RU2663687C2 - Композиции наночастиц альбумина и паклитаксела - Google Patents
Композиции наночастиц альбумина и паклитаксела Download PDFInfo
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- RU2663687C2 RU2663687C2 RU2015131141A RU2015131141A RU2663687C2 RU 2663687 C2 RU2663687 C2 RU 2663687C2 RU 2015131141 A RU2015131141 A RU 2015131141A RU 2015131141 A RU2015131141 A RU 2015131141A RU 2663687 C2 RU2663687 C2 RU 2663687C2
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- albumin
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- pharmaceutical composition
- paclitaxel
- nanoparticles
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Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI1585548T1 (sl) | 2002-12-09 | 2018-11-30 | Abraxis Bioscience, Llc | Sestave in metode odmerjanja farmakoloških sredstev |
| US8735394B2 (en) | 2005-02-18 | 2014-05-27 | Abraxis Bioscience, Llc | Combinations and modes of administration of therapeutic agents and combination therapy |
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| US10213513B2 (en) | 2014-06-16 | 2019-02-26 | Mayo Foundation For Medical Education And Research | Treating myelomas |
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| TW201713360A (en) | 2015-10-06 | 2017-04-16 | Mayo Foundation | Methods of treating cancer using compositions of antibodies and carrier proteins |
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| US11427637B2 (en) | 2016-09-06 | 2022-08-30 | Mayo Foundation For Medical Education And Research | Methods of treating PD-L1 expressing cancer |
| EP3509643A1 (en) | 2016-09-06 | 2019-07-17 | Mayo Foundation for Medical Education and Research | Paclitaxel-albumin-binding agent compositions and methods for using and making the same |
| US11590098B2 (en) | 2016-09-06 | 2023-02-28 | Mayo Foundation For Medical Education And Research | Methods of treating triple-negative breast cancer using compositions of antibodies and carrier proteins |
| CN106420665B (zh) * | 2016-10-28 | 2019-04-16 | 浙江省林业科学研究院 | 一种包裹紫杉烷类药物的白蛋白纳米颗粒载体的制备方法 |
| CN118649239A (zh) | 2017-10-03 | 2024-09-17 | 克里蒂泰克公司 | 局部递送抗肿瘤颗粒与全身递送免疫治疗剂相结合用于治疗癌症 |
| SG11202009145PA (en) | 2018-03-20 | 2020-10-29 | Abraxis Bioscience Llc | Methods of treating central nervous system disorders via administration of nanoparticles of an mtor inhibitor and an albumin |
| US20220401374A1 (en) * | 2019-09-13 | 2022-12-22 | Purdue Research Foundation | Compositions and methods for cancer treatment by enhancing antitumor immunity using tannic acid-based nanocapsules |
| AU2020375810A1 (en) * | 2019-10-28 | 2022-05-12 | Abraxis Bioscience, Llc | Pharmaceutical compositions of albumin and rapamycin |
| CA3161105A1 (en) * | 2019-11-11 | 2021-05-20 | Abraxis Bioscience, Llc | Biomarkers for nanoparticle compositions |
| US20230074885A1 (en) * | 2020-02-05 | 2023-03-09 | The Johns Hopkins University | Bortezomib-loaded nanoparticles |
| WO2024118542A1 (en) * | 2022-11-28 | 2024-06-06 | Takeda Vaccines, Inc. | A method for the quantitative determination of human serum albumin monomer in virus-containing pharmaceutical compositions |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011119988A1 (en) * | 2010-03-26 | 2011-09-29 | Abraxis Bioscience, Llc | Methods of treatment of hepatocellular carcinoma |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5728553A (en) * | 1992-09-23 | 1998-03-17 | Delta Biotechnology Limited | High purity albumin and method of producing |
