Xiao Yi, Chen Suhua, Zhang Simeng, Wang Guofang, Yi Haomin, Xin Gui-Zhong, Yang Xiaoping
Key Laboratory of Study and Discovery of Small Targeted Molecules of Hunan Province, Department of Pharmacy, School of Medicine, Hunan Normal University, Changsha, 410013, Hunan, China; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, 02138, USA.
Hunan Provincial Maternal and Child Health Care Hospital, Changsha, 410008, Hunan, China.
Talanta. 2021 Aug 15;231:122399. doi: 10.1016/j.talanta.2021.122399. Epub 2021 Apr 9.
Straightforward and accurate measurement of medical biomarkers is of essential importance in clinical diagnostics and treatments. However, the major challenge is the diversity in dynamic range of different biomarkers ranging from pg mL to μg mL in various body fluids and tissues among patients. Here, we develop a mesoporous silica (MS)-mediated controllable electrochemiluminescence (ECL) quenching of immunosensor that allows accurate immunoassays with simplicity, sensitivity and tunable sensing range. MS is employed to enhance the sensitivity and tune ECL quenching to broaden the detection range just by altering luminophore (Ru(bpy)) and coreactant (DBAE) concentration without additional modifications. The immunoassay is followed: homogeneous sandwich immunoreaction, magnetic separation, and ECL quenching detection. As a proof-of-concept, simple and sensitive detection of IgG is achieved ranging from pg mL to μg mL, and applications of the strategy are extended by the combination of ECL immunosensor with commercial ELISA kit. This study will not only be expected to serve as a new avenue for the assay of physiological and clinical implications of immunological biomarkers, but also benefit a wide range of applications that require a tunable detection range and ultrahigh sensitivity.
在临床诊断和治疗中,对医学生物标志物进行直接且准确的测量至关重要。然而,主要挑战在于不同生物标志物在患者各种体液和组织中的动态范围差异很大,从皮克每毫升到微克每毫升不等。在此,我们开发了一种介孔二氧化硅(MS)介导的免疫传感器可控电化学发光(ECL)猝灭方法,该方法能够以简单、灵敏且可调节的传感范围进行准确的免疫测定。通过仅改变发光体(Ru(bpy))和共反应剂(DBAE)的浓度,而无需额外修饰,利用MS来提高灵敏度并调节ECL猝灭以拓宽检测范围。免疫测定过程如下:均相夹心免疫反应、磁分离以及ECL猝灭检测。作为概念验证,实现了对皮克每毫升到微克每毫升范围内IgG的简单且灵敏的检测,并且通过将ECL免疫传感器与商业ELISA试剂盒相结合扩展了该策略的应用。这项研究不仅有望为免疫生物标志物的生理和临床意义检测提供新途径,还将惠及广泛需要可调检测范围和超高灵敏度的应用。