AU2007214359A1 - Esters of L-carnitine or alkanoyl L-carnitines useful as cationic lipids for the intracellular delivery of pharmacologically active compounds - Google Patents

Description

Australian Patents Act 1990 Regulation 3.2A ORIGINAL COMPLETE SPECIFICATION STANDARD PATENT Invention Title "Esters of L-carnitine or alkanoyl L-caritines useful as cationic lipids for the intracellular delivery of pharmacologically active compounds" The following statement is a full description of this invention, including the best method of performing it known to us:- P/00/011 Q \OPER\MA.2007\August\30322327 Div doc 31/8/07 P\OPER\MAL\2EM)7\30322327 DIv doc-31 //2X)7 -1- Esters of L-carnitine or alkanoyl L-carnitines useful as cationic lipids for the intracellular delivery of pharmacologically active compounds.

This is a divisional of Australian Patent Application No. 2004224958, the entire contents of which are incorporated herein by reference.

The invention described herein relates to a class of new esters of L-camitine and acyl L-carnitines and their use as cationic lipids suitable for favouring the intracellular Sdelivery of pharmacologically active compounds, facilitating their transmembrane transport, or for promoting their interaction with specific cell membrane sites (receptors).

The invention described herein also relates to further known esters of L-carnitine and acyl L-carnitines, useful for the same purposes as the above-mentioned new compounds.

What is meant here by the term "intracellular delivery" is cellular transfection with polynucleotides or plasmids of natural origin or modified, endowed with therapeutic activity (gene delivery) or the introduction of drugs or immunogenic peptides into the cells.

Many of the pharmacologically active substances, such as, for instance, polypeptides and proteins or drugs in general need to penetrate into the cells to exert their effects by influencing cell functions at subcellular or molecular level. For these molecules the cell membrane constitutes a selectively impermeable barrier. The cell membrane, in fact, performs a protective function, preventing the entry of potentially toxic substances, but also the passage of compounds with therapeutic activity. The complex composition of the cell membrane includes phospholipids, glycolipids and proteins; D its function is influenced by cytoplasmatic components such as Ca** and other ions, ATP, microfilaments, microtubules, enzymes and proteins that bind Ca*. The interaction between the structural and cytoplasmatic components of the cells and the response to external r 5 signals are responsible for the selectivity shown by and among the S various different cell types. The barrier effect of the membranes can Sbe overcome by combining substances in complexes with lipid formulations that reproduce the composition of naturally occurring membrane lipids. These lipids are capable of fusing with the o membranes and of releasing the substances combined with them into the cells. The lipid complexes are capable not only of facilitating intracellular transfer by means of fusion with the membranes, but can also diminish the charge repulsion between the membrane and the molecule that has to penetrate into the cell. Amphipathic lipids, such as membrane phospholipids, form lipid vesicles or liposomes in the aqueous systems.

Liposomes are vesicles in which an aqueous volume is entirely enclosed by one or more membranes composed of lipid molecules, usually phospholipids. Phospholipids, which consist in a hydrophilic ?o head and a pair of carbon chains (hydrophobic tail), are the main components of biological membranes. In aqueous solution the hydrophobic tails autoassociate to exclude water, while the 3 hydrophilic heads interact with the medium, spontaneously forming populations of vesicles of varying diameters. The lipids are generally T: zwitterionic, neutral or anionic. These vesicles can be used as carriers of drugs, small molecules, proteins, nucleotides and r plasmids.

t Over recent years, the cationic liposomes, a class of positively charged vesicles prepared from synthetic lipids, have been extensively used for the transfer of genetic material into the cells.

The negative charge of DNA can interact with the positive charges of the cationic lipids, forming a stable DNA-liposome complex. The simplicity and versatility of this technology have made liposomes an important vehicle for the delivery of genes for gene therapy in human subjects. Currently, most of the vectors used for gene therapy and approved by the NIH Recombinant Advisory Committee include viral and synthetic systems.

Viral infection involves a series of complex mechanisms in order to be able to attack a specific cell and carry the DNA into the nucleus. The rationale for the use of viral vectors for gene therapy is based on the possibility of replacing the viral genes with genes that code for a therapeutic function, without eliminating the ability of the viral particle to infect the cells. The limitations of viral therapy have to do with those viral elements that may be immunogenic, cytopathic S and recombinogenic.

Great hopes are placed in the use of cationic lipids for gene therapy. These vectors possess great potential compared with those s of biological origin, since they are much safer, less toxic and are also capable of incorporating genes of large size. As compared with S biological-type vectors, however, they have a low intracellular gene transcription yield. It should be borne in mind, however, that the use of such transfection systems is in an initial stage of research.

o Cationic lipids play a very important role in the formation of the DNA-lipid complex, in cell-complex interaction, in fusion with the membrane, in DNA release inside the cell and in transcription.

There are important examples of in-vivo applications of cationic liposomes. The first clinical trial on gene therapy was conducted by introducing an expression vector containing the human liposomecomplexed HLA-B7 gene for the treatment of melanoma. Another important application relates to the treatment of pulmonary cystic fibrosis by means of the administration via the pulmonary route or as a nasal spray of the liposome-complexed expression vector

SV-

40C-FTR. Other clinical trials involving the use of liposomes in gene therapy for cancer are currently in progress.

Four constituent elements are generally identified in the Z structure of cationic lipids: the positively charged cationic head, the spacer, the anchor lipid and the linker bond.

The cationic head is responsible for the interactions between Scationic liposomes and DNA, between the DNA-liposome complex and the cell membrane and the other components of the cell. It S consists of mono- or polycationic groups (depending on the number of charges) that can be variably substituted.

The spacer is the part of the molecule that separates the cationic head from the hydrophobic tail and is involved in ensuring optimal contact between the cationic head and the negative charges of the DNA phosphates.

The anchor lipid is the non-polar hydrocarbon part of the molecule and determines the physical properties of the double lipid layer, such as its rigidity and rate of exchange with membrane lipids.

What is meant by "linker bond" is the bond between the hydrocarbon chains and the rest of the molecule. This bond determines the chemical stability and biodegradability of the cationic lipids.

In recent years the use of liposomes has steadily increased in the cosmetics sector. The success of liposomes in this field is due to Sthe fact that these compounds are very well tolerated by the skin.

N1 12 They are used both as vehicles for active ingredients and as compounds favouring the absorption of the latter.

rn The scientific and patent literature is rich in references to the .1 preparation and use of liposomes; there are, however, very few Sreferences describing the use of carnitine derivatives useful for gene 3 delivery, whereas for drug delivery no documents are available N1 dealing with known techniques for the preparation of compounds remotely resembling those according to the invention described herein.

Patent application EP 0 279 887 describes the use of a derivative of carnitine, i.e. phosphatidyl carnitine, optionally in mixtures with other phospholipids and lipids (cholesterol, phosphatidyl choline, phosphatidyl serine), for the preparation of liposomes.

In the example provided regarding the preparation of liposomes, liposomes of phosphatidyl carnitine are produced which incorporate propranolol, a drug known to be active as an antihypertensive, anti-angina and antiarrhythmia agent. The carnitine derivative is used here on account of the pronounced myocardial tropism of carnitine. This tropism makes it possible to I *07f 7KhL IPEClW&.?0 I'p. amO 12'07:04 -7avoid the liposomes being metabolised by the liver, rather than reaching the desired target site.

The presence of phosphatidyl camitine also makes it possible to administer the liposomes orally, since they are resistant to intestinal lipases.

In J. Med. Chem 1998 Jun 18; 41 (13):2207-15, a number of esters of L-camitine useful for gene delivery are described, but they are not described or proposed as useful agents for drug delivery.

WO 96/39193 describes novel targeting drug agents that are targeted for entry into the mitochondria via the camitine-acylcarnitine traslocase system, but does not suggest them as useful agent for preparing liposomes.

EP 559 625 BI describes a number of esters of L-camitine and acyl L-camitines endowed with selective gastrointestinal tract muscle-relaxing activity.

In recent years molecular biologists have identified numerous defects at the chromosomal level that cause hereditary diseases in human subjects.

An important sector of modem medicine is concerned with the treatment of these hereditary genetic-based diseases by means of the use of gene therapy protocols.

As already mentioned, cationic liposomes are extensively used for the intracellular delivery of pharmacologically active compounds, facilitating transmembrane transport or promoting their interaction with specific cell membrane sites (receptors).

SThese vectors have great potential as compared to those of ,biological origin, since they are much safer, less toxic and are also capable of incorporating genes of large size. As compared to biological-type vectors, however, they have a low intracellular gene Stranscription yield.

SMoreover, gene transfer mediated by conventional cationic Slipids requires that plasmid DNA and cationic lipids be kept separate, and that their mixing be effected immediately before gene transfer.

Attempts to stabilise these polynucleotide complexes have so far failed to yield encouraging results; in fact, they remain stable only for a short period.

In the field of gene therapy or gene delivery and drug delivery, there is therefore a strongly perceived need for stable, reproducible Ssite-specific systems which are also active after a suitable period of time.

It has now been found that a class of cationic lipids powerfully active in promoting the intracellular delivery of pharmacologically active compounds comprises the new esters of L-carnitine and acyl L-carnitines.

These new compounds are stable and highly selective because they are site-specific in reaching the target organ.

0' 'SPI O 71111 t- -9- This characteristic makes them particularly useful for the transport of active compounds directly to the site where they can exert their pharmacological activity.

According to one embodiment of the present invention there are provided compounds of formula (I) 0

H

3 C R1

H

3 C N R2 o H 3 C 0 0 H 2

R

(I)

where: n is an integer from 1 to 3; R is hydrogen or alkanoyl, straight or branched, with 2-6 carbon atoms; RI and R 2 which may be the same or different, represent a saturated or unsaturated straight acyl chain, with 3-20 carbon atoms; and X- is the anion of a pharmacologically acceptable acid.

Examples of R are acetyl, propionyl, butyryl, valeryl and isovaleryl.

Examples of RI and R 2 are hexanoyl, undecanoyl, myristoyl, palmitoyl or oleoyl.

