Anti-hepatocarcinoma effects of chrysin loaded solid lipid nanoparticle against H22 tumor bearing mice

被引:0
作者
Wang, Zhiping [1 ]
Fan, Hua [2 ]
Li, Yan [3 ]
Wang, Yifei [4 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Hinabiotech Co Ltd, Guangzhou 511400, Guangdong, Peoples R China
[3] Guangzhou Univ Chinese Med, Sch Chinese Mat Med, Guangzhou 510006, Guangdong, Peoples R China
[4] Jinan Univ, Inst Med Biol, Guangzhou 510632, Guangdong, Peoples R China
来源
PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON MATERIAL, MECHANICAL AND MANUFACTURING ENGINEERING | 2015年 / 27卷
关键词
solid lipid nanoparticles; Chrysin; Cytotoxicity; Antitumor activity; H22; cells; tumor bearing mice; FLAVONOID CHRYSIN; INDUCE APOPTOSIS; CANCER CELLS; IN-VIVO; CYTOTOXICITY; CARCINOMA; GROWTH; PROLIFERATION; ARREST;
D O I
暂无
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Hepatocarcinoma, a malignant cancer, threaten human life badly. It is a current issue to seek the effective natural remedy from plant to treat cancer due to the resistance of the advanced hepatocarcinoma to chemotherapy. Chrysin (Chr), a major symbol ingredient in Chinese Propolis, has a wide range of pharmacological properties and is considered to have anti-hepatocarcinoma effects. However its low oral bioavailability restricts its wide application. In this report, Chr-loaded solid lipid nanoparticles (Chr-SLN) composed of Chr, cremophor EL and glyceryl behenate were prepared by high pressure homogenization technique. The in vivo anti-hepatocarcinoma effects of Chr-SLN relative to efficacy of bulk Chr were evaluated. The particle size and zeta potential of Chr-SLN were 479.7 nm and -26.3 mV, respectively. The results showed higher antitumor efficacy against H22 solid tumor bearing mice. These results suggest that the delivery of Chr-SLN is a promising approach for treating tumors.
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页码:1020 / 1024
页数:5
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