Scurlock Rodger D, Ohlson Greg B, Worthen David K
AZ DPS Central Regional Crime Lab, Toxicology Unit, 2102 W. Encanto Blvd., Phoenix, Arizona 85005, USA.
J Anal Toxicol. 2006 May;30(4):262-6. doi: 10.1093/jat/30.4.262.
A method is described for the simultaneous analysis of Delta(9)-tetrahydrocannabinol (THC) and its carboxylic acid metabolite, 11-nor-9-carboxy-Delta(9)-tetrahydrocannabinol (THCA) as their trimethylsiyl derivatives using 2-dimensional chromatography and electron ionization-mass spectrometric detection. The addition of a Deans switch to a standard GC oven allows the use of two chromatographic columns of differing stationary phase to greatly reduce matrix interference. The analytes are extracted from 1 mL of whole blood by first precipitating the blood proteins with the addition of acetonitrile followed by solid-phase extraction. The limit of quantitation for both THC and THCA was determined to be 1.0 ng/mL. The between-run precision at 1.0 ng/mL (N = 30) was 7.7% and 7.4% for THC and THCA, respectively. The method is linear from 1 to 100 ng/mL.
描述了一种使用二维色谱法和电子电离质谱检测法同时分析Δ⁹-四氢大麻酚(THC)及其羧酸代谢物11-去甲-9-羧基-Δ⁹-四氢大麻酚(THCA)的三甲基硅烷基衍生物的方法。在标准气相色谱炉中添加迪恩斯切换装置,可使用两种不同固定相的色谱柱,大大减少基质干扰。通过先加入乙腈沉淀血液蛋白质,然后进行固相萃取,从1 mL全血中提取分析物。THC和THCA的定量限均确定为1.0 ng/mL。THC和THCA在1.0 ng/mL(N = 30)时的批间精密度分别为7.7%和7.4%。该方法在1至100 ng/mL范围内呈线性。