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采用结合-游离相检测的一步法、免洗涤、基于磁珠的免疫测定法。

One-step, wash-free, bead-based immunoassay employing bound-free phase detection.

作者信息

Johannsen Benita, Karpíšek Michal, Baumgartner Desirée, Klein Vanessa, Bostanci Nagihan, Paust Nils, Früh Susanna M, Zengerle Roland, Mitsakakis Konstantinos

机构信息

Hahn-Schickard, Georges-Koehler-Allee 103, 79110 Freiburg, Germany.

BioVendor-Laboratorní Medicína a.s., Research & Diagnostic Products Division, Karasek 1767/1, Reckovice, 62100, Brno, Czech Republic; Masaryk University, Faculty of Pharmacy, Palackeho Trida 1946/1, 61242, Brno, Czech Republic.

出版信息

Anal Chim Acta. 2021 Apr 8;1153:338280. doi: 10.1016/j.aca.2021.338280. Epub 2021 Feb 5.

Abstract

We present a simple and fast one-step heterogeneous immunoassay, with performance characteristics that can enable easy and versatile adaptation to miniaturized, automated point-of-care systems. This novel analytical method uses magnetic and fluorescent beads as capture and detection agents respectively. Its main feature is the measurement of the fluorescent signal in the bound-free phase for (semi-)quantitative detection of analytes. Thus, no washing is required and the workflow consists only of sample and reagent supply, incubation, separation and detection. The immunoassay concept is demonstrated with C-reactive protein (CRP), a systemic inflammation marker. CRP in only 5 μL of undiluted serum was measured in the range 20-140 mg L (includes clinically relevant cut-off values). The limit of detection (LOD) was 22.1 ± 6.3 mg L (incubation 15 min). A CRP certified reference material was measured on five different days. Intra- and inter-assay coefficients of variation were 4.6 ± 1.9% and 5.6% respectively. To demonstrate the compatibility of the assay concept with additional matrices and concentration ranges, three oral inflammation markers, namely matrix metalloproteinases 8 and 9 (MMP-8, MMP-9) and tissue inhibitor of metalloproteinases 1 (TIMP-1), were measured in saliva in the ranges 0.47-30 ng mL for MMP-8 and MMP-9, and 0.69-44 ng mL for TIMP-1. LODs were 0.24 ng mL, 0.38 ng mL and 0.39 ng mL respectively (incubation 20 min). Multiplexing capacity of the assay concept was also shown with these markers. The demonstrated excellent reproducibility of the results, combined with the versatility and low complexity of the introduced immunoassay concept, make it an attractive candidate for applied analytical chemistry and automated point-of-care testing.

摘要

我们展示了一种简单快速的一步式异质免疫分析方法,其性能特征能够轻松且灵活地适用于小型化、自动化的即时检测系统。这种新型分析方法分别使用磁性珠和荧光珠作为捕获剂和检测剂。其主要特点是在结合-游离相中测量荧光信号,用于(半)定量检测分析物。因此,无需洗涤,工作流程仅包括样品和试剂供应、孵育、分离和检测。以全身炎症标志物C反应蛋白(CRP)为例展示了该免疫分析概念。在仅5μL未稀释血清中测量CRP的范围为20 - 140mg/L(包括临床相关临界值)。检测限(LOD)为22.1±6.3mg/L(孵育15分钟)。在五个不同日期测量了CRP认证参考物质。批内和批间变异系数分别为4.6±1.9%和5.6%。为了证明该分析概念与其他基质和浓度范围的兼容性,在唾液中测量了三种口腔炎症标志物,即基质金属蛋白酶8和9(MMP - 8、MMP - 9)以及金属蛋白酶组织抑制剂1(TIMP - 1),MMP - 8和MMP - 9的范围为0.47 - 30ng/mL,TIMP - 1的范围为0.69 - 44ng/mL。检测限分别为0.24ng/mL、0.38ng/mL和0.39ng/mL(孵育20分钟)。这些标志物也展示了该分析概念的多重检测能力。所展示的结果的出色重现性,结合所引入免疫分析概念的多功能性和低复杂性,使其成为应用分析化学和自动化即时检测的有吸引力的候选方法。

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