RU2001132111A - Композиции, подавляющие развитие кровеносных сосудов и способы их использования - Google Patents
Композиции, подавляющие развитие кровеносных сосудов и способы их использования Download PDFInfo
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- RU2001132111A RU2001132111A RU2001132111/14A RU2001132111A RU2001132111A RU 2001132111 A RU2001132111 A RU 2001132111A RU 2001132111/14 A RU2001132111/14 A RU 2001132111/14A RU 2001132111 A RU2001132111 A RU 2001132111A RU 2001132111 A RU2001132111 A RU 2001132111A
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- Prior art keywords
- stent
- composition according
- obstruction
- blood vessels
- coated
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract 40
- 210000004204 blood vessel Anatomy 0.000 title claims abstract 23
- 238000000034 method Methods 0.000 claims abstract 24
- 229930012538 Paclitaxel Natural products 0.000 claims abstract 14
- 229960001592 paclitaxel Drugs 0.000 claims abstract 14
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 claims abstract 14
- 206010006440 Bronchial obstruction Diseases 0.000 claims abstract 5
- 230000001740 anti-invasion Effects 0.000 claims abstract 2
- 206010028980 Neoplasm Diseases 0.000 claims 9
- 210000000013 bile duct Anatomy 0.000 claims 6
- 210000003238 esophagus Anatomy 0.000 claims 6
- 210000003708 urethra Anatomy 0.000 claims 6
- 230000015572 biosynthetic process Effects 0.000 claims 5
- 229920000642 polymer Polymers 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 230000002792 vascular Effects 0.000 claims 4
- 201000011510 cancer Diseases 0.000 claims 3
- 229920001577 copolymer Polymers 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 229920000747 poly(lactic acid) Polymers 0.000 claims 3
- 239000004626 polylactic acid Substances 0.000 claims 3
- 102000001938 Plasminogen Activators Human genes 0.000 claims 2
- 108010001014 Plasminogen Activators Proteins 0.000 claims 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 2
- 210000000621 bronchi Anatomy 0.000 claims 2
- 210000004087 cornea Anatomy 0.000 claims 2
- 230000010102 embolization Effects 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 229940127126 plasminogen activator Drugs 0.000 claims 2
- 229920001610 polycaprolactone Polymers 0.000 claims 2
- 239000004632 polycaprolactone Substances 0.000 claims 2
- 230000000250 revascularization Effects 0.000 claims 2
- 239000007787 solid Substances 0.000 claims 2
- 238000001356 surgical procedure Methods 0.000 claims 2
- 210000003437 trachea Anatomy 0.000 claims 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims 1
- 241001465754 Metazoa Species 0.000 claims 1
- 102000005353 Tissue Inhibitor of Metalloproteinase-1 Human genes 0.000 claims 1
- 108010031374 Tissue Inhibitor of Metalloproteinase-1 Proteins 0.000 claims 1
- 102000005354 Tissue Inhibitor of Metalloproteinase-2 Human genes 0.000 claims 1
- 108010031372 Tissue Inhibitor of Metalloproteinase-2 Proteins 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000003246 corticosteroid Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000005038 ethylene vinyl acetate Substances 0.000 claims 1
- 239000004519 grease Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000004005 microsphere Substances 0.000 claims 1
- 239000002077 nanosphere Substances 0.000 claims 1
- 231100001223 noncarcinogenic Toxicity 0.000 claims 1
- 231100001222 nononcogenic Toxicity 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 229940127557 pharmaceutical product Drugs 0.000 claims 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims 1
- 238000005507 spraying Methods 0.000 claims 1
- FIAFUQMPZJWCLV-UHFFFAOYSA-N suramin Chemical compound OS(=O)(=O)C1=CC(S(O)(=O)=O)=C2C(NC(=O)C3=CC=C(C(=C3)NC(=O)C=3C=C(NC(=O)NC=4C=C(C=CC=4)C(=O)NC=4C(=CC=C(C=4)C(=O)NC=4C5=C(C=C(C=C5C(=CC=4)S(O)(=O)=O)S(O)(=O)=O)S(O)(=O)=O)C)C=CC=3)C)=CC=C(S(O)(=O)=O)C2=C1 FIAFUQMPZJWCLV-UHFFFAOYSA-N 0.000 claims 1
- 229960005314 suramin Drugs 0.000 claims 1
- 239000002870 angiogenesis inducing agent Substances 0.000 abstract 2
- 230000001772 anti-angiogenic effect Effects 0.000 abstract 2
- 206010044291 Tracheal obstruction Diseases 0.000 abstract 1
- 150000004508 retinoic acid derivatives Chemical class 0.000 abstract 1
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Claims (39)
1. Композиция, включающая (a) фактор, подавляющий развитие кровеносных сосудов; и (b) полимерный носитель.
