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新型生物人工水凝胶的药物释放

Drug release from new bioartificial hydrogel.

作者信息

Gayet J C, Fortier G

机构信息

Département de chimie-biochimie, Université du Québec à Montréal, Canada.

出版信息

Artif Cells Blood Substit Immobil Biotechnol. 1995;23(5):605-11. doi: 10.3109/10731199509117975.

Abstract

The use of high water content (> 96%) hydrogels obtained from copolymerisation of bovine serum albumin and poly(ethylene glycol) as a controlled release system has been investigated. Such hydrogels allowed release of soluble and hydrophobic substances, even proteins. Release is shown to occur by a diffusion controlled mechanism, leading to half-life times of release ranging between 0.8 hour for theophylline and 4.2 hours for lysozyme, when a 2.4 mm thick disc of BSA-PEG (MW of 10000) was used. The effect of the porosity of the hydrogel on the diffusive properties of theophylline and hydrocortisone has been evaluated by varying the molecular weight of the poly(ethylene glycol). It was shown that poly(ethylene glycol) of high molecular weight leads to more porous hydrogels in which the diffusion is faster.

摘要

对通过牛血清白蛋白与聚乙二醇共聚获得的高含水量(>96%)水凝胶作为控释系统的应用进行了研究。这种水凝胶能够释放可溶性和疏水性物质,甚至蛋白质。释放过程显示是由扩散控制机制发生的,当使用2.4毫米厚的BSA-PEG(分子量为10000)圆盘时,茶碱的释放半衰期为0.8小时,溶菌酶的释放半衰期为4.2小时。通过改变聚乙二醇的分子量,评估了水凝胶孔隙率对茶碱和氢化可的松扩散特性的影响。结果表明,高分子量的聚乙二醇会导致形成孔隙率更高的水凝胶,其中扩散速度更快。

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