AU1145999A - Method for treating proliferative diseases by therapy - Google Patents
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- AU1145999A AU1145999A AU11459/99A AU1145999A AU1145999A AU 1145999 A AU1145999 A AU 1145999A AU 11459/99 A AU11459/99 A AU 11459/99A AU 1145999 A AU1145999 A AU 1145999A AU 1145999 A AU1145999 A AU 1145999A
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/31—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
- C07C323/32—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to an acyclic carbon atom of the carbon skeleton
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/12—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by a special physical form, e.g. emulsion, microcapsules, liposomes, characterized by a special physical form, e.g. emulsions, dispersions, microcapsules
- A61K51/1282—Devices used in vivo and carrying the radioactive therapeutic or diagnostic agent, therapeutic or in vivo diagnostic kits, stents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B59/00—Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
- C07B59/004—Acyclic, carbocyclic or heterocyclic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur, selenium or tellurium
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- C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C251/36—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atoms of the oxyimino groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C251/38—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atoms of the oxyimino groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of a saturated carbon skeleton
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- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic System
- C07F13/005—Compounds without a metal-carbon linkage
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
Description
WO 99/13920 PCT/EP98/05741 Process for Therapeutic Treatment of Proliferative Diseases The invention pertains to the field of treatment of proliferative diseases and especially the treatment of vascular diseases such as, for example, arteriosclerosis. It is known that ionizing radiation inhibits the proliferation of cells. A considerable number of neoplastic and non-neoplastic diseases have already been treated in this way (Fletcher, Textbook of Radiotherapy, Philadelphia, PA: Lea and Febiger, 1980, Hall, Radiobiology for the Radiologist, Philadelphia, PA: Lippincott, 1988). An attempt has also already been made to treat arteriosclerotic diseases using this process. Arteriosclerosis is an inflammatory, fibroproliferative disease that is responsible for 50% of all deaths in the USA, Europe, and Japan (Ross 1993, Nature 362: 801-809). In its peripheral manifestation, it threatens the upkeep of the extremities; with its coronary manifestation, the risk of fatal myocardial infarction exists; and with supra-aortic infection, there is the threat of stroke. At this time, arteriosclerosis is treated in various ways. In addition to conservative measures (e.g., lowering the cholesterol level in the blood) and the bypass operation, mechanical dilatation (angioplasty), as well as the intravascular removal of atheromatous tissue (atherectomy) of stenotic segments in peripheral arteries and the coronaries have been established as alternatives in regular clinical practice. As stated below, the above-mentioned methods are associated with a considerable number of drawbacks, however. The value of mechanical recanalization processes is greatly diminished by vascular occlusions as a result of vascular tears and dissections, as well as acute thromboses (Sigwart et al. 1987, N. Engl. J. Med. 316: 701-706). Long-term success is jeopardized by the reoccurrence of constrictions (restenoses). The CAVEAT study thus revealed that of 1012 patients, the restenosis rate six months after intervention in coronary atherectomy was 50% and in coronary angioplasty even 57% (Topol et al. 1993, N. Engl. J. Med. 329: 221-227). In addition, abrupt vascular occlusion occurred in this study in 7% of the atherectomy patients and in 3% of the angioplasty patients. Nicolini and Pepine (1992, Endovascular Surgery 72: 919-940) report a restenosis rate of between 35 and 40% and an acute occlusion rate of 4% after angioplastic intervention. To combat these complications, various techniques have been developed. These include the implantation of metal endoprostheses (stents), (Sigwart et al. 1987, N. Engl. J. Med. 316: 701-706; Strecker et al., 1990, Radiology 175: 97-102). The implantation of stents in large-caliber arteries, e.g., in occlusions in the axis in the pelvis, has already become a treatment modality that is to be applied primarily. The use of stents in femoral arteries has shown disappointing results, however, with a primary openness rate of 49% and a reocclusion frequency of 43% (Sapoval et al., 1992, Radiology 184: 833-839). Similar unsatisfactory results have been achieved with currently available stents in coronary arteries (Kavas et al. 1992, J. Am. Coll. Cardiol. 20: 467-474). Up until now, no pharmacological or mechanical interventions have been able to prevent restenosis (Muller et al. 1992, J. Am. Coll. Cardiol. 19: 418-432, Popma et al. 1991, Circulation 84: 14226-1436). The reason for the restenoses frequently occurring after mechanical intervention is assumed to be that interventions induce a proliferation and migration of smooth muscle cells in the vascular wall. The latter result in a neointimal hyperplasia and the observed restenoses in the treated vessel sections (Cascells 1992, Circulation 86, 723-729, Hanke et al. 1990, Circ. Res. 67, 651-659, Ross 1993, Nature 362, 801-809). An alternative process for treating arteriosclerotic diseases uses ionizing radiation. The use of ionizing radiation of external origin on restenosis is associated with the drawback, however, that upon administration the radiation dose is not limited just to the desired spot; rather, the surrounding (healthy) tissue is also undesirably exposed to the radiation. Thus, to date, various studies have come up with little to increase the chances of success (Gellmann et al. 1991, Circulation 84 Suppl. II: 46A-59A, Schwartz et al. 1992, J. Am. Coll. Cardiol. 19: 1106-1113). These drawbacks, which occur when external radiation sources are used, can be overcome if gamma radiation is directly used with restenosis via, e.g., a catheter in the vascular area. With this form of administration with iridium-192, a high radiation dose of 20 Gy is applied to the restenosis foci. Some works report on the almost complete prevention of restenosis after this intervention (Wiedermann et al. 1994, Am. J. Physiol. 267: H125 H132, Bbttcher et al. 1994, Int. J. Radiation Oncology Biol. Phys. 29: 183-186, Wiedermann et al. 1994, J. Am. Coll. Cardiol. 