Preferred examples of compounds according to the invention are: ester of L-carnitine bromide with 2-hydroxyacetyl-1,3-dipalmitoyl glycerol (ST 770); ester of acetyl L-carnitine bromide with 2-hydroxyacetyl-1,3dipalmitoyl glycerol (ST 771); ester of propionyl L-carnitine bromide with 2-hydroxyacetyl-1,3dipalmitoyl glycerol (ST 772); ester of isobutyryl L-carnitine bromide with 2-hydroxyacetyl-1,3 dipalmitoyl glycerol (ST 773); ester of isovaleryl L-carnitine bromide with 2-hydroxyacetyl-1,3dipalmitoyl glycerol (ST 774); ester of L-carnitine bromide with 1, 3 -dihexanoyl-2-hydroxycetyl glycerol (ST 810); ester of acetyl L-carnitine bromide with 1,3-dihexanoyl-2hydroxyacetyl glycerol (ST 809).

ester of propionyl L-carnitine bromide with 1,3-dihexanoyl-2hydroxyacetyl glycerol (ST 808).

What is meant by an anion of a pharmacologically acceptable acid is any anion of an acid that does not give rise to unwanted toxic or side effects.

O These acids are well known to pharmacologists and to experts t) in pharmaceutical technology.

Examples of these anions, though not exclusively the ones listed, are: chloride; bromide; iodide; aspartate; acid aspartate; 'n citrate; acid citrate; tartrate; acid tartrate; phosphate; acid phosphate; fumarate; acid fumarate; glycerophosphate; glucose O phosphate; lactate; maleate; acid maleate; mucate; orotate; oxalate; acid oxalate; sulphate; acid sulphate; trichloroacetate; trifluoroacetate; methane sulphonate; pamoate and acid pamoate.

Compounds of formula in the form of liposomes, are agents useful both for the delivery of naturally occurring or modified plasmids or nucleotides useful in gene therapy, or which code for a peptide or protein useful as a vaccine, and for the general delivery of drugs, such as, for instance, anticancer drugs, antiviral agents, antibacterial agents, antifungals, antiprotozoans, drugs useful for the therapy of cardiovascular system diseases, or immunogenic peptides and other drugs useful in therapy.

The liposomes containing the compound of formula are prepared by means of conventional techniques, well-known to the person having ordinary skill in the art; see for example Allen T.M.

Drugs 56, 747-56 (1998). The liposomes according to the present invention may be prepared also by using other components wellrknown in the practice of liposome technology. In one embodiment of

(N

OJD the present invention, the liposomes may contain helper lipids, a term which is well understood in this art. Examples of helper lipids are cholesterol, l-palmitoyl-2-oleoyl phosphatidyl choline or dioleyl phosphatidyl choline.

The liposomes according to the present invention are suitably 0 presented as compositions. In the embodiment pertaining to delivery of pharmacologically active compounds, the compositions are understood as pharmaceutical ones, optionally comprising pharmaceutically acceptable vehicles and/or excipients.

Compounds of formula in the form of liposomes, may also be useful in the preparation of cosmetic compositions, both comprising the liposome per se as cosmetic active agent and for the delivery of substances with cosmetic activity, such as, for instance, hydrating agents, nutrients, substances for facial cleansing, antiwrinkle agents, anticellulitis agents and anti-stretch-mark agents.

Liposomes comprising the compounds of formula can be administered orally or parenterally, intravenously, intramuscularly, subcutaneously, transdermally, or in the form of nasal or mouth sprays.

Ci The invention described herein also relates to additional Scationic lipids with general formula already known for a different Suse (EP 559 625 mentioned above).

According to the present invention, the compounds of formula .c (II) are esters of L-carnitine, useful for the preparation of liposomes which possess potent activity in drug delivery and present 0 characteristics of stability and selectivity in reaching the target organ comparable to those of the compounds of formula described above. The same advantageous properties are applicable in case of cosmetics.

These compounds have the general formula (II): H3C. 0 HC 3/ H 3C 0 13

(II)

where:

R

3 is a saturated or unsaturated, straight or branched acyl chain, with 4-26 carbon atoms;

R

4 is a saturated or unsaturated, straight or branched alkyl chain, with 4-26 carbon atoms; and X- is the anion of a pharmacologically acceptable acid.

SPreferred examples of R 3 are nonanoyl, dodecanoyl, myristoyl, O palmitoyl, stearoyl or oleoyl.

Preferred examples of R 4 are nonyl, undecyl, tetradecyl, hexadecyl or oleyl.

Examples of specific compounds of formula according to the invention described herein are: palmitoyl L-carnitine chloride undecyl ester (ST 983); stearoyl L-carnitine chloride undecy ester (ST 1055); stearoyl L-carnitine chloride tetradecyl ester (ST 1351); palmitoyl L-carnitine chloride tetradecyl ester (ST 1379); miristoyl L-carnitine chloride tetradecyl ester (ST 1380); palmitoyl L-carnitine bromide hexadecyl ester (ST 1390); oleyl L-carnitine chloride oleyl ester (ST 1392).

A number of compounds of formula namely ST 1380, ST 1390 and ST 1392, are known and described in the above-cited J.

Med. Chem. 1998 Jun 18;41(13):2207-15, as useful agents for the preparation of liposomes for cellular transfection endowed with therapeutic activity, but have never been described as useful agents for the preparation of liposomes for drug delivery.

The skilled person with average experience in the field of pharmaceutical formulations is well aware of the difficulties encountered in preparing liposome-drug complexes; in fact, it is P 1\PER\MKWISPEC]7601 dc.29 0/04 0 impossible to establish a priori whether a liposome which is useful for gene delivery can be used for drug delivery owing to the numerous problems which must be overcome to obtain a liposome capable of complexing a drug and which will deliver it preferentially to the 0 organ where it has to exert its curative activity.

C 5 Compounds of formula in the form of liposomes, are useful agents for the Sdelivery of drugs, such as, for instance, anticancer, antiangiogenic, antiviral, antibacterial, Santifungal, antiprotozoan agents, or drugs useful for the therapy of cardiovascular diseases, O or immunogenic peptides, and other drugs useful in therapy.

Compounds of formula (II) in the form of liposomes, are also useful in the preparation of cosmetic compositions as cosmetic agents per se or for the delivery of substances with cosmetic activity, such as, for instance, hydrating agents, nutrients, facial cleansing agents, and anti-wrinkle, anticellulitis and anti-stretch-mark agents.

Said liposomes may optionally comprise helper lipids as in the case of the liposomes comprising compounds of formula (II).

According to a preferred embodiment of the invention there is provided use of a liposome comprising a compound of formula (II)

H

3

C

H

3 CN O'R4

H

3 C X O O R3

(II)

where:

R

3 is a saturated or unsaturated, straight or branched acyl chain, with 4-26 carbon atoms;

R

4 is a saturated or unsaturated, straight or branched alkyl chain, with 4-26 carbon atoms; and X- is the anion of a pharmacologically acceptable acid, for the transport of drugs or of substances with cosmetic activity.

According to another preferred embodiment of the invention there is provided use of a liposome comprising a compound of formula (III): P 'OPER\MKRISPECI\76301 4iv doc.29/O'04

H

3

C

H3C- R6

H

3 C X- 0 0 4 3

(III)

where:

R

5 is a saturated or unsaturated, straight or branched acyl chain, with 4-26 carbon atoms;

R

6 is a saturated or unsaturated, straight or branched alkyl chain, with 4-26 carbon atoms; and X is the anion of a pharmacologically acceptable acid; with the proviso that: when R 5 is stearoyl R 6 is not stearyl, when R 5 is oleoyl, R 6 is not stearyl, when R 5 is palmitoyl, R 6 is not palmitoyl, when R 5 is myristoyl, R 6 is not myristoyl, when R 5 is lauroyl, R 6 is not lauryl, when R 5 is oleoyl, R 6 is not oleyl, for the transport of a naturally occurring or modified plasmid or polynucleotide.

Liposomes comprising compounds of formula (II) can be administered orally or parenterally, intravenously, intramuscularly, subcutaneously, transdermally, or in the form of nasal or mouth sprays.

Q The invention described herein also relates to additional Scationic lipids with general formula (III), already known for a different use (EP 559 625 mentioned above).

According to the present invention, the compounds of formula c (III) are esters of L-carnitine, useful for the preparation of liposomes Nc which possess potent activity in promoting drug delivery and present O characteristics of stability and selectivity in reaching the target organ comparable to those of the compounds of formula described above.

These compounds have the general formula (III):

H

3 C 0 H X 4 H3C 3

(III)

where: Rs is a saturated or unsaturated, straight or branched acyl chain, with 4-26 carbon atoms;

R

6 is a saturated or unsaturated, straight or branched alkyl chain, with 4-26 carbon atoms; and X- is the anion of a pharmacologically acceptable acid; with the proviso that: when Rs is stearoyl, R 6 is not stearyl, Swhen Rs is oleoyl, R 6 is not stearyl, Swhen R 5 is palmitoyl, R 6 is not palmityl, when Rs is myristoyl, R 6 is not myristyl, when R 5 is lauroyl, R 6 is not lauryl, C C r when Rs is oleoyl, R 6 is not oleyl.

Nc The disclaimed compounds in the form of liposomes are O disclosed in J. Med. Chem. 1988, 41, 2207-2215 exclusively for gene delivery.

Preferred examples of Rs are nonanoyl, dodecanoyl, myristoyl, palmitoyl, stearoyl or oleoyl.

Preferred examples of R 6 are nonyl, undecyl, tetradecyl, hexadecyl or oleyl.

Preferred examples of compounds of formula (III) according to the invention described herein are: 1s palmitoyl L-carnitine chloride undecyl ester (ST 983); stearoyl L-carnitine chloride undecyl ester (ST 1055); stearoyl L-carnitine chloride tetradecyl ester (ST 1351); palmitoyl L-carnitine chloride tetradecyl ester (ST 1379).

Compounds of formula (III) are useful agents for the delivery of naturally occurring or modified plasmids or nucleotides useful in gene therapy or which code for a peptide or protein useful as a vaccine.

Compounds of formula (III) can be administered orally or parenterally, intravenously, intramuscularly, subcutaneously, transdermally, or in the form of nasal or mouth sprays.