2. Композиция по п.1, в которой указанным фактором, подавляющим развитие кровеносных сосудов, является антиинвазивный фактор.
3. Композиция по п.1, в которой указанным фактором, подавляющим развитие кровеносных сосудов, является ретеновая кислота и ее производные.
4. Композиция по п.1, в которой указанный фактор, подавляющий развитие кровеносных сосудов, выбирают из группы, включающей сурамин, тканевый ингибитор металлопротеиназы-1, тканевый ингибитор металлопротеиназы-2, ингибитор-1 плазминогенового активатора, ингибитор-2 плазминогенового активатора.
5. Композиция, включающая: (а) таксол, и (b) полимерный носитель.
6. Композиция по любому из пп.1-5, которая приготавливается в виде микросфер со средним размером от 0,1 до 200 мкм.
7. Композиция по любому из пп.1-5, которая приготавливается в виде пленки со средним толщиной от 100 мкм до 2 мм.
8. Композиция по любому из пп.1-5, которая представляет собой жидкость при температуре выше 45°С и которая представляет собой твердое вещество или полутвердое вещество при температуре 37°С.
9. Композиция по любому из пп.1-5, в которой указанным полимерным носителем является (полиэтилен-винилацетат), сшитый 40%-тами винилацетата.
10. Композиция по любому из пп.1-5, в которой указанным полимерным носителем является сополимер молочной и гликолевой кислот.
11. Композиция по любому из пп.1-5, в которой указанным полимерным носителем является поликапролактон.
12. Композиция по любому из пп.1-5, в которой указанным полимерным носителем является полимолочная кислота.
13. Композиция по любому из пп.1-5, в которой указанным полимерным носителем является сополимер поли(этилен-винилацетата), сшитого 40%-тами винилацетата, и полимолочной кислоты.
14. Композиция по любому из пп.1-5, в которой указанным полимерным носителем является сополимер полимолочной кислоты и поликапролактона.
15. Способ эмболизации кровеносного сосуда, заключающийся в доставке в указанный сосуд терапевтически эффективного количества композиции по любому из пп.1-14, так что указанный кровеносный сосуд эффективно закупоривается.
16. Способ по п.15, где указанный кровеносный сосуд питает опухоль.
17. Стент, имеющий в общем случае трубчатую структуру, поверхность которой покрыта композицией по любому из пп.1-14.
18. Способ расширения просвета расположенного внутри тела канала, заключающийся в размещении в канале стента, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией по любому из пп.1-14, так что указанный канал расширяется.
19. Способ устранения непроходимости сосудов, заключающийся в размещении сосудистого стента в канал сосуда, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией по любому из пп.1-14, так что указанная непроходимость сосуда устраняется.
20. Способ устранения непроходимости желчных протоков, заключающийся в размещении стента в желчном протоке, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией по любому из пп.1-14, так что указанная непроходимость желчного протока устраняется.
21. Способ устранения непроходимости мочеиспускательного канала, заключающийся в размещении уретрального стента в мочеиспускательном канале, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией по любому из пп.1-14, так что указанная непроходимость мочеиспускательного канала устраняется.
22. Способ устранения непроходимости пищевода, заключающийся в размещении стента в пищеводе, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией по любому из пп.1-14, так что указанная непроходимость пищевода устраняется.
