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Formulation and evaluation of floating in situ gelling system of losartan potassium

机译:氯沙坦钾漂浮原位胶凝体系的制备与评价

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The present investigation deals with the formulation and evaluation of sodium alginate and pectin based In situ gel of Losartan Potassium. Sodium alginate and guar gum were used as a polymer and CaCO3 was used as a crosslinking agent. The formulation of gel depends upon factors like temperature modulation, pH changes, presence of ions and ultra-violet irradiation, from which drug gets released in sustained and controlled manner. The objective of this study was to develop a novel in- situ gel. The system utilizes polymers that exhibit sol-to-gel phase transition due to change in specific Physico-chemical parameters. In-situ gel was formed at a biological pH. In vitro release studies were conducted in simulated gastric fluid and cumulative amount of drug release was analyzed by spectrophotometry. From designed set of experiments, it was evident that formulation containing 2 of sodium alginate and 1.5 of Guar gum control the release of drug for longer duration. The in-situ gel exhibited the expected, viscosity, drug content, pH, in vitro gelling capacity, in vitro floating ability and sustained drug release. The drug release from the in situ gels follows the Fickian diffusion type of release.
机译:本研究涉及海藻酸钠和果胶基氯沙坦钾原位凝胶的制备和评价。海藻酸钠和瓜尔豆胶用作聚合物,CaCO3用作交联剂。凝胶的配方取决于温度调节、pH 值变化、离子的存在和紫外线照射等因素,药物从中以持续和可控的方式释放。本研究的目的是开发一种新的原位凝胶。该系统利用的聚合物由于特定物理化学参数的变化而表现出溶胶到凝胶的相变。原位凝胶在生物pH值下形成。在模拟胃液中进行体外释放研究,并通过分光光度法分析药物释放的累积量。从设计的一组实验中可以明显看出,含有 2% 海藻酸钠和 1.5% 瓜尔豆胶的制剂可以更长时间地控制药物的释放。原位凝胶表现出预期的粘度、药物含量、pH值、体外凝胶能力、体外漂浮能力和药物持续释放。原位凝胶的药物释放遵循 Fickian 扩散类型的释放。

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