Zheng Yufang, Axelsson Magnus A B, Andresen Bergström Moa
Department of Laboratory Medicine, Unilabs, Malarsjukhuset, Eskilstuna 631 88, Sweden.
Region Västra Götaland, Sahlgrenska University Hospital, Laboratory of Clinical Chemistry, Bruna Stråket 16, Gothenburg 413 45, Sweden.
J Anal Toxicol. 2025 Jan 20;49(1):14-25. doi: 10.1093/jat/bkae087.
Liquid chromatography-mass spectrometry (LC-MS) methods for detection of multiple drugs of abuse (DoA) in oral fluid (OF) samples are being implemented in many clinical routine laboratories. Therefore, there is a need to develop new multianalyte methods with simple sample pretreatment and short analysis times. The purpose of this work was to validate a method detecting 58 DoA to be used with two different OF sampling kits, the saliva collection system (SCS) from Greiner Bio-One and Quantisal from Immunalysis, using the same sample pretreatment and analytical method. A set of 110 samples collected with the SCS kit was further compared to an high-resolution mass spectrometry (LC-HRMS) method in another laboratory. The method was successfully validated, with precision and accuracy of ≤15% and z-scores of <2 for external controls. Using a sensitive LC-MS-MS instrument, the detection limits were <1 µg/l in neat oral fluid. In the comparative study between the LC-MS-MS and LC-HRMS methods using SCS samples, a good agreement was observed. Discrepancies were limited to lower concentration ranges, attributable to differences in cut-off thresholds between the methods. This work contributes to the development of LC-MS multianalyte methods for OF samples, which are suitable for clinical routine laboratories.
液相色谱-质谱联用(LC-MS)法用于检测口腔液(OF)样本中的多种滥用药物(DoA),目前许多临床常规实验室都在采用。因此,有必要开发新的多分析物方法,实现简单的样本预处理和较短的分析时间。本研究的目的是验证一种可检测58种DoA的方法,该方法使用相同的样本预处理和分析方法,与两种不同的OF采样试剂盒配合使用,即Greiner Bio-One公司的唾液采集系统(SCS)和Immunalysis公司的Quantisal。将用SCS试剂盒采集的110份样本与另一家实验室的高分辨率质谱(LC-HRMS)方法进行了进一步比较。该方法成功通过验证,外部对照的精密度和准确度≤15%,z分数<2。使用灵敏的LC-MS-MS仪器,纯口腔液中的检测限<1µg/l。在使用SCS样本的LC-MS-MS和LC-HRMS方法的对比研究中,观察到了良好的一致性。差异仅限于较低浓度范围,这归因于两种方法之间截断阈值的差异。这项工作有助于开发适用于临床常规实验室的OF样本LC-MS多分析物方法。