Kuwayama Kenji, Miyaguchi Hajime, Yamamuro Tadashi, Tsujikawa Kenji, Kanamori Tatsuyuki, Iwata Yuko T, Inoue Hiroyuki
National Research Institute of Police Science, 6-3-1 Kashiwanoha, Kashiwa, Chiba, 277-0882, Japan.
Rapid Commun Mass Spectrom. 2015 Nov 30;29(22):2158-66. doi: 10.1002/rcm.7363.
A primary metabolite of Δ(9) -tetrahydrocannabinol, 11-nor-9-carboxytetrahydrocannabinol (THC-COOH), serves as an effective indicator for cannabis intake. According to the recommendations of the Society of Hair Testing, at least 0.2 pg/mg of THC-COOH (cut-off level) must be present in a hair sample to constitute a positive result in a drug test. Typically, hair is digested with an alkaline solution and is subjected to gas chromatography/tandem mass spectrometry (GC/MS/MS) with negative ion chemical ionization (NICI).
It is difficult to quantify THC-COOH at the cut-off level using liquid chromatography/tandem mass spectrometry (LC/MS/MS) without acquisition of second-generation product ions in triple quadrupole-ion trap mass spectrometers, because large amounts of matrix components in the low-mass range produced by digestion interfere with the THC-COOH peak. Using the typical pretreatment method (alkaline dissolution) and micro-pulverized extraction (MPE) with a stainless bullet, we compared the quantification of THC-COOH using GC/MS/MS and LC/MS/MS.
MPE reduced the amount of matrix components in the low-mass range and enabled the quantification of THC-COOH at 0.2 pg/mg using a conventional triple quadrupole liquid chromatograph coupled to a mass spectrometer. On the other hand, the MPE pretreatment was unsuitable for GC/MS/MS, probably due to matrix components in the high-mass range. The proper combination of pretreatments and instrumental analyses was shown to be important for detecting trace amounts of THC-COOH in hair.
In MPE, samples can be prepared rapidly, and LC/MS/MS is readily available, unlike GC/MS/MS with NICI. The combination of MPE and LC/MS/MS might therefore be used in the initial screening for THC-COOH in hair prior to confirmatory analysis using GC/MS/MS with NICI.
Δ(9)-四氢大麻酚的主要代谢产物11-去甲-9-羧基四氢大麻酚(THC-COOH)是大麻摄入的有效指标。根据毛发检测协会的建议,毛发样本中必须至少含有0.2 pg/mg的THC-COOH(截断水平),药物检测结果才呈阳性。通常,毛发用碱性溶液消化,然后采用负离子化学电离(NICI)的气相色谱/串联质谱法(GC/MS/MS)进行检测。
在三重四极杆-离子阱质谱仪中,如果不采集第二代产物离子,使用液相色谱/串联质谱法(LC/MS/MS)很难对截断水平的THC-COOH进行定量,因为消化产生的低质量范围内大量的基质成分会干扰THC-COOH峰。我们采用典型的预处理方法(碱性溶解)和使用不锈钢子弹进行的微粉碎萃取(MPE),比较了使用GC/MS/MS和LC/MS/MS对THC-COOH的定量。
MPE减少了低质量范围内的基质成分数量,并能够使用常规的三重四极杆液相色谱仪与质谱仪联用,对0.2 pg/mg的THC-COOH进行定量。另一方面,MPE预处理不适用于GC/MS/MS,可能是由于高质量范围内的基质成分。结果表明,预处理和仪器分析的适当组合对于检测毛发中痕量的THC-COOH很重要。
在MPE中,可以快速制备样品,而且与带有NICI的GC/MS/MS不同,LC/MS/MS很容易获得。因此,MPE和LC/MS/MS的组合可用于在使用带有NICI的GC/MS/MS进行确证分析之前,对毛发中的THC-COOH进行初步筛查。