CEDIA--homogeneous immunoassays for the 1990s and beyond.

W A Coty, R Loor, N Bellet, P L Khanna, P Kaspar, M Baier
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Abstract

New homogeneous enzyme immunoassays have been developed for cortisol, digoxin, digitoxin, theophylline, phenytoin, and phenobarbital using the cloned enzyme donor immunoassay technology. As applied to Boehringer Mannheim/Hitachi analysis systems these methods provide rapid, accurate and precise quantification of analytes, with minimal interferences from endogenous serum constituents and low cross-reactivities to structurally-related hormonal precursors, drug metabolites and natural compounds. Additional significant features of the new assays are linear standard curves and two-point calibration. The six CEDIA assays join the two currently available CEDIA assays for determination of the thyroid parameters T4 and T Uptake. Additional new therapeutic drug and anemia monitoring assays are under development, demonstrating the versatility of the cloned enzyme donor immunoassay technology. These tests, in concert with Boehringer Mannheim/Hitachi analyzers, provide a high throughput, random access immunoassay system. The menu of available assays should continue to increase during the 1990s, providing efficient automation while allowing consolidation of testing on a limited number of instrument systems.

CEDIA——20世纪90年代及以后的均质免疫测定。
利用克隆酶供体免疫测定技术,开发了新的均相酶免疫测定皮质醇、地高辛、地高辛、茶碱、苯妥英和苯巴比妥。当应用于勃林格曼海姆/日立分析系统时,这些方法提供了快速、准确和精确的分析物定量,内源性血清成分的干扰最小,与结构相关的激素前体、药物代谢物和天然化合物的交叉反应性低。新测定法的其他重要特征是线性标准曲线和两点校准。这六种CEDIA检测方法加入了目前可用的两种CEDIA检测方法,用于测定甲状腺参数T4和T摄取。其他新的治疗药物和贫血监测分析正在开发中,证明了克隆酶供体免疫测定技术的多功能性。这些测试,配合勃林格曼海姆/日立分析仪,提供高通量,随机访问免疫分析系统。在20世纪90年代,可用的检测方法应继续增加,提供有效的自动化,同时允许在有限数量的仪器系统上合并检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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