Holt P J, Bruce N C, Lowe C R
Institute of Biotechnology, University of Cambridge, United Kingdom.
Anal Chem. 1996 Jun 1;68(11):1877-82. doi: 10.1021/ac951207r.
Illicit heroin is trafficked as a solid particulate drug, while heroin abuse is monitored by testing urine samples for its principal metabolites, morphine and morphine-3-glucuronide. Two novel bacterial enzymes were used in the development of a linked-enzyme assay for heroin and its metabolites: heroin esterase, which converts heroin to morphine, and morphine dehydrogenase, which oxidizes morphine to morphinone with the concomitant reduction of NADP+. A bioluminescent assay involving heroin esterase, morphine dehydrogenase, and the bacterial luciferase from Vibrio harveyi was developed and shown to be sensitive to 89 ng/mL heroin and 2.0 ng/mL morphine. Excellent correlation with the results from 83 authentic samples submitted for urine drug screening at a hospital laboratory was obtained. The bioluminescent assay exhibited greater specificity and speed than current immunological screening methods. A novel format of the bioluminescent assay involving immobilized enzymes was sensitive to 101 ng (250 pmol) of heroin and responded well to particulate heroin. This form of the test was sensitive enough to respond to one or two typical particles of illicit heroin.
非法海洛因作为一种固体颗粒药物进行贩卖,而对海洛因滥用情况的监测是通过检测尿液样本中的主要代谢物吗啡和吗啡 - 3 - 葡萄糖醛酸苷来进行的。在开发一种用于检测海洛因及其代谢物的连锁酶测定法时使用了两种新型细菌酶:将海洛因转化为吗啡的海洛因酯酶,以及将吗啡氧化为吗啡酮并伴随NADP⁺还原的吗啡脱氢酶。开发了一种涉及海洛因酯酶、吗啡脱氢酶和哈维弧菌细菌荧光素酶的生物发光测定法,该方法对89 ng/mL的海洛因和2.0 ng/mL的吗啡敏感。与一家医院实验室提交的83份用于尿液药物筛查的真实样本结果具有良好的相关性。该生物发光测定法比目前的免疫筛查方法具有更高的特异性和更快的速度。一种涉及固定化酶的新型生物发光测定法对101 ng(250 pmol)海洛因敏感,并且对颗粒状海洛因反应良好。这种测试形式足够灵敏,能够对一两个典型的非法海洛因颗粒做出反应。