°C in an ice bath. Pivaloyl chloride (3.14 g, 0.026 mol) was slowly added and the solution was warmed to room temperature. After 24 hours, the solvent was removed under reduced pressure. The resulting dark oil was triturated with petroleum ether but no solidification occurred. Identity of the product was confirmed by NMR analysis. The product was dissolved 1n aqueous methanol (10%) and extracted with ethyl ether to remove -144a highly colored contaminant before using as the starting material in Example 29 below.

EXAMPLE 28 Preparation of 1-Methyl-3-|N-[(1'-ethoxycarbonyl)-2' 5 (4'1-isobutyryloxyphenyl) ethyl]fcarbamoylpyridinium tri f1uoroacetate: The product of Example 26 (6 g, 0.013 mol) was dissolved in 50 mL of trifluoroacetic acid cooled to O’C in an ice bath. To that solution, with stirring, was slowly added isobutyryl chloride (2.77 g, 2.76 mL). The solution was stirred overnight at ambient temperature and the solvent was removed under reduced pressure. The oil was stirred overnight with petroleum ether and then dried in vacuo, but no solidification occurred. Identity of the product was confirmed by NMR analysis. The product was dissolved in aqueous methanol (10%) and extracted with ethyl ether to remove a highly colored contaminant before using in Example 30 below. -145EXAMPLE 29 Preparation of 1-Methyl-3-|N-[(11-ethoxycarbonyl)-2*(4''-pi val oyloxyphenyl)ethy1] lcarbamoyl -1,4-di hydropyridi ne: The product of Example 27 (4.07 g, 0.0079 mol) was dissolved in 100 mL of 25% aqueous methanol. Nitrogen gas was bubbled through the solution. To the solution, stirring in an ice bath, was then added NaHCOs (2.02 g, 0.024 mol). Ethyl ether (100 mL) was added, followed by the addition of Na2S204 (4.12 9» 0.024 mol). The yellow biphasic solution was stirred for 30 minutes, then the layers were separated and the aqueous layer was extracted twice with 75 mL portions of ethyl ether. The combined organic fractions were dried over NagSO^ and the solvent was removed under reduced pressure to afford a solid foam which was oxidized by ethanolic silver nitrate. Anal. calc, for CggHggNgOg •l/2H20: C, 65.23; H, 7.33. Found: C, 65.76; H, 7.28; N, 6.95. -146EXAMPLE 30 Preparation of 1-Methyl-3-(N-[(11-ethoxycarbonyl)-2*(4''-1 sobutyryloxyphenyl)ethyl] }carbamoyl-1,4di hydropyri di ne: The product of Example 28 (2.20 g, 0.0044 mol) was dissolved in 100 mL of aqueous methanol. The solution was cooled in an ice bath with a stream of N? passing through it. To this solution, NaHC03 (1.11 g, 0.0132 mol) and ether (100 mL) were added. Then, sodium dithionite (2.30 g, 0.0132 mol) was added and the solution was stirred for 30 minutes. The layers were separated and the aqueous phase was washed with ethyl ether. The combined organic layers were dried over anhydrous Na2S04 and reduced in volume. The resultant orange oil was oxidized by ethanolic silver nitrate. Identity of the product was confirmed by NMR analysis.

EXAMPLE 31 Preparation of Chloromethyl [2S-(2a,5a,6fl)]-3,3d imethyl-7-oxo-6-[(2,6-dimethoxy)benzamido]-4-thia-lazabi cyclo[3.2.0]heptane-2-carboxy!ate: To a solution of 4.02 g (0.01 mol) methicillin sodium salt in 10 mL water and 10 mL CHgClg. 2.4 g sodium bicarbonate and 0.34 g tetrabutylammonium hydrogen sulfate were added. Then, 1.9 g (0.0115 mol) chloromethyl chlorosulfate dissolved in 3 mL CH2C12 were added with stirring, over a 5 minute period, keeping the temperature below 30°C. After an additional 30 minutes of stirring, the organic phase was separated, washed twice with water and dried over MgS04. By removing the solvent in vacuo, 4.24 g of the -147desired product were obtained as a yellow solid, melting at 88-90°C.

EXAMPLE 32 Preparation of Chloromethyl C2S-(2a,5a,6 β)]-3,35 dimethyl-6-(5-methyl-3-phenyl-4-i soxazolecarboxamido)7-oxo-4-thia-l-azabi cyclo[3.2.0]heptane-2-carboxylate: Substantial repetition of the procedure of Example using 2.12 g (0.005 mol) oxacillin sodium salt with 1.2 g NaHCOg, 0.17 g tetrabutylammonium hydrogen sulfate and 0.95 g chioromethylchiorosulfate afforded 0 1.87 g of the desired product melting at 78-80 C (dec.) EXAMPLE 33 Preparation of Chloromethyl [2S-(2a,5α,βg)]-6-[3-( 215 chi orophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3di methyl -7-oxo-4-thia-l-azabi cyclo[3.2.0]heptane-2carboxylate: Using the same procedure as in Example 31, but substituting 2.38 g (0.005 mol) cloxacillin sodium salt (1 mol water), 1.2 g NaHC03, 0.17 g Bu4NHS04 and 0.95 g chloromethyl chlorosulfate gave 2.27 g of the desired product melting at 97-100°C (dec.). -148EXAMPLE 34 Preparation of Chloromethyl [2S-(2a,5<»,6B)]-6-[3-(2,6dichl orophenyl)-5-methyl-4-i soxazol ecarboxamido]-3,3dimethyl-7-oxo-4-thia-l-azabi cyclo[3.2.0]heptane-25 carboxyl ate: Similarly, following the procedure of Example 31 but using 2.55 g (0.005 mol) did oxaci 11 i n Na salt (1 mol water) with 1.7 g NaHCOg, 0.17 g BU4NHSO4 and 0.95 g chloromethyl chlorosulfate, 2.43 g of product were obtained melting at 98-101°C (dec.).

EXAMPLE 35 Preparation of [ ( 3-Pyridi nyl carbonyl) oxyjmethyl ['2S(2a,5a,6B)]-3,3-dimethyl-7-oxo-6-[(2,6-dimethoxy)benzamido]-4-thia-l-azabicyclo[3.2.0]heptane-2-cairboxy15 1 ate : Three and eight-tenth grams (0.0089 mol) of the methicillin chloromethyl ester produced in Example 31 and 1.6 g (0.01 mL) potassium nicotinate in 70 mL OMF were stirred 6 days at room temperature (20-25°C). 300 mL ethyl acetate were added, the resultant solid was removed by filtration and the solution was extracted 4 times with 50 mL concentrated aqueous NaCl and dried over MgSO^. The solvent was removed in vacuo and the resultant residue was purified by chromatography (silica gel). Obtained as a white solid were 3 g of the desired product melting at 151-157°C. -149EXAMPLE 36 Preparation of [(3-Pyridinylcarbonyl)oxy]methy! [2S(2a,5a,6g)]-3,3-dimethyl-6-(5-methyl-3-pheny1-4-i soxazolecarboxamido)-7-oxo-4-thi a-l-azabi cyclo[3.2.015 heptane-2-carboxyl ate : Following the procedure of Example 35, but utiliz ing 1.81 g (0.004 mol) of the oxacillin chloromethyl ester produced in Example 32 and 0.75 g (0.0046 mol) K nicotinate, afforded, after purification by chromato10 graphy, 0.75 g of the desired product as a white solid melting at 79-82°C (dec.).

EXAMPLE 37 Preparation of [(3-Pyridinylcarbonyl )oxy]methyl [2S(2a,5a,6B)]-6-[3-(2-chlorophenyl)-5-methyl-4-isoxazole carboxamidol-3,3 dimethyl-7-oxo-4-thia-l-azabicyclo[3.2.0]heptane-2-carboxylate: Using the procedure of Example 35, but substituting 2.1 g (0.0043 mol) of the cloxacillin chloromethyl ester produced in Example 33 and 0.8 g (0.005 mol) K nicotinate, gave 1.2 g of product melting at 83 85°C (dec.).

EXAMPLE 38 Preparation of [(3-Pyridinylcarbonyl)oxy]methyl [2S(2a,5a,68)]-6-[3-(2,6-dichlorophenyl)-5-methy1-4-isoxa· zo1ecarboxamido]-3,3-dimethy1-7-oxo-4-thia-l-azabicyclo[3.2.0]heptane-2-carboxylate: Similarly, following the procedure of Example 35 but using 2.27 g (0.0047 mol) of the did oxaci 11 i n chloromethyl ester produced in Example 34 and 0.87 g -150(0.0054 mol) K nicotinate afforded 1.1 g of the product as a white solid melting at 87-90°C (dec.).

EXAMPLE 39 Preparation of [2S-(2a,5a,66)3-3-C[C[[3,3-Dimethyl-75 oxo-6-C(2,6-dimethoxy)benzamido]-4-thia-l-azabi cycl o[3.2.0]hept-2-ylIcarbonyl]oxy]methoxyIcarbonyl ]-lmethylpyridinium iodide: One and one-fourth grams (0.0024 mol) of the methicillin derivative produced in Example 35 in 35 mL nitromethane and 1.14 g (0.5 mL) (0.008 mol) methyl iodide were reacted in a closed system at room temperature (20-25°C) for 7 days. The solvent was removed in vacuo, the resultant residue was stirred with ether, filtered off, washed with ether and dried. There were thus obtained 1.6 g of yellow hygroscopic product melting at 95-100°C and being further characterized by the structural formula: XH o' -151EXAMPLE 40 Preparation of [2S-(2a,5a,66)]-3-[[C[[3,3-dimethyl-6(5-methy 1-3-phenyl-4-isoxazol ecarboxamido)-7-oxo-4thia-l-azabi cyclo[3.2.0]hept-2-yl]carbonyl]oxy]5 methoxy]carbony13-1-methylpyridini um iodide: Using the procedure of Example 39, but substituting 0.5 g (0.0009 mol) of the oxacillin derivative produced in Example 36 in 25 mL nitromethane and 0.45 g (0.2 mL) (0.003 mol) CH3I produced, after 6 days, 0.6 g of the desired product melting at 75-80°C and having the formula: EXAMPLE 41 Preparation of [2S-(2a,5a,68)]-3-CCCCC6-[3-(2-chloro15 phenyl )-5-methyl-4-isoxazo1ecarboxamido3-3,3-dimethyl7-oxo-4-thia-l-azabicyclo[3.2.0]hept-2-yl]carbonyl]oxyjmethoxyjcarbonyl]-1-methylpyridini um iodide: Similarly, using the procedure of Example 39, but substituting 0.44 g (0.0008 mol) of the cloxacillin derivative produced in Example 37 in 25 mL nitromethane and 0.45 g (0.2 mL) (0.003 mol) CH3I, gave 0.45 g of product melting at 90-95°C (dec.) and having the formula : EXAHPLE 42 Preparation of [2S-(2q,5a,6g)-3-[[CC[6-C3-(2,6dichlorophenyl )-5-methyl-4-isoxazolecarboxamido]-3,35 dimethyl-7-oxo-4-thi a-l-azabi cyclo[3.2.0]hept-2-ylΙο a rbonyl ]oxy]methoxyJcarbonyl]-l-methylpyri di ni um iodide: In a similar manner, using the procedure of Example 39, but substituting 0.5 g (0.007 mol) of the did oxaci 11 i n derivative produced in Example 38 in 25 mL nitromethane and 0.45 g (0.2 mL) (0.003 mol) CH3I gave 0.55 g of product melting at 95-100°C (dec.) and having the formula: -153EXAHPLE 43 Preparation of [[(1,4-Dihydro-l-methyl-3-pyridinyl) carbonyl]oxylmethyl C2S-(2a,5a,6 6)]-3,3-diwethy1-7-oxo6-[(2,6-dimethoxy)benzamido]-4-thi a-l-azabicycl o5 C3.2.0]heptane-2-carboxylate: 0.45 g (0.0007 mol) of the product of Example 39 dissolved in a mixture of deaerated 25 mL ethyl acetate and 70 mL water were reduced with a mixture of 0.34 g (0.004 mol) NaHC03 and 0.48 g (0.0028 mol) sodium dithionite at 0-5°C over 70 minutes. The disappearance of the 268 nm maxima and increase of 366 nm maxima in the U.V. spectra were followed. The 1ayers were separated and the aqueous layer was extracted with 2 x 25 mL ethyl acetate, then the organic layers were extracted with 2 x 20 mL cold, deaerated water. After drying over Na2SO4, the solvent was removed in vacuo. 0.25 g of the product was obtained as a yellow solid melting at 88-90°C (dec.). The product had the formula : L3 -154EXAHPLE 44 Preparation of [[(1,4-Dihydro-l-methyl-3-pyridinyl )carbony1]oxy]methy1 [2S-(2a,5a,6 fl)]-3,3-dimethy1-6-(5methyl-3-phenyl-4-isoxazolecarboxamido)-7-oxo-4-thia-l5 azabi cycl o[3.2.0]heptane-2-carboxy1ate: Similarly, repetition of the general procedure of Example 43 using 0.17 g (0.00025 mol) of the product of Example 40, 0.08 g (0.0001 mol) NaHC03 and 0.51 g (0.001 mol) Na2S204, in 15 mL water and 15 mL ethyl acetate, afforded 0.1 g of product melting at 93-100°C (dec.). The product had the formula: EXAMPLE 45 Preparation of [[(1,4-Dihydro-l-methyl-3-pyridinyl)15 carbonyl]oxy]methy1 [2S-(2a,5o,6g)]-6-[3-(2ch1orophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3dimethyl-7-oxo-4-thia-l-azabicyclo[3.2.0]heptane-2carboxylate: In a similar manner, following the procedure of 20 Example 43, but substituting 0.18 g (0.00025 mol) of the product of Example 41, 0.089 NaHCO3 and 0.17 g Na2S204, gave 0.13 g of product as a yellow solid, -155melting at 80-85°C (dec.) and having the structural formula : EXAMPLE 46 Preparation of [[(1,4-Di hydro-1-methyl-3-pyridinyl) carbonyl]oxy]methyl C2S-(2a,5a,6g)]-6-[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl 7-oxo-4-thia-l-azabi cyclo[3.2.0]heptane-2-carboxy1ate : In like manner, repetition of the procedure of 10 Example 43 using 0.19 g (0.00025 mol) of the product of Example 42, 0.08 g NaHCOg, 0.17 g NagSgO^ yielded 0.14 g of desired product melting at 98-102°C (dec.) and having the formula: ci Cl CH -156EXAHPLE 47 Preparation of [(3-Pyridinylcarbonyl)oxyjmethy1 (2S(2o,5a,6 6)3-3,3-dimethyl-7-oxo-6-C(phenyl acetyl) ami noJ4-thi a-l-azabi cyclo[3.2.Ojheptane-2-carboxyl ate: A suspension of 3.83 g (0.01 mol) of the chloromethyl ester of benzylpenicillin, namely chloromethyl [2_S-( 2 a, 5 a, 6 6)3-3,3-dimethyl-7-oxo-6-(( phenyl acetyl) aminoJ-4-th1a-l-azabi cyclo[3.2.Ojheptane-2-carboxylate, and 1.93 g (0.012 mol) potassium pyrid1ne-3-carboxyl ate in 100 mL of dimethylformamide was stirred at 20-25°C for 6 days. Then, 300 mL of ethyl acetate were added and the solid was removed by filtration. The solution was extracted 4 times with concentrated aqueous sodium chloride solution, then dried over MgSO^. The solvent was removed in vacuo to give 4.5 g of foamy solid. Purification by chromatography over silica gel using ethyl acetate as eluent afforded 2.5 g of product melting at 127-130’C.

