Zhang HuiFen Hannah, Loh Jia Ying Hilda, Moy Hooi Yan, Lui Chi Pang
Analytical Toxicology Laboratory, Analytical Toxicology Division, Health Sciences Authority, Singapore.
Drug Test Anal. 2025 Aug;17(8):1344-1356. doi: 10.1002/dta.3840. Epub 2024 Dec 14.
This study presents the development and validation of a drug testing method in hair, employing a semi-automated sample preparation procedure and gas chromatography-tandem mass spectrometry (GC-MS/MS) for simultaneous multidrug analysis in hair. The method aims to detect and quantify multiple drugs in hair, including amphetamine, methamphetamine, 3,4-methylenedioxyamphetamine, 3,4-methylenedioxymethamphetamine, ketamine, norketamine, cocaine, benzoylecgonine, morphine, codeine and 6-monoacetylmorphine, using a comprehensive procedure involving decontamination, pulverization, clean-up using supported-liquid extraction (SLE) and a two-step derivatization process. The method validation included specificity, linearity, limit of detection (LOD), limit of quantification (LOQ), precision, accuracy, carryover, robustness and stability. The results indicate a linearity range of 0.1-5 ng/mg for all drugs except methamphetamine, which has a linearity range of 0.2-5 ng/mg. The accuracy and precision of the method are within ±20%, with the LOQ at 0.2 ng/mg for methamphetamine, 0.1 ng/mg for amphetamine and MDMA and 0.05 ng/mg for the rest of the drugs. The LODs were found to be 0.1 ng/mg for methamphetamine, 0.05 ng/mg for amphetamine and MDMA and 0.025 ng/mg for other drugs. This method has demonstrated its accuracy by comparing the quantitative test results with the expected results, using hair samples from the proficiency test service providers. This test method offers efficient testing of multiple drugs in a single analysis, significantly improves the hair analysis workflow in a routine testing laboratory by reducing turnaround time and the amount of hair sample required.
本研究介绍了一种头发药物检测方法的开发与验证,该方法采用半自动样品制备程序和气相色谱 - 串联质谱法(GC-MS/MS)对头发中的多种药物进行同步分析。该方法旨在通过包括去污、粉碎、使用支持液液萃取(SLE)净化以及两步衍生化过程的综合程序,检测和定量头发中的多种药物,包括苯丙胺、甲基苯丙胺、3,4 - 亚甲基二氧基苯丙胺、3,4 - 亚甲基二氧基甲基苯丙胺、氯胺酮、去甲氯胺酮、可卡因、苯甲酰爱康宁、吗啡、可待因和6 - 单乙酰吗啡。方法验证包括特异性、线性、检测限(LOD)、定量限(LOQ)、精密度、准确度、残留、稳健性和稳定性。结果表明,除甲基苯丙胺外,所有药物的线性范围为0.1 - 5 ng/mg,甲基苯丙胺的线性范围为0.2 - 5 ng/mg。该方法的准确度和精密度在±20%以内,甲基苯丙胺的LOQ为0.2 ng/mg,苯丙胺和摇头丸为0.1 ng/mg,其余药物为0.05 ng/mg。发现甲基苯丙胺的LOD为0.1 ng/mg,苯丙胺和摇头丸为0.05 ng/mg,其他药物为0.025 ng/mg。通过将定量测试结果与预期结果进行比较,使用能力验证服务提供商提供的头发样本,该方法证明了其准确性。这种测试方法在单次分析中提供了对多种药物的高效检测,通过减少周转时间和所需头发样本量,显著改善了常规检测实验室中的头发分析工作流程。