Kanso Hussein, Inguimbert Nicolas, Istamboulie Georges, Barthelmebs Lise, Calas-Blanchard Carole, Noguer Thierry
Univ. Perpignan Via Domitia, Biocapteurs-Analyses-Environnement, 66860, Perpignan, France; Laboratoire de Biodiversité et Biotechnologies Microbiennes, USR 3579 Sorbonne Universités (UPMC) Paris 6 et CNRS Observatoire Océanologique, 66650, Banyuls-sur-Mer, France.
Univ. Perpignan Via Domitia, Centre de Recherche Insulaire et Observatoire de l'Environnement (CRIOBE), USR CNRS 3278, 66860, Perpignan, France.
Anal Biochem. 2017 Nov 15;537:63-68. doi: 10.1016/j.ab.2017.08.023. Epub 2017 Sep 8.
New chemiluminescence-based immunoassays for sensitive detection of 17-β estradiol (E2) and ethinylestradiol (EE2) are described on the basis of the use of biotinylated estrogen derivatives. Estrogen derivatives bearing a carboxylic group (E2-COOH and EE2-COOH) on C-3 position were synthesized, covalently bound to aminated biotin and subsequently immobilized on avidin-coated microtiter plates. The assay principle was based on competition between free and immobilized estrogens for their binding to primary antibodies, with subsequent revelation using horseradish peroxidase (HRP)-labeled secondary antibodies. Under optimized conditions, the chemiluminescence immunoassays showed a highly sensitive response to E2 and EE2, with respective detection limits of 0.5 and 1.2 ng L. The LOD achieved using biotinylated E2 was in the same order of magnitude as those obtained using commercially available E2-bovine serum albumin conjugate (E2-BSA). The developed devices were successfully applied to analysis wastewater treatment plants effluents (WWTP) with negligible matrix effect.
基于生物素化雌激素衍生物的使用,描述了用于灵敏检测17-β雌二醇(E2)和乙炔雌二醇(EE2)的新型化学发光免疫分析方法。合成了在C-3位带有羧基的雌激素衍生物(E2-COOH和EE2-COOH),将其与胺化生物素共价结合,随后固定在抗生物素蛋白包被的微量滴定板上。该分析原理基于游离雌激素和固定化雌激素竞争与一抗结合,随后使用辣根过氧化物酶(HRP)标记的二抗进行显色。在优化条件下,化学发光免疫分析对E2和EE2表现出高度灵敏的响应,检测限分别为0.5和1.2 ng/L。使用生物素化E2获得的检测限与使用市售E2-牛血清白蛋白缀合物(E2-BSA)获得的检测限处于同一数量级。所开发的装置成功应用于分析污水处理厂出水(WWTP),基质效应可忽略不计。