Thermosensitive and pH-sensitive Drug Release from Taxifolin-Containing Collagen-Acrylic Hydrogels

O. V. Luneva, Ksenija Bikova, Alexander I. Kashurin, V. V. Motovilov, M. Uspenskaya
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Abstract

The variety of skin diseases encourage the creation of new coatings, the search for a suitable wound dressing. Significant success has been achieved with hydrogel dressings containing biologically active compounds for the healing of wounds of varying severity. The aim of this work was to obtain taxifolin-containing hydrogels based on acrylic acid and collagen as the basis for a wound dressing. The gelation time, sorption kinetics based on a pseudo-second order model and a mathematical model, as well as the drug release of the obtained samples based on the Korsmeyer-Peppas, Higuchi, Baker-Lonsdale, Hopfenberg, Weibull models, respectively, with variation of solvent pH and sorption temperature have been studied. Sorption characteristics of polymer hydrogel matrix containing 0.5 wt.% taxifolin reaches the values from 25 to 30 g/g, respectively at the various pH solvent. The release of taxifolin in the buffer solutions with pH=5.8 and pH=7.2 carries out in two stages. The best release of the drug substance is observed for the sample containing taxifolin in an alkaline medium and is described by the Hopfenberg model.
含taxifolin的胶原-丙烯酸水凝胶的热敏和ph敏药物释放
各种各样的皮肤病促使人们创造新的涂层,寻找合适的伤口敷料。含有生物活性化合物的水凝胶敷料在不同严重程度的伤口愈合方面取得了显著的成功。本研究的目的是获得以丙烯酸和胶原蛋白为基础的含taxifolin的水凝胶,作为伤口敷料的基础。研究了胶凝时间、基于拟二阶模型和数学模型的吸附动力学以及基于Korsmeyer-Peppas、Higuchi、Baker-Lonsdale、Hopfenberg、Weibull模型的药物释放随溶剂pH和吸附温度的变化。含0.5 wt.%紫杉醇的聚合物水凝胶基质在不同pH溶剂下的吸附特性分别达到25 ~ 30 g/g。taxifolin在pH=5.8和pH=7.2缓冲液中的释放分两个阶段进行。在碱性介质中观察到含有杉木素的样品中原料药的最佳释放,并用Hopfenberg模型描述。
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