Ji Jiao-Jiao, Xu Duoqi, Yan Hui, Xiang Ping, Shen Min
Department of Forensic Toxicology, Shanghai Key Laboratory of Forensic Medicine, Academy of Forensic Science, Shanghai, China.
Department of Forensic Medicine, Shanghai Medical College, Fudan University, Shanghai, China.
Front Chem. 2023 May 5;11:1115247. doi: 10.3389/fchem.2023.1115247. eCollection 2023.
Hair testing is well established for the assessment of past drug exposure; however, more research is needed to understand drug incorporation mechanisms and drug entry pathways into hair. In this study, a micro-segmental LC-MS/MS method was used to analyze a 0.4 mm segment of hair after a single oral administration of zolpidem. Five single hairs were plucked at 1 day, 3 days, 7 days, and 28 days after administration from the vertex posterior of three subjects, and 5 single hairs were also plucked from the parietal, left temporal, and right temporal regions of the head at 28 days. Proximal S1 (0-0.4 mm) in hair plucked at 1 day had the highest level of zolpidem at 1.5-2.4 pg/mm; much lower concentrations (< 1 pg/mm) were detected at proximal S2-S8 (0.4-3.2 mm). The drug concentration decreased gradually in S1 for 7 days after drug intake and disappeared by 28 days, suggesting that the drug from the bloodstream initially combined with the hair follicle and then gradually moved to the hair tip as the hair grew. The zolpidem concentration-hair segment profiles exhibited a large peak (root side) and a small peak (tip side) for the four sampling times in all three subjects, indicating that drug incorporation in the hair bulb occurred mainly from the blood but probably also entered the hair through sweat and sebum. Zolpidem was also detected in all hairs from the vertex posterior in all three subjects but was not detected in 1 hair from the parietal region and 2 hairs from the left temporal region. The consistency in drug detection, drug concentration level, and peak position was better in hair from the vertex posterior than from the other three regions, indicating that the vertex posterior is a suitable sampling region for estimating drug intake.
毛发检测在评估过去的药物暴露情况方面已得到充分确立;然而,需要更多研究来了解药物掺入机制以及药物进入毛发的途径。在本研究中,采用微分段液相色谱 - 串联质谱法分析单次口服唑吡坦后0.4毫米长的毛发段。在给药后第1天、3天、7天和28天,从三名受试者头顶后部拔取5根单根毛发,在第28天还从头部的顶叶、左颞叶和右颞叶区域拔取5根单根毛发。给药后第1天拔取的毛发近端S1(0 - 0.4毫米)中唑吡坦水平最高,为1.5 - 2.4皮克/毫米;在近端S2 - S8(0.4 - 3.2毫米)处检测到的浓度要低得多(<1皮克/毫米)。药物摄入后7天内,S1中的药物浓度逐渐下降,到28天时消失,这表明血液中的药物最初与毛囊结合,然后随着毛发的生长逐渐向发梢移动。在所有三名受试者的四个采样时间点,唑吡坦浓度 - 毛发段图谱均呈现一个大峰(根部侧)和一个小峰(梢部侧),表明毛球中药物掺入主要来自血液,但也可能通过汗液和皮脂进入毛发。在所有三名受试者头顶后部的所有毛发中均检测到唑吡坦,但在顶叶区域的1根毛发和左颞叶区域的2根毛发中未检测到。头顶后部毛发在药物检测、药物浓度水平和峰位置方面的一致性比其他三个区域更好,表明头顶后部是估计药物摄入量的合适采样区域。