Rapid sandwich ELISA-based in vitro diagnostic procedure for the highly-sensitive detection of human fetuin A

被引:30
|
作者
Vashist, Sandeep Kumar [1 ,2 ]
Schneider, E. Marion [3 ]
Luong, John H. T. [4 ]
机构
[1] Univ Freiburg, Dept Microsyst Engn IMTEK, Lab MEMS Applicat, D-79110 Freiburg, Germany
[2] HSG IMIT, Inst Mikro & Informat Techn, D-79110 Freiburg, Germany
[3] Univ Hosp Ulm, Sekt Expt Anaesthesiol, D-89081 Ulm, Germany
[4] Natl Univ Ireland Univ Coll Cork, Biol Chem Res Facil ABCRF, Dept Chem & Analyt, Innovat Chromatog Grp,Irish Separat Sci Cluster I, Cork, Ireland
来源
关键词
Rapid sandwich ELISA; In vitro diagnostics; Human fetuin A; APTES; EDC; A ALPHA-2HS-GLYCOPROTEIN; METABOLIC SYNDROME; DIALYSIS PATIENTS; ADHESIVE PROTEIN; LIVER-CIRRHOSIS; TUMOR-CELLS; IMMUNOASSAY; ASSOCIATION; LEVEL; MORTALITY;
D O I
10.1016/j.bios.2014.06.058
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A rapid sandwich enzyme-linked immunosorbent assay (ELISA)-based in vitro diagnostic (IVD) procedure has been developed for human fetuin A (HFA), an important disease biomarker for inflammatory diseases as well as malignancies. In this simplified and cost-effective procedure, the EDC-activated anti-HFA antibody (Ab) was admixed with 1% (v/v) 3-aminopropyltriethoxysilane (APTES) in 1:1 (v/v) and dispensed in a KOH-pretreated microtiter plate (MTP). APTFS formed a stable complex with the capture antibody that was in turn covalently bonded on the KOH-treated surface in 30 min. The resulting immunoassay (IA) format detects HFA with a dynamic range of 0.1-243 ng mL(-1), and a limit of detection (LOD) and analytical sensitivity of 0.3 ng mL(-1) and 1.0 ng mL(-1), respectively. For the determination of HFA spiked in diluted human whole blood and serum, and HFA in ethylenediaminetetraacetic acid (EDTA)-plasma of patients, the obtained analytical precision is similar to that of the conventional sandwich ELISA. The anti-HFA Ab-bound MTPs, stored at 4 degrees C in 0.1 M PBS, pH 7.4, retained its biological activity for 8 weeks, thereby demonstrating excellent storage stability. This generic sandwich ELISA procedure can be extended for rapid, simplified and cost-effective detection of other disease biomarkers. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:73 / 78
页数:6
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