RU2009136992A - Наночастица, содержащая рапамиции и альбумин, в качестве противоракового агента - Google Patents
Наночастица, содержащая рапамиции и альбумин, в качестве противоракового агента Download PDFInfo
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- RU2009136992A RU2009136992A RU2009136992/15A RU2009136992A RU2009136992A RU 2009136992 A RU2009136992 A RU 2009136992A RU 2009136992/15 A RU2009136992/15 A RU 2009136992/15A RU 2009136992 A RU2009136992 A RU 2009136992A RU 2009136992 A RU2009136992 A RU 2009136992A
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- Prior art keywords
- therapy
- cancer
- kinase inhibitor
- nanoparticles
- albumin
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- 238000000034 method Methods 0.000 claims abstract 39
- 229940043355 kinase inhibitor Drugs 0.000 claims abstract 12
- 239000003757 phosphotransferase inhibitor Substances 0.000 claims abstract 12
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- 102000014914 Carrier Proteins Human genes 0.000 claims abstract 8
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims abstract 4
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- 229940071846 neulasta Drugs 0.000 claims 1
- BWKDAMBGCPRVPI-ZQRPHVBESA-N ortataxel Chemical compound O([C@@H]1[C@]23OC(=O)O[C@H]2[C@@H](C(=C([C@@H](OC(C)=O)C(=O)[C@]2(C)[C@@H](O)C[C@H]4OC[C@]4([C@H]21)OC(C)=O)C3(C)C)C)OC(=O)[C@H](O)[C@@H](NC(=O)OC(C)(C)C)CC(C)C)C(=O)C1=CC=CC=C1 BWKDAMBGCPRVPI-ZQRPHVBESA-N 0.000 claims 1
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- WBXPDJSOTKVWSJ-ZDUSSCGKSA-L pemetrexed(2-) Chemical compound C=1NC=2NC(N)=NC(=O)C=2C=1CCC1=CC=C(C(=O)N[C@@H](CCC([O-])=O)C([O-])=O)C=C1 WBXPDJSOTKVWSJ-ZDUSSCGKSA-L 0.000 claims 1
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- DKPFODGZWDEEBT-QFIAKTPHSA-N taxane Chemical class C([C@]1(C)CCC[C@@H](C)[C@H]1C1)C[C@H]2[C@H](C)CC[C@@H]1C2(C)C DKPFODGZWDEEBT-QFIAKTPHSA-N 0.000 claims 1
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Classifications
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/436—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
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- A—HUMAN NECESSITIES
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- A61K31/66—Phosphorus compounds
- A61K31/683—Diesters of a phosphorus acid with two hydroxy compounds, e.g. phosphatidylinositols
- A61K31/685—Diesters of a phosphorus acid with two hydroxy compounds, e.g. phosphatidylinositols one of the hydroxy compounds having nitrogen atoms, e.g. phosphatidylserine, lecithin
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Abstract
1. Способ лечения рака у индивидуума, включающий в себя (а) первую терапию, предусматривающую введение этому индивидууму эффективного количества композиции, содержащей наночастицы, которые содержат рапамицин или его производное и белок-носитель, и (b) вторую терапию, выбранную из группы, состоящей из химиотерапии, лучевой терапии, хирургии, гормональной терапии, генотерапии, иммунотерапии, трансплантации костного мозга, трансплантации стволовых клеток, прицельной терапии, криотерапии, ультразвуковой терапии и иммунотерапии. ! 2. Способ по п.1, где эта вторая терапия является химиотерапией. ! 3. Способ по п.2, где этот способ предусматривает введение химиотерапевтического агента, выбранного из группы, состоящей из антиметаболитных агентов, агентов на основе платины, алкилирующих агентов, ингибиторов киназ, антрациклиновых антибиотиков, винкаалкалоидов, ингибиторов протеасом и ингибиторов топоизомераз. ! 4. Способ по п.3, где этот способ предусматривает введение ингибитора киназ. ! 5. Способ по п.4, где этот ингибитор киназ является ингибитором киназы AKT. ! 6. Способ по п.5, где этот ингибитор киназы AKT является перифозином. ! 7. Способ по п.4, где этот ингибитор киназ является ингибитором тирозинкиназ. ! 8. Способ по п.7, где этот ингибитор тирозинкиназ является эрлотинибом. ! 9. Способ по п.2, где этот способ предусматривает введение ингибитора пути mTOR. ! 10. Способ по п.9, где этот ингибитор пути mTOR является ингибитором mTORC2. ! 11. Способ по п.2, где химиотерапия предусматривает введение химиотерапевтического агента, выбранного из группы, состоящей из адриамицина, колхицина, циклофосфамида, актиномицина, блеомицина, даунорубицина,
Claims (33)
1. Способ лечения рака у индивидуума, включающий в себя (а) первую терапию, предусматривающую введение этому индивидууму эффективного количества композиции, содержащей наночастицы, которые содержат рапамицин или его производное и белок-носитель, и (b) вторую терапию, выбранную из группы, состоящей из химиотерапии, лучевой терапии, хирургии, гормональной терапии, генотерапии, иммунотерапии, трансплантации костного мозга, трансплантации стволовых клеток, прицельной терапии, криотерапии, ультразвуковой терапии и иммунотерапии.
