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Relationship between oral fluid and blood concentrations of drugs of abuse in drivers suspected of driving under the influence of drugs

机译:疑似在药物影响下驾驶的驾驶员口服液与血药浓度之间的关系

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摘要

In recent years, the interest in the use of oral fluid as a biological matrix has increased significantly, particularly for detecting driving under the influence of drugs (DUID). In this study, the relationship between the oral fluid and the blood concentrations of drugs of abuse in drivers suspected of DUID is discussed. Blood and oral fluid samples were collected from drivers Suspected of DUID or stopped during random controls by the police in Belgium, Germany, Finland, and Norway for the ROSITA-2 project. The blood samples were analyzed by gas chromatography-mass spectrometry (GC-MS) or liquid chromatography-mass spectrometry (LC-MS), sometimes preceded by immunoassay screening of blood or urine samples. The oral fluid samples were analyzed by GC-MS or LC-MS(/MS). Scatter plots and trend lines of the blood and oral fluid concentrations and the median, mean, range, and SD of the oral fluid to blood (OF:B) ratios were calculated for amphetamines, benzodiazepines, cocaine, opiates, and Delta(9)-2 tetrahydrocannabinol. The ratios found in this study were comparable with those that were published previously, but the range was wider. The ORB ratios of basic drugs such as amphetamines, cocaine, and opiates were > 1 [amphetamine: median (range) 13 (0.5-182), methylenedioxyamphetamine: 4 (1-15), methylenedioxymethamphetamine: 6 (0.9-88), methamphetamine: 5 (2-23), cocaine: 22 (4-119), benzoylecgonine: 1 (0.2-11), morphine: 2 (0.8-6), and codeine: 10 (0.8-39)]. The ratios for benzodiazepines were very low, as could be expected as they are highly protein bound and weakly acidic, leading to low oral fluid concentrations [diazepam: 0.02 (0.01-0.15), nordiazepam: 0.04 (0.01-0.23), oxazepam: 0.05 (0.03-0.14), and temazepam: 0.1 (0.06-0.54)]. For tetrahydrocannabinol, an OF:B ratio of 15 was found (range 0.01-569). In this study, the time of last administration, the dose, and the route of administration were unknown. Nevertheless, the data reflect the variability of the OF:B ratios in drivers thought to be under the influence of drugs. The wide range of the ratios, however, does not allow reliable calculation of the blood concentrations from oral fluid concentrations.
机译:近年来,使用口服液作为生物基质的兴趣显着增加,特别是对于检测药物(DUID)影响下的驾驶。在这项研究中,讨论了怀疑是DUID的驾驶员的口服液与滥用药物的血药浓度之间的关系。比利时,德国,芬兰和挪威的警察针对ROSITA-2项目从怀疑是DUID的驾驶员那里收集了血液和口腔液体样本,或在进行随机控制期间将其停止。通过气相色谱-质谱法(GC-MS)或液相色谱-质谱法(LC-MS)分析血液样本,有时还需要对血液或尿液样本进行免疫分析筛选。通过GC-MS或LC-MS(/ MS)分析口腔液样品。计算了苯丙胺,苯二氮卓,可卡因,鸦片和Delta(9)的血液和口腔液浓度的散点图和趋势线以及口腔液与血液的中值,平均值,范围和SD(OF:B)比(9) -2四氢大麻酚。这项研究中发现的比率与先前发表的比率相当,但范围更广。基本药物(例如苯丙胺,可卡因和鸦片)的ORB比率> 1 [苯丙胺:中位数(范围)13(0.5-182),亚甲二氧基苯丙胺:4(1-15),亚甲二氧基甲基苯丙胺:6(0.9-88),甲基苯丙胺:5(2-23),可卡因:22(4-119),苯甲酰芽子碱:1(0.2-11),吗啡:2(0.8-6)和可待因:10(0.8-39)]。苯二氮卓类药物的比例非常低,这是可以预料的,因为它们具有高蛋白结合力和弱酸性,导致低的口服液浓度[地西p:0.02(0.01-0.15),去甲西p:0.04(0.01-0.23),奥沙西m:0.05 (0.03-0.14)和替马西m:0.1(0.06-0.54)]。对于四氢大麻酚,发现OF:B比率为15(范围为0.01-569)。在这项研究中,最后一次给药的时间,剂量和给药途径尚不清楚。然而,这些数据反映出认为受药物影响的驾驶员中OF:B比率的变异性。但是,比率的范围很宽,无法从口服液浓度可靠地计算出血液浓度。

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