Magnetic bead-based fluorescence immunoassay for aflatoxin B1 in food using biofunctionalized rhodamine B-doped silica nanoparticles

被引:63
作者
Tang, Dianping [1 ]
Yu, Yongliang [2 ]
Niessner, Reinhard [1 ]
Miro, Manuel [3 ]
Knopp, Dietmar [1 ]
机构
[1] Tech Univ Munich, Inst Hydrochem, Chair Analyt Chem, D-81377 Munich, Germany
[2] Northeastern Univ, Res Ctr Analyt Sci, Shenyang 110004, Peoples R China
[3] Univ Balearic Isl, Fac Sci, Dept Chem, Palma de Mallorca 07122, Illes Balears, Spain
关键词
BIO-BARCODE ASSAY; PROTEIN; SIZE;
D O I
10.1039/c0an00221f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simple and sensitive fluorescence immunoassay for the detection of aflatoxin B-1 (AFB(1), as a model compound) in food was developed using AFB(1)-bovine serum albumin conjugate (AFB(1)-BSA)-functionalized magnetic beads as immunosensing probes. The recognition elements were prepared by doping of rhodamine B (RB) fluorophore into silica nanoparticles followed by immobilization of monoclonal anti-AFB(1) antibodies on the silica shell. Based on a competitive-type immunoassay format, the assay was performed both in low-binding polypropylene 96-well microtiter plates (MTPs) and in an automated sequential injection (SI) format. Similar detection limit (LOD) of 0.2 ng mL(-1) vs. 0.1 ng mL(-1) but narrower dynamic working linear range of 0.5-7 ng mL(-1) vs. 0.5-30 ng mL(-1) was obtained toward AFB(1) standards with the flow setup compared to the MTP format. Intra-batch assay precision was substantially improved (<= 5.3% vs. <= 8.7%) by resorting to the SI manifold. The proposed method features unbiased identification of negative (blank) and positive samples. No significant differences at the 95% confidence level were encountered in the analysis of naturally contaminated peanut samples between the proposed immunoassay and liquid chromatography for determination of AFB(1).
引用
收藏
页码:2661 / 2667
页数:7
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