23. Способ устранения трахеально-бронхиальной непроходимости, заключающийся в размещении трахеально-бронхиального стента в трахее или бронхе, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией по любому из пп.1-14, так что указанная трахеальнобронхиальная непроходимость устраняется.
24. Способ лечения места иссечения опухоли, заключающийся в нанесении композиции по любому из пп.1-14 на границы иссечения опухоли после, операции, так что подавляется местный рецидив рака и образование в указанном месте новых кровеносных сосудов.
25. Способ по п.24, где указанной композицией, подавляющей развитие кровеносных сосудов является термопаста.
26. Способ по п.24, в котором стадия нанесения включает разбрызгивание композиции наносфер, включающих составы, подавляющие развитие кровеносных сосудов, на границы иссечения опухоли.
27. Способ лечения реваскуляризации роговицы, заключающийся в нанесении на роговицу терапевтически эффективного количества композиции по любому из пп.1-14, так что образование кровеносных сосудов подавляется.
28. Способ по п.27, в котором указанная композиция также содержит кортикостероид для местного назначения.
29. Способ подавления развития кровеносных сосудов у пациентов с неонкогенными заболеваниями, определяемыми развитием кровеносных сосудов, который заключается в назначении терапевтически эффективного количества композиции, содержащей таксол, пациенту, страдающему от неонкогенного заболевания, определяемого развитием кровеносных сосудов, такого как образование новых кровеносных сосудов.
30. Способ эмболизации кровеносного сосуда при неонкогенных заболеваний, определяемых развитием кровеносных сосудов, который заключается в доставке в указанный сосуд терапевтически эффективного количества композиции, содержащей таксол, так что указанный кровеносный сосуд эффективно закупоривается.
31. Способ расширения просвета расположенного внутри тела канала, заключающийся в размещении в канале стента, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией, содержащей таксол, так что указанных проход расширяется.
32. Способ устранения непроходимости сосудов, заключающийся в размещении сосудистого стента в канал сосуда, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией, содержащей таксол, так что указанная непроходимости сосуда устраняется.
33. Способ устранения непроходимости желчных протоков, заключающийся в размещении стента в желчном протоке, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией, содержащей таксол, так что указанная непроходимость желчного протока устраняется.
34. Способ устранения непроходимости мочеиспускательного канала, заключающийся в размещении уретрального стента в мочеиспускательном канале, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией, содержащей таксол, так что указанная непроходимость мочеиспускательного канала устраняется.
35. Способ устранения непроходимости пищевода, заключающийся в размещении стента в пищеводе, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией, содержащей таксол, так что указанная непроходимость пищевода устраняется.
36. Способ устранения трахеально-бронхиальной непроходимости, заключающийся в размещении трахеально-бронхиального стента в трахее или бронхе, при этом стент имеет в общем случае трубчатую структуру, поверхность которой покрыта композицией, содержащей таксол, так что указанная трахеально-бронхиальная непроходимость устраняется.
37. Способ лечения места иссечения опухоли, заключающийся в нанесении композиции, содержащей таксол, на границы иссечения опухоли после операции, так что подавляется местный рецидив рака и образование в указанном месте новых кровеносных сосудов.
38. Способ лечения реваскуляризации роговицы, заключающийся в нанесении на роговицу терапевтически эффективного количества композиции, содержащей таксол, так что образование кровеносных сосудов подавляется.
39. Фармацевтическое средство, включающее (a) таксол в контейнере и (b) размещенное на контейнере извещение, форма которого определяется правительственным учреждением, регулирующим производство, использованием и продажу фармацевтических препаратов, при этом в извещении должно быть указано, что указанный таксол разрешен указанным правительственным учреждением к использованию при лечении неонкогенных заболеваний человека и животных, определяемых развитием кровеносных сосудов.
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RU2001132111/15A RU2304433C2 (ru) | 1993-07-19 | 2001-11-28 | Композиции, подавляющие развитие кровеносных сосудов, и способы их использования |
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