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Influence on variation in process parameters for the design of xanthan-gum-facilitated ethyl cellulose microparticles for intestinal specific delivery

机译:黄原胶促进肠道特异性递送的乙基纤维素微粒设计工艺参数变化的影响

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Xanthan-gum-facilitated aspirin-loaded ethyl cellulose microparticles were prepared by multiple-emulsion solvent evaporation technology and the impact on variation in process parameters was investigated systematically. Scanning electron microscopy was performed to determine the surface morphology of the microparticles before and after dissolution study. X-ray diffraction (XRD), differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) analysis were performed, and yield value, swelling study, encapsulation efficiency, flow properties and dissolution profiles of the prepared formulations were evaluated. The size of microparticles varied between 247 and 410 μm, and 58.34% drug entrapment efficiency was achieved depending on the variation in process parameters. The drug release in acid solutions was slower than in alkaline solution. The microparticles provided extended drug release in alkaline dissolution medium, and the drug release was found to be controlled by Fickian diffusion mechanism. XRD and DSC analyses revealed the amorphous nature of drug in the microparticles. FTIR data indicated the stable character of the encapsulated drug in the microparticles. Thus, variation in process parameters showed a slow and prolonged release of aspirin in simulated intestinal fluid.
机译:利用多乳液溶剂蒸发技术制备了黄原胶促进的阿司匹林负载乙基纤维素微粒,并系统地研究了其对工艺参数变化的影响。在溶解研究之前和之后,进行扫描电子显微镜以确定微粒的表面形态。进行了X射线衍射(XRD),差示扫描量热法(DSC),傅立叶变换红外光谱(FTIR)分析,并评估了所制备制剂的产率值,溶胀研究,包封效率,流动性质和溶出曲线。微粒的大小在247至410μm之间变化,取决于工艺参数的变化,可实现58.34%的药物截留效率。酸性溶液中的药物释放比碱性溶液中的药物释放慢。微粒在碱性溶解介质中提供了延长的药物释放,并且发现药物释放受菲克扩散机制控制。 XRD和DSC分析揭示了微粒中药物的无定形性质。 FTIR数据表明微粒中封装药物的稳定特性。因此,工艺参数的变化表明阿司匹林在模拟肠液中的释放缓慢而延长。

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