Smith M L, Hughes R O, Levine B, Dickerson S, Darwin W D, Cone E J
Office of the Armed Forces Medical Examiner, Armed Forces Institute of Pathology, Washington, DC 20306-6000.
J Anal Toxicol. 1995 Jan-Feb;19(1):18-26. doi: 10.1093/jat/19.1.18.
Opiate testing for morphine and codeine is performed routinely in forensic urine drug-testing laboratories in an effort to identify illicit opiate abusers. In addition to heroin, the 6-keto-opioids, including hydromorphone, hydrocodone, oxymorphone, and oxycodone, have high abuse liability and are self-administered by opiate abusers, but only limited information is available on detection of these compounds by current immunoassay and gas chromatographic-mass spectrometric (GC-MS) methods. In this study, single doses of hydromorphone, hydrocodone, oxymorphone, and oxycodone were administered to human subjects, and urine samples were collected before and periodically after dosing. Opiate levels were determined in a quantitative mode with four commercial immunoassays, TDx opiates (TDx), Abuscreen radioimmunoassay (ABUS), Coat-A-Count morphine in urine (CAC), and EMIT d.a.u. opiate assay (EMIT), and by GC-MS. GC-MS assay results indicated that hydromorphone, hydrocodone, oxymorphone, and oxycodone administration resulted in rapid excretion of parent drug and O-demethylated metabolites in urine. Peak concentrations occurred within 8 h after drug administration and declined below 300 ng/mL within 24-48 h. Immunoassay testing indicated that hydromorphone, hydrocodone, and oxycodone, but not oxymorphone, were detectable in urine by TDx and EMIT (300-ng/mL cutoff) for 6-24 h. ABUS detected only hydrocodone, and CAC failed to detect any of the four 6-keto-opioid analgesics. Generally, immunoassays for opiates in urine displayed substantially lower sensitivities for 6-keto-opioids compared with GC-MS. Consequently, urine samples containing low to moderate concentrations of hydromorphone, hydrocodone, oxymorphone, and oxycodone will likely go undetected when tested by conventional immunoassays.
在法医尿液药物检测实验室中,常规进行吗啡和可待因的阿片类药物检测,以识别非法阿片类药物滥用者。除海洛因外,包括氢吗啡酮、氢可酮、羟吗啡酮和羟考酮在内的6-酮类阿片具有很高的滥用可能性,且被阿片类药物滥用者自行服用,但目前关于通过免疫测定和气相色谱-质谱联用(GC-MS)方法检测这些化合物的信息有限。在本研究中,给人体受试者单次服用氢吗啡酮、氢可酮、羟吗啡酮和羟考酮,并在给药前和给药后定期收集尿液样本。使用四种商业免疫测定法(TDx阿片类药物检测法(TDx)、阿布斯克里恩放射免疫测定法(ABUS)、尿液中吗啡的涂层计数法(CAC)和EMIT d.a.u.阿片类药物测定法(EMIT))以及GC-MS以定量模式测定阿片类药物水平。GC-MS分析结果表明,服用氢吗啡酮、氢可酮、羟吗啡酮和羟考酮后,母体药物和O-去甲基代谢物在尿液中迅速排泄。给药后8小时内出现峰值浓度,并在24-48小时内降至300 ng/mL以下。免疫测定测试表明,TDx和EMIT(截断值为300 ng/mL)在6-24小时内可在尿液中检测到氢吗啡酮、氢可酮和羟考酮,但无法检测到羟吗啡酮。ABUS仅检测到氢可酮,而CAC未能检测到这四种6-酮类阿片类镇痛药中的任何一种。一般来说,尿液中阿片类药物的免疫测定法对6-酮类阿片的灵敏度远低于GC-MS。因此,当通过传统免疫测定法检测时,含有低至中等浓度氢吗啡酮、氢可酮、羟吗啡酮和羟考酮的尿液样本可能会漏检。