The procedure for the preparation of compounds of formula (I) according to the invention is represented in the following reaction diagram, being intended that this diagram applies to the whole general formula The skilled person can easily obtain all the groups meant in R, R 1 and R 2 since all the necessary regents are commercially available or disclosed in literature and reaction conditions are generally applicable to the whole scope of the present invention any modification, if necessary is normally achieved within the general common knowledge.

CH.OF

-2 CjCo-(CF.),,CH CH.CC0(CH:),,CH, CH.C0(CEi.),CH 1 CH-0H.

CH.0c0(CH.)"CE, f C -0 CH.0CO(C'{:),,CH, -B aH,

CX-OH

CH.OCO(CH.L.)"CH

-CIOCCI-{Br CIX.0C0CH.Br LCE.0C0(CH.),,CH)

C)

CH,

0 O H.; /00 Ci?, 0 I I 0 CH.OC(C*H.),ClH CH0OC(cp.).,CH, ch:0c0(CX:)"ClH.

0 cH.0C0(CK'),CH, 0) d) With reference to the above reaction diagram 1, the OJf preparation of compounds of formula according to the invention is illustrated here below.

EXAMPLE 1 In Preparation of the ester of propionyl L-carnitine bromide with 2hydroxy acetyl 1,3 dipalmitoyl glycerol (ST 772) a) Preparation of 1,3-dihydroxypropan-2-one 1,3-dipalmitate (1) Dihydroxyacetone (7g; 0.078 mol) was dissolved in 300 mL of anhydrous chloroform at 0°C (external temperature) under anhydrous nitrogen flow.

To the solution thus obtained palmitoyl chloride (44 g; 0.16 mol) and anhydrous pyridine (15 mL) were added dropwise.

The resulting mixture, the temperature of which was brought up to ambient temperature, was maintained under stirring for 24 hours.

The mixture was then extracted in the following order: with 300 mL of an aqueous solution of 0.5% hydrochloric acid, 300 mL of an aqueous solution of 5% sodium bicarbonate and lastly with 300 mL of water.

The separated organic phase was dehydrated on anhydrous sodium sulphate, filtered on a cellulose filter and concentrated to dryness, obtaining crude product O Pure product was obtained by crystallisation from 500 mL Sof ethyl alcohol.

30.4 g of product were obtained.

Yield: 73% m.p. 80-81°C HINMR (CDC13): 0.9 (6H, t, CH 3

CH

2 1.3 (48H, m, (CH2)n=24); 1.55 (4H, m, -OCOCH 2 CH2-); 2.4 (4H, t, -OCOCH 2 4.7 (4H, s, -OCCH 2 b) Preparation of 1,2,3-trihydroxypropane- 1,3-dipalmitate (2) Water (7.5 mL) was added slowly to product (5 g, 9 mmol), dissolved in tetrahydrofuran (125 mL) and toluene (25 mL) under stirring.

The temperature of the milky white suspension obtained was brought to 5°C (external temperature) and sodium borohydride (500 mg; 13 mmol) was added in small portions. The suspension was maintained under stirring for 30 minutes at 5 0

C.

Glacial acetic acid was then added slowly until the effervescence produced by the decomposition of the excess sodium borohydride ceased, finally obtaining a solution.

Chloroform (100 mL) was added to the solution, obtaining the formation of a biphasic system.

r- SThe lower organic phase consisting of CHC13 was separated, Ob being extracted in the following order: with water (25 mL), sodium bicarbonate (25 mL of 10% aqueous solution) and water (25 mL).

The organic solution containing was dehydrated on sodium 'n sulphate, filtered and concentrated to dryness, obtaining a wax-like product.

SProduct was obtained by acetone crystallisation of the waxlike crude product.

4.8 g of product were obtained.

Yield: 94%.

m.p. 71-72 C HINMR(CDC13): 0.9 (6H, t, CH 3

CH

2 1.3 (48H, m, (CH 2 )n= 24 1.55 (4H, m, -OCOCH 2 CH2-); 2.4 (4H, t, -OCOCH 2 4.2 (5H, m

CHCH

2 1 c) Preparation of 1,3-dipalmitoyl-2-bromoacetyl glycerol (3) Product (2.5 g; 4.4 mmol) was solubilised in anhydrous chloroform (50 mL) under stirring and at 0°C (external temperature).

To the solution thus obtained were slowly added pyridine (0.42 ml) and dropwise 3 ml of a chloroform solution containing brornoacetylchloride (0.43 mL; 5.2 mmol).

The reaction mixture was held for 30 minutes at 0°C (external temperature) and for 30 minutes at ambient temperature.

23

O

O The reaction mixture was then treated in the following order with: an aqueous solution of 1% hydrochloric acid (50 mL approx.), San aqueous solution of 5% sodium bicarbonate (50 mL approx.) and water.

c Product was purified by acetone crystallisation, after Nc dehydrating the reaction mixture (with sodium sulphate) and 0 concentrating to dryness.

g of product were obtained.

Yield: 89%.

m.p. 46-47°C H1NMR (CDC13): 0.9 (6H, t, CH 3 CH2-); 1.3 (48H, m, (CH2)n=24); 1.55 (4H, m, -OCOCH2CH2-); 2.4 (4H, t, -OCOCH2-); 3.9 (2H, s,

OCH

2 COO-) 4.2-4.4 (5H, m, -CHCH20-); 5.25 (1H, m, d) Preparation of the ester L-propionyl carnitine bromide with 2- 1s hydroxyacetvl-1,3-dipalmitoylglvcerol (4) L-propionyl carnitine inner salt (0.95 g, 4.4 mmol) previously vacuum dried at 40°C was suspended in anhydrous dimethylformamide (20 mL approx.).

Product (3 g, 4.7 mmol) was added to the suspension in small portions. The suspension was heated slowly to 38°C and held in these conditions until a solution was obtained.

SAfter 10 minutes the solution was brought to 0°C for Sminutes. A precipitate was obtained, which was filtered and washed with ethyl ether and dissolved in chloroform (100 mL). The opalescent solution obtained (30 mL) was filtered on celite and l n concentrated. To this latter solution was added hexane (100 mL), Sand the precipitate of product obtained was filtered and vacuum dried at 3.19 g of the titre compound were obtained.

Yield: m.p. =127-128°C 25 D--3.9 (C chloroform) Elemental analysis of C 47

H

8 8BrNOio C% H% N% Br% Calculated 62.23 9.78 1.54 8.81 Found 62.73 10.15 0.79 8.77 HI NMR (CDC13) :0.9-0.95 (6H,t, CH 3

CH

2

CH

2 1.1-1.2 (3H,t,

CH

3

CH

2 CO); 1.2-1.4 (24H, m, CH 2 n=24); 1.5-1.6 (4H, m,

OCCH

2

CH

2 2.3-2.4 (4H, t, -OCCH 2

CH

2 2.4-2.45 (4H,

CHCH

2 2.95 (2H, d, -CH2COH 2

CCH

2 COO-); 3.5 (9H, s, N (CH 3 3 4.2 (4H, m, -CH20COCH 2 4.35 (2H,m, -CH 2 4,65 (2H,d,d,

OCH

2 5.25 (1H,m, -OCH 2

CHCH

2 5.75 (1H, m, -CHCH 2 O EXAMPLES 2-7 SThe following compounds were prepared in the same way as in the preceding example: ester of L-carnitine bromide with 2-hydroxyacetyl- 1,3-dipalmitoyl c glycerol (ST 770); ester of acetyl L-carnitine bromide with 2-hydroxyacetyl-1,3dipalmitoyl glycerol (ST 771); ester of isobutyryl L-carnitine bromide with 2-hydroxyacetyl-1,3 dipalmitoyl glycerol (ST 773); ester of isovaleryl L-carnitine bromide with 2-hydroxyacetyl-1,3dipalmitoyl glycerol (ST 774); ester of L-carnitine bromide with 1,3-dihexanoyl-2-hydroxyacetyl glycerol (ST 810); ester of acetyl L-carnitine bromide with 1,3-dihexanoyl-2hydroxyacetyl glycerol (ST 809).

propionyl L-carnitine bromide ester with 1,3-dihexanoyl-2hydroxyacetyl glycerol (ST 808), One preferred embodiment of the invention described herein consists in the preparation of liposomes with anticancer drugs, and particularly liposomes that act as vehicles for camptothecins, for example those disclosed in WO 97/31003. In a more preferred 0 embodiment, the invention described herein provides liposomes for delivering camptothecins with general formula (IV): R R R 9

N

HO

H 3

C

(IV)

where: R 7 is a -C(Rii)=N-O(n)Rio group, in which Rio is hydrogen or a Ci-Cs alkyl or C 1

-C

5 alkenyl group, straight or branched, or a C 3 Cio cycloalkyl group, or a straight or branched (C 3 -Co1) cycloalkyl-

(C

1

-C

5 alkyl group, or a C 6

-C

1 4 aryl, or a straight or branched (C 6

C

1 4 aryl- C 1

-C

5 alkyl group, or a heterocyclic or straight or branched heterocycle-(Ci-Cs) alkyl group, said heterocyclic group containing at least one heteroatom selected from atoms of nitrogen, optionally substituted by a (Ci-Cs) alkyl group, and/or oxygen and/or sulphur; said alkyl, alkenyl, cycloalkyl, aryl, aryl-alkyl, heterocyclic or heterocyclo-alkyl groups being optionally substituted with other groups selected from: halogen, hydroxy, Ci-Cs alkyl, C 1 Cs alkoxy, phenyl, cyano, nitro, -NR 1 2

R

1 3 where R 12 and R 13 which may be the same or different, are hydrogen, straight or branched C Ci-Cs) alkyl, the -COOH group or one of its pharmaceutically icceptable esters; or the -CONR14Ris group, where R 14 and Ris, SNvhich may be the same or different, are hydrogen, straight or Saranched (Ci-Cs) alkyl; or Rio is a C 6 -Clo aroyl residue, optionally substituted by one or r more groups selected from: halogen, hydroxy, straight or branched N Ci-Cs alkyl, straight or branched Ci-Cs alkoxy, phenyl, cyano, nitro,

-NR

16 R7, where R16 and R 1 7, which may be the same or different, are hydrogen, straight or branched Ci-Cs alkyl; SRio is a polyaminoalkyl residue; or Rio is a glycosyl residue; n is the number 0 or 1; Ril is hydrogen, straight or branched Ci-Cs alkyl, straight or branched Ci-Cs alkenyl, C 3 -Cio cycloalkyl, straight or branched

(C

3

C

1 o) cycloalkyl

(C

1

-C

5 alkyl, C 6

-C

1 4 aryl, straight or branched

(C

6

C

14 aryl (Ci-C5) alkyl; Rg and Rg, which may be the same or different, are hydrogen, hydroxyl, straight or branched Ci-Cs alkoxy; their Ni-oxides, single isomers, particularly the syn and anti isomers of the -C(Ri)=N-On)Rio group, their possible enantiomers, diastereoisomers and related mixtures, their pharmaceutically acceptable salts and their active metabolites.

