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首页> 外文期刊>International journal of legal medicine >Validation of an LC-MS/MS method for the determination of zopiclone, N-desmethylzopiclone and 2-amino-5-chloropyridine in whole blood and its application to estimate the original zopiclone concentration in stored specimens
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Validation of an LC-MS/MS method for the determination of zopiclone, N-desmethylzopiclone and 2-amino-5-chloropyridine in whole blood and its application to estimate the original zopiclone concentration in stored specimens

机译:验证全血Zopiclone,N-去甲基丙酮醇和2-氨基-5-氯吡啶的测定的LC-MS / MS方法及其应用,以估算储存标本中原始唑酮浓度的施用

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摘要

2-Amino-5-chloropyridine (ACP) is a degradation product of zopiclone (ZOP) and its two main metabolites N-desmethylzopiclone (NDZOP) and zopiclone N-oxide (ZOPNO). ACP may be formed when specimens are stored. ZOP instability in blood makes interpretation of concentrations difficult especially in cases of prolonged sample storage. This study investigated how ACP could be used to estimate the original concentration of ZOP in authentic samples. For that purpose, an analytical liquid chromatography tandem mass spectrometry (LC-MS/MS) method for the quantitation of ACP, ZOP, and NDZOP in blood was developed and validated. Due to poor extraction recovery, ZOPNO was not included in the analytical method. The method was then applied to investigate ACP formation, ZOP and NDZOP degradation in stored ZOP post-dosed authentic whole blood and two mathematical models were used to calculate the original concentration of ZOP. During storage, ACP was formed in amounts equimolar to the ZOP and NDZOP degradation. Results from samples in which ACP had been formed were used to test two models to estimate the original ZOP concentration. The correlation tests of the models showed strong correlations to the original ZOP concentration (r = 0.960 and r = 0.955) with p < 0.01 and explained more than 90 % of the ZOP concentration. This study showed that the equimolar degradation of ZOP and NDZOP to ACP could be used to estimate the original concentration of ZOP.
机译:2-氨基-5-氯吡啶(ACP)是ZOPICLONE(ZOP)的降解产物及其两种主要代谢物N-去甲基丙酮(NDZOP)和ZOPICLONE N-氧化物(ZOPNO)。储存样品时可以形成ACP。血液中的ZOP不稳定性使得浓度的解释尤其是在延长样品储存的情况下难以。本研究调查了ACP如何用于估计真实样品中ZOP的原始浓度。为此目的,开发并验证了用于定量ACP,ZOP和NDZOP的分析液相色谱串联质谱(LC-MS / MS)方法。由于提取差,ZOPNO不包括在分析方法中。然后将该方法应用于研究ACP形成,ZOP和Ndzop降解储存的ZOP后剂型正宗的全血,并使用两种数学模型来计算ZOP的原始浓度。在储存期间,ACP以ZOP和NDZOP降解的量成分形成。使用ACP形成的样品的结果用于测试两种模型以估计原始ZOP浓度。该模型的相关试验显示出与原始ZOP浓度(R = 0.960和r = 0.955)的强相关性,P <0.01并解释了ZOP浓度的90%以上。该研究表明,ZOP和Ndzop至ACP的等摩尔降解可用于估计ZOP的原始浓度。

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