溴酚蓝紫外可见分光光度法测定普瑞巴林的纯度和剂型

Swapna A. Surendran, Akshay K, A. V., D. S, Vismaya Venugopalan
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引用次数: 0

摘要

建立了一种简便、准确、经济、快速、灵敏的溴酚蓝紫外-可见分光光度法测定普瑞巴林纯度和剂型的新方法。该方法在线性度、准确度、精密度、坚固性、定量限和定量限等方面均按照ICH指南进行了验证。此法制备普瑞巴林所用溶剂为蒸馏水。该方法是基于溴酚蓝试剂与普瑞巴林形成棕色离子对络合物。离子对配合物是在pH为3的邻苯二甲酸酯缓冲液存在下生成的。在室温下呈现出稳定的褐色。发育的棕色配合物在592nm处吸光度最大。在50、60、70、80、90µg/ml浓度范围内呈线性关系,回归系数为0.995。日内和日间的精密度研究表明,百分比相对标准偏差在可接受范围内。回收率研究在50%、100%和150%三个百分比水平下进行。结果表明,该方法是准确的。检测限(LOD)为10.91µg/ml,定量限(LOQ)为33.06µg/ml。使用不同的分析人员进行了坚固性研究;确保该方法是坚固的。该方法可用于该药的常规质量控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A new Validated UV-visible Spectrophotometric Method for the Estimation of Pregabalin in its pure and dosage form using Bromophenol blue
A new simple, accurate precise, cost effective, rapid and sensitive UV-Visible spectrophotometric method was developed for the estimation of Pregabalin in its pure and dosage form using Bromophenol blue. The developed method was validated as per ICH guideline in terms of linearity, accuracy, precision, ruggedness, LOD and LOQ. In this method the solvent used for the preparation of Pregabalin was distilled water. The method is based on the formation of brown colored ion-pair complex of Pregabalin with Bromophenol Blue reagent. The ion pair complex was produced in presence of Acid Phthalate Buffer of pH 3. The developed brown colour was stable at room temperature. The developed brown coloured complex showed maximum absorbance at 592nm. Linearity was found in the concentration range of 50, 60, 70, 80 and 90µg/ml with regression coefficient value 0.995. Precision studies for intra-day and inter-day shows that percentage relative standard deviation was within range of acceptable limit. The recovery studies were carried out at three percentage levels that is 50%, 100% and 150% levels. The results shows that the method was found to be accurate. The limit of detection (LOD) was found to be 10.91µg/ml and limit of quantification (LOQ) was found to be 33.06µg/ml. A ruggedness study was carried out using different analysts; assure that the method was rugged. Hence the method can be applied for routine quality control of the drug.
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