0 Compounds of formula (IV) are described in European patent

(N

Napplication no. 99830124.6, filed on 9th March 1999.

As regards the compounds of formula (IV) in which n is 1 and Rio is as defined above, with the exception of aroyl, these compounds can be prepared starting from camptothecin 7-aldehyde S(formula IVa, Rn hydrogen) o camptothecin 7-keto (formula IVa, R 1 Sother than hydrogen).

N

R

RR

HO

H 3

C

(IVa) where R 7 is the -C(Rii)=0 group, and R 11 is as defined in formula

R

8 and R9 are as defined in formula The formula (IVa) compound is reacted with the formula (Va) compound RioO-NH2, where Rio is as above, to yield compounds of formula in which R7 is the -C(RI )=N-O-Rio group, Rio is defined as in formula except for aroyl.

29 O The reaction can be carried out with conventional methods Sknown to experts in the field, the process consisting in the normal formation of oximes. Preferably, the molar ratio of camptothecin 7aldehyde o 7-keto to hydroxylamine should be in the 1:3 to 3:1 IV 5 range. The relevant hydroxylamine salts can also be used. The Cc, reaction is carried out in the presence of a base, for example, an 0 inorganic base such as potassium carbonate, or an organic base, such as triethylamine or diazabicyclononane, using polar solvents, preferably methanol or ethanol, and carrying out the reaction at a o temperature ranging from ambient temperature to the boiling point temperature of the solvent, optionally in the presence of dehydrating agents, e.g. sodium or magnesium sulphate, molecular sieves. If required, the reaction can also be carried out in the presence of a catalyst, e.g. a Lewis acid.

Alternatively, the above-mentioned compounds can be prepared from the oxime of camptothecin 7-aldehyde (obtained as described in Sawada et al Chem. Pharm. Bull. 39, 2574 (1991)), or 7-ketone or from the corresponding 7-acylcamptothecin by reaction with an Rio-X halide, where X is preferably iodine, in a polar solvent, e.g. tetrahydrofuran or alcohols, and in the presence of a base, e.g.

sodium hydride or potassium carbonate.

As regards the compounds of formula (IV) in which n is 1 and SRio is aroyl, as defined in formula these compounds can be prepared starting from camptothecin 7 -oxime, the preparation of which was described in the previous paragraph, with Rio-COCI acyl chlorides, in polar solvents, and in the presence of a base, preferably pyridine, or directly in pyridine, as described by Cho et al. J. Org.

Chem. 62, 2230 (1997).

As regards the compounds of formula (IV) in which n is 0 and Rio is as defined above, with the exception of aroyl, the compounds o can be prepared starting from camptothecin 7-aldehyde (formula IVa, Ru 1 hydrogen) or camptothecin-7-keto (formula IVa, R 11 other than hydrogen).

R R 7 8

R

HO

HC

where R 7 is the -C(Rll)=O group, and R 11 is as defined in formula Ra and R9 are as defined in formula The formula (IVa) 31 D compound is reacted with the formula (Vb) compound Rio-NH2, Swhere Rio is as defined above, to yield compounds of formula in which R7 is the -C(Rii)=N-Rio group, Rio is defined as in formula (IV), except for aroyl. The reaction can be carried out with conventional methods known to experts in pharmaceutical technology, the t ,A process consisting in the normal formation of imines. Preferably, the molar ratio of camptothecin 7-aldehyde or 7-keto to imine should be in the 1:3 to 3:1 range. The relevant amine salts can also be used.

The reaction is carried out in the presence of a base, for example, an inorganic base, such as potassium carbonate, or an organic base, such as triethylamine or diazabicyclononane, using polar solvents, preferably methanol or ethanol, and carrying out the reaction at a temperature ranging from ambient temperature to the boiling point temperature of the solvent, optionally in the presence of dehydrating is agents, e.g. sodium or magnesium sulphate, molecular sieves. If required, the reaction can also be conducted in the presence of a catalyst, e.g. a Lewis acid as described, for example, by Moretti and Torre, Synthesis, 1970, 141; or by Kobayashi et al, Synlett, 1977, 115).

Camptothecin 7-aldehyde and camptothecin 7-oxime are described in European patent application EP 0056692 and in the above cited article by Sawada et al, Chem. Pharm. Bull. 39, 2574 J (1991).

SThe Ni-oxides of the compounds of formula (IV) are prepared according to known heteroaromatic nitrogen oxidation methods, -f 5 preferably by oxidation with acetic or trifluoroacetic acid and hydrogen peroxide, or by reaction with organic peroxyacids Albini S and S. Pietra, Heterocyclic N-oxides, CRC, 1991).

As regards the varying significance of Rio, present in the different formula V reagents, these reagents are commercially available, or can be prepared according to methods familiar from the literature, which the expert in the sector can resort to, as a supplement to his or her own knowledge of the subject.

Pharmaceutically acceptable salts are obtained with conventional methods described in the literature, and which require i no further description.

EXAMPLE 8 7 -benzyloxyiminomethylcamptothecin (CPT 172) 500 mg (1.33 mmol) of 7 -formylcamptothecin are dissolved in 100 ml of ethanol. 15 ml of pyridine and 638 mg (4 mmol) of Obenzylhydroxylamine hydrochloride are added. The solution is refluxed for 5 hours. The solvent is vacuum evaporated and the 1.) CN residue thus obtained is purified by flash chromatography on silica Sgel using a 4:6 mixture of hexane/ethyl acetate as the eluant.

rn Yield: o\ 200-205°C dec.

SThe product obtained consists of an approximately 8:2 mixture Sof the two syn and anti isomers (isomer A: Rf 0.32; isomer B, Rf S0.19, on Merck 60 F254 silica gel; eluant: hexane:ethyl acetate 3:7).

HPLC: the analyses were carried out on an apparatus equipped with a quaternary pump (HP 1050) with a Rheodyne injector (20 p1 loop) and a diode-array detector (HP 1050) run by the HPLC- ChemStation program. Spectra acquisition was done from 200 to 600 nm and the chromatograms were recorded at 360 and 400 nm.

A C18 reverse-phase column (Rainin C18; 25x0.4 cm, Varian) was used with an RP18 precolumn. The analysis was carried out with a linear elution gradient, starting from acetonitrile:water 30:70 to acetonitrile 100% in 20 min, with a flow rate of 1 ml/min. The retention times were: 12.51 min for isomer B and 14.48 min for isomer A.

1 H-NMR (300 MHz; DMSO-d6): 8: 0.88 H 3 -18A+H 3 -18B), 1.87 8m,

(H

2 -19A+H 2 -19B), 5.18 H 2 5.21 (8s, H 2 -Ph 5.30 (H 2 -Ph A), 5.40 H 2 5.45 H2.17A+H 2 -17B), 6.53 -OH A+-OH 7.3- 7.6 Ar A+ Ar B+H-14A+ H-14B), 7.75 H-l1A+H-11B), 7.85-7- 34 95 H-10A+H-10B), 7.98 (dd, H-12B), 8.18-8.27 H-12A+H9-

(N

8.45 CH=N 8.59 (dd, H-9A), 9.38 CH=N A).

Mass m/z 481 100) 374 (30) 330 (70) 300 (30) 273 (20) 243 91 (34).

tf EXAMPLE 9 S7-butoxyiminomethylcamptothecin (CPT 184) S400 mg (1.06 mmol) of 7-formylcamptothecin are dissolved in ml of ethanol. 12 ml of pyridine and 400 mg (3.18 mmol) of O-tbutylhydroxylamine hydrochloride are added. The solution is refluxed for 4 hours. The solvent is vacuum evaporated and the residue thus obtained is purified by flash chromatography on silica gel using a 4:6 mixture of hexane/ethyl acetate as the eluant.

322 mg (0.72 mmol) of yellow solid are obtained.

Yield: 68% i, 250°C dec.

The product obtained consists of an approximately 8:2 mixture of the two syn and anti isomers (isomer A: Rf 0.31; isomer B, Rf 0.24, on Merck 60 F254 silica gel; eluant: hexane:ethyl acetate 3:7).

HPLC: the analyses were carried out on an apparatus equipped with a quaternary pump (HP 1050) with a Rheodyne injector (20 fl loop) and a diode-array detector (HP 1050) run by the HPLC- O ChemStation program. Spectra acquisition was done from 200 to 600 nm and the chromatograms were recorded at 360 and 400 nm.

A C18 reverse-phase column (Rainin C18; 25x0.4 cm, Varian) was used with an RP18 precolumn. The analysis was carried out s with a linear elution gradient, starting from acetonitrile:water 30:70 S to acetonitrile 100% in 20 min, with a flow rate of 1 ml/min. The retention times were: 12.92 min for isomer B and 14.61 min for isomer A.

IH-NMR (300 MHz; DMSO-d 6 6: 0.88 H 3 -18A+H 3 -18B), 1.30 t- Sbut.B), 1.47 t-but.A), 1.87 H2-19A+H 2 -19B), 5.18 H 2 -5 B), 5.37 (H 2 -5 5.42 H2-17A+H 2 -17B), 6.54 -OH A+-OH 7.35 (s H-14A), 7.36 H-14B) 7.69-7.83 H-11A+H-11B), 7.85-7.98 H-10A+H-10B), 8.07 (dd, H-9B), 8.16-8.27 H-9A+H-12B) 8.40 CH 8.62 (dd, H-12A), 9.31 CH A).

.j Mass m/z 448 28) 391 (40) 374 (100) 362 (40) 330 (34) 57 (17).

