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由乙基吗啡生成吗啡:对尿液中药物滥用检测的意义。

Morphine formation from ethylmorphine: implications for drugs-of-abuse testing in urine.

作者信息

Popa C, Beck O, Brodin K

机构信息

Department of Clinical Pharmacology, Karolinska Hospital, Stockholm, Sweden.

出版信息

J Anal Toxicol. 1998 Mar-Apr;22(2):142-7. doi: 10.1093/jat/22.2.142.

Abstract

In drugs-of-abuse testing, opiates constitute a delicate and controversial task because morphine may occur in urine for several reasons. Ethylmorphine (EtM), which is used as an antitussive drug in many countries, is metabolically converted to morphine. The present study was performed in order to document intra- and interindividual differences in morphine formation after single-dose intake of EtM at two different doses (25 and 50 mg). The urinary excretion of opiates was measured during 48 h with EMIT and gas chromatography-mass spectrometry in 10 healthy volunteers. The mean values of totally recovered EtM and morphine in hydrolyzed urine during 48 h were 42 and 47% of the given dose at high and low dose level, respectively. The ratio between total recovered morphine and EtM ranged from 19 to 131% with a mean value of 48%. The rate of positive outcome in the EMIT opiate-screening assay was 100% during the first 24 h for both doses, and it was still high (> or = 67%) in the 24-48 h time interval. It was found that the decline in urinary EtM is more rapid than for morphine, which leads to an increasing morphine/EtM ratio in urine over time. THe mean value of the morphine/EtM ratio was found to be greater than 1 during the 12-24 h interval and finally increased to greater than 10. There was an intra-individual concordance in morphine/EtM ratio between doses, but there was marked interindividual variation. Morphine/EtM ratios that were greater than 1 were only seen when the concentration of morphine was below 300 micrograms/mmol creatinine. Our results demonstrate that morphine is formed from EtM at a high and variable rate and may be present in urine in concentrations greater than those of EtM even shortly after drug intake.

摘要

在药物滥用检测中,阿片类药物检测是一项微妙且有争议的任务,因为吗啡可能因多种原因出现在尿液中。在许多国家用作止咳药的乙基吗啡(EtM)在代谢过程中会转化为吗啡。本研究旨在记录单次摄入两种不同剂量(25毫克和50毫克)EtM后吗啡形成的个体内和个体间差异。在10名健康志愿者中,采用酶放大免疫测定技术(EMIT)和气相色谱 - 质谱联用技术,在48小时内测量阿片类药物的尿排泄量。在高剂量和低剂量水平下,48小时内水解尿液中完全回收的EtM和吗啡的平均值分别为给药剂量的42%和47%。总回收吗啡与EtM的比例在19%至131%之间,平均值为48%。两种剂量在最初24小时内EMIT阿片类药物筛查试验的阳性率均为100%,在24 - 48小时时间段内仍很高(≥67%)。研究发现,尿液中EtM的下降比吗啡更快,这导致尿液中吗啡/EtM的比例随时间增加。在12 - 24小时时间段内,吗啡/EtM比例的平均值大于1,最终增至大于10。不同剂量之间个体内吗啡/EtM比例具有一致性,但个体间存在显著差异。仅当吗啡浓度低于300微克/毫摩尔肌酐时,才会出现大于1的吗啡/EtM比例。我们的研究结果表明,吗啡以高且可变的速率由EtM形成,甚至在服药后不久,尿液中吗啡的浓度可能高于EtM。

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