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

被引:15
|
作者
Johannsen, Benita [1 ]
Karpisek, Michal [2 ,3 ]
Baumgartner, Desiree [4 ]
Klein, Vanessa [1 ,6 ]
Bostanci, Nagihan [5 ]
Paust, Nils [1 ,4 ]
Frueh, Susanna M. [1 ,4 ]
Zengerle, Roland [1 ,4 ]
Mitsakakis, Konstantinos [1 ,4 ]
机构
[1] Hahn Schickard, Georges Koehler Allee 103, D-79110 Freiburg, Germany
[2] BioVendor Lab Med AS, Res & Diagnost Prod Div, Karasek 1767-1, Brno 62100, Czech Republic
[3] Masaryk Univ, Fac Pharm, Palackeho Trida 1946-1, Brno 61242, Czech Republic
[4] Univ Freiburg, IMTEK Dept Microsyst Engn, Lab MEMS Applicat, Georges Koehler Allee 103, D-79110 Freiburg, Germany
[5] Karolinska Inst, Dept Dent Med, Div Oral Dis, Sect Periodontol & Dent Prevent, Alfred Nobels Alle 8, S-14104 Stockholm, Sweden
[6] Eurofins Genom Germany GmbH, Anzinger Str 7a, D-85560 Ebersberg, Germany
基金
欧盟地平线“2020”;
关键词
Immunoassay; Bound-free phase; Micro/nanoparticles; Oral biomarkers; Inflammation; Saliva; C-REACTIVE PROTEIN; PERIODONTAL-DISEASE; MATRIX METALLOPROTEINASES; HOMOGENEOUS IMMUNOASSAY; SENSITIVE DETECTION; TISSUE INHIBITORS; PRACTICAL GUIDE; MMP-8; ASSOCIATION; SALIVA;
D O I
10.1016/j.aca.2021.338280
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 mu L of undiluted serum was measured in the range 20-140 mg L-1 (includes clinically relevant cut-off values). The limit of detection (LOD) was 22.1 +/- 6.3 mg L-1 (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(-1) for MMP-8 and MMP-9, and 0.69-44 ng mL(-1) for TIMP-1. LODs were 0.24 ng mL(-1), 0.38 ng mL(-1) and 0.39 ng mL-1 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. (C) 2021 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
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页数:9
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