Development of nobiliside A loaded liposomal formulation using response surface methodology

International Journal of Pharmaceutics

Volumn 371, Issue 1-2, 2009, Pages 197-203

  Xiong, Yang ^a,b   Guo, Dan ^a   Wang, Lili ^b   Zheng, Xiaoli ^a   Zhang, Yue ^a   Chen, Jianming ^a  

^a SECOND MILITARY MEDICAL UNIVERSITY   (China)

^b ZHEJIANG CHINESE MEDICAL UNIVERSITY   (China)

Author keywords

Acute toxicity; Encapsulation efficiency; Hemolysis; Liposome; Nobiliside; Response surface methodology

Indexed keywords

CHOLESTEROL; DRUG CARRIER; LIPOSOME; NOBILISIDE A; PHOSPHATIDYLCHOLINE; SAPONIN DERIVATIVE; SEPHADEX; SODIUM CHLORIDE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CARDIOTOXICITY; CONTROLLED STUDY; DOSE RESPONSE; DRUG FORMULATION; DRUG SAFETY; DRUG STRUCTURE; FEMALE; HEMOLYSIS; INSTITUTE FOR CANCER RESEARCH MOUSE; LD 50; MALE; MOUSE; NANOENCAPSULATION; NONHUMAN; PRIORITY JOURNAL; RESPONSE SURFACE METHOD;

ANIMALS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DRUG COMPOUNDING; DRUG STABILITY; ERYTHROCYTES; FEMALE; HEMOLYSIS; LETHAL DOSE 50; LIPOSOMES; MALE; MICE; MICE, INBRED ICR; MICROSCOPY, ELECTRON, TRANSMISSION; MOLECULAR STRUCTURE; PARTICLE SIZE; RABBITS; SAPONINS; SURFACE PROPERTIES; ULTRASONICS;

EID: 62749188232     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2008.12.031     Document Type: Article

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