EXAMPLE 48 Preparation of [2S-(2a,5a,6g)]-3-CCCCC3,3-0imethyl-7oxo-6-C(phenylacety1)amino]-4-thia-l-azabicyclo[3.2.0]hept-2-yl]carbonyl]oxy]methoxyJcarbonyl]-l-methy1pyridinium iodide: Two and one-half grams (0.053 mol) of the product of Example 47 dissolved in 100 mL of dry nitromethane were reacted with 2.25 g (1 mL, 0.016 mol) of methyl Iodide In a closed system at 20-25°C for 6 days, at the end of which time thin layer chromatography showed complete reaction. The solvent was removed in vacuo and the solid residue was slurried with ether, filtered -157and dried in vacuo over P205. The product, melting at 90-95°C (dec.), was obtained as a yellow solid (2.91 g). It was assigned the structural formula: EXAMPLE 49 Preparation of [[(1,4-Dihydro-l-methyl-3-pyridinylCarbonyl ]oxy lmethyl [2S-(2a,5a,6g)]-3,3-dimethyl-7-oxo-6[(phenylacetyl)ami no]-4-thia-l-azabi cyclo[3.2,0]heptane-2-carboxylate: The quaternary salt prepared in Example 48 (3.25 g, 0.0053 mol) was dissolved in a mixture of 350 mL of water and 150 mL of ethyl acetate. The resultant mixture was cooled at 0-5eC and deaerated with nitrogen, then a mixture of 2.67 g (0.032 mol) of sodium bicarbonate and 3.69 g (0.021 mol) of sodium dithionite was added over a 2-3 minute period. The reaction mixture was stirred for 1 hour under the same conditions as before, then the layers were separated, the aqueous layer was extracted twice with 50 mL portions of ethyl acetate, and the combined organic extracts were washed twice with 30 mL portions of cold, deaerated water. Drying over sodium sulfate and removal of the solvent in vacuo afforded 1.7 g of yellow solid melting 98-100*C and having the formula: EXAHPLE 50 Preparation of Chioromethyl N-[3-(10,ll-dihydro)-5Hdibenz[b,f]azepin-5-y1)lpropyl-N-methylcarbamate : Method A: Oesipramine hydrochloride (1.5 g, 0.005 mol) was dissolved in 20 mL of methylene chloride, cooled at 05°C. Then 1 g NaHCOg was added, followed by 0.92 g (0.007 mol) chloromethyl chloroformate. The reaction mixture was stirred for 1 hour, then the salts were removed by filtration and the solution was extracted twice with 10 mL portions of 5% HCI. The organic layer was dried over MgS04 and the solvent was removed in vacuo to give the desired compound as a colorless oily substance in 76% yield (1.35 g).

Method 6: Imipramine hydrochloride (1.59 g, 0.005 mol) was dissolved in 15 mL of water, then 5 mL of 4% sodium hydroxide solution was added, with cooling. The resultant imipramine base was extracted twice with 10 mL portions of benzene. The solution was concentrated -159to 10 mL, then a solution of 0.7 g (0.0054 mol) chloromethyl chloroformate in 5 mL benzene was added with cooling at 10°C. The reaction mixture was stirred at 20-25°C for 30 minutes, then was refluxed for 1 hour.

A small amount of imipramine hydrochloride resulted and was filtered off. The solution was extracted twice with 20 mL portions of 4% HCl and dried over MgSO^. Removal of solvent in vacuo afforded 1.2 g (66%) of product having the same characteristics as that obtained by Method A.

EXAMPLE 51 Preparation of 1-Chloroethyl N-[3-(10,ll-dihydro-5Hdibenz[b,f]azepin-5-y1)lpropy1-N-methylcarbamate : Following the general procedure of Example 50, but 15 using 1.5 g (0.005 mol) of desipramine hydrochloride and 0.86 g (0.006 mol) chloroethyl chloroformate and carrying out the reaction at 5-10°C for 2 hours, gave 1.6 g (86%) of the title compound as a colorless oil.

EXAMPLE 52 Preparation of [{N-[3-(10,ll-Dihydro-5H-dibenz[b ,flazepin-5-yl)lpropy!-N-methylami no [carbonyloxylmethyl 3-pyridinecarboxylate: The product of Example 50 (1.35 g, 0.0037 mol) dissolved in 5 mL dimethylformamide was added to a solution prepared from 0.57 g (0.046 mol) nicotinic acid and 0.45 g triethylamine in 5 mL dimethylformamide. The mixture was stirred for 24 hours at 2530°C, then 30 mL of ethyl acetate were added. The precipitated salts were removed by filtration and the -160solution was extracted 4 times with 15 mL portions of saturated aqueous sodium chloride solution. Drying over MgS04 and removal of the solvent in vacuo afforded 1 g (611) of pure product as an oil.

EXAMPLE 53 Preparation of [1-{N-[3-(10 ,ll-01hydro-5H-dibenz[b,f]azepin-5-yl)Ipropy1-N-methylami no }carbonyloxylethyl 3-pyridinecarboxyl ate: Following the general procedure of Example 52, but 10 using 1.05 g (0.0028 mol) of the product of Example 51, 0.45 g (0.036 mol) of nicotinic acid and 0.36 g of triethylamine in 10 mL dimethylformamide and carrying out the reaction at 25-30’C for 48 hours, gave 0.5 g of the title compound as a yellow oil.

EXAMPLE 54 Preparation of 3-[ |N-[3-(10,11-Dihydro-5H-dibenz[b,f]azepin-5-yl)Ipropy1-N-methylamlno}carbony1oxylmethoxycarbony1-1-methylpyridinium iodide: Eight-tenths gram (0.0018 mol) of the product of 20 Example 52 in 30 mL of nitromethane was methylated with 0.8 mL of methyl iodide at 25-30eC for 48 hours. The solvent was removed in vacuo and the residue was slurried with ethyl ether, filtered and dried over ρ2θ5· The quaternary salt was obtained in 83% yield (0.88 g) as a light yellow solid melting at 172-175eC (dec.) and having the structural formula: EXAMPLE 55 Preparation of 3-[l-{N-[3-(10,ll-0ihydro-5H-dibenz[b , f]a2epin-5-y1)lpropy1-N-methylami nofcarbonyloxy]5 ethoxycarbonyl-1-methylpyridinium iodide: Following the general alkylation procedure of Example 54, but using 0.5 g (0.0011 mol) of the product of Example 53 in 15 mL nitromethane with 0.5 mL methyl iodide, and carrying out the reaction at 20-25°C for 6 days, afforded 0.33 g (50%) of the desired quaternary salt as a dark yellow solid melting at 101-103°C (dec.) and having the structural formula: -162EXAMPLE 56 Preparation of [fN-C3-(10 ,ll-Dihydro-5H-dibenz[b,fjazepin-5-yl )Ipropyl-N-methylamino)carbony1oxy]methyl 1,4-di hydro-1-methyl-3-pyridi necarboxyl ate: Three-tenths gram (0.0005 mol) of the product of Example 54 in 30 mL water and 15 mL ethyl acetate was reduced with 0.25 g (0.003 mol) NaHCOj and 0.35 g (0.002 mol) sodium dithionite at 0-5°C, with deaeration, for a 60 minute period. The layers were separated and the aqueous layer was extracted twice with 30 mL portions of ethyl acetate. The combined organic layers were then extracted twice with 20 mL portions of cool deaerated water. Drying over Na2S04 and removal of the solvent in vacuo afforded 0.22 g (95%) of the title compound, melting at 59-63°C (dec.) and having the structural formula: EXAMPLE 57 Preparation of [1-{N-[3-(10,11-Dihydro-5H-dibenz[b,f]20 azepin-5-yl)Ipropyl-N-methylami no }carbonyloxy]ethyl 1,4-dihydro-l-methyl-3-pyridi necarboxylate: Following the procedure of Example 56, but using 0.1 g (0.0017 mol) of the product of Example 55 1n 10 mL water and 6 ml ethyl acetate, 0.11 g NaHC03 and 0.15 -163g ^262()4 and carring out the reaction for a 60 minute period, gave 0.07 g (88%) of the title compound as a yellow solid, melting at 60-65’C (dec.) and having the structural formula: EXAMPLE 58 Preparation of N-(2-Hydroxyethyl)-3-pyridinecarboxami de : A solution of 49.2 g (0.32525 mol) ethyl nico10 tinate and 72 g (1.17 mol) ethanolamine was heated at 70°C for 60 hours. The excess ethanolamine was removed under reduced pressure and the resulting viscous cream oil was stirred with ether for 48 hours. The resulting white solid was removed by filtration, affording 46 g (85.1%) of the title compound melting at 75-78°C.

EXAMPLE 59 Preparation of 3-[21 -(2-propyl )pentanoyloxy]ethylcarbamoyl pyri d i ne: To a stirred solution of 1.0 g (0.006021 mol) of 20 the product of Example 58 and 0.61 g (0.00598 mol) triethylamine in 40 mL dry dichloromethane, 1.96 g (0.012047 mol) of (2-propyl)pentanoyl chloride were -164added and the mixture was refluxed for 4 hours. The resultant solution was washed sequentially with 30 mL 5% NaHC03, 30 mL 5% HCl and 30 mL water. The organic layer was dried over MgS04 and the solvent was removed under reduced pressure to give 0.6 g (34.3%) of the product as a pale brown oil.

EXAMPLE 60 Preparation of l-Methyl-3-[2'-(2l,-propyl)pentanoyloxy]ethylcarbamoylpyridinium iodide: To a solution of 1 g (0.00342 mol) of the product of Example 59 in 20 mL of dry ethyl acetate, 0.73 g (0.00513 mol) of methyl iodide was added. The reaction mixture was stirred overnight at room temperature. The pale yellow solid which formed was removed by filtra15 tion and recrystallized from ethyl acetate to give 1.35 g (90.9%) of the quaternary salt as a yellow crystalline solid. The product had the formula: as confirmed by IR, NMR and UV analyses. -165EXAMPLE 61 Preparation of 1-Methyl-3-[2‘-(2-propy1)pentanoyloxy]~ ethylcarbamoyl-1,4-dihydropyridine: To 50 mL of vigorously stirred, degassed, ice-cold 5 deionized water, a solution of 3.0 g (0.006909 mol) of the quaternary product of Example 60 in 50 mL of ethyl acetate was added. Throughout the reaction, the temperature and pH were maintained at 0°C and 8 respectively, while nitrogen was bubbled through the reaction mixture. A mixture of 3.5 g (0.04145 mol) of sodium bicarbonate and 4.8 g (0.02763 mol) of sodium dithionite was added portionwise. After 45 minutes, the organic layer was separated and the aqueous layer was extracted with 100 mL of ice-cold ethyl acetate.

The combined organic extracts were washed with ice-cold water and dried over MgSO^. Solvent was removed under reduced pressure to give 2.1 g (98.8%) of the product as a pale yellow solid having the structural formula: as confirmed by IR, NMR and UV analyses. -166EXAMPLE 62 Preparation of 3-Pyridinecarboxyl1c acid (2-hydroxy)ethyl ester hydrochloride: To 120 mL cold (-10°C) ethylene glycol, 16 mL of 5 thionyl chloride were added dropwise. Upon completion of the addition, 24.6 g (0.2 mol) of nicotinic acid were added portionwise and the reaction mixture was. heated overnight at 60°C. Then, 700 mL of hot tetrahydrofuran were added and the mixture was cooled. The solid which formed was removed by filtration and washed with ether to give 28.5 g of the title compound as white crystals.

