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首页> 外文期刊>Chemicke Zvesti >Biodegradable and biocompatible agarose-poly (vinyl alcohol) hydrogel for the in vitro investigation of ibuprofen release
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Biodegradable and biocompatible agarose-poly (vinyl alcohol) hydrogel for the in vitro investigation of ibuprofen release

机译:可生物降解和生物相容性琼脂糖 - 聚(乙烯醇)水凝胶用于对布洛芬释放的体外研究

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摘要

Biodegradable and biocompatible interpenetrating hydrogels consisting of agarose and poly (vinyl alcohol) (PVA) were synthesized using N,N'-methylene bisacrylamide as the cross-linker. Different hydrogels of agarose were prepared with varying concentration of PVA, cross-linker, and initiator ammonium persulfate. The concentration of each of the component was optimized on the basis of their nature of swelling. Surface morphology of the prepared hydrogel was examined by FESEM analysis and structural changes were confirmed by FTIR, XRD and TGA/DSC technique. Prepared hydrogels showed excellent swelling and pH-dependent drug release. Ibuprofen was used as a model drug to investigate the release behavior from hydrogels. Pre-synthesized IBU and β-cyclodextrin (1:1) inclusion complex was loaded directly into the hydrogel and its release study was performed in different pH solutions. The release data were fitted using various kinetic models such as zeroorder, first-order, Higuchi model and Korsemeyer-Peppas model and examined the release mechanism. The biodegradation and cytotoxicity assay studies confirmed the degradable and non-toxic nature of modified hydrogel.
机译:使用N,N'-亚甲基双式丙烯酰胺作为交联剂,合成可生物降解和生物相容性的间隔水凝胶和聚(乙烯醇)(PVA)合成。制备不同的琼脂糖水凝胶,其具有不同浓度的PVA,交联剂和引发剂铵过硫酸铵。根据其肿胀的性质,优化每个组分的浓度。通过FESEM分析检查制备水凝胶的表面形态,并通过FTIR,XRD和TGA / DSC技术确认了结构变化。制备的水凝胶显示出优异的溶胀和依赖性药物释放。布洛芬用作模型药物以研究水凝胶的释放行为。预合成的IBU和β-环糊精(1:1)将包含复合物直接加载到水凝胶中,并在不同的pH溶液中进行释放研究。使用各种动力学模型(如​​ZERORANDE,一阶,HIGUCHI模型和Korsemeyer-Peppas模型)安装了释放数据,并检查了释放机制。生物降解和细胞毒性测定研究证实了改性水凝胶的可降解和无毒性质。

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