PREPARATION OF LIPOSOMES The compounds according to the invention can be used to prepare multilamellar liposomes (MLV) and unilamellar liposomes (SUV), both in the form of dry powders and as suspensions in aqueous solutions.

The compounds according to the invention, prepared as described in examples 1-7, are used to prepare the liposomes according to the following procedure. A suitable amount of the 0 compound is dissolved in chloroform; the solution is vacuum concentrated to dryness in a rotary evaporator until a lipid film is obtained. The lipid film is dried under high vacuum until the last remaining traces of solvent have been eliminated and then dissolved in tert-butylic alcohol or with water. The solution thus obtained is lyophilised, obtaining a soft, dry powder.

The powders are hydrated with a suitable amount of aqueous solution, obtaining the liposome of the compound used, which is o then complexed with the polynucleotide or with the drug desired.

Another method of preparation of liposomes consists in adsorbing a lipid film, consisting of a compound according to the invention in a solvent, on a suitable inert support such as sorbitol, mannitol or other pharmacologically acceptable carbohydrates. The Is mixture is vacuum dried, obtaining a solid which can be easily and very rapidly hydrated prior to use.

Preparations in the form of dry powders present the advantage of being stable for long periods, and are easy to use.

Moreover, the compounds according to the invention can be used to prepare liposomes complexed with DNA or with the drug desired, in the form of dry powders, according to the following procedure. The compound according to the invention is dissolved in tert-butylic alcohol or with water; the solution thus obtained is mixed with DNA or the drug desired and the mixture is lyophilised, S obtaining the complex which we can define as proliposome-DNA or proliposome-drug, in the form of a soft, dry powder.

The powders thus obtained (proliposomes) can be used for the 1 preparation of pharmaceutical compositions which can be administered via aerosol, or which, alternatively, when reconstituted with water, or with a suitable buffer solution, can be administered parenterally or orally.

o Liposomes complexed with DNA or with drugs, in solid form, can also be obtained with the method of adsorption of the lipid film on an inert support such as sorbitol, mannitol or other carbohydrates by means of the method described above.

Testing of liposome formation Liposome formation was tested by means of a colorimetric method, using a water-soluble dye, according to the following procedure. An aqueous solution of the water-soluble dye Arsenazo III was obtained 776.37; 2.3 mg/mL).

This solution was used instead of water to hydrate the lipid films coming from the above-mentioned preparation.

An aliquot of the suspension containing the liposome encapsulating the dye was diluted 100-fold with water.

Two mL of the liposome suspension were used to obtain the 3 first optical density reading at 660 nm; the reading was obtained in relation to an equal sample defined as a blank. 200 il of a CaC12 solution (15 mg/mL; 100 mM) were added to the first sample, and the optical density was measured at 660 nm against the blank, to which 200 pl of water were added. The absorbance value obtained was indicated as reading 2. We proceeded by adding to the sample 100 il of a solution of Triton X-100 5% v/v; 0.26% final concentration) and to the blank 200 il of water; the optical density o reading at 660 nm furnished the optical density value defined as reading 3. To calculate the percentage of encapsulated dye, the following formula was used: dye encapsulated Reading 3 Reading 2 x 100 Reading 3 The percentage of encapsulated dye provides a measure of liposome formation and on average is approximately 40%: the liposome size check was performed using Laser Light Scattering with a positive outcome.

EXAMPLES OF PREPARATION OF LIPOSOMES Preparation of liposomes of palmitoyl L-carnitine chloride undecyl ester (ST 983) in the form of: 0 a) Lyophilised powders j! 65 mg, 0.11 mmol of palmitoyl L-carnitine chloride undecyl ester were dissolved in 20 mL of chloroform, in a 100 mL flask.

The solution was evaporated until a lipid film was obtained I3 which was vacuum dried for 3 hours The product thus obtained was dissolved in tert-butylic alcohol and this solution was rapidly cooled 0 to -70 0 C with liquid nitrogen and lyophilised for 24 hours.

A spongy soft white solid was obtained.

b) Adsorbed powders 143 mg, 0.231 mmol of palmitoyl L-carnitine chloride undecyl ester were dissolved in 10 mL of chloroform. The solution thus obtained was poured in small portions into a 100 mL flask containing 750 mg of sorbitol. At the end of the addition of the various portions of chloroform solution, the chloroform was rapidly evaporated.

The solid thus obtained was vacuum dried for 3 hours.

893 mg of a solid white product were obtained.

Prior to use, the product is hydrated rapidly with a suitable volume of water to obtain an isotonic solution.

c) MLV suspensions mg, 0.11 mmol of palmitoyl L-carnitine chloride undecyl ester were dissolved in 20 mL of chloroform, in a 100 mL flask.

The solution thus obtained was evaporated until a lipid film tJo was obtained which was then vacuum dried for 3 hours.

The lipid film was hydrated with 10 mL of water, at 30 0 C, for 3 hours, obtaining an MLV suspension.

tI 5 The MLV suspension, suitably diluted, was complexed with a ec¢ polynucleotide or with a drug and used for biological assays.

0 e) SUV suspensions mg, 0.11 mmol of palmitoyl L-carnitine chloride undecyl ester were dissolved in 20 mL of chloroform, in a 100 mL flask.

3 The solution thus obtained was evaporated until a lipid film was obtained which was then vacuum dried for 3 hours.

The lipid film was hydrated with 10 mL of water, at 30 0 C, for 3 hours, obtaining an MLV suspension.

The MLV suspension was extruded 10 times through a polycarbonate filter with a pore size of 200 nm. The unilamellar liposome suspension thus obtained was complexed with a polynucleotide or a drug and used for biological assays.

f) Testing of physical stability of liposomes The physical stability of the liposome suspension was tested by means of turbidimetry for a period of 30 days.

An absorbance measurement at 600 nm for a certain time interval was performed for each suspension to be tested. The mean i absorbance value measured at time 0 remained constant for all the j formulations tested.

The molecules considered presented compliant values over the time periods considered MLV and SUV liposome suspensions can be prepared by combining the compounds according to the invention with helper lipids such as cholesterol, 1-palmitoyl-2-oleoyl phosphatidyl choline (POPC) or dioleyl phosphatidyl choline (DOPE).

The compounds are combined with helper lipids for the purposes of obtaining liposomes with stabler membranes. Here below, in the section describing the preparation of liposomes, an example of a preparation is given, in which a compound according to the invention is combined with a helper lipid such as cholesterol or

POPC.

EXAMPLES OF PREPARATION OF LIPOSOMES FOR DRUG

DELIVERY

EXAMPLE Preparation of taxol-ST 983 MLV liposomes (1:40) mg, 0.0234 mmol of taxol and 556 mg, 0.9417 mmol of ST 983 were dissolved in 20 mL of chloroform.

The solution was concentrated until a lipid film was obtained on the surface of the glass flask.

42 After eliminating the last traces of chloroform with the aid of a vacuum pump, 20 mL of tert-butylic alcohol were added to the lipid film and the solution thus obtained was subdivided into 19 fractions which were immediately frozen at -70 0 C with liquid nitrogen and 5 lyophilised for 24 hours. Each fraction of solid contained taxol (1.05 mg) and ST 983 (29.2 mg).

To obtain the final liposome suspension, the lyophilised product was hydrated at the time of use with water (450 pL) or other saline solutions, stirred for 10 min and left to rest for 30 min to o allow completion of the swelling (hydration) process.

MLV liposomes were obtained.

Testing of physical stability of the preparation The physical stability of the preparation was tested by means of turbidimetry with the recording of a TDC (Time Drive Curve) at S800 nm, at 20 for 20 hours.

A constant turbidity trend, indicative of stability of the preparation, was recorded, with no precipitation phenomena.

Testing of chemical stability of taxol in the preparation The chemical stability of taxol was tested by HPLC.

The chromatographic conditions were as follows: Column: pBondapack C-18 Eluant: acetonitrile:water 70:30 Detector UV-VIS 227 nm Flow rate: 1 mL/min Retention time: 4.5 min The taxol concentration, determined against a standard, was 2.13 mg/mL.

The percentage of encapsulated taxol was 98%.

EXAMPLE 11 Preparation of taxol-ST 983 SUV liposomes mg, 0.0234 mmol of taxol and 556 mg, 0.9417 mmol of ST 983 were dissolved 20 mL of chloroform.

The solution was concentrated until a lipid film was obtained on the surface of the glass flask.

After eliminating the last traces of chloroform with a highvacuum pump, 20 mL of tert-butylic alcohol were added to the lipid film and the solution thus obtained was subdivided into 19 fractions which were immediately frozen at a -70°C with liquid nitrogen and lyophilised for 24 hours. Each fraction of solid contained taxol (1.05 mg) and ST 983 (29.2 mg).

To obtain the final SUV liposome suspension the lyophilised product, hydrated with a PBS solution (1 mL), was sonicated for min at 0° C.

44 Filtration was then performed on a 400 nm filter to eliminate tJ traces of titanium released by the sonicator probe.

S Testing of physical stability of the preparation The physical stability of the preparation was tested by means of turbidimetry with recording of a TDC (Time Drive Curve) at 800 nm, at 20 0 C, for 20 hours.

(N

A constant turbidity trend, indicative of stability of the preparation, was recorded, with no precipitation phenomena.

Testing of chemical stability of taxol in the preparation The chemical stability of taxol was tested by HPLC.

The chromatographic conditions were as follows: Column: pBondapack C-18 Eluent: acetonitrile:water 70:30 Detector UV-VIS 227 nm Flow rate: 1 mL/min Retention time: 4.5 min HPLC analysis of the SUV liposome suspension yielded the same results as the corresponding MLV liposome suspension, and in this case, too, the percentage of encapsulated taxol was 98%.

HPLC analysis repeated after 24 hours revealed no new peaks other than the taxol peak, indicating stability of the active ingredient.

EXAMPLE 12 b Preparation of taxol-ST 983-cholesterol liposomes (1:15) These types of liposomes were prepared in order to obtain complexes with stabler membranes.

5 6 mg, 0.0101 mmol of taxol, 62.2 mg, 0.105 mmol of ST 983 and 40 mg of cholesterol were dissolved in 10 mL of chloroform.

The solution thus obtained was concentrated until a lipid film was obtained on the surface of the glass flask.

