Kim Eun-mi, Lee Ju-seon, Choi Sang-kil, Lim Mi-ae, Chung Hee-sun
Narcotics Analysis Section, National Institute of Scientific Investigation, 331-1 Shinwol 7-dong, Yangcheon-gu, Seoul 158-707, Republic of Korea.
Forensic Sci Int. 2008 Jan 30;174(2-3):197-202. doi: 10.1016/j.forsciint.2007.04.217. Epub 2007 Jun 5.
Ketamine (KT) is widely abused for hallucination and also misused as a "date-rape" drug in recent years. An analytical method using positive ion chemical ionization-gas chromatography-mass spectrometry (PCI-GC-MS) with an automatic solid-phase extraction (SPE) apparatus was studied for the determination of KT and its major metabolite, norketamine (NK), in urine. Six ketamine suspected urine samples were provided by the police. For the research of KT metabolism, KT was administered to SD rats by i.p. at a single dose of 5, 10 and 20mg/kg, respectively, and urine samples were collected 24, 48 and 72 h after administration. For the detection of KT and NK, urine samples were extracted on an automatic SPE apparatus (RapidTrace, Zymark) with mixed mode type cartridge, Drug-Clean (200 mg, Alltech). The identification of KT and NK was by PCI-GC-MS. m/z238 (M+1), 220 for KT, m/z 224 (M+1), 207 for NK and m/z307 (M+1) for Cocaine-D(3) as internal standard were extracted from the full-scan mass spectrum and the underlined ions were used for quantitation. Extracted calibration curves were linear from 50 to 1000 ng/mL for KT and NK with correlation coefficients exceeding 0.99. The limit of detection (LOD) was 25 ng/mL for KT and NK. The limit of quantitation (LOQ) was 50 ng/mL for KT and NK. The recoveries of KT and NK at three different concentrations (86, 430 and 860 ng/mL) were 53.1 to 79.7% and 45.7 to 83.0%, respectively. The intra- and inter-day run precisions (CV) for KT and NK were less than 15.0%, and the accuracies (bias) for KT and NK were also less than 15% at the three different concentration levels (86, 430 and 860 ng/mL). The analytical method was also applied to real six KT suspected urine specimens and KT administered rat urines, and the concentrations of KT and NK were determined. Dehydronorketamine (DHNK) was also confirmed in these urine samples, however the concentration of DHNK was not calculated. SPE is simple, and needs less organic solvent than liquid-liquid extraction (LLE), and PCI-GC-MS can offer both qualitative and quantitative information for urinalysis of KT in forensic analysis.
氯胺酮(KT)近年来被广泛用于致幻,还被滥用作“约会强奸”药物。研究了一种使用带自动固相萃取(SPE)装置的正离子化学电离-气相色谱-质谱联用(PCI-GC-MS)分析法,用于测定尿液中的KT及其主要代谢物去甲氯胺酮(NK)。警方提供了6份疑似氯胺酮的尿液样本。为研究KT的代谢情况,分别以5、10和20mg/kg的单剂量腹腔注射给SD大鼠施用KT,并在给药后24、48和72小时收集尿液样本。为检测KT和NK,尿液样本在自动SPE装置(RapidTrace,Zymark)上,使用混合型柱Drug-Clean(200mg,Alltech)进行萃取。通过PCI-GC-MS对KT和NK进行鉴定。从全扫描质谱图中提取m/z238(M+1)、220用于KT,m/z 224(M+1)、207用于NK以及m/z307(M+1)用于可卡因-D(3)作为内标,下划线标注的离子用于定量分析。KT和NK的萃取校准曲线在50至1000 ng/mL范围内呈线性,相关系数超过0.99。KT和NK的检测限(LOD)均为25 ng/mL。定量限(LOQ)为50 ng/mL。KT和NK在三种不同浓度(86、430和860 ng/mL)下的回收率分别为53.1%至79.7%和45.7%至83.0%。KT和NK的日内和日间精密度(CV)均小于15.0%,在三种不同浓度水平(86、430和860 ng/mL)下,KT和NK的准确度(偏差)也均小于15%。该分析方法还应用于实际的6份疑似氯胺酮尿液标本以及给大鼠施用氯胺酮后的尿液样本,测定了KT和NK的浓度。在这些尿液样本中也确认了脱氢去甲氯胺酮(DHNK),但未计算其浓度。SPE操作简单,与液液萃取(LLE)相比所需有机溶剂更少,并且PCI-GC-MS可为法医分析中尿液中KT的分析提供定性和定量信息。