EXAMPLE 63 Preparation of 3-[21 -(2-Propyl)pentanoyloxyjethoxy15 carbonyl pyridine : To a solution of 10.0 g (0.0491 mol) of the product of Example 62 in 150 mL of dry CH^Cl^. 10.7 g (0.09819 mol) of triethylamine were added. After all of the solid was dissolved, 11.92 g (0.07364 mol) of 220 propylpentanoyl chloride were added and the reaction mixture was stirred at room temperature for 36 hours. Sequential washing with 5% NaHC03, 5% HCl and water afforded an organic layer which was then dried over anhydrous MgS04. Solvent was removed under reduced pressure to give a yellow-brown oil that was triturated with a 40:60 mixture of ether and petroleum ether to yield 9.7 g of the product as an orange oil. -167EXAMPLE 64 Preparation of l-Methy1-3-C2,-(2-Propyl)pentanoyloxy3ethoxycarbony1pyridinium iodide: To a solution of 2.0 g (0.006816 mol) of the product of Example 63 in 10 mL of dry acetone, 1.45 g (0.01022 mol) of methyl iodide were added and the mixture was refluxed overnight. Removal of solvent under reduced pressure afforded 1.84 g of the quaternary salt as a brown oil. The product had the structural formula: EXAMPLE 65 Preparation of 1-Methyl-3-[21-(2-propy1)pentanoyloxy]ethoxycarbonyl-1,4-di hydropyrid i ne: To 50 mL of vigorously stirred, degassed, ice-cold deionized water, a solution of 1.84 g (0.004226 mol) of the quaternary product of Example 64 in 50 mL of ethyl acetate was added. Throughout the reaction, the temperature and pH were maintained at O’C and 8, respectively, while argon was bubbled through the reaction mixture. A mixture of 2.13 g (0.02536 mol) of NaHCOg and 2.94 g (0.0169 mol) of Na2SgO4 was added portionwise. After 55 minutes, the organic layer was separated and the aqueous layer was extracted with 100 mL of Ice-cold ethyl acetate. The combined organic -168layers were washed with ice-cold water and dried over MgSO^. The solvent was removed under reduced pressure to give 0.9 g of the title compound as a yellow oil. The product had the formula: EXAMPLE 66 Preparation of 3,17g-Bis[(3-pyridinylcarbonyl)oxyl-19nor-17a-pregna-l,3,5(10)-trien-20-yne: To 2.0 g (6.7 mmol) of ethinyl estradiol dissolved in 50 mL of dry pyridine were added 6.16 g (0.027 mol) of nicotinic anhydride and a catalytic quantity of 4(dimethylami no)pyridine (OMAP). The solution was warmed gently to 50°C to effect solution. After 2 weeks, the pyridine solution was poured over ice and the solid produced was collected by filtration. The solid was dried over PgO^ in vacuo to give 3 g (85%) of an off-white powder.

EXAMPLE 67 Preparation of 3-Hydroxy-17S-[(3-pyridinylcarbonyl)20 oxy]-19-nor-17a-pregna-1,3,5(10)-trien-20-yne: To 200 mL of 0.5% methanolic KHC03, 2.0 g (3.9 mmol) of the product of Example 66 were added. After 6 -169hours, the slurry was diluted with 200 mL of water and the mixture was extracted with chloroform. The organic layers were combined, dried over MgSO^ and concentrated in vacuo. The resulting oil was triturated with hexane to give 1.48 g (94%) of a white solid. NMR and UV spectra and elemental analysis confirmed the identity of the title compound.

EXAMPLE 68 Preparation of 1-Methyl-3-{[(19-nor-l7a-pregna10 l,3,5(10)-trien-20-yn-17B-y1)oxy]carbonyl [pyridinium iodide: To 50 mL of acetone, 1.0 g (2.5 mmol) of the product of Example 67 was added, followed by 2 mL of methyl iodide. The reaction mixture was refluxed for 12 hours. The solid which formed was collected by filtration, yielding 1.15 g (85%) of the quaternary salt as a yellow solid having the structural formula HO The assigned structure was confirmed by UV and NMR 20 spectral analyses and by elemental analysis. -170EXAHPLE 69 Preparation of 3-Hydroxy-176- {[(1-methyl-1,4di hydropyridin-3-yl)carbonyl]oxy}-19-nor-17a-pregnal,3,5(10)-trien-20-yne: To a cooled suspension of 1.0 g (1.8 mmol) of the product of Example 68 in 100 mL of 50:50 water: tertbutanol, 0.77 g of NaHC03 and 0.96 g of Na2S204 were added. The reaction mixture was stirred at 0°C For 1 hour, then was extracted twice with 100 mL portions of CH2C12. The organic extracts were combined, dried over MgS04 and concentrated under reduced pressure to give 520 mg (69%) of the title compound as a yellow foam.

The product was assigned the structure HO which was in accord with UV and NMR values as well as elemental analysis. -171EXAMPLE 70 Preparation of 3,17B-Bis[(3-pyridinylcarbonyl)oxy]estra-l,3,5(10)-triene: To 5.3 g (0.03 mol) of nicotinoyl chloride in 30 5 mL of dry pyridine at 0°C were added 2.0 g (0.0073 mol) of β-estradiol. The reaction mixture was refluxed for 1 hour, then was poured over 100 mL of ice water, and the resulting precipitate was collected by filtration. The precipitate was dried in vacuo over ρ2θ5» affording 3.18 g (90%) of the title compound melting at 148-150°C.

EXAMPLE 71 Preparation of l.l'-Oimethyl-S^'-ICCestra-l^SflO)triene-3,17B-diy1)dioxy]dicarbonyl |dipyridinium di iodide: To 50 mL of acetone and 2 mL (0.032 mol) of methyl iodide, 2.0 g (0.004 mol) of the product of Example 70 were added. The solution was heated at reflux overnight. The precipitate which formed was filtered, washed with acetone and dried to give 2.75 g (88%) of the quaternary salt melting at 251-252°C and having the structural formula as confirmed by UV, NMR and elemental analyses. -172EXAMPLE 72 Preparation of 3,176-Bls {[(l-methyl-l ,4-di hydropyrii di n3-yl )carbonyl]oxy}estra-l,3,5(10)-triene: One gram (1.31 mmol) of the product of Example 71 5 was dissolved in 100 mL of dry acetonitrile. To that solution, which was flushed with nitrogen, 0.28 g (1.31 mmol) of 1-( phenyl methyl )-4-( ami nocarbonyl )-1,2-dihydropyridine was added, and the reaction mixture was stirred at 0°C for 1 hour. Removal of the solvent under reduced pressure afforded a solid, which was suspended in methylene chloride and removed by filtration. The filtrate was chromatographed several times on a neutral alumina column prepared with methylene chloride. Purification and evaporation of the solvent in vacuo gave a solid foam. The product had the formula as confirmed by UV, NMR and elemental analyses -173EXAMPLE 73 Preparation of 3-(Pheny1 carbonyloxy)-178-C(3-pyridinylcarbonyl)oxy3estra-l,3,5(10)-triene: Estradiol benzoate (2.5 g, 6.6 mmol) was dissolved 5 in 50 mL of dry pyridine, then 1.66 g of nicotinic anhydride and a catalytic amount of 4-(dimethylamino)pyridine (OMAP) were added. The reaction mixture was stirred for 5 days at room temperature, then was poured into ice water. The solid which formed was collected by filtration and dried in vacuo, yielding 3.01 g (94%) of the product as a white solid melting at 151-154°C.

EXAMPLE 74 Preparation of 1-Methyl-3-(f[3-(pheny1 carbonyloxy)estra-l,3,5(10)-trien-17 8-yl]oxy Icarbonyl)pyridini um iodide: The product of Example 73 (1.5 g, 3.1 mmol) was suspended in 2.5 mL of acetone. Then, 2 mL of methyl iodide were added and the reaction mixture was refluxed overnight. The yellow solid (1.8 g, 93%) was collected by filtration and dried in vacuo. UV, NMR and elemental analyses confirmed that the product had the assigned structure: -174EXAMPLE 75 Preparation of 3-(Phenylcarbonyloxy)-178-{[l-methyI 1,4-dihydropyridin-3-yl)carbonyl]oxy }estra-l,3,5(10)triene: The quaternary salt prepared in Example 74 (1.2 g, 1.93 mmol) was suspended in 100 ml of 50:50 tert-butyl alcohol/water. Then, 0.81 g of NaHCO^ and 1.0 g of Na2S204 were added and the reaction was allowed to continue for 1.5 hours. The resultant solution was extracted with CH2C12, and the organic phase was dried over MgS04 and concentrated in vacuo to afford 650 mg of title compound as a yellow foam. The identity of the product was confirmed by UV, NMR and elemental analyses. It was assigned the structure: EXAMPLE 76 Preparation of N-(2-{4-[Bis(2-ch1oroethyl)amino]butanoyloxy} ethy1)-3-pyridinecarboxamide: Chlorambucil (20 g, 0.0657 mol) was dissolved in 800 mL of dry acetonitrile, then 13.1 g (0.079 mol) of N-(2-hydroxyethyl)-3-pyridinecarboxamide were added. Acetonitrile was added until the solution was clear.

The total volume of acetonitrile used at this stage was -175850 mL. To the stirred solution, maintained over argon, there were added 1.492 g (0.0723 mol) of dicyclohexylcarbodiimide and 0.802 g (0.0066 mol) of 4(dimethylami no)pyridine (OMAP). The reaction mixture was stirred overnight at room temperature under dry conditions, and the progress of the reaction was followed by thin layer chromatography. At the end of the reaction period, the solid which formed was removed and washed with 50 mL of cold acetonitrile. The filtrate was evaporated in vacuo at 30°C, and the yellow solid thus obtained was dissolved in a minimum amount (15 mL) of 8:2 chioroform/tetrahydrofuran and applied to a column packed with 900 g of silica gel.

The column was eluted with 8:2 chioroform/tetrahydro15 furan. The adduct and chlorambucil were eluted within the first 500 mL, and the desired ester was then collected upon evaporation of the eluent under vacuum. The title compound was obtained in 82.7% yield as a yellow solid melting at 73-75°C. It had the formula -176EXAMPLE 77 Preparation of 1-Methy1-3-[(N-|2-[4-( (4-bis(2-chloroethyl) ami no]{phenyl)butanoyloxy]ethyl }) carbamoyl]pyridinium methanosulfate: The product of Example 76 (2 g, 0.04 mol) was dissolved in 200 mL dry acetonitrile. Dimethyl sulfate (0.613 g, 0.0486 mol) was added and the mixture was refluxed overnight. The reaction was followed by thin layer chromatography (8:2 ch1oroform/tetrahydrofuran) until no more unquaternized ester remained. Evaporation of the solvent in vacuo gave a residue which was washed several times with dry ether. The red viscous liquid which remained was stored over argon for further use. Yield 97.35%. The product was identified as the desired quaternary salt by NMR analysis. It was assigned the structural formula: (cich2ch2)2n ch3so4' EXAMPLE 78 Preparation of 1-Methyl-3-[(N-{2-[4-({4-[bis(2-chl oroethyl)]amino }phenyl)butanoyloxy]ethy1 })carbamoy1]-1,4d i hydropyri di ne: The quaternary salt prepared in Example 77 (2.49 g, 0.0043 mol) was dissolved 1n 350 mL of water. Nitrogen was bubbled through the solution throughout the reaction period. The aqueous solution was cooled -177over ice to 5°C, then 2.17 g (0.026 mol) of NaHC03 were added over a 5 minute period, followed by 2.997 g (0.017 mol) of sodium dithionite over a 10 minute period. The reaction mixture was maintained at 5°C for 120 minutes, then the layers were separated. The aqueous layer was extracted 4 times with ethyl acetate. The ethyl acetate extracts were combined, dried over MgS04 and evaporated to dryness in vacuo.

The semi-solid thus obtained was washed several times with dry ether to give the title compound as a yellow solid melting at 90-92°C and having the structural formula: EXAMPLE 79 Preparation of N-(4-Hydroxycyc1ohexy1)-3-pyridinecarboxami de : Trans-4-aminocyclohexanol hydrochloride (5.05 g, 0.033 mol) was suspended in 50 mL of ethanol, then 33 mL of IN NaOH were added slowly while cooling the reaction mixture to 10°C. The homogeneous mixture was evaporated to dryness, then three portions of a 50:50 mixture of benzene and acetone were added and evaporated to dryness in vacuo each time. The dry solid was extracted with 100 mL of chloroform and filtered, and the filtrate was evaporated to dryness.

The residue was triturated with ether and dried to give -1783.50 g (91.23%) of the free aminocyclohexanol melting at 111-U2°C.

Nicotinic acid (2.14 g, 0.017 mol) was suspended in 75 mL of dry tetrahydrofuran, then 1.76 g of freshly distilled triethylamine were added. The clear solution thus obtained was cooled to -4°C in an ice bath under argon, then ethyl chloroformate (1.88 g, 0.014 mol) in 10 mL of tetrahydrofuran was added such that the temperature did not go above 0°C. The free aminocyclohexanol (2.0 g, 0.017 mol) was added as a powder to the cold reaction mixture, which was allowed to come to room temperature and stirred for 2 hours.

The precipitate which formed was collected by filtration, dissolved in 28 mL of hot water and recrystallized as 3.25 g (85%) of fine colorless needles melting at 208-210°C and having the formula as confirmed by elemental analysis.

