Transarterial Chemoembolization Using Docetaxel-Loaded Phytantriol Cubic Phase Precursor for the Treatment of Hepatocellular Carcinoma

被引:7
作者
Han, Ke [1 ,2 ,3 ]
Wang, Zhouhua [1 ]
Peng, Xinsheng [1 ,4 ]
Chen, Bao [1 ]
Wen, Xinguo [1 ]
Dong, Yixuan [1 ]
Wu, Chuanbin [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Res & Dev Ctr Pharmaceut Engn, Guangzhou 510006, Guangdong, Peoples R China
[3] Guangzhou Med Coll, Affiliated Hosp 2, Guangzhou 510260, Guangdong, Peoples R China
[4] Guangdong Med Coll, Sch Pharmaceut Sci, Dongguan 523808, Peoples R China
基金
中国国家自然科学基金;
关键词
controlled release; site-specific delivery; cancer chemotherapy; pharmacodynamics; pharmacokinetics; hydrogels; viscosity; cell culture; phytantriol; cubic phase; LIVER-TUMOR; NANOPARTICLES; DELIVERY; MICELLES; RELEASE; RABBITS; POWDER;
D O I
10.1002/jps.22456
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The purpose of this study was to evaluate the transarterial chemoembolic agent based on docetaxel-loaded phytantriol cubic phase precursor (DTX PCPP) by in vitro cytotoxicity study and in vivo evaluation of antitumor efficacy as well as the histological examination. The methythiazolyl tereazolium bromide assay in Hep G2 cell line revealed that DTX PCPP generated high cytotoxicity by causing cell apoptosis and G2/M phase arrest. In vivo studies conducted in rabbits bearing VX2 tumors, which were treated with DTX PCPP, used as a transarterial chemoembolic agent, showed a significant antitumor efficacy and prominent higher DTX concentrations in tumor and liver than those in other organs. The histology presented typical necrosis in tumor that demonstrated excellent therapeutic effect. In conclusion, the DTX PCPP could achieve an excellent antitumor effect with low systemic toxicity for the treatment of hepatocellular carcinoma and therefore implied the prospect of DTX PCPP for clinical applications. (C) 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:2240-2247, 2011
引用
收藏
页码:2240 / 2247
页数:8
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