23: 1491-1498, Liermann et al. 1994, Cardiovasc. Intervent. Radiol. 17: 12-16). A drawback to this method is, however, that the radiation dose of 20 Gy that is applied in this case is very high. Since the lesions are dispersed irregularly on the vascular wall, uniform administration of a defined dose is not possible using this technique. Moreover, treatment of large caliber vessels is not possible since, because of the dose reduction from the iridium source, the dose that can be administered is not adequate. Another possible way of inhibiting restenosis is the implantation of P-32-doped stents (Fischell et al. Stents III, Entwicklung, Indikationen und Zukunft, Konstanz [Development, Indications, and the Future, Constancy]: Kollath and Liermann, 1995). In this work, an activity of 0.2 kBq P-32 per centimeter of stent length was enough (corresponding to a radiation dose of 0.25 Gy) to achieve maximum inhibition of smooth vascular muscle cells in vitro. It was thus possible to show that not only y emitters but also B-emitters prevent the proliferation of smooth muscle cells. An advantage of this method is that the radiation dose administered is considerably lower than in all previously mentioned interventions. At this low dose, the endothelial cells that line the vascular bed are not damaged (Fischell et al. Stents III, Entwicklung, Indikationen und Zukunft, Konstanz: Kollath and Liermann, 1995). This form of intervention is possible only once, however, namely when the stent is positioned. In addition, it is limited only to those interventions in which stents are used. The restenoses that occur in the far more common types of interventions, such as atherectomies and angioplasties, cannot be treated with this method. Because of the small range of action of the B-radiation, it is not possible to administer a uniform dose of energy to the entire lesion. In addition to radiation therapy, a number of other therapeutic strategies are also used for inhibiting neointimal hyperplasias (restenoses). The latter comprise standard medicines for suppression of restenoses such as antithrombotic agents, platelet aggregation inhibitors, calcium antagonists, anti-inflammatory and antiproliferative substances, but also gene-therapy approaches. In this case, the inhibition of growth stimulators, e.g., by antisense oligonucleotides or the enhancement of inhibiting factors by expression-vector-plasmids and the virus-mediated gene integration, is possible. Also, Aptamer oligonucleotides can be used for inhibiting a wide variety of receptor-mediated processes, which play a decisive role in restenosis. With great energy and care, substances have been studied over the years that were administered under strictly controlled conditions as a long-term treatment since the desired purpose was theoretically to reduce the restenosis rate (Herrmann et al., 1993, Drugs 46: 18-52). More than 50 controlled studies with different substance groups were performed, without yielding definite proof that the substances examined could seriously reduce the restenosis rate. This also applies for topical administration, in which the substances are brought via a special balloon catheter to the site of action that is desired in each case. It has been shown, however, that the previously used substances are washed too quickly from the vascular wall to be able to be therapeutically effective. Moreover, additional vascular wall alterations, which even act to promote restenosis, are induced by these pressure mediated liquid injections. The object of this invention was therefore to develop a process for the treatment of proliferative diseases that overcomes the drawbacks of previously known treatment processes. - This object is achieved by this invention. A process for therapeutic treatment of proliferative diseases was developed that is characterized in that first an administration catheter is placed at the site of the lesion, and a radioactive substance is topically administered via the catheter, then the catheter is removed, and the radioactive substance remains at the site of the lesion. Since radioactive substances are transported via an administration catheter right to the wall of a blood vessel and remain there, the concentration of the radionuclide lasts long enough to inhibit the proliferation of the cells and thus a restenosis. The process according to the invention has some important advantages in comparison to known treatment processes. In comparison to a considerable number of studied compounds from a wide variety of classes, the topical administration of certain substances and with certain catheters results in a surprisingly high radioactive dose at the desired, pathologically altered spot. This procedure results in a highly effective radiation dose with a low systemic load. The radioactive substances have a long dwell time at the administration site, which results in a highly effective dose on the spot. They are dispersed in particular and uniformly in the pathological regions. The unbonded radioactive substances are quickly eliminated. Since certain radioactive substances, which are described in more detail below, pass into the wall of the arteriosclerotically altered vessels, not only the cells of the intima that face the lumen, but also those of the media and adventitia are kept from proliferating. The proportion of the administered dose that passes through the cell membrane results in a high radiation dose, which is effective close to the cell core. Owing to the sensitivity of proliferating cells to ionizing radiation, the process according to the invention is suitable not only for treatment of arteriosclerotic diseases, but also for the treatment of other proliferative diseases, such as, e.g., tumor diseases.
Suitable radioactive substances are those that have sufficiently high lipophilia to remain adhered to the plaque. For example, radiolabeled metal complexes are suitable, such as, e.g., metal complexes of bis-amine-oxime derivatives of general formula I R HN )nNH R 2RR R N N RR I I OH OH () in which n = 0 - 3, and radicals R 1 to R 8 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic
C
1
-C,
0 O alkyl, C 1
-C,
00 alkenyl,
C
1
-C
10 O alkinyl, C 1 -Co 0 aryl, C,-Co 0 alkylaryl and/or C,
C,
0 arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine and/or iodine atoms, and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde or alkoxy groups with up to 30 carbon atoms and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se, and whereby radicals R 2 and R 3 , R 4 and R 5 as well as R 6 and R 7 together optionally can stand for an oxygen atom. These compounds, together with a radionuclide, form a metal complex, which is then used for topical administration in the treatment of proliferative diseases.
