胶束
生物利用度
紫杉醇
体内
药理学
化学
P-糖蛋白
细胞毒性
体外
化疗
医学
多重耐药
水溶液
生物化学
内科学
生物
有机化学
生物技术
抗生素
作者
Ting Zhao,Hongli Zhou,Wanyan Wu,Xu Song,Tao Gong
标识
DOI:10.1080/03639045.2021.1879831
摘要
Bromotetrandrine (W198) was reported as a P-glycoprotein (P-gp) inhibitor. We aimed to prepare oral W198 micelles following by paclitaxel (PTX) micelles (W198/PTX micelles) to improve the clinical application of PTX.The poor water solubility, intestinal permeability, and multidrug resistance (MDR) of PTX can be improved in the multistage oral delivery system.The novel W198/PTX oral micelles were developed by water-bath ultrasound method and were evaluated in vivo and in vitro in 4T1 orthotopic tumor-bearing mice model.PTX micelles and W198 micelles were prepared to be round and uniform. W198 micelles pre-administrated group showed higher cellular uptake efficiency of PTX on Caco-2 cells and more prominent cytotoxicity compared with W198-untreated group on 4T1 cells. The oral bioavailability of W198/PTX micelles group was nearly 5.7-folds higher than the PTX micelles only group. In addition, W198/PTX micelles showed enhanced anticancer efficacy.We established a multistage oral delivery system to improve oral bioavailability and anticancer efficacy of PTX.
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