EXAMPLE 80 Preparation of N-|4-[4-( |4-[Bis(2-chloroethyl)]amino}phenyl )butanoyloxyjcyclohexyl )-3-pyridinecarboxamide: Chlorambucil (1.38 g, 0.0045 mol) and N-(4hydroxycyclohexyl)-3-pyr1d1necarboxamide (1.1 g, 0.0049 mol) were mixed together with 1.03 g (0.00459 mol) of -17910 dicyclohexylcarbodiimide and 55 mg (0.00045 mol) of 4(dimethylamino)pyridine (OMAP) in 50 mL of freshly distilled acetonitrile. The reaction mixture was stirred at room temperature in the presence of argon for 2 days. The progress of the reaction was followed by thin layer chromatography using 8:2 chloroform/tetrahydrofuran. At the end of the reaction period, the precipitate was removed by filtration and the filtrate was evaporated to dryness in vacuo at low temperature. The residue was applied to a silica column and eluted with 8:2 chioroform/tetrahydrofuran. The appropriate eluting portions were combined and evaporated to dryness in vacuo. The product (1.86 g, 81%) was obtained as a light cream-colored powder melting at 120-122°C and having the formula HNC N The identity of the product was confirmed by elemental analysi s. -180EXAHPLE 81 Preparation of 1-Methy1-3-(N-{4-[4-(4-{[bis(2-chloroethyl)Jamino {phenyl)butanoyloxylcyclohexyl {carbamoyl)pyridinium methanosulfate: The product of Example 80 (1 g, 0.0019 mol) was dissolved in 30 mL of dry acetonitrile and 0.249 g (0.0019 mol) of dimethyl sulfate was added. The mixture was refluxed under argon until thin layer chromatography (8:2 chioroform/tetrahydrofuran on silica) indicated quaternization was complete (about one and one-half days). The solvent was evaporated in vacuo, leaving an orange residue which was washed several times with anhydrous ether and evaporated i n vacuo. The quaternary salt (1.04 g, 80.6%) was yellow mass. It had the obtained as a sticky structural formula: (cich2ch2)2n EXAMPLE 82 Preparation of 1-Methyl-3-(N-{4-[4-(4-{[bis(2-chloroethyl )laminolphenyl)butanoyloxy]cyclohexyl {carbamoyl)1,4-dihydropyridine: The quaternary salt prepared in Example 81 (0.34 g, 0.0005 mol) was dissolved 1n 0.5 mL of acetonitrile and taken up 1n 20 mL of degassed water (bubbling N^) cooled to O’C. To the stirring solution, sodium -181bicarbonate (0.27 g, 0.003 mol) was added, followed first by 0.37 g (0.002 mol) of sodium dithionite and then by 20 mL of ethyl acetate. After 90 minutes, the organic phase was removed and the aqueous phase was extracted 3 to 4 times with ethyl acetate. The ethyl acetate extracts were combined, dried over sodium sulfate and evaporated in vacuo. The residual solid was washed several times with anhydrous ether and dried. The residue thus obtained was applied to a neutral alumina column and eluted with chloroform under pressure. Evaporation of chloroform left 0.18 g (65%) of a hygroscopic yellow solid of the formula The identity of the product was confirmed by UV 15 analysis.

EXAMPLE 83 Preparation of N-(2-Hydroxy)propy1-3-pyridinecarboxami de : To 4.29 g (0.039 mol) of nicotinic acid suspended 20 in 120 mL of dry tetrahydrofuran, 4.04 g (0.039 mol) of freshly distilled triethylamine was added in one portion. The resultant clear solution was cooled to -4”C 1n an 1ce bath under argon. Ethyl chloroformate (4.33 g, 0.039 mol) in 25 mL of tetrahydrofuran was -182added at such a rate that the temperature of the solution did not exceed 0°C. Then, 3 g (0.039 mol) of 1amino-2-propanol were added directly to the cold reaction mixture. The reaction mixture was allowed to come to room temperature and stirred for 2 hours. The precipitate was removed by filtration and the filtrate was evaporated in vacuo. The oily residue was washed several times with anhydrous ether and allowed to stand. The title compound was obtained as a white, hygroscopic, low-melting, waxy solid melting at 40°C (6.11 g, 85%) and having the formula EXAMPLE 84 Preparation of N-|2-[4-({4-[Bis(2-chloroethy1)]amino }phenyl )butanoyloxy]propyl }-3-pyridinecarboxamide: Chlorambucil (1.0 g, 0.003 mol) and N-(2-hydroxy ) propyl-3-pyridinecarboxamide (0.065 g, 0.0036 mol) were combined with 0.68 g (0.003 mol) of dicyclohexylcarbodiimide and 41 mg (0.0003 mol) of 4-(dimethy1 ami πo)pyridine (OMAP) in 40 mL of freshly distilled acetonitrile. The reaction mixture was stirred at room temperature in the presence of argon for 2 days, the progress of the reaction being followed by thin layer chromatography on silica using 8:2 methylene chloride/ethyl acetate. At the end of the reaction period, -183the precipitate was removed by filtration and the filtrate was evaporated to dryness in vacuo at 30°C.

The residue was applied to a silica column and eluted with 8:2 methylene chioride/ethyl acetate. The appropriate eluting portions were combined and evaporated to dryness in vacuo. The title compound was obtained as a sticky material in 84% yield (1.53 g).

It had the structural formula: EXAMPLE 85 Preparation of 1-Methy1-3-[(N-{2-(4-( {4-Cbis(2-chloroethyl )]ami no [phenyl)butanoyloxy]propyl | )carbamoyl]pyridinium methanosulfate : The product of Example 84 (2.2 g, 0.0047 mol) was dissolved in 45 mL of dry acetonitrile, dimethyl sulfate (0.59 g, 0.0047 mol) was added and the mixture was refluxed under argon. The progress of the reaction was followed by thin layer chromatography using 8:2 methylene chioride/ethyl acetate. After one and one-half days, the solvent was removed by evaporation in vacuo, leaving an orange residue. The residue was washed thoroughly with anhydrous ether and was dried in vacuo. The product, obtained as a yellow sticky mass in 92.47% yield, had the structural formula: -184(C1CH2CH2)2N EXAMPLE 86 Preparation of 1-Methy1-3-C(N-{2-[4-( |4-[bis(2-chloroethyl)]amino}phenyl)butanoyloxy]propyl })carbamoyl]-l,45 di hydropyridine: The quaternary salt prepared in Example 85 (2.39 g, 0.004 mol) was dissolved in 1 mL of acetonitrile and then taken up in 100 mL of degassed water (bubbling Ng) and cooled to 0°C in an ice-water bath. Sod’um bicarbonate (2.03 g, 0.024 mol) was added to the stirring solution, followed by 2.81 g (0.016 mol) of sodium dithionite. To the resultant mixture, 60 mL of ethyl acetate were added. The reaction was allowed to continue for 90 minutes, then the phases were separated and the aqueous phase was extracted 3 or 4 times with 30 mL portions of ethyl acetate. The combined ethyl acetate extracts were dried over sodium sulfate and evaporated in vacuo. The residue was applied to a neutral alumina column and eluted with chloroform under pressure. The appropriate fractions were evaporated to give a hygroscopic yellow solid in 60% yield. The product had the formula: -185(C1CH2CH2)2N N ' £h. ‘3 as confirmed by UV analysis.

EXAMPLE 87 Preparation of N-(2-Hydroxy-2-pheny1) ethyl-3-pyridinecarboxami de : Nicotinic acid (1.79 g, 0.014 mol) was suspended in 60 mL of dry tetrahydrofuran and 1.48 g (0.014 mol) of freshly distilled triethylamine were added. The clear solution which resulted was cooled to -4°C in an ice bath and argon was bubbled through it continuously. Ethyl chloroformate (1.58 g, 0.014 mol) in 10 mL of tetrahydrofuran was added at such a rate that the temperature did not exceed 0°C. Then, 2.0 g (0.014 mol) of 2-amino-1-pheny1 ethanol were added as a solution in 5 mL of tetrahydrofuran. The reaction mixture was allowed to warm to room temperature and was stirred for 2 hours. The precipitate which formed was removed by filtration and the filtrate was evaporated in vacuo to give 3.22 g (91.1%) of a white crystalline solid melting at 122-124°C and having the formula o ι . -186Elemental analysis confirmed the identity of the product.

EXAMPLE 88 Preparation of N-( |2-Phenyl-2-[4-({4-[bis(2-chloro5 ethyl)]aminolphenyl)butanoyloxy] }ethyl)-3-pyridinecarboxami de: Chlorambucil (1.0 g, 0.003 mol) and N-(2-hydroxy2-phenyl)ethyl-3-pyridinecarboxamide (0.88 g, 0.003 mol) were combined with 0.68 g (0.003 mol) of dicyclo10 hexy1carbodiimide and 41 mg (0.0003 mol) of 4(dimethy1 ami no)pyridine (OMAP) in 35 mL of freshly distilled acetonitrile. The reaction mixture was stirred at room temperature under argon for 3 days.. Thin layer chromatography using 8:2 methylene chioride/ethyl acetate was used to follow the progress of the reaction. The precipitate which formed was removed by filtration and the acetonitrile was evaporated in vacuo. The residue thus obtained was applied to a silica column and eluted with 8:2 methylene chioride/ethyl acetate. The appropriate fractions were collected and evaporated in vacuo to give a light tan powder (1.21 g, 70%) melting at 99101°C and having the formula -187EXAHPIE 89 Preparation of 1-Methy1-3-[(N-{2-pheny1-2-[4-( |4-[bis(2-c hl oroethy 1) ]ami no } phenyl) but an oyl oxy] }ethyl ) carbamoyl Ipyridi ni um methanosulfate: The product of Example 88 (0.5 g, 0.00094 mol) was dissolved in 20 mL of dry acetonitrile and 0.12 g (0.00094 mol) of dimethyl sulfate was added. The mixture was refluxed under argon for 2 days, then the solvent was removed by evaporation in vacuo. The residue which was obtained was washed several times with anhydrous ether and dried to give 0.54 g (91%) of a sticky light yellow product having the formula EXAMPLE 90 Preparation of 1-Methyl-3-[(N-{2-phenyl-2-[4-( {4[bis(2-chloroethyl)]ami no }phenyl)butanoyloxy] }ethyl)carbamoyl-1,4-dihydropyridine: The quaternary salt prepared in Example 89 (0.53 g, 0.0008 mol) was dissolved in 0.5 mL of acetonitrile and taken up 1n 20 mL of degassed, deionized water cooled to 0°C. Sodium bicarbonate was added to the stirring solution at 0°C, followed by 0.56 g (0.0032 mol) of sodium dithionite. Then, 20 mL of ethyl -188acetate were added and the reaction was allowed to continue for 2 hours. The organic phase was removed and the aqueous phase was extracted several times with ethyl acetate (total volume 70 ml), until color was no longer observed in the organic phase. The ethyl acetate extracts were combined and dried over sodium sulfate and evaporated in vacuo. The residue was applied to a neutral alumina column and eluted with chloroform. Evaporation of chloroform gave 0.2 g (45%) of a hygroscopic orangish yellow compound of the formula The identity of the product was confirmed by UV spectral analysis.

EXAMPLE 91 Preparation of N-(2-Hydroxyethyl)-3-pyridinecarboxam i d e : A neat mixture of 2-aminoethanol (6.1 g, 0.10 mol) and ethyl nicotinate (15.1 g, 0.10 mol) was refluxed overnight. As the mixture was cooled to room temperature, the product precipitated as a crystalline solid. It was filtered, washed with ether and then recrystallized from 2-propanol/ether. The final product was collected by vacuum filtration and washed with ether. The dried, white compound weighed 10.7 g, -189resulting in a 64.5% yield; mp 88.5-89.5°C (lit. value 92°C).

EXAMPLE 92 Preparation of ( + )N-C2-(6-Methoxy-g-methyl-2-naphthal enyl acetoxy) ethyl ]-3-pyri d inecarboxamide: Naproxen (2.30 g, 1GL.0 mmol) was coupled with the product of Example 91 (1.71 g, 10.0 mmol) using dicyclohexylcarbodiimide (2.30 g, 11.0 mmol) and 4-(dimethyl am i η o) py r i d i n e (122 mg, 1.00 mmol) in acetonitrile (150 mL). The reaction was stirred at room temperature for 48 hours. The precipitate was filtered, rinsed with acetonitrile and dried to a weight of 2.3 g. The solvent was removed under reduced pressure and the residual clear oil was stirred with anhydrous ether. The resulting white solid was vacuum filtered, washed with ether and air-dried. The crude product weighed 2.80 g. The compound was recrystal1ized from 2-propanol. The final product was filtered, washed with 0.5% aqueous sodium bicarbonate, water, and finally with ether. The compound was dried in a desiccator over P2O5. The recrystallized material weighed 2.40 g resulting in an overall yield of 63.4%; mp 79-82°C.

EXAMPLE 93 Preparation of N-(2-{[l-(p-Chlorobenzoyl)-5-methoxy-2methyl-3-indolyl]acetoxy} ethy1)-3-pyridinecarboxamide: A reaction of indomethacin (1.79 g, 5.00 mmol) and the product of Example 91 (0.830 g, 5.00 mmol) was carried out, using dicyclohexylcarbodiimide (1.10 g. -1905.50 mmol) as the coupling agent and acetonitrile as the solvent. The first two reactants were dissolved completely and the solution was then cooled to 0°C., The dicyclohexylcarbodiimide was added and the mixture was stirred overnight. The reaction was allowed to continue for 48 hours. The precipitate (1.2 g) was removed by vacuum filtration. The solvent was removed from the filtrate under reduced pressure leaving an oily residue. The product was solidified by stirring with anhydrous ether. It was filtered, air-dried and recrystallized from ethanol/ether. The final product was vacuum filtered, washed with ether, and air dried. The product weighed 1.65 g, giving a 65.2% yield; mp 123-125°C.

EXAMPLE 94 Preparation of 1-Methyl-3-{N-[2-(6-methoxy-α-methy1-2naphthalenylacetoxy)ethyljcarbamoyl [pyridinium iodide: The quaternization of the naproxen ester prepared in Example 92 (1.0 g, 2.6 mmol) was carried out using methyl iodide (2.3 g, 16 mmol) in acetone (45 mL). The solution was heated to reflux for 20 hours. Methyl iodide (1.1 g, 8.0 mmol) was again added to the reaction flask. The precipitated product was filtered after an additional 4 hours of reaction time. The offwhite powder was dried. The material weighed 2.2 g and was found to be analytically pure without recrystallization. The solvent was removed from the acetone filtrate and the residue was solidified with anhydrous ether. The resulting dark yellow powder was dissolved 1n water and washed with ether (4 x 30 mL). The water was then removed under vacuum giving 0.2 g of a lighter -191yellow powder. The overall yield of the reaction was 93%; mp 169-170°C. The product had the structural formula as further confirmed by UV, NMR and elemental analyses.

