Hyaluronic Acid-RGD Peptide Conjugated Mesoporous Silica-coated Gold Nanorods for Cancer Dual-targeted Chemo-photothermal Therapy

被引:0
|
作者
周汇敏 [1 ]
高玉香 [2 ]
徐海星 [1 ]
LI Xin [1 ]
Lü Yahui [1 ]
MA Tian [1 ]
CAI Xinjie [1 ]
LI Rui [1 ]
WANG Xiaobing [3 ]
许沛虎 [1 ]
机构
[1] School of Chemistry,Chemical Engineering and Life Sciences,Wuhan University of Technology
[2] School of Materials and Science Engineering,Wuhan University of Technology
[3] Wuhan Kanghua Century Pharmaceutical Company
基金
中国国家自然科学基金;
关键词
hyaluronic acid; RGD; mesoporous silica-coated gold nanorods; chemotherapy; photothermal therapy;
D O I
暂无
中图分类号
R73-3 [肿瘤学实验研究]; TB383.1 [];
学科分类号
070205 ; 080501 ; 100214 ; 1406 ;
摘要
A multifunctional drug delivery system(GNRs@mSiO2-HA-RGD) was developed by conjugating targeting ligand hyaluronic acid(HA) and RGD with mesoporous silica-coated gold nanorods(GNRs@mSiO2) for dual-targeted chemo-photothermal therapy. The physiochemical properties of the prepared nanoparticles were characterized by FTIR, UV-vis spectra, and1H NMR. Doxorubicin hydrochloride(DOX), an anticancer drug, was used as the model drug to investigate the drug loading, in vitro drug release profiles and cytotoxicity. The experimental results show that DOX-GNRs@mSiO2-HA-RGD is synthesized with a mean diameter of 116 nm and a sufficient load capacity of about 19.8%. It also has p H-enzyme sensitive and NIRtriggered drug release manner. Cellular uptake indicates that DOX-GNRs@mSiO2-HA-RGD exhibits a higher cellular uptake via CD44 receptor and integrin receptor mediated endocytosis compared with the GNRs@mSiO2modified with one receptor or no receptor. In comparison with chemotherapy or photothermal therapy alone, DOX-GNRs@mSiO2-HA-RGD displayes the synergistic effects and achieves a higher therapeutic efficacy. It can be expected that DOX-GNRs@mSiO2-HA-RGD is a potential dual-targeted chemo-photothermal therapeutic platform for effective cancer treatment.
引用
收藏
页码:512 / 523
页数:12
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