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Development and Validation of UV Spectrophotometric Method for Estimation Ibandronate sodium in Pharmaceutical Formulation

机译:紫外分光光度法估算药物制剂中伊班膦酸钠的研制与验证

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A simple, accurate, precise, rapid spectrophotometric method for estimation of Ibandronate sodium in pharmaceutical formulation. Ibandronate sodium is one off the nitrogen carrying bisphosphonate. It prevents osteoclast-conciliate bone resorption, Paget’s disease, postmenopausal osteoporosis. The maximum wavelength (λmax) of ibandronate sodium is 218nm. Linearity was observed in the concentration range 2-100μg/ml. The coefficient of variation value was found to be 0.3499. Amount of drug estimated from tablet formulation were in precise with label claim. The method was statistically validated as per ICH guidelines and can be successively applied for analysis for tablet formulation. The proposed method is economical and sensitive for estimation of ibandronate sodium in pharmaceutical formulation.
机译:一种简单,准确,精确,快速的分光光度法,用于评估药物制剂中的伊班膦酸钠。伊班膦酸钠是一种脱氮的双膦酸钠。它可防止破骨细胞纤毛吸收,佩吉特氏病,绝经后骨质疏松症。伊班膦酸钠的最大波长(λmax)为218nm。在2-100μg/ ml的浓度范围内观察到线性。发现变异系数值为0.3499。从片剂中估计的药物量与标签要求完全一致。该方法已按照ICH指南进行了统计验证,可连续用于片剂的分析。所提出的方法对于估计药物制剂中伊班膦酸钠的经济性和敏感性。

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