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用于原位形成聚乙烯醇基水凝胶的迈克尔型加成反应。

Michael-type addition reactions for the in situ formation of poly(vinyl alcohol)-based hydrogels.

作者信息

Tortora Mariarosaria, Cavalieri Francesca, Chiessi Ester, Paradossi Gaio

机构信息

Dipartimento di Scienze e Tecnologie Chimiche, Università di Roma Tor Vergata, Via della Ricerca Scientifica, 00133 Roma, Italy.

出版信息

Biomacromolecules. 2007 Jan;8(1):209-14. doi: 10.1021/bm0607269.

Abstract

Michael-type addition reactions offer the possibility to obtain in situ formation of polymeric hydrogels in the absence of a radical mechanism for the networking process. We explored such a synthetic route for obtaining a poly(vinyl alcohol) (PVA)-based hydrogel as a potential biomaterial for applications in vitro-retinal replacement surgery. The presence of radicals in the reaction medium can represent a risk for in situ surgical treatment. To circumvent this problem we have applied nucleophilic addition to ad hoc modified PVA macromers. The gel formation has been studied with respect to the timing required in this surgery and in terms of the structural characteristics of the obtained network.

摘要

迈克尔型加成反应提供了在不存在用于交联过程的自由基机制的情况下原位形成聚合物水凝胶的可能性。我们探索了这样一种合成路线,以获得基于聚乙烯醇(PVA)的水凝胶,作为用于体外视网膜置换手术的潜在生物材料。反应介质中自由基的存在可能对原位手术治疗构成风险。为了规避这个问题,我们将亲核加成应用于经过特殊改性的PVA大分子单体。我们研究了凝胶形成与该手术所需时间以及所得网络的结构特征之间的关系。

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