Hydroxyapatite/mesoporous silica coated gold nanorods with improved degradability as a multi-responsive drug delivery platform

被引:77
|
作者
Song, Zhixuan [1 ]
Liu, Yang [2 ]
Shi, Jun [1 ]
Ma, Teng [1 ]
Zhang, Zheng [1 ]
Ma, He [1 ]
Cao, Shaokui [1 ]
机构
[1] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Gore-shell nanoparticles; Gold nanorods; Hybrid silica/hydroxyapatite; Degradation; NIR-/pH-responsiveness; Drug delivery; CHEMO-PHOTOTHERMAL THERAPY; MESOPOROUS SILICA; CANCER-THERAPY; IN-VITRO; HYBRID MICROPARTICLES; NANOPARTICLES; CYTOTOXICITY; RELEASE; BIOCOMPATIBILITY; NANOSTRUCTURES;
D O I
10.1016/j.msec.2017.11.012
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
In this study, gold nanorods/mesoporous silicaAydroxyapatite (Au/SiO2/HAP) hybrid nanoparticles with AuNR core and SiO2/HAP hybrid inorganic shell for multi-responsive drug delivery had been prepared. The morphology and structure of the nanoparticles were characterized by TEM, XPS, XRD, FT-IR and N-2 adsorption-desorption isotherms. The degradation of the hybrid nanoparticles could be significantiy improved by the dissolution of HAP from the hybrid skeleton in acid environment. In vitro drug release results indicated that Au/SiO2/HAP nanoparticles exhibited high drug loading efficiency, excellent near-infrared (NIR)-and ptfcre-sponsive drug release properties. Compared to the drug release of Au/SiO2 nanoparticles over 12 h (about 6.35%), AU/SiO2/HAP nanoparticles displayed a higher drug release of 37.62% upon NIR irradiation at pH 4.5 due to the NIR-responsiveness of AuNRs and the pH-responsiveness of HAP in acid media. The cell viability results also indicated that the Au/SiO2/HAP nanoparticles exhibited the excellent biocompatibility. The present paper provides a facile route to fabricate a hybrid drug carrier with high drug loading efficiency, excellent pH sensitivity, NIR-sensitivity, biodegradability and biocompatibility.
引用
收藏
页码:90 / 98
页数:9
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