Gottås André, Arnestad Marianne, Halvorsen Per Steinar, Bachs Liliana C, Høiseth Gudrun
Division of Forensic Medicine, Norwegian Institute of Public Health, Pb 4404 Nydalen, 0403 Oslo, Norway ; Department of Pharmacology, Oslo University Hospital, Oslo, Norway.
Division of Forensic Medicine, Norwegian Institute of Public Health, Pb 4404 Nydalen, 0403 Oslo, Norway.
Forensic Toxicol. 2016;34(2):277-285. doi: 10.1007/s11419-016-0315-z. Epub 2016 Apr 7.
Vitreous humor (VH) is an alternative matrix for drug analysis in forensic toxicology. However, little is known about the distribution of xenobiotics, such as opioids, into VH in living organisms. The aim of this study was to simultaneously measure heroin and metabolite concentrations in blood and VH after injection of heroin in a living pig model. Six pigs were under non-opioid anesthesia during the surgical operation and experiment. Ocular microdialysis was used to acquire dialysate from VH, and a venous catheter was used for blood sampling. Twenty milligrams of heroin was injected intravenously with subsequent sampling of blood and dialysate for 6 h. The samples were analyzed by ultra-performance liquid chromatography-tandem mass spectrometry. Heroin was not detected in VH; 6-monoacetylmorphine (6-MAM) and morphine were first detected in VH after 60 min. The morphine concentration in VH thereafter increased throughout the experimental period. For 6-MAM, was reached after 230 min in VH. In blood, 6-MAM reached after 0.5 min, with a subsequent biphasic elimination phase. The blood and VH 6-MAM concentrations reached equilibrium after 2 h. In blood, morphine reached after 4.3 min, with a subsequent slower elimination than 6-MAM. The blood and VH morphine concentrations were in equilibrium about 6 h after injection of heroin. In conclusion, both 6-MAM and morphine showed slow transport into VH; detection of 6-MAM in VH did not necessarily reflect a recent intake of heroin. Because postmortem changes are expected to be small in VH, these experimental results could assist the interpretation of heroin deaths.
玻璃体液(VH)是法医毒理学中药物分析的一种替代基质。然而,关于诸如阿片类药物等外源性物质在生物体内向玻璃体液中的分布情况,人们了解甚少。本研究的目的是在活体猪模型中注射海洛因后,同时测量血液和玻璃体液中海洛因及其代谢物的浓度。六头猪在手术操作和实验过程中处于非阿片类麻醉状态。采用眼微透析技术从玻璃体液中获取透析液,并使用静脉导管进行采血。静脉注射20毫克海洛因,随后在6小时内采集血液和透析液样本。通过超高效液相色谱 - 串联质谱法对样本进行分析。在玻璃体液中未检测到海洛因;6 - 单乙酰吗啡(6 - MAM)和吗啡在60分钟后首次在玻璃体液中被检测到。此后,玻璃体液中的吗啡浓度在整个实验期间持续升高。对于6 - MAM,在玻璃体液中230分钟后达到峰值。在血液中,6 - MAM在0.5分钟后达到峰值,随后进入双相消除期。血液和玻璃体液中的6 - MAM浓度在2小时后达到平衡。在血液中,吗啡在4.3分钟后达到峰值,随后消除速度比6 - MAM慢。注射海洛因约6小时后,血液和玻璃体液中的吗啡浓度达到平衡。总之,6 - MAM和吗啡向玻璃体液中的转运均较慢;在玻璃体液中检测到6 - MAM不一定反映近期摄入过海洛因。由于预计玻璃体液中的死后变化较小,这些实验结果有助于对海洛因致死情况进行解读。