After eliminating the last traces of chloroform with a highvacuum pump, 6.3 mL of tert-butylic alcohol were added to the lipid film and the solution thus obtained was subdivided into 5 fractions which were immediately frozen at a -70°C with liquid nitrogen and lyophilised for 24 hours. Each fraction of solid contained taxol (1.2 mg), ST 983 (12.44 mg) and cholesterol (8 mg).

,3 To obtain the final liposome suspension, the lyophilised product was hydrated at the time of use with water (1000 pL) or other saline solutions, stirred for 10 min and left to rest for 30 min to allow completion of the swelling (hydration) process.

MLV liposomes were obtained.

Testing of physical stability of the preparation SThe physical stability of the preparation was tested by means tOJ of turbidimetry with recording of a TDC (Time Drive Curve) at 800 nm, at 20 for 6 hours.

A constant turbidity trend, indicative of stability of the f preparation, was recorded, with no precipitation phenomena.

1- EXAMPLE 13 Preparation of taxol-ST 772 SUV liposomes (1:70) mg, 0.0234 mmol of taxol and 1485 mg, 1.638 mmol of ST 772 were dissolved in 20 mL of chloroform.

The solution was concentrated until a lipid film was obtained on the surface of the glass flask.

After eliminating the last traces of chloroform with a highvacuum pump, 20 mL of tert-butylic alcohol were added to the lipid film. To obtain a clear solution, it had to be heated to 60 0 C. The 1a solution was immediately frozen at a -70°C with liquid nitrogen and lyophilised for 24 hours.

To obtain the final SUV liposome suspension the lyophilised product, hydrated with a PBS solution (20 mL), was sonicated for min at 0°C.

Filtration was then performed on a 400 nm filter to eliminate traces of titanium released by the sonicator probe.

Testing of physical stability of the preparation O The physical stability of the preparation was tested by means Jo1 of turbidimetry with recording of a TDC (Time Drive Curve) at 800 nm, at 20 0 C, for 6 hours.

A constant turbidity trend, indicative of stability of the I preparation, was recorded, with no precipitation phenomena.

SEXAMPLE 14 0 Preparation CPT 83-ST 983 MLV liposomes (1:40) 6.3 mg, 0.0168 mmol of CPT 83 (7-carbonitrile camptothecin, described in WO 97/31003) and 400 mg, 0.667 mmol of ST 983 were dissolved in 20 mL of chloroform.

The solution was concentrated until a lipid film was obtained on the surface of the glass flask.

After eliminating the last traces of chloroform with the aid of a vacuum pump, 26 mL of tert-butylic alcohol were added to the lipid film and the solution thus obtained was subdivided into 12 fractions which were immediately frozen at -70°C with liquid nitrogen and lyophilised for 24 hours. Each fraction of solid contained CPT 83 (0.525 mg) and ST 983 (33.33 mg).

To obtain the final liposome suspension, the lyophilised product was hydrated at the time of use with water (1000 pL) or other saline solutions and stirred for 10 min.

MLV liposomes were obtained.

Testing of physical stability of the preparation P) The physical stability of the preparation was tested by means 1_ of turbidimetry with the recording of a TDC (Time Drive Curve) at 800 nm, at 20 for 20 hours.

rn 5 A constant turbidity trend, indicative of stability of the 1preparation, was recorded, with no precipitation phenomena.

Testing of chemical stability of CPT 83 in the preparation.

The chemical stability of CPT 83 was tested by HPLC.

The chromatographic conditions were as follows: Column: Supelcosil LC-ABZ Eluent: phosphate buffer 20 mM:methanol 40:60, pH 7.3 Detector UV-VIS 360 nm Flow rate: 1 mL/min Retention time: 4.033 min The CPT 83 concentration, determined against a standard, was 0.502 mg/mL.

The percentage of encapsulated CPT 83 was 99%.

EXAMPLE Preparation of CPT 83-ST 983 SUV liposomes (1:40) 6.3 mg, 0.0168 mmol of CPT 83 and 400 mg, 0.667 mmol of ST 983 were dissolved in 20 mL of chloroform.

c The solution was concentrated until a lipid film was obtained on the surface of the glass flask.

SAfter eliminating the last traces of chloroform with a highvacuum pump, 26 mL of tert-butylic alcohol were added to the lipid C film and the solution thus obtained was subdivided into 12 fractions Swhich were immediately frozen at a -70°C with liquid nitrogen and

O

N- lyophilised for 24 hours. Each fraction of solid contained CPT 83 (0.525 mg) and ST 983 (33.33 mg).

To obtain the final SUV liposome suspension the lyophilised Sproduct, hydrated with water (1000 iL), was sonicated for 40 min at o0C.

Filtration was then performed on a 400 nm filter to eliminate traces of titanium released by the sonicator probe.

Testing of chemical stability of CPT 83 in the preparation The chemical stability of CPT 83 was tested by HPLC.

The chromatographic conditions were as follows: Column: Supelcosil LC-ABZ Eluent: phosphate buffer 20 mM:methanol 40:60, pH 7.3 Detector UV-VIS 360 nm Flow rate: 1 mL/min Retention time: 4.033 min The CPT 83 concentration, determined against a standard, was -Q 0.3 mg/mL.

The percentage of encapsulated CPT 83 was 59%.

HPLC analysis repeated after 24 hours revealed no new peaks other than the CPT 83 peak, indicating stability of the compound.

S Testing of physical stability of the preparation SThe physical stability of the preparation was tested by means of turbidimetry with recording of a TDC (Time Drive Curve) at 600 nm, at 20'C, for 20 hours.

A constant turbidity trend, indicative of stability of the preparation, was recorded, with no precipitation phenomena.

EXAMPLE 16 Preparation of CPT 184-ST 983 MLV liposomes (1:40) 7.29 mg, 0.0168 mmol of CPT 184 and 400 mg, 0.677 mmol of ST 983 were dissolved in 20 mL of chloroform.

The solution was concentrated until a lipid film was obtained on the surface of the glass flask.

After eliminating the last traces of chloroform with the aid of a vacuum pump, 26 mL of tert-butylic alcohol were added to the lipid film and the solution thus obtained was subdivided into 12 fractions which were immediately frozen at -70 0 C with liquid nitrogen and lyophilised for 24 hours. Each fraction of solid contained CPT 184 (0.607 mg) and ST 983 (33.33 mg).

To obtain the final liposome suspension, the lyophilised product was hydrated at the time of use with water (1000 pL) or other saline solutions and stirred for 10 min.

MLV liposomes were obtained.

Testing of physical stability of the preparation The physical stability of the preparation was tested by means of turbidimetry with the recording of a TDC (Time Drive Curve) at o 600 nm, at 20 for 20 hours.

A constant turbidity trend, indicative of stability of the preparation, was recorded, with no precipitation phenomena.

Testing of chemical stability of CPT 184 in the preparation.

The chemical stability of CPT 184 was tested by HPLC.

The chromatographic conditions were as follows: Column: Supelcosil LC-ABZ Eluent: phosphate buffer 20 mM:methanbl 40:60, pH 7.3 Detector UV-VIS 360 nm Flow rate: 1 mL/min Retention time: 25.5 min The CPT 184 concentration, determined against a standard, was 0.600 mg/mL.

The percentage of encapsulated CPT 184 was 99%.

EXAMPLE 17 Preparation of CPT 184-ST 983 SUV liposomes (1:40) 7.29 mg, 0.0168 mmol of CPT 184 and 400 mg, 0.667 mmol of s ST 983 were dissolved in 20 mL of chloroform.

1 The solution was concentrated until a lipid film was obtained on the surface of the glass flask.

After eliminating the last traces of chloroform with a highvacuum pump, 26 mL of tert-butylic alcohol were added to the lipid o film and the solution thus obtained was subdivided into 12 fractions which were immediately frozen at a -70°C with liquid nitrogen and lyophilised for 24 hours. Each fraction of solid contained CPT 184 (0.607 mg) and ST 983 (33.33 mg).

To obtain the final SUV liposome suspension the lyophilised !s product, hydrated with water (1000 iL), was sonicated for 40 min at

O°C.

Filtration was then performed on a 400 nm filter to eliminate traces of titanium released by the sonicator probe.

Testing of chemical stability of CPT 184 in the preparation The chemical stability of CPT 184 was tested by HPLC.

The chromatographic conditions were as follows: Column: Supelcosil LC-ABZ Eluent: phosphate buffer 20 mM:methanol 40:60, pH 7.3 Detector UV-VIS 360 nm Flow rate: 1 mL/min Retention time: 25.5 min s The CPT 184 concentration, determined against a standard, was 0.36 mg/mL.

The percentage of encapsulated CPT 184 was HPLC analysis repeated after 24 hours revealed no new peaks other than the CPT 184 peak, indicating stability of the active o ingredient.

Testing of physical stability of the preparation The physical stability of the preparation was tested by means of turbidimetry with recording of a TDC (Time Drive Curve) at 600 nm, at 20°C, for 20 hours.

A constant turbidity trend, indicative of stability of the preparation, was recorded, with no precipitation phenomena.

In the following examples, liposomes were prepared by using helper lipids and/or cryoprotecting agents.

EXAMPLE 18 Preparation of CPT 184-ST 983 liposomes In a 2 1 flask, 100 ml of methylchloroform were added to 20 mg of CPT 184 and 600 mg of ST 983 and the mixture was slightly warmed until complete dissolution. The solution obtained was concentrated in a rotavapor until a lipid film was obtained, which c was further dried for two hours at a high-vacuum pump. The lipid film was hydrated with a lactose solution (6 g/300 ml water) at 45 0

C

and left under stirring in the rotavapor for about 2 hours. The suspension was then sonicated for 2 hours, each cycle lasting half an hour. Subsequently, the product was filtered through a 200 nm filter and lyophilised.

Testing of chemical stability of CPT 184 in the preparation The chemical stability of CPT 184 was ascertained by HPLC.

The product was stable during 24 hours of the test.

Testing of physical stability of the preparation The physical stability of the preparation was tested by means of turbidimetry. The product was stable throughout the 24 hours of the test. Particle size also was stable (mean value of 100 nm).

