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Biologically active oxazolones and their chemical immobilization on xanthat

机译:具有生物活性的恶唑酮及其在xanthat上的化学固定

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摘要

The aim of the present paper is the characterization of two oxazolones resulting from the N-(m-, p-nitrobenzoyl)-L-asparagic acids, as to their biological action, as well as to their immobilization-by esteric bonds - on xanthan, in order to obtain a new polymer-drug system with controlled release of the active component. The influence of some parameters of the immobilization reaction (oxazolone/xanthan weight ratio, dicyclohexylcarboddiimide/oxazolone mole ratio) on the coupling efficiency was studied. The in vitro tests made evident the active component to be released from the macromolecular, support according to a "zero order" kinetics.
机译:本文的目的是表征N-(间-,对硝基苯甲酰基)-L-天冬酰胺酸产生的两种恶唑酮的生物学作用以及它们通过酯键固定在黄原胶上的特性,以便获得具有控制性释放活性成分的新型聚合物-药物系统。研究了固定化反应的一些参数(恶唑酮/黄原胶重量比,二环己基碳二亚胺/恶唑酮摩尔比)对偶联效率的影响。体外试验表明活性成分按照“零级”动力学从大分子载体上释放出来。

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