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:LC-MS / MS法测定全血中佐匹克隆,N-去甲基佐匹克隆和2-氨基-5-氯吡啶的方法的验证及其在估算样本中佐匹克隆原始浓度中的应用

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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)是佐匹克隆(ZOP)及其两个主要代谢产物N-去甲基佐匹克隆(NDZOP)和佐匹克隆N-氧化物(ZOPNO)的降解产物。储存标本时可能会形成ACP。血液中ZOP的不稳定性使浓度的解释变得困难,尤其是在长时间保存样品的情况下。这项研究调查了如何使用ACP来估计真实样品中ZOP的原始浓度。为此,开发并验证了用于定量分析血液中ACP,ZOP和NDZOP的分析型液相色谱串联质谱(LC-MS / MS)方法。由于提取回收率差,因此分析方法未包含ZOPNO。然后将该方法用于调查储存的ZOP给药后真实全血中ACP的形成,ZOP和NDZOP的降解,并使用两个数学模型计算ZOP的原始浓度。在储存过程中,形成的ACP的量与ZOP和NDZOP的降解等摩尔。形成ACP的样品的结果用于测试两个模型,以估算原始ZOP浓度。模型的相关性测试显示与原始ZOP浓度(r = 0.960和r = 0.955)有很强的相关性,p <0.01,并解释了90%以上的ZOP浓度。这项研究表明,ZOP和NDZOP等摩尔降解为ACP可用于估算ZOP的原始浓度。

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