Hull Mindy J, Griggs David, Knoepp Stewart M, Smogorzewska Agata, Nixon Andrea, Flood James G
Clinical Chemistry and Toxicology, Department of Pathology and Laboratory Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
Am J Forensic Med Pathol. 2006 Dec;27(4):359-62. doi: 10.1097/01.paf.0000233534.59330.c2.
This is a report of postmortem false-positive reactivity using an enzyme-multiplied urine phencyclidine (PCP) immunoassay (EMIT II+) due to a single-agent fatal tramadol overdose. An autopsy of a 42-year-old male who died alone at home revealed no identifiable lethal anatomic abnormalities, thus leading to toxicologic analysis. Femoral blood was obtained for drug testing by high-performance liquid chromatography (HPLC) and showed a tramadol level of 14.0 mg/L, 2 orders of magnitude greater than the therapeutic range (0.1 to 0.3 mg/L). Urine was also obtained and EMIT II+ immunoassay revealed positivity for PCP at 88 mAU/min. However, confirmatory testing by HPLC failed to identify PCP in either the urine or serum. To verify the suspicion that this was a false-positive PCP result, stock solutions of tramadol and its major metabolite (O-desmethyltramadol) at concentrations of 100 mg/L in 10% methanol/H2O were compared with a blank solution (10% methanol/H2O) for EMIT II+ PCP reactivity and demonstrated reactivities of 44 mAU/min and 27 mAU/min, respectively. While these individual results were below the cutoff reactivity for a positive EMIT II+ PCP result (ca. 85 mAU/min), they were much more reactive than the blank calibrator (set at 0 mAU/min). Therefore, we conclude that the immunoreactivity of tramadol and its metabolites in aggregate is responsible for the PCP immunoassay interference and false-positive result.
这是一份关于因单药致命性曲马多过量导致酶放大尿液苯环利定(PCP)免疫测定(EMIT II +)出现尸检假阳性反应的报告。一名42岁男性在家中独自死亡,尸检未发现可识别的致命解剖学异常,因此进行了毒理学分析。采集股静脉血通过高效液相色谱法(HPLC)进行药物检测,结果显示曲马多水平为14.0 mg/L,比治疗范围(0.1至0.3 mg/L)高2个数量级。同时也采集了尿液,EMIT II +免疫测定显示PCP阳性,反应率为88 mAU/min。然而,HPLC确证检测未能在尿液或血清中鉴定出PCP。为了验证这是PCP假阳性结果的怀疑,将浓度为100 mg/L的曲马多及其主要代谢物(O - 去甲基曲马多)的储备液溶于10%甲醇/水与空白溶液(10%甲醇/水)进行EMIT II + PCP反应性比较,结果显示反应率分别为44 mAU/min和27 mAU/min。虽然这些单独结果低于EMIT II + PCP阳性结果的临界反应率(约85 mAU/min),但它们比空白校准物(设定为0 mAU/min)的反应性高得多。因此,我们得出结论,曲马多及其代谢物的总体免疫反应性是导致PCP免疫测定干扰和假阳性结果的原因。