Hydrotropy – A Solubility Enhancement Tool for the Estimation of Cefdinir in its Suspension Dosage Form by UVSpectroscopy

A. Susmitha, E GireeshKumar.
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Abstract

Present work describes development and validation of a simple, novel, accurate, precise, economical and reproducible spectrophotometric method in ultraviolet region for the assay of Cefdinir in suspension formulation using sodium bicarbonate and distilled water (1:9) as hydrotropic solvent. Cefdinir exhibits absorption maxima at 287nm in hydrotropic solvent. Beer’s law was found to be obeyed in the concentration range of 2.5-17.5μg/ml. The developed method was validated as per the ICH guidelines. The calibration plot was linear over the concentration range investigated (2.5–17.5μg/ml) for Cefdinir in hydrotropic solvent with correlation coefficient, r 2 , 0.99903. The method is accurate, precise and economical. In this proposed method, there was no interference from common pharmaceutical excipients. The proposed method is therefore successfully used for the routine analysis of the Cefdinir in its suspension dosage form.
紫外光谱法测定头孢地尼悬浮液剂型的溶解度增强工具
建立了一种简便、新颖、准确、精密度高、经济、重现性好的紫外分光光度法,以碳酸氢钠和蒸馏水(1:9)为溶剂测定头孢地尼悬浮液中的含量。头孢地尼在亲水溶剂中在287nm处表现出最大吸收。在2.5 ~ 17.5μg/ml浓度范围内符合Beer定律。所开发的方法按照ICH指南进行了验证。头孢地尼在亲水溶剂中的浓度范围(2.5 ~ 17.5μg/ml)与标定曲线呈线性关系,相关系数r = 2,0.99903。该方法准确、精密度高,经济实用。该方法不受常用药用辅料的干扰。因此,所提出的方法成功地用于头孢地尼悬浮液剂型的常规分析。
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