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基于生物素-链霉亲和素放大时间分辨荧光免疫分析测定己烯雌酚。

Determination of diethylstilbestrol based on biotin-streptavidin-amplified time-resolved fluoro-immunoassay.

机构信息

College of Chemistry and Chemical Engineering, Liaocheng University, People's Republic of China.

出版信息

Luminescence. 2012 Jan-Feb;27(1):28-33. doi: 10.1002/bio.1320. Epub 2011 Jun 22.

Abstract

A rapid and sensitive time-resolved fluoroimmunoassay (TR-FIA) based on the biotin-streptavidin amplification system was developed for the determination of diethylstilbestrol (DES). Europium-labelled streptavidin derivatives combined with europium and anhydride of diethylene triamine penta-acetic acid were used to label streptavidin; biotin was coupled with goat anti-rabbit IgG to form a biotin-goat anti-rabbit IgG bridge between streptavidin-europium and the anti-DES antibody in the immunoassay. The DES assay was carried out by measuring the fluorescence of Eu(3+) -SA at 615 nm. The presented method produced a wide linear range, 0.001-1000.0 ng/mL, and a detection limit up to 0.81 pg/mL for DES. The method was applied to determine DES in serum samples, with recoveries of 97.4-107.8% and RSD 1.32-4.04%. The assay results by the present method showed that biotin-streptavidin amplified TR-FIA for DES detection; it may offer high sensitivity and promising alternative special methods in biological samples.

摘要

建立了一种基于生物素-链霉亲和素放大系统的快速灵敏时间分辨荧光免疫分析(TR-FIA)方法,用于测定己烯雌酚(DES)。用铕标记的链霉亲和素衍生物与铕和二乙烯三胺五乙酸酐结合,标记链霉亲和素;生物素与兔抗山羊 IgG 偶联,在免疫分析中形成链霉亲和素-铕和抗 DES 抗体之间的生物素-兔抗山羊 IgG 桥。通过测量 615nm 处 Eu(3+) -SA 的荧光来进行 DES 测定。该方法产生了宽的线性范围,0.001-1000.0ng/mL,检测限低至 0.81pg/mL。该方法用于测定血清样品中的 DES,回收率为 97.4-107.8%,RSD 为 1.32-4.04%。本方法的测定结果表明,生物素-链霉亲和素放大 TR-FIA 用于 DES 检测;它可能为生物样品提供高灵敏度和有前途的替代特殊方法。

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