A nontoxic disulfide bond reducing method for lipophilic drug-loaded albumin nanoparticle preparation: Formation dynamics, influencing factors and formation mechanisms investigation

International Journal of Pharmaceutics

Volumn 443, Issue 1-2, 2013, Pages 80-86

  Jiang, Liqun ^a   Xu, Yisheng ^b   Liu, Qi ^a   Tang, Yue ^a   Ge, Liang ^a   Zheng, Chunli ^a   Zhu, Jiabi ^a   Liu, Jianping ^a  

^a CHINA PHARMACEUTICAL UNIVERSITY   (China)

^b NATIONAL INSTITUTE OF BIOLOGICAL SCIENCES   (China)

Author keywords

Bovine serum albumin; Cysteine; Disulfide bond reducing method; Nanoparticle; Paclitaxel

Indexed keywords

BOVINE SERUM ALBUMIN; CYSTEINE; NANOCARRIER; PACLITAXEL;

ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; DISULFIDE BOND; DRUG SYNTHESIS; HUMAN; IN VITRO STUDY; LIPOPHILICITY; MOLECULAR DYNAMICS; NANOENCAPSULATION; PARTICLE SIZE; PH; PRIORITY JOURNAL; QUANTUM YIELD; TEMPERATURE;

CHEMISTRY, PHARMACEUTICAL; CYSTEINE; DISULFIDES; DRUG CARRIERS; DRUG COMPOUNDING; NANOPARTICLES; OXIDATION-REDUCTION; PACLITAXEL; PARTICLE SIZE; SERUM ALBUMIN, BOVINE; SOLUBILITY; SURFACE PROPERTIES;

EID: 84873027054     PISSN: 03785173     EISSN: 18733476     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2012.12.035     Document Type: Article

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