Baptista Maria João, Monsanto Paula Verâncio, Pinho Marques Estela Gouveia, Bermejo Ana, Avila Sofia, Castanheira Alice Martelo, Margalho Cláudia, Barroso Mário, Vieira Duarte Nuno
Laboratory of Forensic Toxicology, National Institute of Legal Medicine, Largo da Sé Nova, 3000-213 Coimbra, Portugal.
Forensic Sci Int. 2002 Aug 14;128(1-2):66-78. doi: 10.1016/s0379-0738(02)00154-8.
A sensitive analytical method was developed for quantitative analysis of delta(9)-tetrahydrocannabinol (delta(9)-THC), 11-nor-delta(9)-tetrahydrocannabinol-carboxylic acid (delta(9)-THC-COOH), cannabinol (CBN) and cannabidiol (CBD) in human hair. The identification of delta(9)-THC-COOH in hair would document Cannabis use more effectively than the detection of parent drug (delta(9)-THC) which might have come from environmental exposure. Ketamine was added to hair samples as internal standard for CBN and CBD. Ketoprofen was added to hair samples as internal standard for the other compounds. Samples were hydrolyzed with beta-glucuronidase/arylsulfatase for 2h at 40 degrees C. After cooling, samples were extracted with a liquid-liquid extraction procedure (with chloroform/isopropyl alcohol, after alkalinization, and n-hexane/ethyl acetate, after acidification), which was developed in our laboratory. The extracts were analysed before and after derivatization with pentafluoropropionic anhydride (PFPA) and pentafluoropropanol (PFPOH) using a Hewlett Packard gas chromatographer/mass spectrometer detector, in electron impact mode (GC/MS-EI). Derivatized delta(9)-THC-COOH was also analysed using a Hewlett Packard gas chromatographer/mass spectrometer detector, in negative ion chemical ionization mode (GC/MS-NCI) using methane as the reagent gas. Responses were linear ranging from 0.10 to 5.00 ng/mg hair for delta(9)-THC and CBN, 0.10-10.00 ng/mg hair for CBD, 0.01-5.00 ng/mg for delta(9)-THC-COOH (r(2)>0.99). The intra-assay precisions ranged from <0.01 to 12.40%. Extraction recoveries ranged from 80.9 to 104.0% for delta(9)-THC, 85.9-100.0% for delta(9)-THC-COOH, 76.7-95.8% for CBN and 71.0-94.0% for CBD. The analytical method was applied to 87 human hair samples, obtained from individuals who testified in court of having committed drug related crimes. Quantification of delta(9)-THC-COOH using GC/MS-NCI was found to be more convenient than GC/MS-EI. The latter may give rise to false negatives due to the detection limit.
开发了一种灵敏的分析方法,用于定量分析人发中的δ⁹-四氢大麻酚(δ⁹-THC)、11-去甲-δ⁹-四氢大麻酚羧酸(δ⁹-THC-COOH)、大麻酚(CBN)和大麻二酚(CBD)。头发中δ⁹-THC-COOH的鉴定比母体药物(δ⁹-THC)的检测更能有效地证明大麻的使用情况,因为母体药物可能来自环境暴露。将氯胺酮作为CBN和CBD的内标添加到头发样本中。将酮洛芬作为其他化合物的内标添加到头发样本中。样本在40℃下用β-葡萄糖醛酸酶/芳基硫酸酯酶水解2小时。冷却后,样本采用液-液萃取程序进行萃取(碱化后用氯仿/异丙醇,酸化后用正己烷/乙酸乙酯),该程序是在我们实验室开发的。使用惠普气相色谱仪/质谱检测器,在电子轰击模式(GC/MS-EI)下,对用五氟丙酸酐(PFPA)和五氟丙醇(PFPOH)衍生化前后的提取物进行分析。衍生化的δ⁹-THC-COOH也使用惠普气相色谱仪/质谱检测器,在负离子化学电离模式(GC/MS-NCI)下,以甲烷作为反应气进行分析。对于δ⁹-THC和CBN,响应在0.10至5.00 ng/mg头发范围内呈线性,对于CBD为0.10 - 10.00 ng/mg头发,对于δ⁹-THC-COOH为0.01 - 5.00 ng/mg(r²>0.99)。批内精密度范围为<0.01%至12.40%。δ⁹-THC的萃取回收率范围为80.9%至104.0%,δ⁹-THC-COOH为85.9%至100.0%,CBN为76.7%至95.8%,CBD为71.0%至94.0%。该分析方法应用于87份人发样本,这些样本来自在法庭上作证承认犯有毒品相关罪行的个人。发现使用GC/MS-NCI对δ⁹-THC-COOH进行定量分析比GC/MS-EI更方便。由于检测限的原因,后者可能会产生假阴性结果。