Doxorubicin-loaded dual-functional hyaluronic acid nanoparticles: Preparation, characterization and antitumor efficacy in vitro and in vivo

被引:33
|
作者
Tian, Guixiang [1 ,2 ]
Sun, Xiue [2 ]
Bai, Jingkun [1 ]
Dong, Jinhua [1 ,3 ]
Zhang, Bo [4 ]
Gao, Zhiqin [1 ,3 ]
Wu, Jingliang [1 ,3 ]
机构
[1] Weifang Med Univ, Sch Biosci & Technol, Weifang 261053, Shandong, Peoples R China
[2] Weifang Med Univ, Dept Psychol, 7166 Baotong West St, Weifang 261053, Shandong, Peoples R China
[3] Weifang Med Univ, Key Lab Biol Med Univ Shandong Prov, Weifang 261053, Shandong, Peoples R China
[4] Weifang Med Univ, Sch Pharm, Weifang 261053, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
hyaluronic acid; nanoparticles; liver-targeting; pH-responsive; INTRACELLULAR DELIVERY; ALBUMIN NANOPARTICLES; COPOLYMER MICELLES; TARGETED DELIVERY; TUMOR; CONJUGATE; SIRNA; CHITOSAN; RELEASE; CARRIER;
D O I
10.3892/mmr.2018.9687
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A novel GHH copolymer was synthesized using hyaluronic acid modified with glycyrrhetinic acid and L-histidine (His), and doxorubicin-loaded GHH nanoparticles (DOX/GHH) were prepared for liver-targeted drug delivery and pH-responsive drug release. In the present study, GHH nanoparticles were characterized, and their pH-responsive behaviors were evaluated at different pH levels. The antitumor effect of the DOX/GHH nanoparticles was investigated in vitro and in vivo. Results showed that the DOX/GHH nanoparticles were spherical, and the particle sizes ranged from 238.1 to 156.7 nm with an increase in the degree of substitution of His. The GHH nanoparticles were obviously internalized into human hepatoblastoma cells. In vitro cytotoxicity assay results showed that the DOX/GHH nanoparticles exhibited a dose-dependent antitumor effect. Compared with free DOX, the DOX/GHH nanoparticles displayed higher antitumor efficacy. These results indicate that GHH nanoparticles could be a promising nano-delivery carrier of hydrophobic drugs for liver-targeted therapy.
引用
收藏
页码:133 / 142
页数:10
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