Effect of experimental parameters on the encapsulation of aclarubicin A loaded PLGA nanoparticles prepared by a double emulsion method

Chinese Journal of Antibiotics

Volumn 30, Issue 6, 2005, Pages 338-340

  Chen, Shu ^a   Zhang, Zhi Rong ^a   Shi, Hai Tao ^a   Lu, Ying Ming ^a  

^a SICHUAN UNIVERSITY   (China)

Author keywords

Aclarubicin A; Encapsulation efficiency; Nanoparticle; PLGA

Indexed keywords

ACETONE; ACLARUBICIN; DICHLOROMETHANE; EMULSIFYING AGENT; NANOPARTICLE; OLEIC ACID; ORGANIC SOLVENT; POLYGLYCOLIC ACID; SODIUM SULFATE;

ARTICLE; DRUG SYNTHESIS; EMULSION; ENCAPSULATION;

EID: 23844482488     PISSN: 10018689     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Yamakawa I, Tsushima Y, Machida R. Preparation of neurotensin analogue-containing poly (dl-lactic acid) microspheres formed by oil-in-water solvent evaporation [J]. J Pharm Sci, 1992, 81(9): 899
2. Govender T, Stolnik S, Garnett M, et al. PLGA nanoparticles prepared by nanoprecipitation: drug loading and release studies of a water soluble drug[J]. J Controlled Release, 1999, 57: 171