Soo V A, Bergert R J, Deutsch D G
Clin Chem. 1986 Feb;32(2):325-8.
We describe a quantitative screen for hypnotic-sedative drugs in which we use capillary gas chromatography with a nitrogen-phosphorus detector (GC/NPD) as the primary method and capillary gas chromatography-mass spectrometry (GC-MS) for confirmation. GC retention times of the acid-extracted underivatized drugs were stable (CVs less than 1%), and the detector response varied linearly over a 20-fold concentration range with a mean correlation coefficient for 11 drugs of 0.989. The limits of detection were satisfactory (0.5 mg/L in a 0.5-mL serum sample and 1-microL injection volume), as were precision (average CV 5.2% within day, 6.4% between day). The complementary use of capillary GC-MS not only unambiguously confirms presumptive peaks identified by GC, but also prevents reports of false positives and identifies compounds not included in the quantitative GC screen that may be listed in the GC-MS library.
我们描述了一种用于催眠镇静药物的定量筛选方法,其中我们使用带有氮磷检测器的毛细管气相色谱法(GC/NPD)作为主要方法,并使用毛细管气相色谱-质谱联用仪(GC-MS)进行确证。酸提取的未衍生化药物的GC保留时间稳定(变异系数小于1%),并且检测器响应在20倍浓度范围内呈线性变化,11种药物的平均相关系数为0.989。检测限令人满意(在0.5 mL血清样品和1 μL进样体积下为0.5 mg/L),精密度也令人满意(日内平均变异系数为5.2%,日间为6.4%)。毛细管GC-MS的互补使用不仅能明确确证由GC鉴定出的推定峰,还能防止假阳性报告,并鉴定出定量GC筛选中未包括但可能列于GC-MS库中的化合物。