EXAMPLE 95 Preparation of l-Methyl-3-[N-(2-{[l-(p-chlorobenzoyl)5-methoxy-2-methyl-3-indolyl]acetoxy}ethy1)carhamoy1]pyridinium iodide: The quaternization of the indomethacin ester prepared in Example 93 (0.50 g, 1.0 mmol) was carried out in acetone, using methyl iodide (1.7 g, 12 mmol). The reaction was refluxed overnight. The solvent was removed under reduced pressure and a yellow solid was obtained. The product was recrystallized using ethanol and a very small amount of ether. Small mold-like crystals were obtained which were light yellow in color. The reaction gave 0.43 g or a 66% yield of the purified material; mp 178-179°C. UV, NMR and elemental analyses confirmed that the product had the structural formula: Preparation of l-Hethyl-3-{N-[2-(6-methoxy-a-methyl-2naphtha1enylacetoxy)ethylJcarbamoyl }-l,4-dihydro5 pyridi ne: The quaternary salt prepared in Example 94 (730 mg, 1.5 mmol) was dissolved in degassed, deionized water (200 mL) and acetonitrile (10 mL). Sodium dithionite (780 mg, 4.5 mmol) and sodium bicarbonate (630 mg, 7.5 mmol) were combined and added to the solution at room temperature. The reaction was continued for 1 hour, while nitrogen gas was slowly bubbled through the solution. The partially precipitated product was extracted repeatedly with ether (8 x 30 mL). The extracts were combined, washed with water (25 mL) and dried over magnesium sulfate. The drying agent was filtered and the solvent was removed from the filtrate under reduced pressure. The oily residue was dissolved in methylene chloride (3x5 mL) and removed under reduced pressure. The resulting foam was rinsed with anhydrous ether (3 mL) and the solvent was removed under vacuum. The final product weighed 390 mg, giving a 66% yield. The hygroscopic solid foam was stored under nitrogen at -100°C. It had the struc25 tural formula: as confirmed by UV, NMR and elemental analyses.

EXAMPLE 97 Preparation of 1-Methy 1-3-[N-(2-{[1-(p-chlorobenzoyl) 5 5-methoxy-2-metby!-3-i ndolyl]acetoxy {ethyl)carbamoyl]1,4-dihydropyridine: The indomethacin quaternary salt prepared in Example 95 (140 mg, 0.22 mmol), was dissolved in a minimum amount of water :acetonitri 1e (8:2). The water had been bubbled with nitrogen for 20 minutes prior to its use. Sodium bicarbonate (91 mg, 1.1 mmol) and sodium dithionite (110 mg, 0.65 mmol) were added to the solution while stirring at O’C. The solution was then allowed to warm to room temperature. The reaction was continued for about 1 hour. Some of the product had precipitated during the reaction. This was dissolved in ethyl ether. The water layer was extracted several times with ether until no more yellow color transferred to the organic layer. The ether portions were combined and dried with magnesium sulfate, filtered and the ether was removed under reduced pressure. The resulting oil was dissolved 1n acetone and the solvent was removed (2 x 10 mL) under reduced pressure to form a dry foam. The final product weighed 92 mg. The yield was 82%; mp 60-65’C. The product had the formula: as confirmed by UV, NMR and elemental analyses.

EXAMPLE 98 Preparation of N-[(1-Hydroxycyclohexyl)methy!]-3pyridinecarboxamide: To 1.48 g (0.012 mol) of nicotinic acid suspended in 50 mL of dry tetrahydrofuran, 2.44 g (0.014 mol) of freshly distilled triethylamine were added, with stirring. The resultant clear solution was cooled to -4°C in an ice bath, under argon. Then, 1.3 g (0.012 mol) of ethyl chloroformate in 10 mL of tetrahydrofuran were added at such a rate that the temperature of the reaction mixture did not exceed 0°C. To the cold reaction mixture, 2.0 g (0.012 mol) of 1-aminomethyl-1cyclohexanol hydrochloride were added directly as a powder. The reaction mixture was allowed to warm to room temperature and stirred for 2 hours, then the triethylamine hydrochloride which formed was removed by filtration and the filtrate was evaporated in vacuo to afford a white solid. The solid was recrystallized from water, washed with acetone and ether and dried.

The title compound, obtained in 85% yield (2.4 g), melted at around 110°C, and was further characterized by the structural formula as confirmed by elemental analysis.

EXAMPLE 99 Preparation of N-(fl-[4-((4-[Bis(2-chloroethyl)]amino}5 phenyl ) but anoyloxy]eyelohexyl fmethyl)-3-pyridinecarboxamide : Chlorambucil (1.18 g, 0.0038 mol) and N-[(lhydroxycyclohexy1)methyl]-3-pyridinecarboxamide (0.99 g, 0.004 mol) were combined with 0.8 g (0.0038 mol) of dicyclohexylcarbodiimide and 47 mg (0.00038 mol) of 4-( di methyl ami no)pyridine (DMAP) in 60 mL of freshly distilled acetonitrile. The reaction mixture was stirred at room temperature under argon for 7 days. At the end of that time, the precipitate which formed was separated by filtration and the filtrate was evaporated to dryness at low temperature in vacuo. The residue was applied to a silica column and eluted, first with 8:2 methylene chioride/ethyl acetate, then with 8:2 chioroform/tetrahydrofuran . The appropriate eluting portions were combined and evaporated to dryness in vacuo. The title compound was obtained in 26% yield as a light yellow solid melting at 92-94°C.

It had the structural formula o 0-C-(CH2)3 CH2CH2C1 CH2CH2C1 “Hid) as confirmed by elemental analysis.

EXAMPLE 100 Preparation of 1-Methyl-3-[N-( {l-[4-(4-|[bis(25 chloroethyl)]amino[phenyl )butanoyl oxy]cyclohexyl [methyl[carbamoyljpyridinium methanosulfate: To 0.69 g (0.0013 mol) of the product of Example 99, dissolved, in 25 mL of dry acetonitrile, was added 0.17 g (0.0013 mol) of dimethyl sulfate. The mixture was refluxed until the reaction was complete (approximately 2 days), as evidenced by thin layer chromatography using 8:2 chioroform/tetrahydrofuran. The solvent was removed by evaporation in vacuo to afford an orange residue, which was washed several times with anhydrous ether and dried. The product was obtained as a sticky yellow mass (85%, 0.72 g) having the formula: ch2ch2ci -197EXAMPLE 101 Preparation of 1-Methyl-3-[N-({l-[4-(4-{[bis(2chloroethyl)]ami no {phenyl)butanoyloxy]cyc1ohexyi |methyl {carbamoyl-1,4-dihydropyridine: The quaternary salt prepared in Example 100 (0.78 g, 0.0012 mol) was dissolved in 0.5 mL of acetonitrile and taken up in 20 mL of water degassed with bubbling Ν?, cooled to O’C. To the stirring solution, 0.61 g (0.0072 mol) of sodium bicarbonate was added, followed by 0.84 g (0.0048 mol) of sodium dithionite and 20 mL of ethyl acetate. The reaction was allowed to proceed for 75 minutes, then the layers were separated and the aqueous layer was extracted 3 to 4 times with 20 mL of ethyl acetate. The organic extracts were combined, dried over sodium sulfate and evaporated in vacuo. The residue was applied to a neutral alumina column and eluted with chloroform under pressure. Evaporation afforded the product as a sticky yellow mass (0.31 g, 49%) having the structural f ormul a : /CH2CH2C1 CH2CH2C1 EXAMPLE 102 Preparation of 1-Methyl-3-{[2-(9-guanylmethoxy)ethoxy]carbonyl {pyridinium iodide: Trigonelline anhydride diiodide (1-methylpyri25 dinium-3-carboxylic acid anhydride diiodide) was -198prepared as described by Brewster et al, Synthet i c Communi cat i ons, 17(4) , 451-455 ( 1987 ).

To a solution of 1.0 g (4.4 mmol) of acyclovir in 25 mL of freshly distilled dry pyridine were added 2.27 g (4.4 mmol) of trigonelline anhydride diiodide and a catalytic amount (5.4 mg, 4 mmol) of 4-(dimethylamino)pyridine (DMAP). The resultant suspension was stirred for 4 days under argon at room temperature. As the reaction proceeded, the orange color of the anhydride was replaced with a yellow color. When all of the acyclovir had been consumed, the reaction was stopped, the precipitate (containing the product ester plus the trigonelline formed as a by-product) was removed by filtration and washed with acetone and ether to remove DMAP. The yellow solid was then stirred in dry methanol at room temperature to remove trigonelline, unreacted anhydride and acyclovir. The title compound was obtained in 87% yield (1.82 g), melting at 201-202°C. NMR and UV analyses confirmed that the product had the formula: I -199EXAMPLE 103 Preparation of 1-Methyl-3-{[2-(9-guanylmethoxy)ethoxyjcarbonyl}-l,4-dihydropyridine: To a solution of 1.58 g (3.3 mmol) of the product of Example 102 in 120 mL of degassed water were added 1.69 g (20.1 mmol) of NaHCOg in one portion. The mixture was stirred at 0°C while 2.33 g (13.18 mmol) of sodium dithionite were added over a 5 minute period.

The flask was flushed with nitrogen throughout the reaction process. The dihydropyridine product was insoluble in water and formed cream-colored crystals on top of the water layer. The crystals were separated by filtration and washed, first with ice-cold water and then with anhydrous ether. Drying over PgOg in a dessicator maintained at -15°C afforded 0.626 g (54%) of the title compound melting at 163-165°C. NMR and UV analyses confirmed that the product had the formula: o II CH?0CH2CH20C EXAMPLE 104 Preparation of 51-Pivaloyltrif1uorothymidine: To a stirring solution of 150 mg of trifluorothymidine in 5 mL of pyridine was added a solution of -20090 mg of pivaloyl chloride in 1 mL of pyridine, with cooling. Stirring was continued at room temperature for 10 hours, then the reaction mixture was poured into 20 mL of ice water and extracted with 50 mL of ethyl acetate. The extract was washed with water and dried over sodium sulfate. The ethyl acetate was removed and the residue was purified by silica gel column chromatography using 20:1 chioroform/methanol as eluent. The title compound melted at 130-132°C after recrystal 1iza10 tion from a mixture of ether and n-hexane.

EXAMPLE 105 Preparation of 3'-(3-Pyridylcarbony1)-5'-pivaloyltrif1uorothymidi ne: To a stirring solution of 450 mg of 5'-pivaloyl15 trifluorothymidine in 10 mL of pyridine was added 1.0 g of nicotinoyl chloride hydrochloride under icecooling. The reaction mixture was stirred at room temperature for 3 days, then was poured into 100 mL of ice water and extracted with 100 mL of ethyl acetate.

The extract was washed with water, dried over anhydrous sodium sulfate and then evaporated in vacuo to give an oil. Crystallization from n-hexane afforded 500 mg (87%) of colorless needles melting at 175-177°C. The product had the structure as further confirmed by NMR spectral analysis.

EXAMPLE 106 Preparation of 3'-(1-Methyl-3-pyridiniumcarbony1)-515 pi valoy11 ri f1uorothymidi ne iodide: To 440 mg of the product of Example 105 dissolved in 10 mL of acetone, 1.0 g of methyl iodide was added. The mixture was refluxed for 10 hours, then the precipitate which formed was collected by suction filtration to give 550 mg of the desired product as yellow leaves melting at 188-190°C with decomposition. NMR analysis confirmed that the product had the structural formula: EXAMPLE 107 Preparation of 3'-(l,4-0ihydro-l-methyl-3-pyridinylcarbonyl)-5'-pivaloyltrifluorothymidine: To a stirring solution of 100 mg of the product of Example 106 in a mixture of 20 mL of water and 20 mL of ethyl acetate were added 64 mg of NaHCOj and 115 mg of NagSgO^ under N2 gas. The resultant mixture was stirred at room temperature for 1 hour, then the organic layer was separated and washed with water.. The extract was dried over anhydrous Na2S04 and evaporated in vacuo. The residue was triturated with a mixture of ether and n-hexane and the yellow needles which formed were collected by suction filtration (50 mg, 62%).. The product melted at 168-170°C. NMR analysis confirmed that the product had the structural formula: Preparation of 3'-Azido-3'-deoxy-51 -(3-pyridylcarbonyl)thymidi ne: A mixture of 1.18 g (4.42 mmol) of azidothymidine , 1.11 g (4.86 mmol) of nicotinic anhydride and 0.15 g (1.22 mmol) of N-(dimethy1 ami no)pyridine was combined in 50 mL of pyridine. The reaction mixture was stirred at room temperature overnight. The clear, colorless reaction mixture was concentrated in vacuo to a semisolid opaque mass which was triturated with ether overnight. The suspension was filtered and dried to give 1.97 g of solid. Then, 1.0 g of the solid was chromatographed over 20 g of silica gel using 10% ethanol/chioroform as eluent. The desired fraction was isolated as 0.53 g of a white foam, which was crystallized from a solvent mixture of ethanol, diethyl ether and hexane. The product melted at 138.5-141.5°C and had the structural formula as confirmed by NMR and IR.

EXAMPLE 109 Preparation of 3'-Azido-31-deoxy-51-[(1-methyl-35 pyri di ni um)carbonyl]thymi dine iodide: A mixture of 0.53 g (2.0 mmol) of azidothymidine, 1.02 g (2.2 mmol) of trigonelline anhydride diiodide and 67 mg (0.5 mmol) of N-(dimethyl ami no)pyridine was combined in 25 mL of pyridine. The reaction mixture was stirred at room temperature for 5 days, then was filtered. The filtrate was concentrated in vacuo to a residue which was triturated with acetone overnight..