| US6749868B1 (en) * | 1993-02-22 | 2004-06-15 | American Bioscience, Inc. | Protein stabilized pharmacologically active agents, methods for the preparation thereof and methods for the use thereof |
| CA2362338A1 (en) * | 1998-07-30 | 2000-02-10 | Human Rt. | Pharmaceutically acceptable composition comprising an aqueous solution of paclitaxel and albumin |
| JP4798832B2 (ja) * | 2000-10-24 | 2011-10-19 | 一般財団法人化学及血清療法研究所 | ヒト血清アルブミン多量体の除去方法 |
| ES2577024T3 (es) * | 2009-08-25 | 2016-07-12 | Abraxis Bioscience, Llc | Terapia combinada con composiciones de nanopartículas de taxano e inhibidores de Hedgehog |
| WO2012092712A1 (zh) * | 2011-01-07 | 2012-07-12 | 无锡圆容生物医药股份有限公司 | 一种含有重组人血白蛋白的纳米颗粒冷冻干燥粉末制剂 |
| CN102078306A (zh) * | 2011-01-11 | 2011-06-01 | 无锡圆容生物医药股份有限公司 | 一种含有重组人血白蛋白的紫杉醇纳米颗粒冷冻干燥制剂 |
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011119988A1 (en) * | 2010-03-26 | 2011-09-29 | Abraxis Bioscience, Llc | Methods of treatment of hepatocellular carcinoma |
Non-Patent Citations (5)
| Title |
|---|
| GARRO AG., et al., Reversible exposure of hydrophobic residues on albumin as a novel strategy for formulation of nanodelivery vehicles for taxanes.Int J Nanomedicine. 2011;6:1193-200. doi: 10.2147/IJN.S19163. Epub 2011 Jun 13. * |
| LANGER K., et al., Human serum albumin (HSA) nanoparticles: reproducibility of preparation process and kinetics of enzymatic degradation.Int J Pharm. 2008 Jan 22; 347(1-2):109-17. Epub 2007 Jun 23. * |
| LANGER K., et al., Human serum albumin (HSA) nanoparticles: reproducibility of preparation process and kinetics of enzymatic degradation.Int J Pharm. 2008 Jan 22; 347(1-2):109-17. Epub 2007 Jun 23. GARRO AG., et al., Reversible exposure of hydrophobic residues on albumin as a novel strategy for formulation of nanodelivery vehicles for taxanes.Int J Nanomedicine. 2011;6:1193-200. doi: 10.2147/IJN.S19163. Epub 2011 Jun 13. TANAKA K., et al., Purification of human albumin by the combination of the method of Cohn with liquid chromatography.Braz J Med Biol Res. 1998 Nov; 31(11):1383-8. SHEFFIELD WP., et al., Modulation of clearance of recombinant serum albumin by either glycosylation or truncation. Thromb Res. 2000 Sep 15; 99(6):613-21. * |
| SHEFFIELD WP., et al., Modulation of clearance of recombinant serum albumin by either glycosylation or truncation. Thromb Res. 2000 Sep 15; 99(6):613-21. * |
| TANAKA K., et al., Purification of human albumin by the combination of the method of Cohn with liquid chromatography.Braz J Med Biol Res. 1998 Nov; 31(11):1383-8. * |
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| US20190192477A1 (en) | 2019-06-27 |
| US20140186447A1 (en) | 2014-07-03 |
| EP2938340A4 (en) | 2016-08-03 |
| CR20150386A (es) | 2015-10-07 |
| NI201500090A (es) | 2015-12-22 |
| WO2014105644A1 (en) | 2014-07-03 |
| MX2015008361A (es) | 2016-03-11 |
| IL239593A0 (en) | 2015-08-31 |
| SG11201505111TA (en) | 2015-07-30 |
| KR20150100903A (ko) | 2015-09-02 |
| BR112015015319A2 (pt) | 2017-07-11 |
| AU2013370955A1 (en) | 2015-07-16 |
| RU2015131141A (ru) | 2017-02-03 |
| PH12015501486B1 (en) | 2020-12-16 |
| HK1216611A1 (zh) | 2016-11-25 |
| NZ630912A (en) | 2017-05-26 |
| PH12015501486A1 (en) | 2015-09-21 |
| CA2896288A1 (en) | 2014-07-03 |
| JP2016504362A (ja) | 2016-02-12 |
| CN105007912A (zh) | 2015-10-28 |
| EP2938340A1 (en) | 2015-11-04 |
| ZA201504762B (en) | 2016-10-26 |
| JP2018087241A (ja) | 2018-06-07 |
| AU2013370955B2 (en) | 2018-12-06 |
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