Encapsulation of paclitaxel into lauric acid-O-carboxymethyl chitosan-transferrin micelles for hydrophobic drug delivery and site-specific targeted delivery

International Journal of Pharmaceutics

Volumn 457, Issue 1, 2013, Pages 124-135

  Nam, Joung Pyo ^a   Park, Seong Cheol ^a   Kim, Tae Hun ^a   Jang, Jae Yeang ^a   Choi, Changyong ^a   Jang, Mi Kyeong ^a   Nah, Jae Woon ^a  

^a Sunchon National University   (South Korea)

Author keywords

Micelle; O carboxymethyl chitosan; Paclitaxel; PEG; Transferrin

Indexed keywords

CHITOSAN; DRUG CARRIER; LAURIC ACID DERIVATIVE; LAURIC ACID O CARBOXYMETHYL CHITOSAN TRANSFERRIN; PACLITAXEL; TRANSFERRIN; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; ASSAY; CANCER CHEMOTHERAPY; CONFOCAL LASER MICROSCOPY; CYTOTOXICITY; DRUG DELIVERY SYSTEM; DRUG RELEASE; ENCAPSULATION; ENDOCYTOSIS; FLOW CYTOMETRY; GENETIC TRANSFECTION; HEMOLYSIS; HUMAN; HUMAN CELL; HYDROPHOBIC DRUG DELIVERY; IN VITRO STUDY; MICELLE; PARTICLE SIZE; PRIORITY JOURNAL; SUSTAINED DRUG RELEASE;

MICELLE; O-CARBOXYMETHYL CHITOSAN; PACLITAXEL; PEG; TRANSFERRIN;

ANIMALS; ANTINEOPLASTIC AGENTS, PHYTOGENIC; CELL LINE, TUMOR; CELL SURVIVAL; CHITOSAN; DRUG CARRIERS; HEMOLYSIS; HUMANS; LAURIC ACIDS; MICELLES; PACLITAXEL; RATS; TRANSFERRIN;

EID: 84885334230     PISSN: 03785173     EISSN: 18733476     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2013.09.021     Document Type: Article

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