Rational Design of Multifunctional Gold Nanoparticles via Host-Guest Interaction for Cancer-Targeted Therapy

被引:51
作者
Chen, Wei-Hai
Lei, Qi
Luo, Guo-Feng
Jia, Hui-Zhen
Hong, Sheng
Liu, Yu-Xin
Cheng, Yin-Jia
Zhang, Xian-Zheng [1 ]
机构
[1] Wuhan Univ, Key Lab Biomed Polymers Minist Educ, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
Multifunctional; gold nanoparticles; host-guest interaction; targeted therapy; triggered release; MESOPOROUS SILICA NANOPARTICLES; INTRACELLULAR DRUG-DELIVERY; IN-VIVO; DOXORUBICIN RELEASE; POLYMERIC MICELLES; RENAL CLEARANCE; TUMOR; ULTRASMALL; EFFICIENT; PEPTIDE;
D O I
10.1021/acsami.5b04031
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A versatile gold nanoparticle-based multifunctional nanocomposite AuNP@CD-AD-DOX/RGD was constructed flexibly via host guest interaction for targeted cancer chemotherapy. The pH-sensitive anticancer prodrug AD-Hyd-DOX and the cancer-targeted peptide AD-PEG(8)-GRGDS were modified on the surface of AuNP@CD simultaneously, which endowed the resultant nanocomposite with the capability to selectively eliminate cancer cells. In vitro studies indicated that the AuNP@CD-AD-DOX/RGD nanocomposite was preferentially uptaken by cancer cells via receptor-mediated endocytosis. Subsequently, anticancer drug DOX was released rapidly upon the intracellular trigger of the acid microenvirenment of endo/lysosomes, inducing apoptosis in cancer cells. As the ideal drug nanocarrier, the multifunctional gold nanoparticles with the active targeting and controllable intracellular release ability hold the great potential in cancer therapy.
引用
收藏
页码:17171 / 17180
页数:10
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