The resulting suspension was filtered and the filtrate was concentrated in vacuo to a foam, which was treated with water and filtered to remove a small amount of insoluble material. The filtrate was concentrated in vacuo to a solid yellow glass (0.50 g, 49%). NMR and UV analysis confirmed that the product had the formula: -205o EXAMPLE 110 Preparation of 31-Azido-3 1-deoxy-51-[(1-methy1-1,4di hydro-3-pyri di nyl )carbonyl]thymidi ne: The crude azidothymidine quaternary derivative prepared according to the procedure of Example 109 (1.45 g, 2.82 mmol) was dissolved in 50 ml of water and filtered. The filtrate was cooled in an ice bath and saturated with argon. Then, 100 mL of ethyl acetate and 2.90 g of NaHCO^ were added, followed by 1.45 g of Na2S204 after 5 minutes. The reaction was allowed to proceed for 1 hour, then the ethyl acetate layer was removed and fresh ethyl acetate was added. This procedure was repeated to give three organic extracts and a reaction time of 3 hours. The extracts were pooled and concentrated in vacuo to a foam weighing 1.01 g (92%). The foam was crystallized from methanol to give the title compound of the formula melting at 138-140°C. Its structure was confirmed by elemental analysis as well as NMR and UV.

EXAMPLE 111 Preparation of Oopamine dipivalate, oxalate salt: To a stirred mixture of 28.1 g of pivaloyl chloride and 150 mL of trifluoroacetic acid, 18.01 g of dopamine hydrobromide were added. The mixture was stirred for 2 hours, then 14 mL of water were added and the mixture was concentrated in vacuo. The residual oil was dissolved in chloroform and washed with cold 10% KHCO-j solution until CO? evolution ceased. The layers were separated and washed with water and the chloroform layer was dried over MgS04, filtered and evaporated to dryness. The residue was taken up in 100 mL of ethyl acetate and 7 g of oxalic acid were added together with 100 mL of ethyl acetate. The resultant solution was filtered to remove insoluble materials and 1.6 g oxalic acid in 25 mL of ethyl acetate were added. The mixture was concentrated in vacuo and -207 cooled. The crystals which formed were isolated by filtration, giving 13 g of the title compound. Cooling of the mother liquor afforded a second crop of crystals (5.9 g). The product had the formula: CH2CH2NH2 COOH COOH EXAMPLE 112 Preparation of Chloromethyl N-{B-[3,4-bis( pivaly1oxy)phenyljethyl }aminocarboxyl ate : Dopamine dipivalate, oxalate salt (822 mg, 2 mmol) was suspended in 15 mL of dry tetrahydrofuran. Triethylamine (278 mL, 1 mmol) was added, the mixture was stirred for 15 minutes and a further 278 mL (1 mmol) of triethylamine were then added. Addition of CICOgCHgCl (390 mg, 6 mmol) resulted in immediate formation of a heavy white precipitate and the evolution of gas. The reaction mixture was stirred overnight at room temperature, then the precipitate was removed by filtration and the filtrate was washed with 10 mL of 0.1 M hydrochloric acid. Drying over magnesium sulfate and evaporation to dryness afforded 1.1 g of a golden oil of the structural formula The identity of the product was confirmed by elemental analysis .

EXAMPLE 113 Preparation of N-{g-[3,4-Bis( pivalyloxy) phenyl]ethyl }aminocarbonyloxymethy! 3-pyridinecarboxylate: The chloromethyl carbamate prepared in Example 112 (1.26 g, 3.04 mmol) was combined with 10 mL of dry dimethylformamide and that mixture was added to a pre10 mixed solution of nicotinic acid (375 mg, 3.04 mmol) and triethylamine (445 mL, 5% excess) in 15 mL of dry dimethylformamide at room temperature. The reaction mixture was stirred for 4 days, then the precipitate which formed was removed by filtration. The filtrate was evaporated to dryness and the residue was taken up in 20 mL of methylene chloride. That solution was washed twice with 10 mL portions of water. Removal of the solvent in vacuo afforded the title compound of the formula: The identity of the product was confirmed by NMR.

EXAMPLE 114 Preparation of N-fg-[3,4-Bis(piva1y1oxy)pheny1]ethy1 }5 aminocarbonyloxymethyl 1-methyl-3-pyridinium carboxylate iodide: The product of Example 113 (860 mg, 1.78 mmol) was combined with 15 mL of dry acetonitrile and that mixture was treated with 223 mL (3.56 mmol) of methyl iodide. The resultant mixture was stirred for 6 hours at room temperature, then an additional 223 mL (3.56 mmol) of methyl iodide was added and the mixture was stirred overnight. Evaporation to dryness afforded, as an orange-red oil, the title compound of the formula The identity of the product was confirmed by NMR analysi s.

EXAMPLE 115 Preparation of N-{g-[3,4-Bis(pi valyloxy)pheny1jethyl )aminocarbonyl oxymethyl 1,4-dihydro-1-methyl-3-pyridinecarboxyl ate: The quaternary salt prepared in Example 114 (54 mg, 0.084 mmol) in 10 mL of water was treated at O’C under nitrogen with NaHCOg (30 mg, 4 equivalents), Na£S204 (60 mg, 4 equivalents) and ethyl acetate (20 mL). The reaction was allowed to proceed for 1 hour 20 minutes, then the aqueous and organic layers were separated and the aqueous layer was re-extracted with mL of ethyl acetate. The combined organics were dried over magnesium sulfate. Removal of the solvent in vacuo gave a red-orange oil which was taken up in chloroform and partially purified by elution with chloroform from a short neutral alumina column. The desired fraction was subjected to preparative thin layer chromatography on silica using 80:20 chloro-211form/acetone. The highest band was taken as the title compound of the structural formula: The identity of the product was confirmed by HPLC (high 5 pressure liquid chromatography) determinations for its ability to release dopamine from plasma and brain homogenate .

EXAMPLE 116 Preparation of 9-F1uoro-11Β,17-dihydroxy-16α-methy1-2110 [(3-pyridiny1 carbonyl)oxy]pregna-l,4-diene-3,20-dione: Dexamethasone (1 g, 2.5 mmol) was dissolved in 50 mL of dry pyridine. To that solution were added 680 mg (3.0 mmol) of nicotinic anhydride and a trace of 4(dimethy1 ami no)pyridine (DMAP). The reaction was allowed to proceed for 4 hours, then the reaction mixture was poured over ice water and refrigerated overnight. The solid was collected by filtration and dried to give 1.08 g (87%) of product melting at 262265°C and having the structural formula as confirmed by elemental analysis.

EXAMPLE 117 Preparation of 1-Methyl-3-{[(9-f1uoro-11S,17-dihydroxy5 16 α-methylpregna-1,4-diene-3,20-dion-21-yl)oxy]carbonyl }pyridinium iodide: The product of Example 116 (0.74 g, 1.5 mmol) was dissolved in 50 mL of acetone to which 2 mL of methyl iodide was added. A small amount (10 mL) of CH3NO3 was subsequently added to increase solubility. The reaction was allowed to proceed for 2 days, then the solid was collected to give 0.54 g (56% yield) of the title compound melting at 218-221°C and having the formula -213The structure of the product was confirmed by elemental analysis.

EXAMPLE 118 Preparation of 9-F1 uoro-11g,17-dihydroxy-16a-methy1-215 {[(1-methyl -1,4-dihydropyridin-3-yl )carbonyl]oxy}pregna-1,4-diene-3,20-dione: The general reduction procedure of Example 11 of U.S. Patent No. 4,617,298 was followed, using 0.78 mmol of the steroidal quaternary salt prepared in Example 117, 0.33 g of NaHC03 and 0.41 g of Na2SgO4 in 50% aqueous methanol at 0°C, with a nitrogen purge. The product had the structural formula: -214EXAMPLE 119 Preparation of llB,17-Dihydroxy-21-[(3-pyridinylcarbonyl)oxy]pregn-4-ene-3,20-dione: Hydrocortisone (2 g, 5.5 mmol) was dissolved in 50 5 mL of dry pyridine. Then, 1.38 g of nicotinoyl anhydride (6.05 mmol) and a trace of 4-(dimethylamino)pyridine (OMAP) were added and the reaction was allowed to proceed for 4 hours at room temperature. The pyridine solution was poured into ice water and the resulting solid was collected by filtration. The solid was dried over P20g in vacuo to give 2.4 g (93%) of the title compound of the formula as confirmed by elemental analysis and UV spectral 15 analysis. -215EXAMPLE 120 Preparation of l-Methyl-3-{[(llg,17-dihydroxypregn-4ene-3,20-dion-21-yl)oxy]carbonyl [pyridinium iodide: The product of Example 119 (1 g, 2.1 mmol) was 5 dissolved in 50 mL of acetone and 4 mL of methyl iodide were added. The solution was stirred at the reflux temperature overnight. Removal of the solvent gave the title compound as a yellow powder in 98% yield. Elemental analysis confirmed that the product had the formula: EXAMPLE 121 Preparation of 11g,17-0ihydroxy-21-{[(1-methyl-l,4dihydropyridin-3-yl) carbonyl]oxy [pregn-4-ene-3,2015 dione: The general reduction procedure of Example 11 of U.S. Patent No. 4,617,298 was followed, using 0.8 mmol of the steroidal quaternary salt prepared in Example 120, 0.34 g of NaHC03 and 0.42 g of Na2S204 in 50% r 20 aqueous methanol at O’C, with a nitrogen purge. The product had the structural formula: EXAHRLE 122 Preparation of N-(2-Chloroethy1)-N1-[2-(3-pyridinecarbonyl oxy) ethyl ]-N-nitrosourea: A solution of 2-aminoethyl nicotinate dihydrochloride (1.25 g, 52 mmol) and 2,4,5-trichlorophenyl-N(2-chloroethyl)-N-nitrosocarbamate (2 g, 6 mmol) in 40 mL of pyridine was stirred under nitrogen at room temperature for 24 hours. The reaction was monitored by thin layer chromatography (silica, 1:1 chloroform/ethyl acetate, Rf 0.26). The solvent was removed in vacuo and the residue was chromatographed on a silica gel column by eluting, first with benzene to remove unreacted nitrosocarbamate and tri chiorophenol by-product, and then with chloroform, to give the desired product. The resultant oil solidified in the freezer. It melted at 63-64*C and had the formula -217i-«Xa^CH2NHC=O ΓΟΤ ?·” f2 CH, I 2 C, EXAMPLE 123 Preparation of N-(2-Ch1oroethy1)-N'-[2-(l-methyl-3pyridiniumcarbonyloxy)ethyl]-N-nitrosourea iodide: A solution of the product of Example 122 (1.5 g, 5 mmol) in 40 mL of tetrahydrofuran was treated with excess methyl iodide. The mixture was stirred at 50°C for 4 hours. The finely crystalline, yellow solid thus obtained (1.8 g, 82%) melted at 120-121°C and had the structure as confirmed by elemental analysis. -218EXAMPLE 124 Preparation of N-(2-Chloroethyl)-N‘-[2-(1,4-dihydro-lmethyl-3-pyridinecarbonyloxy)ethyl ]-N-nitrosourea: A solution of the quaternary nitrosourea prepared 5 in Example 123 (0.48 g, 1.1 mmol) and 1-benzyl-1,2di hydroi soni coti namide (0.23 g, 1 mmol) in 25 mL of anhydrous methanol was stirred at O’C for 4 hours under nitrogen. The solid which separated was filtered and washed with methanol and ether. The solid was identi10 fied as 1-benzyl-4-carbamoylpyridinium iodide by NMR. The filtrate was evaporated in vacuo at about 30°C and the residue was suspended in methylene chloride. The solid that separated was filtered and washed with methylene chloride. The filtrate was evaporated in vacuo and the residue was dissolved in chloroform.

Flash chromatography on a short column of neutral alumina, using chloroform as eluent, gave a chloroform solution which was evaporated in vacuo to afford 0.2 g (63%) of a gummy residue, identified by NMR as the desired product of the formula CH. '3 An alcoholic solution of silver nitrate was readily reduced by the compound thus obtained. -219EXAHPLE 125 Preparation of N-(2-F1uoroethyl)-N*-[2-(3-pyridinecarbonyl oxy) ethyl]-N-nitrosourea: A solution of. 2-ami noethyl nicotinate dihydro5 chloride (1.5 g, 6.3 mmol) and 2,4,5-trich1oropheny1 -N(2-f1uoroethyl)-N-nitrosocarbamate (2.18 g, 6.9 mmol) in 50 ml of pyridine was stirred under nitrogen at room temperature for 24 hours. The reaction was monitored by thin layer chromatography (silica, 1:1 chloro10 form/ethyl acetate, 0.25). The solvent was removed in vacuo and the residue was chromatographed on a silica gel column by eluting, first with benzene to remove unreacted nitrosocarbamate and trichiorophenol , and then with chloroform to elute the desired product. The compound (1.56 g, 87.4%) melted at 7577°C and was characterized by the structural formula: Wl.

I 2 CH, I 2 F -220EXAMPLE 126 Preparation of N-(2-Fluoroethyl)-N'-[2-(l-methy1-3pyridiniumcarbonyloxy)ethyl]-N-nitrosourea iodide: A solution of the product of Example 125 (1.56 g, .4 mmol) in 40 mL of tetrahydrofuran was treated with excess methyl iodide. The mixture was stirred at 50°C for 4 hours. The finely crystalline, yellow solid thus obtained (2.20 g, 94.1%) melted at 123-125eC and had the structural formula F EXAMPLE 127 Preparation of N-(2-F1uoroethyl)-N'-[2-(l,4-dihydro-lmethyl-3-pyridinecarbonyloxy)ethyl]-N-nitrosourea: A solution of the quaternary nitrosourea prepared 15 in Example 126 (0.426 g, 1 mmol) and 1 -benzy1 -1,2di hydroisonicotinamide (0.21 g, 1 mmol) in 25 mL of anhydrous methanol was stirred at 0°C for 4 hours under nitrogen. The solvent was evaporated in vacuo at about 30°C and the residue was suspended in chloroform, filtered and flash chromatographed on a short column of neutral alumina. The title compound was obtained in r -22155% yield after elution with chloroform and was assigned the structure N I CH. '3 ‘ ‘ u I 2 2 NO consistent with UV analysis.

