Laboratório de Análise de Compostos Orgânicos Poluentes, Departamento de Química, Universidade Federal de Sergipe, 49100-000, Av. Marechal Rondon, s/n. Jardim Rosa Elze, São Cristóvão, SE, Brazil.
Anal Chim Acta. 2010 Jun 18;670(1-2):63-71. doi: 10.1016/j.aca.2010.04.023. Epub 2010 Apr 18.
The development of an analytical method for the determination of Delta(9)-tetrahydrocannabinol (THC), cannabidiol (CBD) and cannabinol (CBN) in samples of human hair is described. Samples were subjected to a procedure based on the combination of headspace solid-phase microextraction (HS-SPME) with gas chromatography linked with mass spectrometry operating in tandem mode (GC-MS/MS). A 10 mg aliquot of sample was firstly decontaminated using petroleum ether, deionized water and dichloromethane (2 mL of each solvent), for 10 min under sonication, and then digested in alkaline solution (1 mol L(-1) NaOH). The method variables evaluated were pH, mass of hair, fiber type, extraction temperature, desorption time, ionic strength, pre-equilibrium time and extraction time. Parameters concerning operation of the tandem mode MS/MS were also assessed and optimized. Validation of the method demonstrated excellent linearity in the range 0.1-8.0 ng mg(-1), with regression coefficients better than 0.994. Precision was determined using two different concentrations (upper and lower limits of the linear range), and RSD values were between 6.6 and 16.4%. Absolute recoveries (measured in triplicate) were in the range 1.1-8.7%, and limits of detection and quantification were 0.007-0.031 ng mg(-1) and 0.012-0.062 ng mg(-1), respectively. The LOQ for THC (0.062 ng mg(-1)) was below the cut-off value (LOQ < or = 0.1 ng mg(-1)) established by the Society of Hair Testing (SOHT), the Society of Toxicological and Forensic Chemistry (STFCh) and the Société Française de Toxicologie Analytique (SFTA). The optimized SPME method was applied in analysis of hair samples from Cannabis drug users, showing that CBN and CBD were present in all samples analyzed.
本文描述了一种用于测定人发样品中 Delta(9)-四氢大麻酚(THC)、大麻二酚(CBD)和大麻酚(CBN)的分析方法的开发。样品首先经过基于顶空固相微萃取(HS-SPME)与气相色谱-串联质谱联用(GC-MS/MS)相结合的程序处理。取 10mg 样品,用石油醚、去离子水和二氯甲烷(每种溶剂 2mL)超声处理 10min 进行去污,然后在碱性溶液(1mol/LNaOH)中消化。评估的方法变量包括 pH 值、头发质量、纤维类型、提取温度、解吸时间、离子强度、预平衡时间和提取时间。还评估和优化了串联模式 MS/MS 操作的参数。方法验证表明,在 0.1-8.0ngmg(-1)范围内具有良好的线性,相关系数均大于 0.994。使用两个不同浓度(线性范围的上限和下限)确定精密度,RSD 值在 6.6-16.4%之间。绝对回收率(重复测定三次)在 1.1-8.7%范围内,检测限和定量限分别为 0.007-0.031ngmg(-1)和 0.012-0.062ngmg(-1)。THC 的 LOQ(0.062ngmg(-1))低于头发检测协会(SOHT)、毒理学和法医化学学会(STFCh)和法国分析毒理学学会(SFTA)规定的 0.1ngmg(-1)的 LOQ。优化后的 SPME 方法应用于大麻药物使用者头发样品的分析,结果表明所有分析样品中均存在 CBN 和 CBD。