Also suitable are the metal complexes of the N 2
S
2 derivatives of general formulas II and III R1 NH NH R18) R R R SH HS Ra 247 Ra R2 N N H H R R23 / \ SH HSR R 22 R2 R 32 R 3 whereby R 9 to R 32 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic C 1
-C
1 o 0 alkyl, C 1 -Co 0 alkenyl, C 1 -Co 0 alkinyl, C 1
-C
1 o 0 aryl, C 1 -Co 0 alkylaryl and/or C 1 -Coo arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine, and/or iodine atoms and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde, or alkoxy groups with up to 30 carbon atoms, and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se, and whereby radicals R 1 and R 12 , R 13 and R 14 , R" and R 16 , as well as R 1 7 and R 18 together optionally can stand for an oxygen atom, and n, m and p, independently of one another, mean 1 or 2. Other suitable compounds, which are suitable for topical treatment after complexing with suitable radioisotopes, are tetrofosmin, sestamibi and furifosmin derivatives. 9"'Tc tetrofosmin can be obtained under the trade name Myovie
T
" from the Amersham Company; 9 "Tc-sestamibi is marketed under the trade name Cardiolite(R) by the DuPont Company; and 99nTc-furifosmin can be purchased under the trade name TechneScan Q-12 from the Mallinckrodt Medical Company. Together with a radionuclide, all these compounds form a metal complex that can then be used for topical administration in the treatment of proliferative diseases. To form a metal complex, radionuclides can be introduced that are alpha-, beta- and/or gamma-radiators, positron radiators, Auger electron-radiators, and fluorescence radiators, whereby B- as well as combined B/y-radiators are preferred for therapeutic purposes. Corresponding radionuclides are known to one skilled in the art. By way of example, the radionuclides of the elements of atomic numbers 27, 29-32, 37-39, 42-51, 62, 64, 70, 75, 77, 82, or 83 can be mentioned. Preferred are the nuclides 99Rc, 1 86Re, 1 88Re, 67 Cu, 90 Y and 107 Ag; especially preferred are nuclides 1 86Re, 1 8sRe and 67 Cu.
The production of bis-amine-oxime derivatives is described in US Patents 5,506,345 and US 5,387,692; the production of N.S 2 derivatives is described in US Patent 5,279,811. The production of tetrofosmin derivatives is described in European Patent Application EP 303 374; the production of furifosmin derivatives is described in US Patent 5,112,595. Sestamibi derivatives and their production are described in International Patent Application WO 89/02433. Other suitable metal complexes have ligands that are derived from ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), or a macrocyclic compound, such as, e.g., tetraazacyclododecane. The production of these compounds is known to one skilled in the art and is, moreover, described in detail in the examples below. Other suitable ligands are, e.g., porphyrin derivatives, as they are described in, e.g., DE 42 32 925 Al and DE 43 05 523 Al. Metal complexes that are suitable for the process according to the invention can also be produced with radionuclides from these ligands. Also suitable are radioactive thallium compounds of isotopes 201 T1, 207 T1, 209 T1, and 210 Tl; especially suitable is 20 1 TlCl. Radiolabeled colloidal solutions are also extremely well suited for the treatment of proliferative diseases and especially for topical administration. Suitable colloidal solutions are the tin colloids that are described in the examples; especially suitable are the tin colloids that can be produced with the aid of a kit from the Amersham Company ("Amerscan Zinnkolloid (WTc) - Markierungskit fUr die Leberszintigraphie (Amerscan Tin Colloid ("Tc) Labeling Kit for Liver Scintigraphy])." Other suitable colloids are, e.g., radioactive gold sol (1 98 Au colloid) and radiolabeled sulfur colloids as well as other physiologically compatible, radioactive colloidal solutions. Suitable radionuclides for radioactive labeling of colloidal solutions are known to one skilled in the art. By way of example, the radionuclides of elements Ag, As, At, Au, Ba, Bi, Br, C, Co, Cr, Cu, F, Fe, Ga, Gd, Hg, Ho, I, In, Ir, Lu, Mn, N, 0, P, Pb, Pd, Pm, Re, Rh, Ru, Sb, Sc, Se, Sm, Sn, Tb, Tc, or Y can be mentioned. Preferred are the nuclides 9"'Tc, 186Re, 1 8Re, 67 Cu, 90 Y, 1 53 Sm, 16 0 Tb, 16 2 Tb, 19 8 Au, and 10 7 Ag. The production of the colloidal solutions is generally done with a redox reaction or the alteration of pH in an aqueous or alcoholic solution in the presence of a radioactive salt. The colloid can be formed in the presence of a stabilizer or subsequently mixed with a surfactant or another stabilizing amphiphilic substance. Other production methods for suitable colloidal solutions are electrochemical methods, such as are described by, e.g., M. T. Reetz et al. in Angew. Chem. [Applied Chemistry] 1995, Vol. 107, p. 2461 ff. The production of the tin colloids is described in the examples below, as well as in the instructions of the labeling kit of the Amersham Company. The production of a gold colloid for diagnostic purposes is described in Patent DE 24 20 531 C3.
The size of the particles formed is in the range between 5 and 1000 nm, and in the case of the tin colloid it is between 300 and 600 nm. As catheters that are suitable for topical administration of the substances according to the invention, the catheters that are sketched in Fig. 3 can be used. Especially suitable are multichamber balloon catheters (such as, e.g., Dispatch", SciMed) and microperforated balloon catheters. In the examples below, the process in the animal experiment is described. In addition, the production of some compounds that are suitable for use in this treatment process is described. In Examples 1 to 5, the process is implemented with 9'"Tc-labeled HMPAO, whereby the ligand HMPAO has the following structure: CHa
CH
3
CH
3 NH HN
CH
3
CH
3 N N CH 3 I I OH OH (see also Radiopharmaceuticals, Chemistry and Pharmacology, edited by Adrian D. Nunn, 1992, page 53).
