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Double-Label Simultaneous Time-Resolved Fluoroimmunoassay of Phenytoin and Phenobarbital

机译:苯妥英和苯巴比妥的双标签同时时间分辨荧光免疫测定

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摘要

A procedure for the simultaneous time-resolved fluoroimmunoassay for phenobarbital and phenytoin, based on the use of europium- and samarium-labeled haptens, has been investigated. These lanthanide ions are bound to the haptens by means of the anhydride of diethylenetriamine-pentaacetic acid. The antibody is immobilized onto immunoplate in which samples are assayed in competitive immunoassay. After the immunoreactions and dissociation with a fluorescence enhancement solution, the fluorescence intensity is measured. The detection limits of the assay are, respectively, 20 ng/ml for phenobarbital and 50 ng/ml for phenytoin. Results obtained with the proposed methods correlate well (CV <10%). The inter-reactions between phenobarbital, phenytoin, and their antibodies are studied.
机译:已经研究了基于label和label标记的半抗原同时测定苯巴比妥和苯妥英钠的时间分辨荧光免疫分析方法。这些镧系元素离子通过二亚乙基三胺-五乙酸的酸酐键合到半抗原。抗体被固定在免疫板上,在该板上进行竞争性免疫分析。免疫反应和荧光增强溶液解离后,测量荧光强度。该测定的检出限分别为苯巴比妥和苯妥英钠分别为20 ng / ml和50 ng / ml。用建议的方法获得的结果具有很好的相关性(CV <10%)。研究了苯巴比妥,苯妥英钠及其抗体之间的相互作用。

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