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Development and Validation of UV Spectrophotometric Method for Simultaneous Estimation of Acyclovir and Silymarin in Niosome Formulation

机译:紫外分光光度法同时估算纳米脂质体中阿昔洛韦和水飞蓟素的研制与验证

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A UV-spectrophotometric method for simultaneous estimation of Acyclovir and Silymarin in niosome formulation has been developed. Methanol is used as solvent for preparation of stock solution and further dilutions are prepared in distilled water. Acyclovir and Silymarin exhibit absorption maxima at 251nm and 287nm respectively. The system obeyed Beer's law over the concentration range of 2-10 μg/ml and 10-50 μg/ml for Acyclovir and Silymarin respectively. Method was validated for linearity, range, accuracy, precision and recovery studies as per ICH norms. Thus the proposed method was found to be rapid, specific, precise, accurate and cost effective quality control tool for the routine analysis of Acyclovir and Silymarin in niosome formulation.
机译:已经开发了一种紫外分光光度法,用于同时估算脂质体制剂中的阿昔洛韦和水飞蓟素。甲醇用作制备原液的溶剂,并在蒸馏水中进行进一步稀释。阿昔洛韦和水飞蓟素分别在251nm和287nm处表现出最大吸收。该系统在阿昔洛韦和水飞蓟素的浓度范围分别为2-10μg/ ml和10-50μg/ ml时遵守比尔定律。该方法已按照ICH规范进行了线性,范围,准确性,精密度和回收率研究的验证。因此,发现所提出的方法是快速,特异性,精确,准确且具有成本效益的质量控制工具,用于常规分析阿昔洛韦和水飞蓟宾在脂质体制剂中的应用。

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