WO 99/13920 PCT/EP98/05741 Example 1 Topical Administration of "'Tc-HMPAO The test animal, a white New Zealand rabbit (internal animal identification no.: 1708, male, 3.7 kg of body weight), was prepared 4 weeks before the actual administration experiment as follows: Under anesthesia (Rompun/Ketavet 1:2, 1 ml/kg of body weight, i.m. administration), the endothelium was damaged with a 2F Fogarthy balloon catheter in the arteria carotis dextra (balloon denudation). Then, the animal received a special diet with an addition of 0.2% cholesterol. The test animal developed an arteriosclerotic lesion on the balloon-denuded spot created by this pretreatment. Topical administration of HMPAO that was labeled with technetium 99m is carried out on the anesthetized test animal (for type of anesthesia, see above) via a coronary perfusion/infusion catheter (dispatch 3.0, Xtra slippery coating, manufacturer: Boston Scientific Corporation, Ratingen) directly on the lesion in the carotid artery. The radioactive dose of 0.48 mCi (= 17.76 MBq) was administered in a volume of 0.85 ml. During the entire experiment, the test animal was under a gamma camera (Elscint SP4 HR) to measure the dispersion of radioactivity in the body. The activity at the lesion is set as a proportion of the total activity (measured at this time in the animal). In the case of this test animal, there was found: 5 minutes post administration 55.38% of the dose at the lesion 4 hours post administration 46.78% of the dose at the lesion 24 hours post administration 21.45% of the dose at the lesion Example 2 Topical Administration of " 9 Tc-HMPAO The test animal, a white New Zealand rabbit (internal animal identification no.: 1856, male, 3.3 kg of body weight), was prepared 4 weeks before the actual administration experiment as follows: Under anesthesia (Rompun/Ketavet 1:2, 1 ml/kg of body weight, i.m. administration), the endothelium was damaged with a 2F Fogarthy balloon catheter in the arteria carotis dextra (balloon denudation). Then, the animal received a special diet with an addition of 0.2% cholesterol. The test animal developed an arteriosclerotic lesion on the balloon-denuded spot created by this pretreatment. The topical administration of the HMPAO that was labeled with technetium 99m is carried out on the anesthetized test animal (for type of anesthesia, see above) via a coronary perfusion/infusion catheter (dispatch 3.0, Xtra slippery coating, manufacturer: Boston Scientific Corporation, Ratingen) directly on the lesion in the carotid artery. The radioactive dose of 1.91 mCi (= 70.67 MBq) was administered in a volume of 1.0 ml (flushing with 0.3 ml of physiological saline solution). During the entire experiment, the test animal was under a gamma camera (Elscint SP4 HR) to measure the dispersion of radioactivity in the body. The activity in the lesion is set as a proportion of the total activity (measured at this time in the animal). In the case of this test animal, there was found: 5 minutes post administration 40.74% of the dose at the lesion 4 hours post administration 35.13% of the dose at the lesion 24 hours post administration 23.69% of the dose at the lesion Example 3 Topical Administration of "oc-HMPAO The test animal is a white New Zealand rabbit (internal animal identification no.: 1584, male, 3.4 kg of body weight). Under anesthesia (Rompun/Ketavet 1:2, 1 ml/kg of body weight, i.m. administration), the endothelium was damaged with a balloon catheter in the infraranal aorta (balloon denudation). Then, over a period of 5 minutes, technetium 99m-labeled HMPAO was administered to the test animal via a microperforated balloon catheter (4 mm Match-35 PTA, Schneider Company, FRG). The radioactive dose of 0.64 mCi (= 23.68 MBq) was administered in a volume of 1 ml. During the entire experiment, the test animal was under a gamma camera (Elscint SP4 HR) to measure the dispersion of radioactivity in the body. The activity in the lesion is set as a proportion of the total activity (measured at this time in the animal). In the case of this test animal, there was found: 5 minutes post administration 38.45% of the dose at the lesion 4 hours post administration 35.64% of the dose at the lesion 24 hours post administration 16.63% of the dose at the lesion Example 4 Topical Administration of "9Tc-HMPAO The test animal was a white New Zealand rabbit (internal animal identification no.: 1587, male, 3.5 kg of body weight). Under anesthesia (Rompun/Ketavet 1:2, 1 ml/kg of body weight, i.m. administration), the endothelium was damaged with a balloon catheter in the infraranal aorta (balloon denudation). Then, over a period of 5 minutes, technetium 99m-labeled HMPAO was administered to the test animal via a microperforated balloon catheter (4 mm Match-35 PTA, Schneider Company, FRG). The radioactive dose of 1.18 mCi (= 43.66 MBq) was administered in a volume of 1 ml. During the entire experiment, the test animal was under a gamma camera (Elscint SP4 HR) to measure the dispersion of radioactivity in the body. The activity in the lesion is set as a proportion of the total activity (measured at this time in the animal). In the case of this test animal, there was found: 5 minutes post administration 37.06% of the dose at the lesion 4 hours post administration 32.03% of the dose at the lesion 24 hours post administration 20.01% of the dose at the lesion Example 5 Topical Administration of 9RTc-HMPAO The test animal was a white New Zealand rabbit (internal animal identification no.: 1586, male, 3.3 kg of body weight). Under anesthesia (Rompun/Ketavet 1:2, 1 ml/kg of body weight, i.m. administration), the endothelium was damaged with a balloon catheter in the infraranal aorta (balloon denudation). Then, over a period of 5 minutes, technetium 99m-labeled HMPAO was administered to the test animal via a microperforated balloon catheter (4 mm Match-35 PTA, Schneider Company, FRG). The radioactive dose of 0.45 mCi (= 16.65 MBq) was administered