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Biodegradable polymeric microspheres of gelatin and carboxymethyl guar gum for controlled release of theophylline

机译:明胶和羧甲基瓜尔胶的可生物降解聚合物微球可控制茶碱的释放

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摘要

Carboxymethyl guar gum (CMGG) was synthesized by carboxy-methylation of guar gum (GG), which was blended with gelatin (GE) to obtain a novel semi-interpenetrating polymer network (semi-IPN) in the form of microspheres prepared by water-in-oil emulsion method to investigate the controlled release of theophylline (THP), an antiasthmatic drug. Electronic spectroscopy revealed the drug encapsulation ranging from 56 to 74 %. Fourier Transform infrared spectroscopy confirmed the carboxymethylation of GG as well as the semi-IPN structure of the blend polymer. Scanning electron microscopy indicated the smooth surfaces with spherical microspheres. Differential scanning calorimetric and X-ray diffraction studies showed the molecular level dispersion of drug in the microspheres. The in vitro drug release profiles were analyzed to study the effect of polymer blend composition, % drug loading and amount of glutaraldehyde added as a crosslinker. The drug release was extended up to 26 h. The in vitro release data performed in acidic and alkaline media were analyzed using the empirical equations to understand the release profiles of THP.
机译:羧甲基瓜尔豆胶(CMGG)是通过瓜尔豆胶(GG)的羧甲基化合成的,然后将其与明胶(GE)混合,以水为原料制备微球形式的新型半互穿聚合物网络(semi-IPN)。油中乳液法研究茶碱(THP)(一种抗哮喘药)的控制释放。电子光谱显示药物包封率为56%至74%。傅里叶变换红外光谱证实了GG的羧甲基化以及共混聚合物的半IPN结构。扫描电子显微镜显示具有球形微球的光滑表面。差示扫描量热法和X射线衍射研究表明药物在微球中的分子水平分散。分析了体外药物释放曲线以研究聚合物共混物组成,药物载量%和作为交联剂添加的戊二醛的量的影响。药物释放延长至26小时。使用经验公式分析了在酸性和碱性介质中进行的体外释放数据,以了解THP的释放曲线。

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