RU2010113969A - Применение trp-6-трипторелина и d-leu6-лейпролида в качестве терапевтических средств - Google Patents
Применение trp-6-трипторелина и d-leu6-лейпролида в качестве терапевтических средств Download PDFInfo
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Abstract
1. Комбинация пептидов Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 и Pyr-His-Trp-Ser-Tyr-D-His(Bzl)-D-Leu-Arg-Pro-NHEt или их солей или гидратов. ! 2. Комбинация по п.1, где пептиды содержатся в комбинации в количестве от 30% по массе к 70% по массе до 70% по массе к 30% по массе. ! 3. Комбинация по п.1 для применения в лекарственном средстве. ! 4. Применение пептида Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 или комбинации по п.1 или 2, или 3 для получения фармацевтической композиции для лечения и/или профилактики злокачественной опухоли, аутоиммунных заболеваний, фиброзов, воспалительных заболеваний, нейродегенеративных заболеваний, инфекционных заболеваний, заболеваний легких, заболеваний сердца и сосудов и болезней обмена веществ. ! 5. Применение пептида по п.4, где злокачественная опухоль, аутоиммунное заболевание, фиброз, воспалительное заболевание, нейродегенеративное заболевание, инфекционное заболевание, заболевание легких, заболевание сердца и сосудов или болезнь обмена веществ выбраны из инфекции Streptococcus pneumoniae, связанных с инфекцией Streptococcus pneumoniae заболеваний, а именно гемолитического уремического синдрома, пневмонии, менингита, осложнения кистозного фиброза, заболеваний среднего уха, инфекций в кровотоке, инфекций синуса и уха, острого синусита, среднего отита, остеомиелита, септического артрита, эндокардита, перитонита, перикардита и абсцесса мозга. ! 6. Применение пептида Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 для получения состава для перорального введения новорожденным, детям ясельного возраста и/или детям дошкольного возраста. ! 7. Применение пептида Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 для получения лиофилизированного состава или буферного жидкого состава. ! 8. Фармацевтическая композиция, со
Claims (12)
1. Комбинация пептидов Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 и Pyr-His-Trp-Ser-Tyr-D-His(Bzl)-D-Leu-Arg-Pro-NHEt или их солей или гидратов.
2. Комбинация по п.1, где пептиды содержатся в комбинации в количестве от 30% по массе к 70% по массе до 70% по массе к 30% по массе.
3. Комбинация по п.1 для применения в лекарственном средстве.
4. Применение пептида Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 или комбинации по п.1 или 2, или 3 для получения фармацевтической композиции для лечения и/или профилактики злокачественной опухоли, аутоиммунных заболеваний, фиброзов, воспалительных заболеваний, нейродегенеративных заболеваний, инфекционных заболеваний, заболеваний легких, заболеваний сердца и сосудов и болезней обмена веществ.
5. Применение пептида по п.4, где злокачественная опухоль, аутоиммунное заболевание, фиброз, воспалительное заболевание, нейродегенеративное заболевание, инфекционное заболевание, заболевание легких, заболевание сердца и сосудов или болезнь обмена веществ выбраны из инфекции Streptococcus pneumoniae, связанных с инфекцией Streptococcus pneumoniae заболеваний, а именно гемолитического уремического синдрома, пневмонии, менингита, осложнения кистозного фиброза, заболеваний среднего уха, инфекций в кровотоке, инфекций синуса и уха, острого синусита, среднего отита, остеомиелита, септического артрита, эндокардита, перитонита, перикардита и абсцесса мозга.
6. Применение пептида Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 для получения состава для перорального введения новорожденным, детям ясельного возраста и/или детям дошкольного возраста.
7. Применение пептида Pyr-His-Trp-Ser-Tyr-Trp-Leu-Arg-Pro-Gly-NH2 для получения лиофилизированного состава или буферного жидкого состава.
8. Фармацевтическая композиция, содержащая комбинацию по п.1 совместно с, по меньшей мере, одним фармацевтически приемлемым носителем, криопротектором, лиопротектором, эксципиентом и/или разбавителем.
9. Фармацевтическая композиция по п.8 в форме лиофилизата или жидкого буферного раствора.
10. Фармацевтическая композиция по п.8 или 9, пригодная для внутривенного введения, перорального введения или для введения посредством ингаляции.
11. Фармацевтическая композиция по п.8 или 9 в форме состава искусственного материнского молока или заменителя материнского молока, пригодная для пероральной доставки новорожденным, детям ясельного возраста и/или детям дошкольного возраста.
12. Фармацевтическая композиция по п.8, или 9, пригодная для лечения и/или профилактики злокачественной опухоли, аутоиммунного заболевания, фиброза, воспалительного заболевания, нейродегенеративного заболевания, инфекционного заболевания, заболевания легких, заболевания сердца и сосудов или болезни обмена веществ.
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