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首页> 外文期刊>Journal of Controlled Release: Official Journal of the Controlled Release Society >Tailor-made polymers for local drug delivery: Release of macromolecular model drugs from biodegradable hydrogels based on poly(ethylene oxide)
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Tailor-made polymers for local drug delivery: Release of macromolecular model drugs from biodegradable hydrogels based on poly(ethylene oxide)

机译:量身定制的用于局部药物递送的聚合物:从基于聚环氧乙烷的可生物降解水凝胶中释放大分子模型药物

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摘要

Hydrogels were synthesized from degradable and non-degradable PEO bismacromonomers. The degradability was provided by hydrolyzable segment between the main PEO chain and the methacrylate or methacrylamide groups at the both PEO chain termini. The hydrolyzable segment consisted of a monomeric alpha-hydroxy acid or a depsipeptide. The polymerization conditions and the choice of a bismacromonomer influenced the cross-linking density of the hydrogels. The release behavior of model macromolecular solutes, FITC dextran and bovine serum albumin (BSA), was studied. The small FITC-dextran 4 kDa was released rapidly front the hydrogel. The larger FITC-dextran 40 kDa and BSA were retained inside the matrix and their release rate was controlled by the degradation. (c) 2004 Elsevier B.V. All rights reserved.
机译:水凝胶是由可降解和不可降解的PEO双大分子单体合成的。通过主PEO链与两个PEO链末端的甲基丙烯酸酯或甲基丙烯酰胺基团之间的可水解链段提供降解性。可水解链段由单体α-羟基酸或二肽组成。聚合条件和双大分子单体的选择影响了水凝胶的交联密度。研究了模型大分子溶质,FITC葡聚糖和牛血清白蛋白(BSA)的释放行为。小FITC-葡聚糖4 kDa在水凝胶前迅速释放。较大的FITC-葡聚糖40 kDa和BSA保留在基质内部,其释放速率受降解控制。 (c)2004 Elsevier B.V.保留所有权利。

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