Hybrid Mesoporous Silica-Based Drug Carrier Nanostructures with Improved Degradability by Hydroxyapatite

被引:208
作者
Hao, Xiaohong [1 ]
Hu, Xixue [2 ]
Zhang, Cuimiao [1 ]
Chen, Shizhu [1 ]
Li, Zhenhua [1 ]
Yang, Xinjian [1 ]
Liu, Huifang [1 ]
Jia, Guang [1 ]
Liu, Dandan [1 ]
Ge, Kun [1 ]
Liang, Xing-Jie [2 ]
Zhang, Jinchao [1 ]
机构
[1] Hebei Univ, Coll Chem & Environm Sci, Chem Biol Key Lab Hebei Prov, Key Lab Med Chem & Mol Diag,Minist Educ, Baoding 071002, Peoples R China
[2] Natl Ctr Nanosci & Technol, CAS Key Lab Biol Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国博士后科学基金;
关键词
silica/hydroxyapatite hybrid nanoparticles; biodegradability; pH sensitivity; anticancer drug carrier; IN-VIVO; CONTROLLED-RELEASE; HEMOLYTIC-ACTIVITY; CANCER-THERAPY; DELIVERY-SYSTEM; NANOPARTICLES; BIODISTRIBUTION; LUMINESCENT; PH; BIOCOMPATIBILITY;
D O I
10.1021/nn507485j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Potential bioaccumulation is one of the biggest limitations for silica nanodrug delivery systems in cancer therapy. In this study, a mesoporous silica nanoparticles/hydroxyapatite (MSNs/HAP) hybrid drug carrier, which enhanced the biodegradability of silica, was developed by a one-step method. The morphology and structure of the nanoparticles were characterized by TEM, DLS, FT-IR, XRD, N-2 adsorption desorption isotherms, and XPS, and the drug loading and release behaviors were tested. TEM and ICP-OES results indicate that the degradability of the nanoparticles has been significantly improved by Ca2+ escape from the skeleton in an acid environment. The MSNs/HAP sample exhibits a higher drug loading content of about 5 times that of MSNs. The biological experiment results show that the MSNs/HAP not only exhibits good bioconnpatibility and antitumor effect but also greatly reduces the side effects of free DOX. The as-synthesized hybrid nanoparticles may act as a promising drug delivery system due to their good biocompatibility, high drug loading efficiency, pH sensitivity, and excellent biodegradability.
引用
收藏
页码:9614 / 9625
页数:12
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