in a volume of 1 ml. During the entire experiment, the test animal is under a gamma camera (Elscint SP4 HR) to measure the dispersion of radioactivity in the body. The activity in the lesion is set as a proportion of the total activity (measured at this time in the animal). In the case of this test animal, there was found: 5 minutes post administration 45.56% of the dose at the lesion 4 hours post administration 36.39% of the dose at the lesion 24 hours post administration 15.24% of the dose at the lesion Example 6 Production of 1-{3-[N-(2-Methoxyethyl)-octadecylsulfamoyl]-2 hydroxy-propyl}-4,7, 10-tetraaza-cyclododecane, Yttrium-90 Complex 5 mg of l-{3-[N-(2-methoxyethyl)-octadecylsulfamoyl]-2 hydroxypropyl}-4,7,10-tetraazacyclododecane (produced according to DE 4340809.5) is dissolved in 500 pl of dimethyl sulfoxide and 50 pl of 0.1M sodium acetate buffer (pH = 4.0). After 37 MBq of yttrium-90-trichloride solution is added, the reaction mixture is heated for 10 minutes to 100 0 C. The Y-90 complex solution that is thus prepared can be used without additional purification. Example 7 a) Production of N,N'-Bisundecyl-diethylene-triamine-pentaacetic acid Diamide 3.57 g (10 mmol) of diethylene-triamine-pentaacetic acid bisanhydride is suspended together with 4.05 g (40 mmol) of triethylamine in 100 ml of absolute dimethylformamide. Then, a solution of 3.42 g (20 mmol) of undecylamine, dissolved in 50 ml of absolute dichloromethane, is added in drops to the reaction mixture at room temperature. The reaction batch is stirred for 6 hours at room temperature, filtered and concentrated by evaporation in a medium-high vacuum. The residue is dissolved three times in 100 ml of dimethylformamide and concentrated by evaporation in a medium-high vacuum in each case. 50 ml of absolute diethyl ether is poured over the foamy reaction product, and it is stirred overnight. It is filtered and dried in a medium-high vacuum. Yield: 6.3 g (90%), white powder. Elementary analysis: Cld: C 61.77 H 9.94 N 10.01 0 18.86 Fnd: C 61.52 H 9.63 N 9.91 0 b) Production of N,N'-bisundecyl-diethylenetriamine-pentaacetic acid diamide, yttrium-90 complex 5 mg of N,N'-bisundecyl-diethylenetriamine-pentaacetic acid diamide (Example 7a) is dissolved in 500 pl of dimethyl sulfoxide and 50 pl of 0.1 M sodium acetate buffer (pH = 4.0). After 37 MBq of yttrium-90 trichloride solution is added, the reaction mixture is allowed to stand for 10 minutes at room temperature. The Y-90 complex solution that is thus prepared can be used without additional purification. Example 8 a) Production of N-Benzyloxycarbonyl-glycyl-N'-undecyl glycinamide 3.63 g (10 mmol) of N-benzyloxycarbonyl-glycyl-glycine-N hydroxysuccinimide ester and 1.71 g (10 mmol) of undecylamine are dissolved in 100 ml of absolute dichloromethane. The reaction mixture is stirred for 6 hours at room temperature. Then, it is diluted with 100 ml of dichloromethane, the organic phase is washed twice with 50 ml of saturated sodium bicarbonate solution and once with 50 ml of water. It is dried on magnesium sulfate, and the solvent is evaporated in a vacuum. The crude product is purified by chromatography on silica gel (eluant: dichloromethane/methanol 95:5). Yield: 3.8 g (90.6%), white powder. Elementary analysis: Cld: C 65.84 H 8.89 N 10.01 0 15.25 Fnd: C 65.71 H 9.02 N 10.10 0 b) Production of Glycyl-N'-undecyl-glycinamide 3 g (7.15 mmol) of N-benzyloxycarbonyl-glycyl-N'-undecyl glycinamide (Example 8a) is dissolved in 100 ml of absolute ethanol. After 300 mg of palladium is added to carbon (10%), it is hydrogenated for 2 hours at room temperature (1 atmosphere of hydrogen). It is filtered and concentrated by evaporation in a vacuum. The resulting amine is used for subsequent reaction without additional purification. Yield: 1.92 g (94.1%), white foam. Elementary analysis: Cld: C 63.12 H 10.95 N 14.72 0 11.21 Fnd: C 63.03 H 11.04 N 14.57 0 c) Production of N-(S-Acetyl-mercaptoacetyl)-glycyl-N'-undecyl glycinamide 285.4 mg (1 mmol) of glycyl-N'-undecyl-glycinamide (Example 8b) and 231.2 mg (1 mmol) of S-acetyl-mercapto-acetic acid-N hydroxy-succinimide ester are dissolved together in 20 ml of absolute dichloromethane. The reaction mixture is stirred for 6 hours at room temperature. Then, it is diluted with 20 ml of dichloromethane, and the organic phase is washed twice with 5 ml of semi-saturated sodium bicarbonate solution and once with 5 ml of water. It is dried on magnesium sulfate, and the solvent is evaporated in a vacuum. The crude product is purified by chromatography on silica gel (eluant: dichloromethane/methanol 93:7). Yield: 362 mg (90.1%), white powder 44 Elementary analysis: Cld: C 56.83 H 8.79 N 10.46 0 15.94 S 7.98 Fnd: C 56.67 H 8.93 N 10.18 0 S 7.72 d) Production of N-(Mercaptoacetyl)-glycyl-N'-undecyl glycinamide 201 mg (0.5 mmol) of N-(S-acetyl-mercaptoacetyl-glycyl-N' undecyl-glycinamide (Example 8c) is dissolved in 15 ml of absolute ethanol. It is saturated with argon, and an ammonia stream is directed through the solution for 30 minutes. Then, it is concentrated by evaporation, and the residue is taken up in 20 ml of dichloromethane. The organic phase is shaken once with 2% aqueous citric acid and dried on sodium sulfate. The solvent is evaporated in a vacuum, and the residue is chromatographed on silica gel (eluant: dichloromethane/methanol 9:1). Yield: 153 mg (85.1%), white powder Elementary analysis: Cld: C 56.79 H 9.25 N 11.69 0 13.35 S 8.92 Fnd: C 56.67 H 9.43 N 11.48 0 S 8.71 e) Production of N-(Mercaptoacetyl)-glycyl-N'-undecyl glycinamide, Re-186 Complex 5 mg of N-(mercaptoacetyl)-glycyl-N'-undecyl-glycinamide (Example 8d) is dissolved in 800 pl of ethanol. After 5 mg of disodium-L-tartrate and 50 pl of 0.1 M sodium hydrogen phosphate buffer (pH = 8.5) are added, 37 MBq of perrhenate and 10 pl of tin dichloride-dihydrate solution (5 mg of SnCl 2 x 2H 2 0/1 ml of 0.1 M HCl) are added. The reaction mixture is heated for 5 minutes to 60 0 