首页> 外文期刊>Analytical Letters >Determination of Carbidopa, Levodopa, and Droxidopa by High-Performance Liquid Chromatography-Tandem Mass Spectrometry
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Determination of Carbidopa, Levodopa, and Droxidopa by High-Performance Liquid Chromatography-Tandem Mass Spectrometry

机译:高效液相色谱 - 串联质谱法测定Carbidopa,Levodopa和Droxidopa

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摘要

Modern treatments of Parkinson's disease include the use of carbidopa and droxidopa along with levodopa that demonstrates the necessity for their binary and simultaneous determination in pharmaceutical tablets and biological matrices. This study presents a rapid, accurate, and precise method for the simultaneous determination of these analytes by liquid chromatography- tandem mass spectrometry method for the first time. Accordingly, performances of two types of analytical columns, namely, octadecylsilane and hydrophilic interaction liquid chromatographic columns, were tested and better resolution was obtained with the former. The pH of aqueous mobile phase (0.5% formic acid) was adjusted to 2.3 to ensure the analytes were in molecular form. Calibration graphs were obtained using multiple reaction mode and detection limits were in the region from 0.002 to 0.007 mu M for both columns. The method developed was applied for quality control samples and tablets and satisfactory recovery values from 100 to 106% were obtained.
机译:现代帕金森病的治疗包括使用Carbidopa和Droxidopa以及Levodopa,左旋多巴证明了其二元和药物片剂和生物基质同时测定的必要性。本研究介绍了通过液相色谱 - 串联质谱法同时测定这些分析物的快速,准确,精确的方法。因此,测试了两种类型的分析柱,即八二烷基硅烷和亲水性相互作用液相色谱塔的性能,并用前者获得更好的分辨率。将流动相(0.5%甲酸)的pH调节至2.3以确保分析物以分子形式。使用多反应模式获得校准图,并且对于这两个柱的检测限制在0.002至0.007μm的区域中。施用的方法用于质量控制样品和片剂,获得100至106%的令人满意的恢复值。

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