Responsive copolymer-graphene oxide hybrid microspheres with enhanced drug release properties

被引:16
作者
Dong, Fuping [1 ,2 ]
Firkowska-Boden, Izabela [1 ]
Arras, Matthias M. L. [1 ,3 ]
Jandt, Klaus. D. [1 ,4 ]
机构
[1] Friedrich Schiller Univ Jena, Otto Schott Inst Mat Res, Fac Phys & Astron, Chair Mat Sci, Lobdergraben 32, D-07743 Jena, Germany
[2] Guizhou Univ, Coll Mat & Met, Dept Polymer Mat & Engn, Guiyang 550025, Peoples R China
[3] Oak Ridge Natl Lab, Biol & Soft Matter Div, Oak Ridge, TN 37831 USA
[4] Friedrich Schiller Univ Jena, Jena Ctr Soft Matter ICSM, Philosophenweg 7, D-07743 Jena, Germany
关键词
POLY(N-ISOPROPYLACRYLAMIDE) HYDROGEL; HOLLOW SPHERES; NANOPARTICLES; DELIVERY;
D O I
10.1039/c6ra25353a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ability to integrate both high encapsulation efficiency and controlled release in a drug delivery system (DDS) is a highly sought solution to cure major diseases. However, creation of such a system is challenging. This study was aimed at constructing a new delivery system based on thermoresponsive poly(N-isopropylacrylamide- co-styrene) (PNIPAAm-co-PS) hollow microspheres prepared via two-step precipitation polymerization. To control the diffusion-driven drug release, the PNIPAAm-co-PS spheres were electrostatically coated with graphene oxide (GO) nanosheets. As a result of the coating the permeability of the copolymer-GO hybrid microspheres was reduced to an extent that suppressed the initial burst release and enabled sustained drug release in in vitro testing. The hybrid microspheres showed improved drug encapsulation by 46.4% which was attributed to the diffusion barrier properties and p-conjugated structure of GO. The system presented here is promising to advance, e.g., anticancer drug delivery technologies by enabling sustained drug release and thus minimizing local and systemic side effects.
引用
收藏
页码:3720 / 3726
页数:7
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