McLaughlin Poppy, Maskell Peter D, Pounder Derrick, Osselton David
Department of Archaeology, Anthropology & Forensic Science, Bournemouth University, Fern Barrow, Poole, Dorset, BH12 5BB, UK.
Abertay University, Bell Street, Dundee, DD1 1HG, UK.
Forensic Sci Int. 2019 Jan;294:211-215. doi: 10.1016/j.forsciint.2018.11.018. Epub 2018 Nov 26.
This paper describes the performance of four Randox drug arrays, designed for whole blood, for the near-body analysis of drugs in a range of post-mortem body specimens.
Liver, psoas muscle, femoral blood, vitreous humor and urine from 261 post-mortem cases were screened in the mortuary and results were obtained within the time taken to complete a post-mortem. Specimens were screened for the presence of amfetamine, barbiturates, benzodiazepines, benzoylecgonine, buprenorphine, cannabinoids, dextropropoxyphene, fentanyl, ketamine, lysergide, methadone, metamfetamine, methaqualone, 3,4-methylenedioxymetamfetamine, opioids, paracetamol, phencyclidine, salicylate, salicylic acid, zaleplon, zopiclone and zolpidem using the DOA I, DOA I+, DOA II and Custom arrays.
Liver and muscle specimens were obtained from each of the 261 post-mortem cases; femoral blood, vitreous humor and urine were available in 98%, 92% and 72% of the cases, respectively. As such, the equivalent of 12,978 individual drug-specific, or drug-group, immunoassay tests were undertaken. Overall >98% of the 12,978 screening tests undertaken agreed with laboratory confirmatory tests performed on femoral blood.
There is growing interest in the development of non-invasive procedures for determining the cause of death using MRI and CT scanning however these procedures are, in most cases, unable to determine whether death may have been associated with drug use. The Randox arrays can provide qualitative and semi-quantitative results in a mortuary environment enabling pathologists to decide whether to remove specimens from the body and submit them for laboratory analysis. Analysis can be undertaken on a range of autopsy specimens which is particularly useful when conventional specimens such as blood are unavailable.
本文描述了四种用于全血检测的兰多克斯药物检测阵列在一系列尸体标本中对药物进行近体分析的性能。
对261例尸检病例的肝脏、腰大肌、股静脉血、玻璃体液和尿液在停尸房进行筛查,并在完成尸检所需的时间内获得结果。使用DOA I、DOA I +、DOA II和定制阵列对标本进行安非他明、巴比妥类药物、苯二氮卓类药物、苯甲酰爱康宁、丁丙诺啡、大麻素、右丙氧芬、芬太尼、氯胺酮、麦角酰二乙胺、美沙酮、甲基苯丙胺、甲喹酮、3,4 - 亚甲基二氧基甲基苯丙胺、阿片类药物、对乙酰氨基酚、苯环己哌啶、水杨酸盐、水杨酸、扎来普隆、佐匹克隆和唑吡坦检测。
从261例尸检病例中均获取了肝脏和肌肉标本;股静脉血、玻璃体液和尿液的获取率分别为98%、92%和72%。因此,共进行了相当于12,978次针对单个药物或药物组的免疫分析检测。在总共进行的12,978次筛查检测中,总体上超过98%的结果与对股静脉血进行的实验室确证检测结果一致。
利用磁共振成像(MRI)和计算机断层扫描(CT)扫描开发用于确定死因的非侵入性程序的兴趣日益浓厚,然而在大多数情况下,这些程序无法确定死亡是否可能与药物使用有关。兰多克斯检测阵列可在停尸房环境中提供定性和半定量结果,使病理学家能够决定是否从尸体上取下标本并送交实验室分析。可以对一系列尸检标本进行分析,这在无法获取常规标本(如血液)时特别有用。