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建立并验证了一种采用同位素稀释液相色谱/串联质谱法测定人血清中苯妥英、苯巴比妥、拉莫三嗪和托吡酯的参考测量程序。

Development and validation of a reference measurement procedure for certification of phenytoin, phenobarbital, lamotrigine, and topiramate in human serum using isotope-dilution liquid chromatography/tandem mass spectrometry.

机构信息

Analytical Chemistry Division, National Institute of Standards and Technology, Gaithersburg, MD 20899-8392, USA.

出版信息

Anal Bioanal Chem. 2011 Oct;401(6):1915-22. doi: 10.1007/s00216-011-5251-5. Epub 2011 Aug 28.

Abstract

Phenytoin (PHT), phenobarbital (PHB), lamotrigine (LTG), and topiramate (TPM) are some of the most widely used antiepileptic drugs (AEDs). Monitoring of their concentrations in serum is important for the treatment of epilepsy. A reference measurement procedure (RMP) for certification of PHT, PHB, LTG, and TPM in serum has been developed and critically evaluated. Isotopically labeled compounds of PHT, PHB, LTG, and TPM are used as internal standards for the four AEDs. The four drugs and their respective labeled internal standards are simultaneously extracted from serum using solid-phase extraction prior to reversed-phase liquid chromatography-tandem mass spectrometry (LC-MS/MS). Chromatographic separation was performed using a C(18) column. Electrospray ionization (ESI) in the positive ion mode for PHT and LTG, and in the negative ion mode for PHB and TPM were used. The recovery of AEDs added to serum (accuracy of the extraction method) was evaluated by recovery studies of measuring the four drugs in spiked samples with known drug levels. The recoveries of the added drugs ranged from 98.6% to 102.0%. The absolute recoveries (extraction efficiencies) of the four drugs with this method ranged from 97% to 100%. Excellent repeatability was obtained for the four drugs with between-set coefficients of variation (CVs) within 1%. The type B components estimates are conservatively large and are considerably larger than the type A component. Therefore, we use the usual metrological expansion factor of 2 to provide an approximate 95% coverage interval. The relative expanded uncertainties for the four AEDs ranged from 2.3% to 2.4%. This LC-MS/MS RMP for PHT, PHB, LTG, and TPM in serum demonstrating good accuracy and precision can be used to assess the accuracy of routine methods used in clinical laboratories.

摘要

苯妥英(PHT)、苯巴比妥(PHB)、拉莫三嗪(LTG)和托吡酯(TPM)是一些最常用的抗癫痫药物(AEDs)。监测其在血清中的浓度对于癫痫的治疗很重要。已经开发并严格评估了一种用于血清中 PHT、PHB、LTG 和 TPM 认证的参考测量程序(RMP)。使用 PHT、PHB、LTG 和 TPM 的同位素标记化合物作为这四种 AED 的内标。在反相液相色谱-串联质谱(LC-MS/MS)之前,使用固相萃取从血清中同时提取这四种药物及其各自的标记内标。使用 C(18)柱进行色谱分离。采用正离子模式的电喷雾电离(ESI)用于 PHT 和 LTG,负离子模式用于 PHB 和 TPM。通过在已知药物水平的加标样品中测量四种药物来评估添加到血清中的 AED 的回收率(提取方法的准确性)。添加药物的回收率范围为 98.6%至 102.0%。该方法对四种药物的绝对回收率(提取效率)范围为 97%至 100%。四种药物的重复性很好,组间变异系数(CVs)在 1%以内。B 型分量估计值保守较大,并且明显大于 A 型分量。因此,我们使用通常的计量扩展因子 2 来提供近似的 95%覆盖区间。四种 AED 的相对扩展不确定度范围为 2.3%至 2.4%。该用于血清中 PHT、PHB、LTG 和 TPM 的 LC-MS/MS RMP 具有良好的准确性和精密度,可用于评估临床实验室中常规方法的准确性。

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