C. The thus prepared solution of the Re-186 complex of N-(mercaptoacetyl)-glycyl-N'-undecyl-glycinamide can be used without additional purification. Example 9 Production of N,N'-Bis[3,6,9,9-tetra(hydroxycarboxymethyl)-1-oxo 3,6,9-triaza-non-1-yl]-mesoporphyrin-IX-13,17-dihydrazide, Y-90 Complex 5 mg of N,N'-bis[3,6,9-tri(hydroxycarboxymethyl)-9 (ethoxycarboxymethyl)-1-oxo-3,6,9-triaza-non-1-yl]-mesoporphyrin IX-13,17-dihydrazide (produced according to DE 42 32 925 Al, Example la) is stirred in 5 ml of 0.1 M NaOH under argon atmosphere for 3 hours at room temperature. After saponification of the bis-ethyl ester (TLC monitoring) has been completed, it is set at pH = 6 with glacial acetic acid, and 37 MBq of yttrium-90 trichloride solution is added to the batch. It is stirred for 15 minutes at room temperature. HPLC analysis indicates 95% incorporation of the radioisotope. Example 10 Production of 5,10,15,20-Tetrakis-[3-(carboxymethoxy)-phenyl] porphyrin, Yttrium-90 Complex 2.0 mg of 5,10,15,20-tetrakis-[3-(carboxymethoxy)-phenyl] porphyrin (produced according to DE 43 05 523 Al, Example 13a) is dissolved in 5 ml of acetic acid and mixed with a hydrochloric acid solution of 1.0 mCi yttrium-90-chloride. The reaction mixture is autoclaved for one hour at 140 0 C, the solvent is evaporated in a vacuum, and the residue is taken up in 5 ml of water. By adding aqueous sodium bicarbonate solution in drops, it is set at pH 7.3, and the red solution that is produced is filtered with a membrane filter. HPLC monitoring of the filtrate can indicate an incorporation rate of > 95% of the activity used in the porphyrin ligands. Example 11 Production of 5,10, 15,20-Tetrakis-[3- (carboxymethoxy-) -phenyl] porphyrin, Copper-67 Complex The production of the complex is described in DE 43 05 523 Al, Example 14. Example 12 Production of a Technetium-99m-tin Colloid 555 MBq of sodium pertechnetate-99m in 2 ml of 0.9% sodium chloride solution is mixed at room temperature with 20 pl of tin(II) chloride solution (5 mg of tin(II) chloride-dihydrate/1 ml of 0.01 M HCl). After 10 minutes, it is diluted with 1 ml of PBS buffer. The solution that is obtained is slightly opalescent.
Example 13 Production of a Rhenium-186-tin Colloid 37 MBq of sodium perrhenate-186 in 2 ml of 0.9% sodium chloride solution is mixed at room temperature with 40 pl of tin(II) chloride solution (5 mg of tin(II) chloride dihydrate/1 ml of 0.01 M HCl). After 10 minutes, it is diluted with 1 ml of PBS buffer. The solution that is obtained is slightly opalescent. Example 14 Topical Administration of a Tin Colloid The test animal is a white New Zealand rabbit (internal animal identification no.: 1852, male, 3.5 kg of body weight). Under anesthesia (Rompun/Ketavet 1:2, 1 ml/kg of body weight, i.m. administration), the endothelium was damaged with a balloon catheter in the infraranal aorta (balloon denudation). Then, over a period of 5 minutes, tin colloid, which was produced according to the kit of the Amersham Company ("Amerscan Zinnkolloid (990c) - Markierungskit fUr die Leberszintigraphie [Amerscan Tin Colloid (WmTc) - Labeling Kit for Liver Scintigraphy]"), was administered to the test animal with a microperforated Match catheter (balloon catheter with a 5 mm diameter; manufacturer: Schneider Company, Dusseldorf). The radioactive dose of 0.4 mCi (= 14.8 MBq) was administered in a volume of 0.1 ml. During the entire experiment, the test animal is under a gamma camera (Elscint SP4 HR) to display the dispersion of radioactivity in the body. In Fig. 1, the situation before administration is depicted in the upper part. The catheter that contains the tin colloid can be seen clearly. The arrow shows the balloon of the catheter, which is at the desired administration spot. In the lower part of the image, the same site is shown 1.5 hours after administration and removal of the catheter. The amount of tin colloid that remains at the administration spot is clearly visible. Example 15 Topical Administration of a Tin Colloid The test animal is a white New Zealand rabbit (internal animal identification no.: 1839, male, 3.7 kg of body weight). Under anesthesia (Rompun/Ketavet 1:2, 1 ml/kg of body weight, i.m. administration), the endothelium was damaged with a balloon catheter in the infraranal aorta (balloon denudation). Then, over a period of 5 minutes, tin colloid, which was produced according to the kit of the Amersham Company ("Amerscan Zinnkolloid (91rc) - Markierungskit fUr die Leberszintigraphie") was administered to the test animal with a microperforated Match catheter (balloon catheter with a 5 mm diameter; manufacturer: Schneider Company, DUsseldorf). The radioactive dose of 0.47 mCi (= 17.39 MBq) was administered in a volume of 0.1 ml. During the entire experiment, the test animal was under a gamma camera (Elscint SP4 HR) to display the dispersion of radioactivity in the body. In Fig. 2, the situation before administration is depicted in the upper part. The catheter that contains the tin colloid can be seen clearly. The arrow shows the balloon of the catheter, which is at the desired administration spot. In the lower part of the image, the same site is shown 1.5 hours after administration and removal of the catheter. The amount of tin colloid that remains at the administration spot is clearly visible.
Claims (6)
1. Process for therapeutic treatment of proliferative diseases, characterized in that first an administration catheter is placed on the site of the lesion, and a radioactive substance is administered topically via the catheter, then the catheter is removed, and the radioactive substance remains on the site of the lesion.
2. Process for therapeutic treatment of arteriosclerotic diseases, wherein first an administration catheter is placed on the site of the lesion, and a radioactive substance is administered topically via the catheter, then the catheter is removed, and the radioactive substance remains on the site of the lesion.
