首页> 美国卫生研究院文献>Designed Monomers and Polymers >Enhanced gastric retention and drug release via development of novel floating microspheres based on Eudragit E100 and polycaprolactone: synthesis and in vitro evaluation
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Enhanced gastric retention and drug release via development of novel floating microspheres based on Eudragit E100 and polycaprolactone: synthesis and in vitro evaluation

机译:通过开发基于Eudragit E100和聚己内酯的新型漂浮微球增强胃retention留和药物释放:合成和体外评估

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摘要

Eudragit E 100 and polycaprolactone (PCL) floating microspheres for enhanced gastric retention and drug release were successfully prepared by oil in water solvent evaporation method. Metronidazole benzoate, an anti-protozoal drug, was used as a model drug. Polyvinyl alcohol was used as an emulsifier. The prepared microspheres were observed for % recovery, % degree of hydration, % water uptake, % drug loading, % buoyancy and % drug release. The physico-chemical properties of the microspheres were studied by calculating encapsulation efficiency of microspheres and drug release kinetics. Drug release characteristics of microspheres were studied in simulated gastric fluid and simulated intestinal fluid i.e., at pH 1.2 and 7.4 respectively. Fourier transform infrared spectroscopy was used to reveal the chemical interaction between drug and polymers. Scanning electron microscopy was conducted to study the morphology of the synthesized microspheres.
机译:通过水包油溶剂蒸发法成功制备了Eudragit E 100和聚己内酯(PCL)漂浮微球,可增强胃retention留和药物释放。甲硝唑苯甲酸酯,一种抗原生动物药物,被用作模型药物。聚乙烯醇用作乳化剂。观察制备的微球的回收率%,水合度%,吸水率%,药物载量%,浮力%和药物释放%。通过计算微球的包封效率和药物释放动力学,研究了微球的理化性质。在模拟的胃液和模拟的肠液中,即分别在pH 1.2和7.4下,研究了微球的药物释放特性。傅里叶变换红外光谱用于揭示药物与聚合物之间的化学相互作用。进行扫描电子显微镜研究合成的微球的形态。

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