Comparative study of colloidal gold and quantum dots as labels for multiplex screening tests for multi-mycotoxin
Astrid Foubert1, Natalia V Beloglazova1, Sarah De Saeger1
1Faculty of Pharmaceutical Sciences, Laboratory of Food Analysis, Ghent University, Ghent, Belgium.
Analytica Chimica Acta
|January 16, 2017
Summary
Quantum dots (QDs) and colloidal gold nanoparticles (CG) were compared for multiplex lateral flow immunoassay (LFIA) to detect mycotoxins in cereals. QD-based LFIA showed superior sensitivity, economic benefits, and easier interpretation for on-site screening.
Area of Science:
- Food Science
- Analytical Chemistry
- Biotechnology
Background:
- Mycotoxin contamination in cereals poses significant risks to food safety and human health.
- Multiplex lateral flow immunoassays (LFIA) offer rapid, on-site detection capabilities for multiple analytes.
- Evaluating different nanoparticle labels is crucial for optimizing LFIA performance.
Purpose of the Study:
- To compare quantum dots (QDs) and colloidal gold nanoparticles (CG) as labels for a multiplex LFIA.
- To develop and validate assays for the simultaneous detection of deoxynivalenol (DON), zearalenone (ZEN), and T2/HT2-toxin (T2/HT2) in cereal matrices.
- To assess the analytical characteristics and practical applicability of QD- and CG-based LFIAs.
Main Methods:
- Development of two multiplex LFIAs utilizing the same immunoreagents but different labels (QDs vs. CG).
- Immobilization of antigens and secondary antibodies on nitrocellulose membranes.
- Conjugation of monoclonal antibodies against DON, ZEN, and T2 with CdSeS/ZnS QDs or CG.
- Analysis of naturally contaminated wheat samples to demonstrate assay applicability.
Main Results:
- Both QD- and CG-based LFIAs successfully detected DON, ZEN, and T2/HT2 in wheat, meeting legal limits.
- QD-based LFIA demonstrated higher sensitivity, consumed fewer immunoreagents, and offered better economic benefits.
- QD-based LFIA provided easier result interpretation with a lower false negative rate (<5%).
Conclusions:
- Both QD and CG are suitable labels for multiplex LFIA of mycotoxins in cereals.
- QD-based LFIA is a more advantageous tool for rapid, cost-effective, and sensitive on-site screening of mycotoxins.
- The developed QD-LFIA aligns with regulatory requirements for analytical method performance in screening purposes.
Related Concept Videos
Immunogold Electron Microscopy
5.7K
Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.
5.7K
Labeling DNA Probes
9.6K
DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
9.6K