3. Process according to claim 1 or 2, wherein the radioactive substance is a metal complex.
4. Process according to claim 1 or 2, wherein the radioactive substance is a metal complex, whose ligand is a bis-amine-oxime derivative of general formula I, (CR 4 R 5 ) -N, R HN n NH R R 2R R N N /'R 8 I I OH OH in which n = 0 - 3, and radicals R 1 to R 8 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic C,-Co 0 alkyl, C,-Cloo alkenyl, C,-C, 00 alkinyl, C 1 -Coo aryl, Cl-Cloo alkylaryl and/or C 1 C100 arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine and/or iodine atoms, and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde or alkoxy groups with up to 30 carbon atoms and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se, and whereby radicals R 2 and R 3 , R 4 and R 5 as well as R 6 and R 7 together optionally can stand for an oxygen atom, and whose central atom is a radionuclide of the elements of atomic numbers 27, 29-32, 37-39, 42-51, 62, 64, 70, 75, 77, 82 or 83.
5. Process according to claim 1 or 2, wherein the radioactive substance is a metal complex, whose ligand is an N 2 S 2 derivative of general formula II, R R R2 NH NH R 1 (R 17n R" n R p R 9 SH HS R 20 (I) whereby R 9 to R 20 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic C 1 -C 1 oo alkyl, C,-Co 0 alkenyl, C,-C 1 0 O alkinyl, C,-Co 0 aryl, C,-Cloo alkylaryl and/or CI-C1O arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine and/or iodine atoms and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde or alkoxy groups with up to 30 carbon atoms, and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se, and whereby radicals R 11 and R 12 , R 13 and R 14 , R 15 and R 1 6 as well as R 17 and R 18 together optionally can stand for an oxygen atom, and n, m and p, independently of one another, mean 1 or 2, and whose central atom is a radionuclide of the elements of atomic numbers 27, 29-32, 37-39, 42-51, 62, 64, 70, 75, 77, 82 or
83. 6. Process according to claim 1 or 2, wherein the radioa.ptive substance is a metal complex, whose ligand is an N 2 S 2 derivative of general formula III, R26 27V R2 R 2 R 24 N N 2 H H R R 23SH HS Ro e 2 -132 31 R R R (M ) whereby R 21 to R 32 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic C 1 -C 00 alkyl, C 1 -C 00 alkenyl, C 1 -C 00 alkinyl, C 1 -C 00 aryl, C 1 -C 00 alkylaryl and/or C 1 -C 00 arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine and/or iodine atoms and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde or alkoxy groups with up to 30 carbon atoms, and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se, and whose central atom is a radionuclide of the elements of atomic numbers 27, 29-32, 37-39, 42-51, 62, 64, 70, 75, 77, 82 or 83. 7. Process according to claim 4, 5, or 6, wherein a central atom, which is selected from the group 99Tc, '8Re, 1 88Re 67 CU, 90 Y and 107 Ag, contains the metal complex that is used. 8. Process according to claim 1 or 2, wherein the radioactive substance is a metal complex, whose ligand is a porphyrin derivative. 9. Process according to claim 1 or 2, wherein the radioactive substance is a thallium compound of isotopes 201 T1, 207 T1, 2 09T1 and 210 T1. 10. Process according to claim 1 or 2, wherein the radioactive substance is 201 TlCl. 11. Process according to claim 1 or 2, wherein the radioactive substance is a tetrofosmin derivative. 12. Process according to claim 1 or 2, wherein the radioactive substance is a sestamibi derivative. 13. Process according to claim 1 or 2, wherein the radioactive substance is a furifosmin derivative. 14. Process according to claim 1 or 2, wherein the radioactive substance is a colloidal solution with particle sizes of between 5 and 1000 nm. 15. Process according to claim 1 or 2, wherein the radioactive substance is 9"'Tc-tin colloid or 1 8Re-tin colloid. 16. Process according to claim 1 or 2, wherein the catheter that is used is a microporous balloon catheter. 17. Process according to claim 1 or 2, wherein the catheter that is used is a multichamber balloon catheter. 18. Use of complexes whose ligand is a bis-amine-oxime derivative of general formula I R 3 HN/(CR4R5 )n "NH Re R N R7 R N N X'R I I OH OH in which n = 0 - 3, and radicals R1 to R 8 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic C 1 -Co 0 alkyl, C 1 -C 00 alkenyl, C 1 -C 00 alkinyl, C 1 -C 00 aryl, C 1 -C 00 alkylaryl and/or C 1 -C 00 arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine and/or iodine atoms and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde or alkoxy groups with up to 30 carbon atoms and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se, and whereby radicals R 2 and R 3 , R 4 and R 5 as well as R 6 and R together optionally can stand for an oxygen atom, and whose central atom is a radionuclide of the elements of atomic numbers 27, 29-32, 37-39, 42-51, 62, 64, 70, 75, 77, 82 or 83, for the production of agents that are administered topically in the treatment of proliferative diseases. 19. Use of complexes whose ligand is an N 2 S 2 derivative of general formula II R 14 R R NH NH R (R N 18pn R' R19 R SH HS Ra20 whereby R 9 to R 20 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic C 1 -C 0 alkyl, C 1 -C 1 0 O alkenyl, C 1 -COO alkinyl, C 1 -C, 0 O aryl, C 1 -CO alkylaryl and/or C 1 -Co 0 arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine and/or iodine atoms and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde or alkoxy groups with up to 30 carbon atoms and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se and whereby radicals R 1 and R 12 , R 1 3 and R 14 , R 15 and R 16 , as well as R17 and R 18 together optionally can stand for an oxygen atom, and n, m and p, independently of one another, mean 1 or 2, and whose central atom is a radionuclide of the elements of atomic numbers 27, 29-32, 37-39, 42-51, 62, 64, 70, 75, 77, 82 or 83, for the production of agents that are administered topically in the treatment of proliferative diseases. 