期刊
JOURNAL OF PHARMACEUTICAL SCIENCES
卷 101, 期 2, 页码 598-609出版社
ELSEVIER SCIENCE INC
DOI: 10.1002/jps.22785
关键词
curcumin; liposomes; anti-inflammatory; antioxidant; vaginal therapy; topical drug delivery; cancer chemoprevention; controlled delivery; nanoparticles; cancer chemoprevention; controlled delivery; drug delivery systems
资金
- Phospholipid Research Center, Heidelberg, Germany
Curcumin is a well-established natural antioxidant and anti-inflammatory agent. Up till now its potential in treatment of vaginal inflammation has not been evaluated. We are aiming at developing liposomal delivery system for curcumin targeting vaginal administration. Liposomes as nanosized phospholipid-based vesicles are expected to solubilize curcumin and enhance its activity, thus serving as an advanced topical formulation in the treatment of vaginal inflammation. Curcumin and curcuminoids were analyzed by the high-performance liquid chromatography method. Liposomes containing curcumin/curcuminoids of various sizes were prepared and characterized. Antioxidant activities of curcumin and liposomal curcumin were compared based on 1,1-diphenyl-2-picrylhydrazyl radical scavenging and superoxide dismutase activities. The anti-inflammatory activities were determined by measuring the inhibition of lipopolysaccharide -induced nitric oxide, interleukin-1 beta, and tumor necrosis factor-a production in macrophage RAW 264.7 cells. Curcumin/curcuminoids were encapsulated in phosphatidylcholine vesicles with high yields. Vesicles in the size range around 200 nm were selected for stability and cell experiments. Liposomal curcumin were found to be twofold to sixfold more potent than corresponding curcuminoids. Moreover, the mixture of curcuminoids was found to be more potent than pure curcumin in regard to the antioxidant and anti-inflammatory activities. Liposomal delivery systems for curcumin are promising formulations for the treatment of vaginal inflammation. (C) 2011 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 101:598609, 2012
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