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首页> 外文期刊>Analytical Letters >A Simple, Rapid, and Validated LC Method for the Estimation of Nimesulide in Human Serum and Its Application in Bioavailability Studies
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A Simple, Rapid, and Validated LC Method for the Estimation of Nimesulide in Human Serum and Its Application in Bioavailability Studies

机译:一种简单,快速,验证的LC方法,用于估计人体血清中的尼美,及其在生物利用度研究中的应用

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摘要

A new, simple, and rapid, sensitive reversed phase liquid chromatographic method was developed for the estimation of nimesulide in blood serum using a 60:40 mixture of acetonitrile and orthophosphoric acid (pH 3.0) as the mobile phase at 230nm. The mobile phase and other chromatographic conditions were optimized to minimize interference from the serum matrix and at the same time provide sufficient sensitivity for the method to be adopted for in vivo studies of oral formulations of nimesulide. Acetonitrile was used to precipitate proteins from serum during sample preparation. Detector response was found to be linear in the region of 100-1000ng/ml. The detection and quantitation limit, as per the error propagation theory, was found to be 50ng/ml and 100ng/ml, respectively. The linear equation obtained by the least square regression method was Area=37.29Conc.(ng/ml)-1699.89 with a retention time of 3.970.04min. The results of the analysis were treated statistically, as per ICH guidelines for validation of analytical procedures, USP-2000. and by recovery studies. An internal standard was not employed in the method, as sample recoveries were in good agreement with their label claims. The results were found to be accurate, reproducible, and free from interference. The developed methods were further used for estimation of nimesulide for oral bioavailability of designed sustained release formulations of nimesulide.
机译:开发了一种新的,简单,快速敏感的反相液相色谱法,用于使用60:40的乙腈和正磷酸(pH3.0)作为230nm的流动相的60:40混合物估计血液血清中的Nimesulide。优化流动相和其他色谱条件以使来自血清基质的干扰最小化,同时为纳米菊酯的口服制剂进行体内研究提供足够的敏感性。在样品制备期间,使用乙腈从血清中沉淀蛋白质。发现探测器响应在100-1000ng / ml的区域中是线性的。根据误差传播理论,发现检测和定量限制分别为50ng / ml和100ng / ml。通过最小二乘回归方法获得的线性方程是面积= 37.29CONC。(Ng / ml)-1699.89,保留时间为3.970.04min。分析结果统计治疗,根据分析程序的验证指南,USP-2000。并通过恢复研究。该方法没有采用内部标准,因为样本回收与其标签索赔良好。发现结果是准确,可重复的,没有干扰。开发的方法进一步用于估计尼菊酯的设计持续释放制剂的口服生物利用度。

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