Raut Prashant P, Charde Shrikant Y, Bishnoi Pradeep
Industrial Research Laboratory, Department of Pharmacy, Birla Institute of Technology and Science, Pilani, Pilani Campus, Rajasthan, - 333 031, India.
Department of Pharmacy, Birla Institute of Technology and Science, Pilani, Hyderabad Campus, Telangana, - 500 078, India.
Biomed Chromatogr. 2016 Oct;30(10):1696-700. doi: 10.1002/bmc.3713. Epub 2016 Mar 15.
The aim of study was to develop a suitable analytical method for simultaneous estimation of levodopa, carbidopa and 3-O-methyl dopa in rat plasma. Chromatographic separation of plasma samples was achieved using a reverse-phase C18 column. The mobile phase used consisted of a mixture of methanol and phosphate buffer (10 mM, pH 3.50) in the ratio of 90:10 v/v. All analytes were estimated by electrochemical detection at +800 mV. The developed method has been validated as per the standard guidelines. Precision study results were found to be satisfactory, with percentage relative standard deviation for repeatability and intermediate precision <3.96 and 6.56%, respectively, for all analytes detected in rat plasma. The developed method in rat plasma was found to be simple, rapid, accurate, precise and specific. The proposed method has been successfully applied for analysis of rat plasma samples obtained during an oral pharmacokinetic study of sustained release pellets of levodopa and carbidopa in rats. Copyright © 2016 John Wiley & Sons, Ltd.
本研究的目的是开发一种合适的分析方法,用于同时测定大鼠血浆中的左旋多巴、卡比多巴和3 - O - 甲基多巴。使用反相C18柱对血浆样品进行色谱分离。所用流动相由甲醇和磷酸盐缓冲液(10 mM,pH 3.50)按90:10 v/v的比例混合而成。所有分析物通过在+800 mV下的电化学检测进行测定。所开发的方法已按照标准指南进行了验证。精密度研究结果令人满意,大鼠血浆中检测到的所有分析物的重复性和中间精密度的相对标准偏差百分比分别<3.96%和6.56%。在大鼠血浆中所开发的方法被发现简单、快速、准确、精密且具有特异性。所提出的方法已成功应用于大鼠口服左旋多巴和卡比多巴缓释微丸药代动力学研究期间获得的大鼠血浆样品的分析。版权所有© 2016约翰威立父子有限公司。