Laboratory of Toxicology, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, 9000, Ghent, Belgium.
Laboratory of Toxicology, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, 9000, Ghent, Belgium.
J Chromatogr A. 2019 Sep 13;1601:95-103. doi: 10.1016/j.chroma.2019.06.022. Epub 2019 Jun 10.
Fully automated dried blood spot (DBS) extraction systems, online coupled to standard liquid chromatography-tandem mass spectrometry (LC-MS/MS) configurations, decrease the hands-on time associated with conventional DBS analysis, resulting in a higher sample throughput, making the technique more compatible with a high-capacity bioanalytical workflow. The aim of this study was to develop and validate an LC-MS/MS method, using a DBS-MS 500 autosampler, for the determination and quantification of four anti-epileptic drugs (carbamazepine, valproic acid, phenobarbital and phenytoin) and one active metabolite (carbamazepine-10,11-epoxide) in DBS samples. Method development included thorough optimization of the fully automated extraction procedure (i.e. extraction solvent, extraction (loop) volume, internal standard application, internal standard drying time, etc.). The method was fully validated based on international guidelines. Accuracy (%bias), as well as precision (%RSD) (with a single exception) were below 13%. Neither carry-over nor unacceptable interferences were observed. All compounds were stable in DBS for at least 1 month when stored at room temperature, 4 °C and -20 °C and for at least 4 days when stored at 60 °C. Internal standard-corrected matrix effects were below 8%, with %RSDs below 9.1%. Reproducible relative recovery values (around 60% for all analytes) were obtained and the effect of the hematocrit on the relative recovery was overall limited. Successful application on capillary patient samples originating from developing countries demonstrated the applicability of the developed procedure in a remote setting.
全自动干血斑(DBS)提取系统与标准液相色谱-串联质谱(LC-MS/MS)在线联用,减少了传统 DBS 分析相关的手动操作时间,提高了样品通量,使该技术更能与高通量生物分析工作流程兼容。本研究旨在开发和验证一种 LC-MS/MS 方法,使用 DBS-MS 500 自动进样器,用于 DBS 样品中四种抗癫痫药物(卡马西平、丙戊酸、苯巴比妥和苯妥英)和一种活性代谢物(卡马西平-10,11-环氧化物)的测定和定量。方法开发包括对全自动提取程序(即提取溶剂、提取(循环)体积、内标应用、内标干燥时间等)进行彻底优化。该方法完全按照国际指南进行了验证。准确度(%偏差)和精密度(%RSD)(只有一个例外)均低于 13%。未观察到交叉污染或不可接受的干扰。当在室温、4°C 和-20°C 下储存至少 1 个月,在 60°C 下储存至少 4 天时,所有化合物在 DBS 中均稳定。内标校正后的基质效应低于 8%,RSD 低于 9.1%。获得了可重复的相对回收率值(所有分析物约为 60%),并且红细胞压积对相对回收率的影响总体上是有限的。来自发展中国家的毛细血管患者样本的成功应用证明了所开发方法在偏远环境中的适用性。