Drug release kinetics from monolayer films of glucose-sensitive microgel

被引:69
|
作者
Liu, Pengxiao [1 ]
Luo, Qiaofang [1 ]
Guan, Ying [1 ]
Zhang, Yongjun [1 ]
机构
[1] Nankai Univ, Key Lab Funct Polymer Mat, Inst Polymer Chem, Coll Chem, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Microgels; Glucose-sensitive; Drug delivery; RESPONSIVE MICROGELS; ACID; PH; NANOPARTICLES; TEMPERATURE; BEARING;
D O I
10.1016/j.polymer.2010.04.011
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
To study the drug release behaviors of glucose-sensitive poly(N-isopropylacrylamide-co-3-acryl-amidophenylboronic acid) (P(NIPAM-PBA)) microgels, P(NIPAM-PBA) microgel monolayers were prepared by the modification of poly(N-isopropylacrylamide-co-acrylic acid) microgel monolayers with 3-aminophenylboronic acid under EDC catalysis. Alizarin Red S CARS) and FITC-labeled insulin (FITC-insulin) were loaded in the monolayers respectively. Their release kinetics under various conditions were measured. For both drugs, at low temperature, the drug release can be described as passive diffusion of the drugs. At temperature higher than the phase transition temperature, however, the drugs are released via a "squeeze-out" mechanism. Glucose-regulated release for both drugs was observed. At all temperatures glucose enhances the release of ARS because it competes with ARS for binding with PBA groups. For FITC-insulin, glucose enhances its release at 4 degrees C, but retards at 37 degrees C. These results will guide the design of self-regulated insulin release systems based on P(NIPAM-PBA) microgels. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2668 / 2675
页数:8
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