Investigation of the cytotoxicity and insulin transport of acrylic-based copolymer protein delivery systems in contact with Caco-2 cultures

被引:65
作者
Foss, AC
Peppas, NA
机构
[1] Univ Texas, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas, Dept Biomed Engn, Austin, TX 78712 USA
[3] Univ Texas, Div Pharmaceut, Austin, TX 78712 USA
关键词
acrylic-based copolymer; copolymer nanospheres; poly(ethylene glycol); Caco-2 cell culture; insulin transport;
D O I
10.1016/j.ejpb.2004.02.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Microparticles or nanospheres of hydrogels of crosslinked poly(methacrylic acid) grafted with poly(ethylene glycol) as well as crosslinked poly(acrylic acid) grafted with poly(ethylene glycol) were prepared for use as oral insulin delivery carriers. The copolymer carriers were synthesized by precipitation/dispersion polymerization that led to gel nanospheres or by bulk polymerization and subsequent size reduction of thin films to obtain gel microparticles. The cytotoxicity of these copolymers was investigated in contact with Caco-2 cell cultures using a metabolic assay to measure the effect of the presence of copolymers on the cell viability. The copolymers were found to exhibit no cytotoxic effect on the cell cultures. Insulin-loaded formulations were also tested for cytotoxicity and insulin transport studies across cell monolayers. The copolymers were shown to open the tight junctions between cells, increasing the available area for diffusion across the cell monolayer, and thus increasing the permeability of insulin across the monolayer. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:447 / 455
页数:9
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