EXAMPLE 128 Preparation of Chloromethyl nicotinate: To a suspension of nicotinic acid (1.23 g, 0.01 mol) in a mixture of 10 mL of water and 20 mL of tetrahydrofuran were added tetrabutylammonium hydrogensulfate (0.34 g, 1 mmol) and sodium bicarbonate (3.19 g, 0.038 mol), with vigorous stirring. Chloromethyl chlorosulfate (1.81 g, 0.011 mol) in 5 mL of tetrahydrofuran was added dropwise, keeping the temperature below 30°C. The reaction mixture was stirred for 1 hour, then the layers were separated and the organic layer was dried by azeotroping with 1:1 acetonitri1e/benzene. The residue was passed through a column of neutral alumina, eluting with chloroform.

The chloroform layer was evaporated to give 1.28 g (74.8%) of an oily residue, which was confirmed by NMR analysis to have the structural formula: EXAMPLE 129 Preparation of 1-(Pyridine-3-carbonyloxymethyl)-5f1uorouraci1: -FU (1.31 g, 0.01 mol) was dissolved in 5 mL of dimethylacetamide and treated with triethylamine (2.78 mL, 0.02 mol). Chloromethyl nicotinate (2.95 g, 0.012 mol) in 5 mL of dimethylacetamide was added in one portion, and the mixture was stirred for 24 hours, filtered, washed with ethyl acetate and evaporated.

The residue was chromatographed on a column of silica gel, using as eluent first benzene, then 3:1 benzene/chloroform , then 1:1 benzene/ch1oroform, then 3:1 chioroform/benzene, then chloroform and finally 99:1 ch1oroform/methanol. Unreacted nicotinate was eluted initially, followed by the 1,3-bis-isomer and finally the 1-isomer. The 1-isomer (1.3 g, 50%) melted at 190 192°C and had the formula -223as confirmed by NMR analysis.

EXAMPLE 130 Preparation of 1,3-Bis(pyridine-3-carbonyloxymethy!)-5f1uorouraci1: -FU (1.31 g, 0.01 mol) was dissolved in 5 mL of dimethyl acetamide and treated with triethylamine (5.6 mL, 0.04 mol). Chloromethyl nicotinate (6.8 g, 0.04 mol) in 15 mL of dimethylacetamide was added in one portion, then the mixture was stirred for 48 hours and filtered, and the filter cake was washed with ethyl acetate. The filtrate was evaporated in vacuo and the residue was diluted with 100 mL of water and extracted with chloroform. The organic layer was evaporated and the residue was dried by azeotroping with 1:1 acetonitri1e/benzene. The residue was chromatographed on a column of neutral alumina, eluting successively with benzene, 1:1 benzene/chloroform, and 50:50:1 benzene/chloroform/methanol, to give 3.2 g (80%) of the bis-isomer of the formula as confirmed by NMR analysis. -224EXAMPLE 131 Preparation of 3-(Pyridine-3-carbonyloxymethyl )-5f1uorouraci1: The 1,3-bis-isomer prepared in Example 130 was 5 dissolved in 10 mL of methanol and mixed with 20 mL of potassium carbonate:sodium bicarbonate buffer (0.1M), pH 10.00. The mixture was stirred at room temperature for 2 hours, by which time thin layer chromatography indicated that the bis-isomer had disappeared completely. The mixture was evaporated and the residue was chromatographed on a column of alumina, eluting successively with chloroform, 99:1 chloroform/methanol and 96:4 chloroform/methanol. The fractions were collected and those containing the 3-isomer were pooled and evaporated to give the compound of the formula as a solid (0.2 g, 30%) melting at 179-180°C. The identity of the product was confirmed by NMR analysis. -225 EXAMPLE 132 Preparation of 1-(1-MethyΊ-3-pyridiniumcarbonyloxymethyl )-5-fl uorouraci 1 iodide: The 1-isomer prepared in Example 129 (1.93 g) was combined with sufficient quantities of methyl iodide and acetonitrile, and the mixture was refluxed for 4 hours, then cooled and filtered to give 2.5 g of a light yellow, fluffy solid. The filtrate was evaporated, triturated with acetonitrile and filtered to give an additional 0.23 g; total yield 2.73 g (92.25%). UV and NMR analyses confirmed that the product had the structural formula: EXAMPLE 133 Preparation of 1-(1,4-Dihydro-1-methy1-3-pyridinylcarbonyloxymethyl)-5-f1uorouracil : The product of Example 132 (1 g) was dissolved in 20 mL of deionized water (degassed with argon) and cooled in an ice-bath, then 20 mL of ethyl acetate were added. To the stirred solution, 1.24 g of sodium bicarbonate were added, followed after about one minute with 1.75 g of sodium dithionite. The reaction was allowed to proceed under argon and was monitored by UV. After approximately 75 minutes, ethanol was added -226and the solid was filtered, washed with water and methylene chloride and dried under argon to give 400 mg of the title compound. UV and NMR analyses confirmed that the product had the structural formula: The aqueous layer was repeatedly extracted with chloroform and combined with the ethyl acetate layer used in the reaction. The solid obtained after removal of the organic solvent was suspended in acetonitrile and filtered to give an additional 250 mg of product melting at 173-174°C.

EXAMPLE 134 Preparation of 3-(1-Methyl-3-pyridiniumcarbonyloxymethyl)-5-f1uorouraci1 iodide: The 3-isomer prepared in Example 131 can be subjected to the general procedure of Example 132 to afford the corresponding quaternary salt of the formula : EXAMPLE 135 Preparation of 3-(1,4-0ihydro-1-methyl-3-pyridinyl carbonyloxymethyl )-5-fluorouracil: The product of Example 134 can be subjected to the general procedure of Example 133 to afford the corresponding dihydropyridine of the formula: I* CH. '3 o COCH.

H -228The parenteral formulations employed in the method of the present invention can be used to treat a variety of conditions, depending upon the pharmacological nature of the drug selected for administration. In the case of the redox carrier-drugs, the pharmacological nature of the parent drug itself from which the carrier drug is derived will be determinative. Thus, with respect to the carrier-drugs, in one preferred embodiment, the redox system is derived from dopamine or L-DOPA or a protected counterpart thereof, and the redox derivative/cyclodextrin parenteral formulation is thus designed to elicit a sustained and brain-specific dopaminergic (e.g. anti-Parkinsonism or antihyperprolactinemia) response in the animal to which the formulation is administered. In analogous fashion,, the redox derivative/cyclodextrin parenteral formulation derived from any other centrally acting drug as defined herein is designed to elicit the kind of pharmacological response which would be obtained by delivery of the drug itself to the brain, i.e. when the centrally acting parent drug is an antitumor/anticancer agent, the instant formulation is employed to elicit an antitumor/anticancer response; when the parent drug is a sympathetic stimulant, the instant formulation is used to elicit a sympathetic stimulant or amphetaminelike response; when the parent drug is an anticonvulsant compound, the instant formulation is used to elicit an anticonvulsant response; when the parent drug is a tranquilizer, the instant formulation is used to elicit a tranqui1izing response; when the parent drug is an antidepressant, the instant formulation is used to elicit an antidepressant response; and so forth. r V -229The parenteral formulations used in the method of the present invention contain a pharmacologically effective amount of at least one selected lipophilic and/or water-labile drug in an aqueous solution containing from about 20% to about 50% of a hydroxypropyi, hydroxyethyl, glucosyl, maltosyl or maltotriosyl derivative of B- or γ-cyclodextrin, preferably of hydroxypropyi -B-cycl odextri n . These formulations are sterile and pyrogen-free, and are prepared in accord with accepted pharmaceutical procedures, for example as described in Remington's Pharmaceutical Sciences, seventeenth edition, ed. Alfonso R. Gennaro, Mack Publishing Company, Easton, PA (1985), pp. 1518-1552. The aqueous sterile injection solutions may further contain anti-oxidants, buffers, bacteriostats, isotonicity adjusters and like additions acceptable for parenteral formulations. Various unit dose and multidose containers, e.g. sealed ampules and vials, may be used, as is well-known in the art. The essential ingredients of the sterile parenteral formulation, i.e. the drug(s), water and selected cyclodextrin, may be presented in a variety of ways, just so long as the solution ultimately administered to the patient contains the appropriate amounts of the essential ingredients. Thus, for example, the drug/cyclodextrin/water formulation may be presented in a unit dose or multidose container, ready for injection. As another example, a concentrated solution of drug/cyclodextrin/water may be presented in a separate container from a diluting liquid (water or cyclodextrin/water) designed so that the contents can be combined to give a formulation containing appropriate amounts for -230injection. As another alternative, the drug or a drug/cyclodextrin combination may be provided in a freeze-dried condition in one container, while a separate container contains diluting liquid (water or cyclodextrin/water, depending on the amount of cyclodextrin in the other container), again designed so that the contents can be combined to give a formulation containing the appropriate amounts of the essential ingredients. In any event, the contents of each container will be sterile.

Generally speaking, the therapeutic dosage ranges for administration of drugs in the parenteral formulations described herein will be the same as or less than (in some Instances, substantially less than) those characteristically used for administration of the drug per se (or, in the case of the carrier-drugs, of the parent drug species per se). Naturally, such therapeutic dosage ranges will vary with the size and species of the patient, the condition for which the formulation is administered, the type of parenteral administration employed and the like. The quantity of given dosage form needed to deliver the desired dose of active ingredients will of course depend upon the concentration of the drug in the parenteral formulation.

Claims (29)

CLAIMS:

1. A method for the preparation of a composition for decreasing the tendency of a lipophilic and/or waterlabile drug to collect in the lungs or other organs due to precipitation at or near the injection site and/or in the lungs or other organs themselves following parenteral administration, said method comprising formulating said drug in an aqueous solution adapted for parenteral administration containing from 20% to 50% of a hydroxypropyl, hydroxyethyl, glucosyl, maltosyl or maltotriosyl derivative of β- or γ-cyclodextrin.

2. A method for the preparation of a composition for decreasing the tendency of a lipophilic and/or water-labile drug to collect in the lungs or other organs due to precipitation at or near the injection site and/or in the lungs or other organs themselves following parenteral administration, said method comprising formulating said drug in an aqueous solution adapted for parenteral administration containing from 20% to 50% of a hydroxypropyl, hydroxyethyl, glucosyl, maltosyl or maltotriosyl derivative of β- or γ-cyclodextrin, with the proviso that when the solution contains from 20% to 50% hydroxypropyl-B-cyclodextrin, the said drug is other than the reduced, biooxidizable, blood-brain barrier penetrating, lipoidal dihydropyridine form of a dihydropyridine *» pyridinium salt redox system for braintargeted drug delivery.

3. A method according to Claim 1 or 2, wherein the aqueous solution is approximately isotonic. -2324. A method according to Claim 1 or 2, wherein said drug is an antineoplastic.

4. 5. A method according to Claim 1 or 2, wherein said drug is a sedative, tranquilizer, anticonvulsant, antidepressant, hypnotic, muscle relaxant or antispasmodic .

5. 6. A method according to Claim 1 or 2, wherein said drug is an androgen, estrogen, progestin or antiinflammatory steroid.

6. 7. A method according to Claim 1 or 2, wherein said drug is a steroidal hypnotic or anesthetic.

7. 8. A method according to Claim 1 or 2, wherein said drug is an anticoagulant, cardiotonic, vasodilator, vasoconstrictor, platelet inhibitor or anti-arrhythmic.

8. 9. A method according to Claim 1 or 2, wherein said drug is an antifungal, antiprotozoal, antibacterial, antibiotic or antiviral.

9. 10. A method according to Claim 1 or 2, wherein said drug is a vitamin/nutritional factor, emetic, antiemetic, diuretic, non-steroidal anti-inflammatory agent, anesthetic, hypoglycemic, radiodiagnostic, carbonic anhydrase inhibitor, narcotic antagonist, narcotic agonist, mixed narcotic agonist-antagonist, pharmacologically active protein, dopaminergic/antiParkinsonism agent or agent for treating Alzheimer's disease.

10. 11. A method according to Claim 4, wherein said drug is chlorambucil, lomustine, melphalan, methotrexate, hexamethylmelamine, teniposide, etoposide, semustine, fazarabine, mercaptopurine, tubulazole, carmofur, carr « -2 3 310 Λ 30 mustine, amsacrine, bruceantin, diaziquone, didemnin B, echinomycin or PCNU.

11. 12. A method according to Claim 5, wherein said drug is a barbiturate or a benzodiazepine.

12. 13. A method according to Claim 5, wherein said drug is phenytoin, pentobarbital, phenobarbital, secobarbital, sulpiride, etomidate, chiordiazepoxide , diazepam, medazepam, oxazepam or lorazepam.

13. 14. A method according to Claim 6, wherein said drug is dexamethasone, hydrocortisone, prednisolone, 17 8estradiol, 17o-ethynylestradiol , ethynylestradiol 3methyl ether, estriol, norethindrone, norethindrone acetate, norgestrel, ethisterone, medroxyprogesterone acetate, progesterone, 17-methyltestosterone or testosterone .

14. 15. A method according to Claim 7, wherein said drug is alfaxalone.

15. 16. A method according to Claim 8, wherein said drug is dicumarol, digoxin, digitoxin, nitroglycerin, flunarizine, alprostadil or prostacyclin.

16. 17. A method according to Claim 9, wherein said drug is ampicillin, penicillin G, ketoconazole, itraconazole, metronidazole benzoate, miconacole, flubendazole or co-trimoxazole.