EXAMPLE 19 Preparation of CPT 184-ST 983 liposomes For 1 ml of liposomal formulation (POPC 1-palmitoyl-2-oleoyl phosphatidyl choline 5 mM; ST 983 1.25 mM; CPT 184 0.25 and trehalose 150 mM), the following procedure was used: 0.11 mg, 0.25 pmoles of CPT 184 were dissolved into 250 pL ethyl acetate, 3.79 mg, 4.89 imoles of POPC were dissolved into 100 iL ethanol and 0.74 mg, 1.25 amoles of ST 983 were dissolved into 100 [L ethanol. The three solutions were mixed together and vortexed. The solvents were evaporated off with a rotavapor at room temperature, 80 mbar. The lipid film was dried for two hours in the dark. The lipid film was suspended in a 1 ml of a 150 mM trehalose dihydrate (Fluka, HPLC 99%) solution, sterilised through a 0.22 nm filter and vortexed for two minutes. The suspension was extruded 21 times through 200 nm polycarbonate filters. The extruded liposome suspension was frozen in liquid nitrogen and o1 lyophilised for 2 nights. A white solid was obtained.

EXAMPLE Preparation of CPT 184-ST 983 liposomes The same procedure of Example 19 was used, except trehalose 500 mM was used.

ANTICANCER ACTIVITY OF ST 983 LIPOSOME-ANTICANCER AGENT COMPLEX As will be seen here below, the ST 983 liposome showed predominant accumulation at the pulmonary level. This characteristic of site-specificity has favoured its use in a murine model of pulmonary carcinogenesis.

The anticancer agent used in this experiment was taxol.

To induce the tumour in ivuo, unanaesthetised Balb/c mice received injections of 3x10 5 cells of murine pulmonary carcinoma M109 in 0.1 ml RPMI-1640 (Sigma) in the quadriceps femoris of the right rear paw.

Ten days after implantation of the tumour the liposome-taxol complex was diluted with phosphate-buffered saline solution (PBS, SIGMA, P-4417) and injected intravenously at a concentration of mg/mL of ST 983 and 75 pjg/mL of taxol.

Taxol (paclitaxel INDENA) used as a control was dissolved in the cremophor vehicle EL (BASF) at a concentration of 20 mg/mL and stored at +4°C for the next 24 hours, protected against the light. At the time of use, it was diluted with phosphate-buffered saline solution (PBS, SIGMA) and injected intravenously in the same volume and concentration conditions as described for taxol transported by the ST 983 liposome.

The cremophor was prepared by diluting 1:1 with ethyl alcohol.

Administrations were given for seven consecutive days starting from day 10 after inoculation of the tumour. The animals were kept under observation up to day 17 post-inoculation and sacrificed by cervical dislocation, and their lungs were removed for determination of the number of metastases. Staining of the lungs to detect metastases was done by incubating the lungs for 10 days in 5 ml of Bouin's solution, consisting of 71% saturated picric acid solution, 4.8% glacial acetic acid (Merck), and 24% 10% formaldehyde (Fluka).

At the end of the incubation period in Bouin's solution, the numbers of metastases were counted.

As compared to the untreated control mice, the cremophortransported taxol showed no reducing effect on the number of pulmonary metastases, though the latter were smaller than those of the untreated controls, whereas taxol complexed with the ST 983 liposome showed a significant reduction in both the number and o size of pulmonary metastases.

Statistical analysis of the data for the number of lung metastases was done using the Mann-Whitney non-parametric tests for unpaired data.

The results obtained are presented in Table 1 here below.

TABLE 1 Lung metastases at 17 th day after M109 tumor inoculation in BALB/c mice after treatment with taxol and taxol/liposome ST983.

Group metastases metastases Mean ±s.d size Controls 21±12 M Taxol 22+9 S Taxol-ST983 10±2 S O M= mean (1-2 mm diameter) SS= small 1 mm diameter) In-vitro cytotoxicity tests The toxicity assays were done on HeLa and M109 cells in 96c 5 well plates. On the day after plating, the cells were treated with the Cl molecules being tested for the next 48 hours. The cells were then O washed with PBS and left in normal growth conditions for 48 hours.

After removal of the growth medium, the cells were incubated on ice with 16% TCA, washed 3 times in H 2 0, treated for 30 minutes with sulforhodamine B (SRB) in 1% acetic acid, washed 3 times in 1% acetic acid alone, incubated for 20 minutes in TRIS 10 mM pH 10.5 and, lastly, readings were taken at 540 nm.

Cytotoxicity tests with CPT 83 In-vitro Cytotoxicity tests with CPT 83 were conducted in order to evaluate the cytotoxicity of the anticancer agent complexed with the liposome, as a preliminary indication of efficient activity.

To evaluate the ability of the liposome to transport CPT 83 in vitro in M109 cells the sulforhodamine B test described above was used.

In addition, the cytotoxicity of CPT 83 dissolved in dimethylsulphoxide (DMSO) was also evaluated as compared to that of the same molecule complexed with the ST 983 liposome.

59 The liposome-CPT 83 complex was used in the cytotoxicity assays at the concentrations indicated in Tables 2.1, 2.2 and 3.3 here below in both the SUV and MLV configurations. The liposome:CPT 83 molar ratio used was 40:1.

The mean cytotoxicity values of the ST 983-CPT 83 complexes in both the SUV and MLV configurations given in Tables 2.1, 2.2 and 2.3 here below, indicate that the ST 983 liposome is capable of transporting CPT 83 in much the same way as DMSO, presenting cytotoxicity levels of the same order of magnitude.

0t TABLE 2.1 Cytotoxicity (SRB) of ST 983 SUV-CPT 83 Concentrations in M ctr 1.3 0.13 0.013 00013 0.911 0.294 0.705 0.908 0.911 0.745 0.198 0.525 0.821 0.83 0.884 0.204 0.801 0.906 0.91 0.833 0.25 0.748 0.856 0.853 0.854 0.254 0.778 0.867 0.873 0.793 0.231 0.739 0.802 0.803 0.792 0.193 0.602 0.827 0.829 0901 0.248 0.69 0.904 0.89 Mean 0.839125 0.352444 0.635333 0.767111 0.7667 s.d. 0.060645 0.034513 0.092925 0.042054 0.040149 The values given in the table refer to the optical density readings at 540 nm.

TABLE 2.2 Cytotqxicity ISR-Rj of ST 983 MLV-CPT 83 concentrations in PM Ctr 1.3 0.13 0.013 0.0013 0.895 0.038 0.04 0.095 0.088 0.82 0.038 0.046 0.109 0.124 0.896 0.041 0.049 0.128 0.127 0.847 0.041 0.042 0.105 0.115 0.863 0.041 0.053 0.111 0.107 0.794 0.043 0.041 0.073 0.095 0.829 0.039 0.044 0.08 0.085 0.893 0.04 1 0.044 0.064 0.065 mean 0.854625 0.04025 0.044875 0.095625 0.10075 s. d. 0.038682 0.001753 0.004357 0.021738 0.021359 The values given in the table refer to the optical density readings at 540 nm.

TABLE 2.3 Cytotoxicity (SRB) of DMSO-CPT 83: Concentrations in pM ctr 13 1.3 0.13 0.013 0.0013 0.898 0.281 0.33 0.406 0.8 0.809 0.774 0.267 0.302 0.407 0.804 0.816 0.857 0.3 0.285 0.57 0.863 0.886 0.787 0.286 0.287 0.383 0.836 0.841 0.808 0.285 0.318 0.474 0.851 0.863 0.745 0.288 0.317 0.467 0.79 0.795 0.775 0.312 0.328 0.429 0.806 0.831 0.864 0.318 0.305 0.421 0.81 0.878 Mean 0.8135 0.292125 0.309 0.444625 0.82 0.839875 s.d. 0.053519 0.016848 0.017205 0.059269 0.026506 0.033237 The values given in the table refer to the optical density readings at 540 nm.

Biological activity of ST 983 liposome-CPT 184 complex The biological activity of liposomes of example 18 (below named liposome A) and of example 20 (below named liposome B) was tested.

Toxicity in healthy mouse Liposomes A and B were given orally, intravenously, in comparison with free CPT 184, at the dose of 1.2 mg/kg according to the q4dx4 scheme. The two liposomes did not have significant effects on the weight of body, lungs, spleen and kidneys. Liposome B, intravenously, and liposome A, orally given affected thymus weight 01) similarly to free CPT 184. Intravenous liposome A had only a ir minimum effect. Haematological parameters did not show significant variations after 24 hours, with both liposomes. Liposome n A, intravenously give according to qd5 scheme showed a toxicity comparable with free CPT 184.

Lung tropism of liposomes Liposomes A and B showed predominant accumulation at the pulmonary level. The liposomes were given i.v. 1.2 mg/kg. Free CPT 184 was given orally 1.2 mg/kg in DMSO. The animals, healthy mice, were sacrificed 24 hours after the last administration. Lungs were excised from the corps and frozen in liquid nitrogen. Once thawed, the organs were pooled and homogenised in a 0.1% acetic acid/acetonitrile 1:5. Homogenates were divided in three aliquots, two of them were added with CPT 184 for recovery calculation. The three samples were centrifuged at 16,000 g for 5 minutes.

Surnatants were gathered and extracted with dichloromethane. The organic phase was dried with a speedvac and the residue was redissolved in acetonitrile in order to have the amount corresponding to one animal in 50 pL for loading in HPLC. HPLC was run on a Waters Symmetry C18 3.5 ipm (4.6x7.5 mm). A Merck fluorimeter was the detector at 370 nm excitation and 510 nm emission. The eluant was water/acetonitrile 60:40, isocratic. Sample volume was 50 iL. CPT 184 recovery was about 70%. Both liposome A and B gave an accumulation level for CPT 184 higher than free CPT 184 in DMSO, as shown in Figure 3.

GENE DELIVERY Preparation of liposome-DNA complex Liposome and plasmid DNA were suitably diluted separately in PBS. The DNA was then added to the liposome and the liposome- DNA complex was left for approximately 30 min at 4°C to facilitate 0o the formation of a stable liposome-DNA interaction.

In the in-vitro experiments, 1,2-dioleoyloxy-3-trimethylammonium propane (DOTAP) was used as a reference cationic lipid; pg of plasmid DNA were used per 2x10 5 HeLa cells, and the liposome concentration was 9 iM.

