Wu Fang, Scroggin Triniti L, Metz Torri D, McMillin Gwendolyn A
Department of Pathology, University of Utah, 15 North Medical Drive East, Salt Lake City, UT 84132, USA.
ARUP Laboratories, 500 Chipeta Way, Salt Lake City, UT 84108, USA.
J Anal Toxicol. 2018 Jan 1;42(1):42-48. doi: 10.1093/jat/bkx078.
In utero exposure to marijuana may cause various short- and long-term health problems, such as stillbirth, low birth weight and decreased cognitive function. Detection of in utero marijuana exposure with a relatively new specimen type, umbilical cord tissue, can be used to plan treatment and guide social management. In this study, a liquid chromatography-tandem mass spectrometry (LC-MS-MS) assay was developed for the simultaneous identification of four cannabinoids in umbilical cord tissue, including ∆9-tetrahydrocannabinol (THC), 11-nor-9-carboxy-∆9--THC (THC-COOH), 11-hydroxy-∆9-THC (11-OH-THC) and cannabinol (CBN). Within- and between-run imprecision, accuracy, linearity, sensitivity, carryover, recovery, matrix effects and specificity were evaluated using drug-free umbilical cord tissue spiked with non-deuterated and deuterated standards. Calibration curves were reproducible and linear (r > 0.995) for all four analytes in the range of 0.2 ng/g lower limit of quantitation (LLOQ) and 30 ng/g upper limit of quantitation (ULOQ). Total imprecisions (% coefficient of variation) were 7.8% (THC), 13.3% (THC-COOH), 11.8% (11-OH-THC) and 10.6% (CBN) at low QC (n = 15, 0.25 ng/g), and were 7.2% (THC), 10.0% (THC-COOH), 9.5% (11-OH-THC) and 5.8% (CBN) at high QC (n = 15, 4 ng/g), respectively. No interfering substances were identified, and no carryover was observed. The average accuracies (N = 25) were 94-95%. The average recoveries observed for THC, THC-COOH, 11-OH-THC and CBN were 74, 82, 58 and 86%, respectively. By analyzing authentic clinical specimens that had been previously tested for cannabinoids by enzyme-linked immunoassay, positive and negative result agreements were 100 and 53.8%. In summary, the presented method can be used for the assessment of in utero exposure to four common cannabinoids.
子宫内暴露于大麻可能会导致各种短期和长期健康问题,如死产、低出生体重和认知功能下降。使用一种相对较新的样本类型——脐带组织来检测子宫内大麻暴露情况,可用于规划治疗和指导社会管理。在本研究中,开发了一种液相色谱-串联质谱(LC-MS-MS)测定法,用于同时鉴定脐带组织中的四种大麻素,包括Δ9-四氢大麻酚(THC)、11-去甲-9-羧基-Δ9-THC(THC-COOH)、11-羟基-Δ9-THC(11-OH-THC)和大麻酚(CBN)。使用添加了非氘代和氘代标准品的无药物脐带组织评估批内和批间精密度、准确度、线性、灵敏度、残留、回收率、基质效应和特异性。在0.2 ng/g定量下限(LLOQ)至30 ng/g定量上限(ULOQ)范围内,所有四种分析物的校准曲线均可重现且呈线性(r>0.995)。低质量控制(n = 15,0.25 ng/g)时,总精密度(变异系数%)分别为7.8%(THC)、13.3%(THC-COOH)、11.8%(11-OH-THC)和10.6%(CBN);高质量控制(n = 15,4 ng/g)时,分别为7.2%(THC)、10.0%(THC-COOH)、9.5%(11-OH-THC)和5.8%(CBN)。未鉴定出干扰物质,也未观察到残留。平均准确度(N = 25)为94-95%。THC、THC-COOH、11-OH-THC和CBN的平均回收率分别为74%、82%、58%和86%。通过分析先前已用酶联免疫测定法检测过大麻素的真实临床标本,阳性和阴性结果一致性分别为100%和53.8%。总之,所提出的方法可用于评估子宫内对四种常见大麻素的暴露情况。