动态光散射
化学
共聚物
甲基丙烯酸
傅里叶变换红外光谱
化学工程
控制释放
毒品携带者
药物输送
聚合
乳液聚合
核化学
生物相容性
材料科学
纳米颗粒
纳米技术
聚合物
有机化学
工程类
作者
Liwei Ma,Mingzhu Liu,Hongliang Liu,Jun Chen,Dapeng Cui
标识
DOI:10.1016/j.ijpharm.2009.10.037
摘要
A simple method has been developed to prepare smart P(N,N-diethylacrylamide-co-methacrylic acid) (P(DEA-co-MAA)) microspheres that consist of well-defined temperature-sensitive cores and pH sensitive shells. The microgels have been prepared by surfactant-free emulsion polymerization using water as the solvent. The core-shell hydrogel microspheres have been characterized by Fourier transform infrared (FTIR) spectroscopy, UV spectrometry, dynamic light scattering (DLS) and transmission electron micrograph (TEM). Preliminary characterization of the biocompatibility of hydrogel microspheres has been done by the cytotoxicity assays using the HeLa human breast cancer cell line as probes. The in vitro drug release indicates that drug release rate, encapsulation efficiency (EE) and release kinetics depend upon the pH value and copolymer composition. According to this study, the hydrogel microspheres based on P(DEA-co-MAA) could serve as suitable candidate for drug site-specific carrier in intestine.
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