Schwilke Eugene W, Barnes Allan J, Kacinko Sherri L, Cone Edward J, Moolchan Eric T, Huestis Marilyn A
Chemistry and Drug Metabolism, Intramural Research Program, National Institute on Drug Abuse, NIH, Baltimore, MD 21224, USA.
Clin Chem. 2006 Aug;52(8):1539-45. doi: 10.1373/clinchem.2006.067983. Epub 2006 Jun 1.
Characterization of opioid excretion in sweat is important for accurate interpretation of sweat tests in drug treatment, criminal justice, and workplace drug testing programs.
Participants (n=20) received placebo, 3 low (60 mg/70 kg) or 3 high (120 mg/70 kg) codeine sulfate doses (used as a model for opioid excretion) within 1 week. Codeine and metabolites in sweat were collected with PharmChek Sweat Patches; hourly patches were applied for 1 to 15 h (n=775) and weekly patches for 7 days (n=118). Patches were analyzed by solid-phase extraction and gas chromatography-mass spectrometry for codeine, norcodeine, morphine, normorphine, and 6-acetylmorphine. Limits of quantification were 2.5 ng/patch (codeine and morphine) and 5 ng/patch (other analytes).
Codeine was the only analyte identified in 12.6% of hourly patches and 83.3% of weekly sweat patches worn during dosing. Weekly patch concentrations (SD) were 38.6 (59.9) ng/patch [median (range), 15.9 (0-225.1) ng/patch] for low and 34.1 (32.7) ng/patch [24.0 (0-96.2) ng/patch] for high codeine doses. Codeine detected 1 week after dosing was 4.6 (5.3) ng/patch [median (range), 4.0 (0-17.1) ng/patch; n=11] after low and 7.7 (7.1) ng/patch [6.9 (0-20.5) ng/patch; n=10] after high doses. In total, 2.6% of hourly, 38.5% of low-dose, and 45.5% of high-dose weekly patches contained codeine at the proposed Substance Abuse and Mental Health Services Administration cutoff.
Codeine was the only analyte detected, at highly variable concentrations, up to 2 weeks after dosing. These results are consistent, considering the complex processes of codeine deposition in sweat. Sweat testing is a useful alternative technique for qualitative monitoring of opioid use.
在药物治疗、刑事司法和工作场所药物检测项目中,准确解读汗液检测结果需要了解阿片类药物在汗液中的排泄特征。
参与者(n = 20)在1周内接受安慰剂、3种低剂量(60mg/70kg)或3种高剂量(120mg/70kg)硫酸可待因(用作阿片类药物排泄模型)。使用PharmChek汗液贴片收集汗液中的可待因及其代谢物;每小时贴片应用1至15小时(n = 775),每周贴片应用7天(n = 118)。通过固相萃取和气相色谱 - 质谱法分析贴片,检测可待因、去甲可待因、吗啡、去甲吗啡和6 - 乙酰吗啡。定量限为2.5ng/贴片(可待因和吗啡)和5ng/贴片(其他分析物)。
在给药期间佩戴的每小时贴片中,12.6%检测到可待因是唯一的分析物,每周汗液贴片中这一比例为83.3%。低剂量可待因每周贴片浓度(标准差)为38.6(59.9)ng/贴片[中位数(范围),15.9(0 - 225.1)ng/贴片],高剂量为34.1(32.7)ng/贴片[24.0(0 - 96.2)ng/贴片]。给药1周后检测到的可待因,低剂量组为4.6(5.3)ng/贴片[中位数(范围),4.0(0 - 17.1)ng/贴片;n = 11],高剂量组为7.7(7.1)ng/贴片[6.9(0 - 20.5)ng/贴片;n = 10]。总体而言,每小时贴片中2.6%、低剂量每周贴片中38.5%、高剂量每周贴片中45.5%的可待因含量达到美国药物滥用和精神健康服务管理局提议的临界值。
可待因是给药后长达2周内检测到的唯一分析物,其浓度变化很大。考虑到可待因在汗液中沉积的复杂过程,这些结果是一致的。汗液检测是定性监测阿片类药物使用的一种有用的替代技术。