Magnetic targeted drug delivery carriers encapsulated with pH-sensitive polymer: synthesis, characterization and in vitro doxorubicin release studies

被引:15
|
作者
Wu, Juan [1 ]
Shen, Yueqing [1 ]
Jiang, Wei [1 ]
Jiang, Wei [1 ]
Shen, Yewen [1 ]
机构
[1] Nanjing Univ Sci & Technol, Natl Special Superfine Powder Engn Res Ctr, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Fe3O4; nanoparticles; poly(acrylic acid); doxorubicin; pH-sensitive; drug release; IRON-OXIDE NANOPARTICLES; BIOMEDICAL APPLICATIONS; CANCER-THERAPY; VIVO; EMULSION; TUMOR; ACID);
D O I
10.1080/09205063.2016.1195159
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Targeted and efficient delivery of drug to tumor is one of the crucial issues in cancer therapy. In this work, we have successfully designed and prepared the pH-sensitive magnetic nanoparticles (MNPs) as targeted anticancer drug carriers, in which the MNPs were coated by poly(acrylic acid) (PAA) and the obtained PAA@MNPs exhibited a size within 100nm, good stability, and superparamagnetic responsibility (M-s 45.97emu/g). Doxorubicin (DOX) can be successfully loaded onto MNPs via electrostatic interaction, and the drug loading content and loading efficiency are 26.4 and 88.1%, respectively. Moreover, the release studies showed that the drug-loaded carriers (MNPs-DOX) had excellent pH sensitivity, 75.6% of the loaded DOX was released at pH 4.0 within 48h. Importantly, MTT assays in HUVEC and MCF-7 cells demonstrated that MNPs-DOX exhibited high anti-tumor activity, while the PAA@MNPs were practically nontoxic. Thus, our results revealed that PAA@MNPs would be a competitive candidate for biomedical application and MNPs-DOX could be used in targeted cancer therapy.
引用
收藏
页码:1303 / 1316
页数:14
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