Preparation and characterization of molecularly imprinted poly(hydroxyethyl methacrylate) microspheres for sustained release of gatifloxacin

被引:17
|
作者
Lu, Xue-Fei [1 ,2 ]
Shi, Yun-feng [1 ,2 ]
Lv, Hong-Ling [3 ]
Fu, Ye-Yun [1 ,2 ]
Ma, Dong [1 ,2 ]
Xue, Wei [1 ,2 ]
机构
[1] Jinan Univ, Inst Biomed Engn, Guangzhou 510632, Guangdong, Peoples R China
[2] Jinan Univ, Guangdong Higher Educ Inst, Key Lab Biomat, Guangzhou 510632, Peoples R China
[3] Second Peoples Hosp Foshan, Foshan 528000, Peoples R China
关键词
SOLID-PHASE EXTRACTION; NANOPARTICLES; POLYMERS; POLYMERIZATION; RECOGNITION; SEPARATION; BIOSENSORS; DELIVERY; LINKING; SYSTEMS;
D O I
10.1007/s10856-014-5191-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Molecularly imprinted poly(hydroxyethyl methacrylate) microspheres (PHEMA MIPMs) were prepared via precipitation polymerization in this article, using gatifloxacin (GFLX), hydroxyethyl methacrylate (HEMA), and ethylene glycol dimethacrylate (EGDMA) as template molecule, functional monomer and cross-linker, respectively. The effects of reaction medium, initial total monomers, cross-linker and molecular imprinting on the polymerization were investigated systematically. The interaction between GFLX and HEMA in pre-solution was studied by UV-Visible spectrophotometer, both size and morphology of products were characterized by a scanning electron microscope. When the total initial monomer concentration was 1 vol%, EGDMA content was 70 mol%, a group of uniform PHEMA MIPMs were prepared at different GFLX/MAA molar ratios, with diameter range from 2.06 +/- A 0.07 to 2.82 +/- A 0.20 mu m. The results of drug loading and in vitro release experiments demonstrated that PHEMA MIPMs could achieve a higher GFLX loading content and a more acceptable sustained release than non-imprinted ones.
引用
收藏
页码:1461 / 1469
页数:9
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