2. Способ по п.1, где эта вторая терапия является химиотерапией.
3. Способ по п.2, где этот способ предусматривает введение химиотерапевтического агента, выбранного из группы, состоящей из антиметаболитных агентов, агентов на основе платины, алкилирующих агентов, ингибиторов киназ, антрациклиновых антибиотиков, винкаалкалоидов, ингибиторов протеасом и ингибиторов топоизомераз.
4. Способ по п.3, где этот способ предусматривает введение ингибитора киназ.
5. Способ по п.4, где этот ингибитор киназ является ингибитором киназы AKT.
6. Способ по п.5, где этот ингибитор киназы AKT является перифозином.
7. Способ по п.4, где этот ингибитор киназ является ингибитором тирозинкиназ.
8. Способ по п.7, где этот ингибитор тирозинкиназ является эрлотинибом.
9. Способ по п.2, где этот способ предусматривает введение ингибитора пути mTOR.
10. Способ по п.9, где этот ингибитор пути mTOR является ингибитором mTORC2.
11. Способ по п.2, где химиотерапия предусматривает введение химиотерапевтического агента, выбранного из группы, состоящей из адриамицина, колхицина, циклофосфамида, актиномицина, блеомицина, даунорубицина, доксорубицина, эпирубицина, митомицина, метотрексата, митоксантрона, фторурацила, карбоплатина, кармустина (BCNU), метил CCNU, цисплатина, этопозида, интерферонов, камптотецина и его производных, фенестерина, топетекана, винбластина, винкристина, тамоксифена, пипосульфана, nab-5404, nab-5800, nab-5801, Иринотекана, HKP, Ортатаксела, гемцитабина, Герцептина, винорелбина, Доксила, капецитабина, Алимта, Авастина, Velcade®, Tarceva®, Neulasta®, Лапатиниба и Сорафениба.
12. Способ лечения рака у индивидуума, предусматривающий введение этому индивидууму эффективного количества композиции, содержащей наночастицы, которые содержат рапамицин или его производное и белок-носитель.
13. Способ по любому из пп.1-12, где этот рак выбран из группы, состоящей из множественной миеломы, рака поджелудочной железы, почечно-клеточной карциномы, рака предстательной железы, рака легкого, меланомы и рака молочной железы.
14. Способ по п.13, где этот рак является раком поджелудочной железы.
15. Способ по любому из пп.1-12, где этот рак не является раком ободочной железы.
16. Способ по любому из пп.1-12, где этот рак является плазмацитомой.
17. Способ по любому из пп.1-12, где количество рапамицина или его производного в эффективном количестве этой композиции находится в диапазоне приблизительно 180- приблизительно 270 мг.
18. Способ по п.1, где таксан не вводят этому индивидууму.
19. Способ по любому из пп.1-12, где этот белок-носитель является альбумином.
20. Способ по п.19, где этот альбумин является сывороточным альбумином человека.
21. Способ по любому из пп.1-12, где средний диаметр наночастиц в этой композиции равен не более чем приблизительно 200 нм.
22. Способ по любому из пп.1-12, где этот индивидуум является человеком.
23. Единичная лекарственная форма для лечения рака, содержащая (а) наночастицы, которые содержат белок-носитель и рапамицин или его производное, где количество рапамицина или его производного в этой единичной лекарственной форме находится в диапазоне приблизительно 180- приблизительно 270 мг, и (b) фармацевтически приемлемый носитель.
24. Единичная лекарственная форма по п.23, где этот белок-носитель является альбумином.
25. Единичная лекарственная форма по п.24, где этот альбумин является сывороточным альбумином человека.
26. Единичная лекарственная форма по любому из пп.23-25, где средний диаметр наночастиц в этой композиции равен не более чем приблизительно 200 нм.
27. Единичная лекарственная форма по любому из пп.23-25, где эта единичная лекарственная форма пригодна для внутривенного введения.
28. Набор, содержащий (а) наночастицы, которые содержат белок-носитель и рапамицин или его производное, где количество рапамицина или его производного в этом наборе находится в диапазоне приблизительно 180- приблизительно 270 мг, и (b) инструкции для применения этого набора в лечении рака.
29. Набор по п.28, где этот рак является раком поджелудочной железы.
30. Набор по п.28, где этот белок-носитель является альбумином.
31. Набор по п.30, где этот альбумин является сывороточным альбумином человека.
32. Набор по любому из пп.28-31, где средний диаметр наночастиц в этой композиции равен не более чем приблизительно 200 нм.
33. Набор по любому из пп.28-31, где эти наночастицы пригодны для внутривенного введения.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2013188763A1 (en) * | 2012-06-15 | 2013-12-19 | The Brigham And Women's Hospital, Inc. | Compositions for treating cancer and methods for making the same |
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