In the in-vivo experiments, both DOTAP and [2,3- (dioleoyl)propyl]trimethylammonium (DOTMA) were used as reference cationic lipids.

The molar ratios defined in the results refer to nmol concentrations of the respective cationic lipids per mg of DNA.

In the in-vivo transfection experiments, 25 [ig of plasmid DNA per animal were used.

The plasmid pCMVluc used in these experiments contained the cDNA of the luciferase gene under the transcriptional control of the cytomegalovirus (CMV) promoter.

Quantitative determination of luciferase activity Protein luciferase activity in cells and tissues was determined using the Boehringer Mannheim kit (cat no. 1669 893).

The cells were washed 3 times in PBS and then removed from the plate with a scraper in lysis buffer (100 mM potassium phosphate pH 7.8. 1 mM dithiothreitol DTT) and submitted to three consecutive cycles of freezing and thawing. After centrifuging in 1.5 mL Eppendorf tubes, the supernatant was used for the luminescence test not more than 5 hours after extraction of the proteins. Luminescence emission measurements were done using a luminometer at 562 nm. After a first freezing in liquid N 2 followed by fine crushing to obtain a powder, the tissues were resuspended in lysis buffer and incubated for 10-15 min in ice.

The samples were then centrifuged in 2 ml Eppendorf tubes and the supernatant was tested for luciferase activity.

Dot-blot analysis Cellular DNA was extracted according to the alkaline lysis procedure described by Sanbrook, Fritsch and Maniatis in Molecular Cloning, 1989.

pg of the DNA extracted from the cells were preabsorbed on Z nylon filters (Boehringer) using the Biorad dot-blot appliance. The filters were then prehybridised for 4 hours at 65°C with a solution containing 0.5 M of sodium pyrophosphate (NaPi), 1 mM EDTA, 7% S SDS. The probe labelled with 3 2 P(alpha) was prepared using plasmid pCMVluc DNA as a template and the random primed Amersham Kit.

The filter was hybridised in the same prehybridisation buffer for 12 hours at 42 0 C using 1x106 CPM/ml. The filter was then submitted to 3 10-min washings at 65 0 C in a buffer containing 40 mM NaPi, 1% SDS. The autoradiographic analysis was carried out with the aid of a phosphor imager which uses phosphor screens activated by betaradiation which are read and quantified by means of a photomultiplier system in conjunction with an image analysis program. The densitometry performed on the dot blot was done using an IP-LabGel image analysis program.

Plasmid DNA transfection tests A number of plasmid DNA transfection tests were carried out both in vitro and in vivo.

Both DOTAP and DOTMA were used as reference cationic lipids, the transfection capacity of which has been amply characterised and described by Abkenet et al., Proc. Natl. Acad. Sci.

USA 1993, 90, 6518. In the in-vivo experiments, various different molar ratios of cationic lipids to plasmid DNA were analysed for the purposes of determining the activity of the cationic lipids and the respective most efficient concentrations for gene transfer. The transfection capability of the various liposomes was evaluated both in vitro and in vivo using the luciferase gene transporter contained in the pCMVluc plasmid, the activity of which, in terms of relative luminescence units (RLU) (described previously) made for easy quantification.

As an alternative, the transfection efficiency of a number of cationic liposomes was evaluated by means of densitometric analysis (phosphor imager) of samples of DNA extracted from transfected cells preabsorbed on nitrocellulose filters (dot-blot) and hybridised with 32 P-labelled plasmid DNA markers, as described previously.

In-vivo transfection tests Dependence of in-vivo transfection efficiency on ST 983 liposome:DNA molar ratio In this experiment, the dependence of liver, lung and heart transfection efficiency on the ST 983 liposome:plasmid DNA molar ratio was evaluated. The following nmol ratios of liposome per pg DNA were tested: 1 2 24:1, 36:1 and 48:1.

Groups of 6 Balb/c mice weighing approximately 20 g were treated intravenously with the above-mentioned amounts of liposome-DNA complex in 200 il volumes of PBS and were sacrificed 24 hours after administration of the complex.

The luciferase activity extracted from the lung, heart and liver tissue revealed a predominantly pulmonary distribution of luciferase at all the molar ratios analysed. In fact, approximately 99% of the total luciferase extracted from the three tissues was located in the lungs. The liposome:DNA molar ratio of 12:1 proved to be the best.

The results obtained are presented in Table 3 here below.

68 TABLE 3 In-vivo transfection efficiency of ST 983 as a function of ST 983:DNA molar ratio (p.g DNA) Lipasoine Mean RLU/mg protein s.d.

Lung ST 983:DNA heart molar ratio liver ST 983 2589 140 1310 385 1035 +/-347 1571 156 8818442 449529 2257856 /-280480 301107 +-21503 112747 ~--5655 458 45 3828742 161332 28875S1 2593 7091 +-249 8351 1-477 5251 +/-489 755 3363 123 12:1 24:1 36:1 48:1 Control 396 55 DOTMA 1352 226 12:1 Dependence of in-vivo transfection efficiency on differences between SRT 983 liposome preparations Luciferase activity values, as relative luminescence units (RLU), extracted from the lungs of Balb/c mice treated intravenously with different ST 983 liposome preparations at a liposome:DNA mola-r ratio of 12: 1, arfe reported in Table 4.

The data obtained, in addition to demonstrating that the ST 983 liposome is capable of transporting plasmid DNAI in vivo, with efficiency ratings higher than and/or comparable to those of DOTMA, also show a degree of variability among the different ST 983 preparations. This may be due to a number of physicochemical characteristics such as the size of the liposomal vesicles, or the relative proportions of the vesicles in relation to the unilamellar (SUV) or multilamellar structure of the different ST 983 preparations. In point of fact, the physicochemical parameters listed Sabove have been amply described as determinants in achieving optimal in-vivo and in-vitro transfection efficiency by R.I. Mahato et al., Human Gene Therapy 9. 1998: 2083.

TABLE 4 ;In-vivo transfection efficiency of ST 983 (different preparations) 01 Liposome Mean RLU/mg protein s.d. ST 983:DNA Lung Molar ratio j ST 983/#72 3118235 184726 12:1 ST 983/#73 7285835 827067 12:1 ST 983/#4 1022117 +/-60402 12:1 Control 1523 98 DOTMA 3410125 189520 12:1 Dependence of in-vivo transfection efficiency on ST 983-DNA liposome complex preincubation time Table 5 presents the relative luminescence units extracted from the liver, lung and heart of mice treated intravenously with ST 983 liposome preincubated with plasmid DNA for 30 minutes or for 3 hours prior to administration. The animals treated with ST 983 preincubated for 3 hours with DNA show an approximately increase in luciferase activity in the lung and heart as compared to those treated with the same liposome preincubated for 30 minutes.

P OPER\MAI.ALC1710322327 Dlv d.o-3l I/2(i)7 S-71- This result suggests that the formation of a stable liposome-DNA complex is a timedependent phenomenon and plays a critical role as a determinant of in-vivo transfection efficiency.

TABLE Efficiency of in-vivo transfection of ST 983 as a function of _liposome/DNA preincubation time Liposome Time Mean RLU/mg protein 6 s.d. T 983:DNA Liver Lung heart molar ratio ST983 30 min. 3526+/-260 874882+/-65917 8118+/-263 12:1 ST983 3h 2497+/-682 4225656+/-211731 37100+/-1853 12:1 Plasmid DNA transfection in HeLa cells with ST 772 liposome Figures 1 and 2 show the plasmid DNA transfection efficiency of the ST 772 liposome in HeLa cells. For this purpose, densitometric analysis of the DNA extracted from the cells transfected with ST 272 and with DOTAP as the reference cationic lipid was carried out. The results of the blot analysis reveal amounts of plasmid DNA of the same order of magnitude as obtained with DOTAP.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The reference in this specification to any prior publication (or information derived from it), or to any matter which is known, is not, and should not be taken as an acknowledgment or admission or any form of suggestion that that prior publication (or information derived from it) or known matter forms part of the common general knowledge in the field of endeavour to which this specification relates.

Claims (9)

1. Use of a compound of formula (III): H 3 C\ 0 HC O R6 HC X S\ 0 (III) where: R 5 is selected from the group consisting of nonanoyl, dodecanoyl, myristoyl, palmitoyl, stearoyl or oleoyl; R6 is selected from the group consisting of nonyl, undecyl, tetradecyl, hexadecyl or oleyl; and X- is the anion of a pharmacologically acceptable acid; for the preparation of a liposome for the transport of a naturally occurring or modified plasmid or polynucleotide.

2. Use according to claim 1, in which X- is selected from the group consisting of chloride; bromide; iodide; aspartate; acid aspartate; citrate; acid citrate; tartrate; acid tartrate; phosphate; acid phosphate; fumarate; acid fumarate; glycerophosphate; glucose phosphate; lactate; maleate; acid maleate; mucate; orotate; oxalate; acid oxalate; sulphate; acid sulphate; trichloroacetate; trifluoroacetate; methane sulphonate; pamoate and acid pamoate.

3. Use according to claims 1-2, in which the compound is selected from the group consisting of: palmitoyl L-caritine chloride undecyl ester; stearoyl L-carnitine chloride undecyl ester; stearoyl L-camitine chloride tetradecyl ester; palmitoyl L-caritine chloride tetradecyl ester. P \OPER\MAL\2l 1(MI0122327 DI doc-3 I/0 (X8r 7 -73-

4. Use according to claim 1, in which the plasmid or polynucleotide codes for a peptide or protein useful as a vaccine.

Use according to claim 1, in which the liposome additionally contains helper lipids.

6. Use according to claim 5, in which said helper lipid is selected from the group consisting of cholesterol, 1-palmitoyl-2-oleoyl phosphatidyl choline or dioleyl phosphatidyl choline.

7. Composition comprising a liposome according to claim 1, for the transport of a naturally occurring or modified plasmid or polynucleotide.

8. Composition according to claim 7, in which the polynucleotide or plasmid codes for a peptide or protein useful as a vaccine.

9. Composition according to claims 7-8, which can be administered orally, parenterally, intravenously, intramuscularly, subcutaneously, transdermally, or in the form of nasal or mouth sprays.