Gunnar Teemu, Mykkänen Sirpa, Ariniemi Kari, Lillsunde Pirjo
Laboratory of Substance Abuse, National Public Health Institute, Mannerheimintie 166, Helsinki 00300, Finland.
J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Jul 5;806(2):205-19. doi: 10.1016/j.jchromb.2004.04.005.
A comprehensively validated procedure is presented for simultaneous semiquantitative/quantitative screening of 51 drugs of abuse or drugs potentially hazardous for traffic safety in serum, plasma or whole blood. Benzodiazepines (12), cannabinoids (3), opioids (8), cocaine, antidepressants (13), antipsychotics (5) and antiepileptics (2) as well as zolpidem, zaleplon, zopiclone, meprobamate, carisoprodol, tizanidine and orphenadrine and internal standard flurazepam, were isolated by high-yield liquid-liquid extraction (LLE). The dried extracts were derivatized by two-step silylation and analyzed by the combination of two different gas chromatographic (GC) separations with both electron capture detection (ECD) and mass spectrometry (MS) operating in a selected ion-monitoring (SIM) mode. Quantitative or semiquantitative results were obtained for each substance based on four-point calibration. In the validation tests, accuracy, reproducibility, linearity, limit of detection (LOD) and limit of quantitation (LOQ), selectivity, as well as extraction efficiency and stability of standard stock solutions were tested, and derivatization was optimized in detail. Intra- and inter-day precisions were within 2.5-21.8 and 6.0-22.5%, and square of correlation coefficients of linearity ranged from 0.9896 to 0.9999. The limit of quantitation (LOQ) varied from 2 to 2000 ng/ml due to a variety of the relevant concentrations of the analyzed substances in blood. The method is feasible for highly sensitive, reliable and possibly routinely performed clinical and forensic toxicological analyses.
本文介绍了一种经过全面验证的方法,用于同时对血清、血浆或全血中51种滥用药物或可能危害交通安全的药物进行半定量/定量筛查。通过高效液液萃取(LLE)分离出苯二氮䓬类药物(12种)、大麻素类药物(3种)、阿片类药物(8种)、可卡因、抗抑郁药(13种)、抗精神病药(5种)、抗癫痫药(2种)以及唑吡坦、扎来普隆、佐匹克隆、甲丙氨酯、卡立普多、替扎尼定和奥芬那君,同时还分离出内标氟西泮。干燥后的提取物通过两步硅烷化进行衍生化处理,并结合两种不同的气相色谱(GC)分离方法进行分析,同时采用电子捕获检测(ECD)和在选择离子监测(SIM)模式下运行的质谱(MS)。基于四点校准获得每种物质的定量或半定量结果。在验证测试中,对准确性、重现性、线性、检测限(LOD)和定量限(LOQ)、选择性以及标准储备溶液的萃取效率和稳定性进行了测试,并对衍生化进行了详细优化。日内和日间精密度分别在2.5 - 21.8%和6.0 - 22.5%范围内,线性相关系数的平方范围为0.9896至0.9999。由于血液中分析物质的相关浓度各不相同,定量限(LOQ)在2至2000 ng/ml之间变化。该方法对于高灵敏度、可靠且可能常规进行的临床和法医毒理学分析是可行的。