Synthesis of poly(ethylene glycol) and poly(vinyl pyrrolidone) co-coated superparamagnetic iron oxide nanoparticle as a pH-sensitive release drug carrier

被引:30
作者
Tu, Zhijiang [1 ]
Zhang, Baolin [1 ]
Yang, Gao [1 ]
Wang, Ming [1 ]
Zhao, Fangyuan [1 ]
Sheng, Dian [1 ]
Wang, Jun [1 ]
机构
[1] Guilin Univ Technol, Key Lab New Proc Technol Nonferrous Met & Mat, Minist Educ, Sch Mat Sci & Engn, Guilin 541004, Peoples R China
基金
中国国家自然科学基金;
关键词
Superparamagnetic iron oxide; PEG; PVP; Colloidal stability; Doxorubicin; pH-sensitive drug carriers; ONE-POT REACTION; MAGNETITE NANOPARTICLES; FE3O4; NANOPARTICLES; NANOCRYSTALS; MRI; FUNCTIONALIZATION;
D O I
10.1016/j.colsurfa.2013.08.019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The superparamagnetic iron oxide nanoparticles (SPIONs) were synthesized by thermal decomposition of the iron (III) acetylacetonate (Fe(acac)(3)) in poly(ethylene glycol) (PEG) solvent containing poly(vinyl pyrrolidone) (PVP). The average size of the SPIONs identified by TEM is in the range of 4-10 nm, which can be controlled by tuning the synthetic temperature and time. The results of FTIR and XPS indicate that the PEG and PVP were tightly attached to the surface of the SPIONs. The SPIONs coated with PEG and PVP performed very good colloidal stability in deionized water, as well as in other physiological buffers. The anticancer drug doxorubicin (DOX) was loaded onto SPIONs and the drug release properties were investigated. The result shows that the DOX has a very high encapsulation efficiency (more than 90%), and the release rate of DOX from drug loaded SPIONs is dramatically enhanced at acidic environment, while less amount of DOX is released at neutral pH 7.4, which indicates that the PEG and PVP co-coated SPIONs have a pH-sensitive drug release capability. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:854 / 861
页数:8
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