17. 18. A method according to Claim 10, wherein said drug is retinol, vitamin A-acetate, cholecalciferol, retinal, an E, D or K vitamin, apomorphine, chlorthalidone, furosemide, spironolactone, indomethacin, piroxicam, flurbiprofen, acetazolamide, lidocaine, acetohexamide , dimenhydri nate, L-DOPA or THA. -23419. A method according to Claim 1 or 2, wherein said drug is the reduced, biooxidizable, blood-brain barrier penetrating, lipoidal dihydropyridine form of a dihydropyridine * pyridinium salt redox system for braintargeted drug delivery.

18. 20. A method according to Claim 19, wherein the aqueous solution is approximately isotonic.

19. 21. A method according to Claim 19, wherein said dihydropyridine form is a compound of the formula [D-DHC] wherein [D] is a centrally acting drug species and [DHC] is the reduced, biooxidizable, blood-brain barrier penetrating, lipoidal form of a dihydropyridine + pyridinium salt redox carrier.

20. 22. A method according to Claim 21, wherein the centrally acting drug species is a dopaminergic agent, an androgenic agent, an anticonvulsant, an anxiolytic agent, a neurotransmitter, an antibiotic or antibacterial agent, an antidepressant, an antiviral agent, an anticancer or antitumor agent, an antiinflammatory agent, an estrogen or a progestin.

21. 23. A method according to Claim 22, wherein the centrally acting drug species is dopamine, testosterone, phenytoin, GABA, valproic acid, tyrosine, methicillin, oxacillin, benzylpenicillin, cloxacillin, di cl oxaci 11in, desipramine, acyclovir, trifluorothymidine, zidovudine, hydroxy-CCNU, chlorambucil, tryptamine, dexamethasone, hydrocortisone, ethinyl estradiol, norethindrone, estradiol, ethisterone, norgestrel, estrone, estradiol 3-methyl ether, estradiol benzoate, i -235norethynodrel , mestranol, indomethaciη , naproxen, FENU, HENU or 5-F'J.

22. 24. A method according to Claim 23, wherein the compound of the formula [D-DHC] is 1-methy1-3-{{N-{S5 [3,4-bis(pivalyloxy)phenyl]ethy1[carbamoyl[[-1,4dihydropyridine, l-methyl-3-{N-[[6-[3,4-bis(isobutyryloxy[phenyl jethylj][carbamoyl-1,4-dihydropyridine, Ν-{β[3,4-bis(pivalyloxy[phenyl jethyl [aminocarbonyloxymethyl 1.4- di hydro-1-methyl-3-pyridinecarboxylate, 17β-[(1,410 di hydro-1-methyl-3-pyri di nylcarbonyl)oxyjandrost-4-en3-one, 178-{[(3-carbamoyl-1’,4'-di hydropyridinyl)acetyljoxy[androst-4-en-3-one, 5,5-dipheny1-3[(1 1 -methyl-1',4'-dihydropyridin-3'-yl[carbonyloxymethylj-2,4-imidazolidinedione, 3-[3‘-carbamoyl-1' , 4' 15 dihydropyridin-l'-yl[acetyloxymethyl]-5,5-dipheny1-2,4imidazolidinedione, 3-[3'-(3 , '-carbamoyl-l , ',4dihydropyridin-1-yljpropionyloxymethylj-5,5-diphenyl2.4- imidazolidinedione, 1-methyl-3-N-[3-(benzyloxycarbonyl[propyljca rbamoyl-1,4-dihydropyridine, 120 methyl-3-{N-[(3'-cyclohexylcarbonyl)propylj[carbamoyl 1.4- di hydropyri di ne, 1-methyl-3-[2'-(2-propyl)pentanoyloxyjethy1 carbamoyl-1,4-di hydropyridi ne, 1-methyl-3[2'-(2-propyl)pentanoyloxyjethoxycarbonyl-l,4-di hydropyri dine, l-[2'-(2”-propyl)pentanoyloxyjethyl-3-car25 boxamide-1,4-dihydropyridine, 1-methyl-3-|N-[(1’ethoxycarbonyl )-2'-(4-pi valoy1oxyphenyl ) ethylj } carbamoyl-1,4-dihydropyridine, 1-methy1-3-{N-[(1’ethoxycarbonyl)-2'-(4-isobutyryloxyphenyl[ethyl]} carbamoyl-1,4-dihydropyridine, [[(1,4-dihydro-1-methyl30 3-pyridinyl[carbonyljoxyjmethyl [2_S_-(2a,5a,6g) j-3,3dimethyl-7-oxo-6-[(2,6-dimethoxy)benzamidoj-4-thia-lazabicyclo[3.2.0jheptane-2-carboxy1 ate , [[(1,4-dihydro-2361-methyl-3-pyri di nyl)carbonylJoxyjmethyl C 2_S_(2a,5a,6S)-3,3-dimethyl-6-(5-methyl-3-phenyl-4isoxazolecarboxamido)-7-oxo-4-thia-l-azabicyclo[3.2.0jheptane-2-carboxylate, [[(l,4-dihydro-l-methyl-3py ri di nyl ) carbonyl J oxy Jmethyl C 2_S_- (2ο,5α,6β)]-3,3dimethyl-7-oxo-6-[(phenylacetyl)aminoJ-4-thia-l-azabicyclo[3.2.0]heptane-2-carboxylate, [((1,4-dihydro-1methyl - 3-pyri di nyl Jcarbonyl J oxy Jmethyl [ 2_S_- (2α,5α,6β)]6-[3-(2-chlorophenyl)-5-methyl-4-isoxazolecarboxamidoJ3,3-dimethyl-7-oxo-4-thia-l-azabicycl o[3.2.Ojheptane-2carboxylate, [[(1,4-di hydro-1-methyl-3-pyridinylJcarbonyl Joxy Jmethyl [ 2_S_- (2a,5a,6B)J-6-[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethy-7oxo-4-thia-l-azabicyclo[3.2.Ojheptane-2-carboxylate, [{N-[3-(10,ll-dihydro- 5JH - d i b e η z [_b_, _f_J azepin-5yl ) J propyl-N-methylami noJcarbonyloxyJmethyl 1,4di hydro-1-me thyl -3-pyridinecarboxylate, [l-{N-[3(10,11-di hydro- 5_H_- d i benz [b_,f_J az epi n- 5-yl )Jpropyl-NmethylaminojcarbonyloxyJethyl l,4-dihydro-l-methyl~3pyri di necarboxy!ate , l-methyl-3-{[2-(9-guanylmethoxy)ethoxyJcarbonyl}-l,4-dihydropyridine, 3'-(1,4-di hydro 1-methyl-3-pyridinylcarbonyl)-5'-pivaloyltrifluorothymidine, 3'-azido-3'-deoxy-5'-(1-methyl-1,4-dihydro3-pyridinylJcarbonylJthymidine, N-(2-chloroethyl)-N'[4-(1,4-dihydro-l-methyl-3-pyridinecarbonyloxy)cyclohexyl J-N-nitrosourea, N-(2-f1uoroethyl)-N'-[2-(1,4di hydro-l-methyl -3-pyridinecarbonyloxy)ethylJ-Nnitrosourea, N-(2-chloroethyl )-N’-[2-(l,4-dihydro-lmethyl-3-pyridinecarbonyloxy)ethylJ-N-nitrosourea, 1methyl-3-[(N-{2-[4-({4-[bis(2-chloroethylJJaminoJphenyl JbutanoyloxyJethyl }) carbamoyl J-l, 4-di hydropy r ° dine, 1-methyl-3-(N-{4-[4-(4-{[bis(2-chloroethyl)]-237aminojphenyl)butanoyloxy]cyclohexyl}carbamoyl)-1,4di hydro pyri dine, l-nethyl-3-[(N-{2-[4-({4-bis(2-chloroethyl )]amino}phenyl)butanoyloxy]propyl }) carbamoyl]-l,4dihydropyridine, l-methyl-3-[(N-{2-phenyl-2-({4-[bi s(25 chloroethyl)]amino}phenyl)butanoyloxy]}ethyl) carbarn oyl ]-l,4-di hydropy rid ine, l-methyl-3-[N-({l-[4-(4{[bis(2-chloroethyl)]amino}phenyl)butanoyloxy]cyclohexyl}methyl )carbamoyl]-l,4-dihydropyridine, 1-methyl3-N-[2-(3-indolyl)ethyl]carbamoyl-l,4-dihydropyridine, 10 9-fluoro-118,17-dihydroxy-16a-methyl-21-{[(l-methyl1.4- dihydropyridin-3-yl)carbonyl ]oxy}pregna-l,4-diene3,20-dione, 116,17-dihydroxy-21-{[(l-methy1-1,4-dihydro pyri din-3-yl )carbonyl]oxy}pregn-4-ene-3,20-dione, 3hydroxy-176-[(1-methyl-1,4-dihydropyridin-3-yl)car15 bony1]oxyestra-1,3,5(10)-triene, 3-hydroxy-178-{[lmethyl-l,4-dihydropyridin-3-yl)carbonyl]oxy}-19-nor17a-pregna-l,3,5(10)-trien-20-yne, 3-[(1-methyl-1,4di hydro-3- pyri di nyl)carbonyloxy]estra-l,3,5(10)-trien17-one, 176-[(1-methyl-1,4-di hydro-3-pyri di nyl)20 carbonyloxyJestra-1,3,5(10)-trien-3-ol 3-methyl ether, 3,176-bis-{[(l-methyl-l,4-dihydropyridin-3-y1)carbonyl]oxy}estra-l,3,5(10)-triene, 3-(phenylcarbony1oxy)-176-{[(1-methy1-1,4-di hydropyr1di n-3-y1)carbony1]oxy Jest ra-1,3,5(10)-tri ene , 3-methoxy-l76-{[125 methy1-1,4-dihydropyridin-3-yl)carbonyl]oxy}-19-nor17a-pregna-l,3,5(10)-triene-20-yne, 176-{[(1-methyl1.4- di hydro pyri di n-3-yl)carbonyl]oxy}-19-norpregn-4-en20-yn-3-one, 176-{[(l-methy1-1,4-dihydropyridin-3-yl)carbonyl]oxy}pregn-4-en-20-yn-3-one, 13-ethyl-176-{[(l30 methy1-1,4-dihydropyridin-3-yl)carbonyl]oxy}-18,19dinorpregn-4-en-20-yn-3-one, 176-{[(1-methyl-1,4di hydro pyri din-3 -yl)carbonyl]oxy}-19-norpregn-5(10)-en-23820-yn-3-one, l-methyl-3-[N-(2-{l-(p-chlorobenzoyl)-5methoxy-2-methyl-3-indolyl jacetoxyJethyl)carbamoylΙΙ,4-di hydro pyridine, l-methyl-3-{N-[2-(6-methoxy-omethyl-2-naphthalenylacetoxy)ethyl]carbamoyl-l,4dihydropyridine, 3-(l,4-dihydro-l-methyl-3-pyridinylcarbonyloxymethyl )-5-f 1 uorouraci 1 or l-(l,4-dihydro-lmethyl-3-pyridinecarbonyloxymethyl)-5-fluorouraci1.

23. 25. A method according to any one of Claims 1 to 18, wherein the sol uti on;? contai ns from 20% to 50% hydroxypropyl- B-cyclodextrin.

24. 26. A method according to Claim 1, wherein said drug is the reduced, biooxidizable, blood-brain barrier penetrating, lipoidal dihydropyridine form of a dihydropyridine * pyridinium salt redox system for brain-targeted drug delivery, and wherein the solution contains from 20% to 50% hydroxypropyl-Bcyclodextri n.

25. 27. An improved parenteral drug formulation having decreased tendency to collect in the lungs or other organs due to precipitation at or near the injection site and/or in the lungs or other organs themselves following parenteral administration, said formulation comprising a lipophilic and/or water-labile drug in an aqueous solution containing from 20% to 50% of a hydroxypropyl, hydroxyethyl, glucosyl, maltosyl or maltotriosyl derivative of B- or γ-cyclodextrin.

26. 28. An improved parenteral drug formulation having decreased tendency to collect in the lungs or other organs due to precipitation at or near the injection site and/or in the lungs or other organs themselves following parenteral administration, said formulation -239comprising a lipophilic and/or water-labile drug in an aqueous solution containing from 20% to 50% of a hydroxypropyl , hydroxyethyl, glucosyl, maltosyl or maltotriosyl cyclodextrin, with the proviso that when 5 the solution contains from 20% to 50% hydroxypropyl-6-cyclodextriη, then said drug is other than the reduced, biooxidizable, blood-brain barrier penetrating, lipoidal dihydropyridine form of a dihydropyridine * pyridinium salt redox system for 10 brain-targeted drug delivery.

27. 29. A parenteral drug formulation according to Claim 27 or 28, wherein the aqueous solution is approximately isotonic. 30. A parenteral drug formulation according to Claim 15 27 or 28, Claims 4 wherein said to 18 . drug is as defined in any one of 31. A parenteral drug formulation according to Claim 27 or 28, Claims 19 wherein said and 21-24. drug is as defined in any one of 20 32. A parenteral drug formulation according to any one of Claims 27 to 30, wherein the solution contains from 20% to 50% hydroxypropyl-6cyclodext ri n . 33. A parenteral drug formulation according to Claim 25 27, wherein said drug is the reduced, biooxidizable, blood-brain barrier penetrating, lipoidal dihydropyridine form of a dihydropyridine * pyridinium salt redox system for brain-targeted drug delivery, and wherein the solution contains from 20% to 50%

28. 30 hydroxypropyl-6-cyclodextri n. '4 -24034. A method according to claim 1 or 2, v substantially as hereinbefore described and exemplified

29. 35. A parenteral drug formulation according to claim 27 or 28, substantially as hereinbefore 5 described and exemplified.