Takeuchi T, Nishikawa T, Matsukawa R, Matsui J
Laboratory of Synthetic Biochemistry, Faculty of Information Sciences, Hiroshima City University, Japan.
Anal Chem. 1995 Aug 1;67(15):2655-8. doi: 10.1021/ac00111a025.
A nonisotopic receptor assay for benzodiazepine drugs using a time-resolved fluorometric technique is described. A novel europium chelate-labeled benzodiazepine (Eu-1012-S) was prepared as a probe ligand for the binding assay based on the competitive inhibition of Eu-1012-S binding by benzodiazepine drugs to their receptors. In this system, the degree of the inhibition was proportional to the affinity of drugs for the receptor. Background fluorescence did not interfere with the measurement, due to the long-lifetime fluorescence of Eu-1012-S. The proposed nonisotopic assay may provide an alternative to radioreceptor assays of benzodiazepines in biological systems and could also be used to screen new benzodiazepine-like compounds from nature.
描述了一种使用时间分辨荧光技术的苯二氮䓬类药物非同位素受体测定法。制备了一种新型铕螯合物标记的苯二氮䓬(Eu-1012-S)作为探针配体,用于基于苯二氮䓬类药物与受体结合对Eu-1012-S结合的竞争性抑制的结合测定。在该系统中,抑制程度与药物对受体的亲和力成正比。由于Eu-1012-S的长寿命荧光,背景荧光不干扰测量。所提出的非同位素测定法可能为生物系统中苯二氮䓬类药物的放射受体测定提供一种替代方法,也可用于从天然物质中筛选新的苯二氮䓬类样化合物。