姜黄素
药代动力学
纳米载体
化学
药理学
细胞凋亡
细胞毒性
脂质体
PI3K/AKT/mTOR通路
紫杉醇
癌症研究
癌症
生物
生物化学
医学
体外
内科学
药品
作者
Song–Lin Li,Chunshu Fang,Jingqing Zhang,Bilin Liu,Zhuanqin Wei,Xiaoqing Fan,Zheng Sui,Qunyou Tan
标识
DOI:10.1016/j.nano.2016.02.007
摘要
Novel catanionic lipid nanosystems (CLNs) incorporating curcumin (CCM) were developed, and improvements in pharmacokinetics and enhanced anti-lung cancer activity were observed. CCM was present in a lipid matrix surrounded by cationic, anionic and zwitterionic surfactants, forming the core-shell nanosystems. Compared with free CCM, the CCM-CLNs had much higher oral and intravenous bioavailabilities due to enhanced absorption and reduced clearance. The CCM-CLNs exhibited greater cytotoxicity in Lewis lung cancer (LLC) cells, which might have been due to increased antiproliferative, proapoptotic and anti-invasive activities and induction of cell cycle arrest. The CCM-CLNs increased the antitumor efficacy of CCM and decreased the tumor growth rate in tumor-bearing mice. This is the first report of induction of apoptosis in LLC cells by CCM through the PI3K/Akt/FoxO1/Bim signaling pathway. Catanionic lipid nanocarriers show promise for the therapeutic delivery of insoluble anti-tumor drugs.
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