20. Use of complexes whose ligand is an N 2 S 2 derivative of general formula III 26 2 Ra R 28 R NRN H HR R23 SH HS R 3 o -213 31 R R R R(I) whereby R 21 to R 32 are the same or different and in each case stand for a hydrogen atom and/or for an unbranched, branched, cyclic or polycyclic C 1 -C, 00 alkyl, C 1 -C 00 alkenyl, C 1 -C 00 alkinyl, C 1 -C 00 aryl, C,-C 00 alkylaryl and/or C 1 -C, 00 arylalkyl radical, which optionally is substituted with fluorine, chlorine, bromine and/or iodine atoms and/or hydroxy, oxo, carboxy, aminocarbonyl, alkoxycarbonyl, amino, aldehyde or alkoxy groups with up to 30 carbon atoms and/or optionally is interrupted and/or substituted by one or more heteroatoms from the series N, P, As, 0, S, Se, and whose central atom is a radionuclide of the elements of atomic numbers 27, 29-32, 37-39, 42-51, 62, 64, 70, 75, 77, 82 or 83, for the production of agents that are administered topically in the treatment of proliferative diseases. j U 21. Use of compounds according to one of claims 18 to 20, wherein the radionuclide is selected from the group 99"'Tc, 1 8Re, 1 ssRe, 6 7CU, 90 Y and 10 7 Ag. 22. Use of colloidal solutions for the production of agents for the treatment of proliferative diseases, wherein the colloidal solution is labeled with a radionuclide of elements Ag, As, At, Au, Ba, Bi, Br, C, Co, Cr, Cu, F, Fe, Ga, Gd, Hg, Ho, I, In, Ir, Lu, Mn, N, 0, P, Pb, Pd, Pm, Re, Rh, Ru, Sb, Sc, Se, Sm, Sn, Tb, Tc or Y. 23. Use of colloidal solutions according to claim 22, wherein the colloidal solution is labeled with a radionuclide that is selected from the group 99"'Tc, 1 8Re, IMRe, 6 7Cu, 90 Y, 153 Sm, 1 6Tb, 16 2 Tb, 198 Au and 107 Ag. 24. Use of colloidal solutions according to claim 22, wherein the colloid is produced by a redox reaction in the presence of a radioactive salt. 25. Use of colloidal solutions according to claim 22, wherein the colloid is produced by changing the pH in an aqueous or alcoholic solution in the presence of a radioactive salt. 26. Use of colloidal solutions according to claim 22, wherein the particle size of the colloidal particles is between 5 and 1000 nm. 27. Use of colloidal solutions according to claim 22, wherein the particle size of the colloidal particles is between 300 and 600 nm. 28. Use of colloidal solutions according to claim 22, wherein the colloidal solution is stabilized with the aid of surfactants or other amphiphilic substances. 29. Use of radiolabeled sulfur colloids for the production of agents for the treatment of proliferative diseases.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
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DE19741695A DE19741695C1 (en) | 1997-09-18 | 1997-09-18 | Treatment of proliferative disorders, i.e. atherosclerosis and tumors |
DE1997141694 DE19741694C2 (en) | 1997-09-18 | 1997-09-18 | Use of complexes whose ligand is a bis-amine oxime derivative or an N¶2¶S¶2¶ derivative and whose central atom is a radionuclide |
DE19741695 | 1997-09-18 | ||
DE19741694 | 1997-09-18 | ||
DE1997142880 DE19742880A1 (en) | 1997-09-23 | 1997-09-23 | Treatment of proliferative or atherosclerotic diseases |
DE19742880 | 1997-09-23 | ||
PCT/EP1998/005741 WO1999013920A2 (en) | 1997-09-18 | 1998-09-10 | Method for treating proliferative diseases by therapy |
Publications (2)
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AU1145999A true AU1145999A (en) | 1999-04-05 |
AU745908B2 AU745908B2 (en) | 2002-04-11 |
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AU11459/99A Ceased AU745908B2 (en) | 1997-09-18 | 1998-09-10 | Method for treating proliferative diseases by therapy |
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EP (1) | EP1011737A2 (en) |
JP (1) | JP2001516730A (en) |
AU (1) | AU745908B2 (en) |
CA (1) | CA2301887A1 (en) |
WO (1) | WO1999013920A2 (en) |
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US6482943B1 (en) | 1999-04-30 | 2002-11-19 | Slil Biomedical Corporation | Quinones as disease therapies |
WO2014197681A1 (en) * | 2013-06-05 | 2014-12-11 | Rheumco Llc | Treatment of immune, inflammatory and degenerative arthritides with tin-117m |
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EP0894012A2 (en) * | 1996-04-17 | 1999-02-03 | Olivier Bertrand | Radioactivity local delivery system |
US5924973A (en) * | 1996-09-26 | 1999-07-20 | The Trustees Of Columbia University In The City Of New York | Method of treating a disease process in a luminal structure |
US5873811A (en) * | 1997-01-10 | 1999-02-23 | Sci-Med Life Systems | Composition containing a radioactive component for treatment of vessel wall |
DE19724223C1 (en) * | 1997-04-30 | 1998-12-24 | Schering Ag | Production of radioactive coated stent, especially at point of use |
DE19718339A1 (en) * | 1997-04-30 | 1998-11-12 | Schering Ag | Polymer coated stents, processes for their manufacture and their use for restenosis prophylaxis |
-
1998
- 1998-09-10 CA CA002301887A patent/CA2301887A1/en not_active Abandoned
- 1998-09-10 EP EP98954267A patent/EP1011737A2/en not_active Withdrawn
- 1998-09-10 AU AU11459/99A patent/AU745908B2/en not_active Ceased
- 1998-09-10 WO PCT/EP1998/005741 patent/WO1999013920A2/en not_active Application Discontinuation
- 1998-09-10 JP JP2000511533A patent/JP2001516730A/en active Pending
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WO1999013920A3 (en) | 1999-05-06 |
AU745908B2 (en) | 2002-04-11 |
WO1999013920A2 (en) | 1999-03-25 |
CA2301887A1 (en) | 1999-03-25 |
JP2001516730A (en) | 2001-10-02 |
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