Thermosensitive poly(N-isopropylacrylamide-co-glycidyl methacrylate) microgels for controlled drug release

被引:48
作者
Li, Penghui [1 ]
Xu, Ruizhen [1 ]
Wang, Wenhao [1 ,2 ]
Li, Xiaolong [3 ]
Xu, Zushun [3 ]
Yeung, Kelvin W. K. [2 ]
Chu, Paul K. [1 ]
机构
[1] City Univ Hong Kong, Dept Phys & Mat Sci, Kowloon, Hong Kong, Peoples R China
[2] Univ Hong Kong, Dept Orthopaed & Traumatol, Div Spine Surg, Pokfulam, Hong Kong, Peoples R China
[3] Hubei Univ, Coll Mat Sci & Engn, Wuhan 430062, Peoples R China
关键词
Thermosensitive; Epoxy groups; Microgels; Drug delivery; POLY N-ISOPROPYLACRYLAMIDE; POTENTIAL APPLICATION; ACRYLIC-ACID; DELIVERY; PARTICLES; BEHAVIOR; NANOPARTICLES; MICROSPHERES; TEMPERATURE; COPOLYMER;
D O I
10.1016/j.colsurfb.2012.07.009
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new type of thermosensitive microgels with epoxy functional groups is designed and synthesized for drug delivery. The thermosensitive poly(N-isopropylacrylamide-co-glycidyl methacrylate) (designated as P(NIPAM-co-GMA)) microgels are prepared by an emulsifier-free emulsion polymerization method and the chemical composition of the copolymer is determined by Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (H-1 NMR). The lower critical solution temperature (LCST) of the microgels is 32 degrees C based on the transmittance changes at 500 nm monitored by UV/visible spectrophotometry. The hydrodynamic diameter and morphology of the microgel particles are examined by dynamic light scattering (DLS) and scanning electron microscopy (SEM), respectively. The drug release properties determined using 5-FU as the drug model in vitro reveal temperature dependence and low cytotoxicity. The thermosensitive microgels have large potential as targeted anti-cancer drug carriers. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:251 / 255
页数:5
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