Method development and validation for estimation of Gliclazide in bulk and tablet form by UV Spectrophotometer

Ravindra Hanwate, Bhupendra Singh, Nilesh Khairnar, Sushmita Chavan
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Abstract

UV Spectrophotometric method has been developed to determine Gliclazide in bulk pure and tablet forms. It is a simple, accurate, reproducible, rapid and less time-consuming method. The maximum wavelength of the drug was found to be 232nm. Beer Lamberts’ law was obeyed in the concentration range of 2-20 µg/ml.  (LOD)The limit of detection and limit of qualification (LOQ) was found to be 0.16 µg/ml and 0.50 µg/ml from this method per cent recovery of the drug was found to be 99.30% which indicates no interaction of the excipients. This method was found accurate, simple, precise and rapid for determination of tablet dosage form. Keywords: validation, Gliclazide, tablets, UV Spectroscopy, LOD, LOQ
利用紫外分光光度计开发和验证估算散装和片剂中格列齐特的方法
本实验采用紫外分光光度法测定纯品和片剂中的格列齐特。该方法简单、准确、重现性好、快速且耗时少。该药物的最大波长为 232 纳米。在 2-20 µg/ml 浓度范围内符合比尔-朗伯定律。 (该方法的检出限和定性限(LOQ)分别为 0.16 µg/ml 和 0.50 µg/ml,药物回收率为 99.30%,表明辅料之间没有相互作用。该方法准确、简便、精确、快速,适用于片剂药物的测定。关键词:验证、格列齐特、片剂、紫外光谱、LOD、LOQ
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