Colbert D L, Gallacher G, Ayling P, Turner G J
Department of Chemical Pathology, St. Bartholomew's Hospital, London, UK.
Clin Chim Acta. 1988 Jan 15;171(1):37-48. doi: 10.1016/0009-8981(88)90289-6.
Two fluoroimmunoassays for the specific detection of morphine in urine are described based on the use of ovine antibodies and fluorescein-labelled normorphine. The first, a polarisation fluoroimmunoassay, is performed by adding 10 microliter of urine to 1.5 ml of a single-reagent, comprising premixed antiserum and tracer, incubation for a few minutes at ambient temperature and measurement of fluorescence polarisation. The assay gives results which compare well with those by thin-layer chromatography, EMIT d.a.u., and the Boehringer opiate drug test. Although adequate for routine screening for drug abuse, the technique is not as sensitive as some radioimmunoassays. Therefore, a second fluoroimmunoassay was developed based on the use of the same antibodies covalently coupled to magnetisable particles to facilitate both the separation of the bound and free fractions and the removal of non-specific interfering substances. Thus, larger sample volumes could be employed and greater sensitivity achieved.
本文描述了两种基于羊抗体和荧光素标记去甲吗啡对尿液中吗啡进行特异性检测的荧光免疫测定法。第一种是偏振荧光免疫测定法,其操作是将10微升尿液加入到1.5毫升单试剂中,该单试剂由预混抗血清和示踪剂组成,在室温下孵育几分钟后测量荧光偏振。该测定法的结果与薄层色谱法、酶放大免疫分析技术(EMIT d.a.u.)以及勃林格阿片类药物检测法的结果相当。虽然该技术足以用于药物滥用的常规筛查,但不如一些放射免疫测定法灵敏。因此,基于使用与可磁化颗粒共价偶联的相同抗体开发了第二种荧光免疫测定法,以促进结合部分和游离部分的分离以及去除非特异性干扰物质。这样就可以使用更大的样本量并实现更高的灵敏度。