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用于检测尿液中苯二氮䓬类药物的酶联免疫吸附测定法。

Enzyme linked immunosorbent assay for detecting benzodiazepines in urine.

作者信息

Laurie D, Mason A J, Piggott N H, Rowell F J, Seviour J, Strachan D, Tyson J D

机构信息

School of Health Sciences, University of Sunderland, UK.

出版信息

Analyst. 1996 Jul;121(7):951-4. doi: 10.1039/an9962100951.

Abstract

A relatively simple ELISA technique was developed for the detection of a range of benzodiazepines (BZs) in urine. The assay employs a mouse anti-oxazepam antibody that is highly specific for the BZs. The limit of detection using 10 microliters samples of urine was 0.3 microgram ml-1 oxazepam. N-Desmethyldiazepam showed equal cross-reactivity to oxazepam, 11 BZs cross-reacted weakly and flurazepam and chlordiazepoxide did not cross-react at levels reported to be found in urine. No cross-reactivity was observed with drugs of abuse and a range of therapeutic drugs commonly found in urine. The assay was used as a screen to detect the presence of BZs in urine from 88 addicts that had been screened by the EMIT technique and a radioreceptor assay (RRA) for BZs. The ELISA produced two false negatives that were EMIT and RRA positive whereas the EMIT produced four different false negatives that were positive by both ELISA and RRA. Thirty-three positives were common to all three assays. The ELISA was also used to monitor nitrazepam-like activity in the urine of a greyhound receiving 5 mg oral medication and the results were compared with those obtained by RRA. Both assays were able to detect nitrazepam-like activity for up to 10 h post-administration.

摘要

开发了一种相对简单的酶联免疫吸附测定(ELISA)技术,用于检测尿液中的一系列苯二氮䓬类药物(BZs)。该测定采用对BZs具有高度特异性的小鼠抗奥沙西泮抗体。使用10微升尿液样本时,检测限为0.3微克/毫升奥沙西泮。N-去甲基地西泮与奥沙西泮具有相同的交叉反应性,11种BZs交叉反应较弱,氟西泮和氯氮䓬在尿液中报道的浓度水平下不发生交叉反应。未观察到与滥用药物和尿液中常见的一系列治疗药物发生交叉反应。该测定用作筛查方法,以检测88名成瘾者尿液中BZs的存在,这些成瘾者已通过BZs的酶倍增免疫测定技术(EMIT)和放射受体测定(RRA)进行过筛查。ELISA产生了两个假阴性结果,而这两个样本通过EMIT和RRA检测为阳性,而EMIT产生了四个不同的假阴性结果,这四个样本通过ELISA和RRA检测均为阳性。所有三种测定共有33个阳性结果。ELISA还用于监测一只口服5毫克药物的灵缇犬尿液中的硝西泮样活性,并将结果与RRA获得的结果进行比较。两种测定在给药后长达10小时内均能检测到硝西泮样活性。

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