雷公藤醇
脂质体
雷公藤
前列腺癌
雷公藤
药理学
前列腺
药品
癌症研究
二甲基亚砜
癌细胞
细胞毒性
体内
化学
癌症
细胞凋亡
医学
生物化学
内科学
立体化学
有机化学
替代医学
糖苷
病理
作者
Joy Wolfram,Krishna Suri,Yi Huang,Roberto Molinaro,Carlotta Borsoi,B. Keyes Scott,Kathryn Boom,Donatella Paolino,Massimo Fresta,Jianghua Wang,Mauro Ferrari,Christian Celia,Haifa Shen
标识
DOI:10.3109/02652048.2013.879932
摘要
Context: Celastrol, a natural compound derived from the herb Tripterygium wilfordii, is known to have anticancer activity, but is not soluble in water. Objective: Formation of celastrol liposomes, to avoid the use of toxic solubilising agents. Materials and methods: Two different formulations of PEGylated celastrol liposomes were fabricated. Liposomal characteristics and serum stability were determined using dynamic light scattering. Drug entrapment efficacy and drug release were measured spectrophotometrically. Cellular internalisation and anticancer activity was measured in prostate cancer cells. Results: Liposomal celastrol displayed efficient serum stability, cellular internalisation and anticancer activity, comparable to that of the free drug reconstituted in dimethyl sulfoxide. Discussion and conclusion: Liposomal celastrol can decrease the viability of prostate cancer cells, while eliminating the need for toxic solubilising agents.
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