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Preparation and Characterization of Gelatin-Tamarind Gum /Carboxymethyl Tamarind Gum Based Phase Separated Hydrogels and Films for Tissue Engineering Application

机译:明胶-罗望子胶/羧甲基罗望子胶的相分离水凝胶和膜的制备与表征,用于组织工程

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摘要

The purpose of this research was to synthesize and characterize gelatin and tamarind gum/carboxymethyl tamarind gum based phase-separated hydrogels and films for tissue engineering applications. The polymeric constructs were thoroughly characterized using bright-field microscope, FTIR spectroscope, differential scanning calorimeter (DSC), mechanical tester and impedance analyzer. The biocompatibility and swelling property also evaluated. The antimicrobial efficiency of ciprofloxacin (model antimicrobial drug) loaded hydrogels and films were studied against E. coli. The in vitro drug release was carried out in pH 7.4. Microstuctural analysis suggested the formation of phase-separated formulations. FTIR studies suggested that carboxymethyl tamarind gum altered the secondary structure of the gelatin molecules. Presence of the polysaccharides within the formulations resulted in the increase in the enthalpy and entropy for evaporation of the moisture from the hydrogels and films. The mechanical studies indicated viscoelastic nature of the polymeric constructs. Electrical analysis suggested an increase in the impedance of the formulations in the presence of the tamarind gum. The presence of carboxymethyl tamarind gum resulted in the decrease in the impedance of the formulations. The hydrogels and films exhibited good biocompatibility, and pH dependent swelling behavior. The drug loaded samples showed good antimicrobial activity and the drug release was pH dependent and diffusion mediated.
机译:这项研究的目的是合成和表征基于明胶和罗望子树胶/羧甲基罗望子树胶的相分离水凝胶和薄膜,用于组织工程应用。使用明场显微镜,FTIR光谱仪,差示扫描量热仪(DSC),机械测试仪和阻抗分析仪对聚合物结构进行了全面表征。还评估了生物相容性和溶胀性。研究了环丙沙星(模型抗菌药物)水凝胶和薄膜对大肠杆菌的抗菌效果。在pH 7.4下进行体外药物释放。显微结构分析表明形成了相分离的制剂。 FTIR研究表明羧甲基罗望子树胶改变了明胶分子的二级结构。制剂中多糖的存在导致从水凝胶和薄膜蒸发水分的焓和熵增加。力学研究表明聚合物构造的粘弹性。电分析表明,在存在罗望子树胶的情况下,制剂的阻抗增加。羧甲基罗望子树胶的存在导致制剂的阻抗降低。水凝胶和薄膜表现出良好的生物相容性,并具有pH依赖性的溶胀行为。载药样品显示出良好的抗菌活性,药物的释放是pH依赖性的,且是扩散介导的。

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    Shaw Gauri Shankar;

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  • 年度 2016
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