Evidence map›Paper›PMID 39451705›Full record

ArticleBiosensors2024

Mycotoxin Detection through Colorimetric Immunoprobing with Gold Nanoparticle Antibody Conjugates.

Vinayak Sharma, Bilal Javed, Hugh J Byrne, Furong Tian

Abstract read
In one paragraph

Article in Biosensors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Vinayak SharmaSchool of Food Science and Environmental Health, Technological University Dublin, D07 H6K8 Dublin, Ireland.
Bilal JavedNanolab, Physical to Life Sciences Research Hub, Technological University Dublin, D08 CKP1 Dublin, Ireland.ORCID 0000-0002-9566-1498
Hugh J ByrneNanolab, Physical to Life Sciences Research Hub, Technological University Dublin, D08 CKP1 Dublin, Ireland.ORCID 0000-0002-1735-8610
Furong TianSchool of Food Science and Environmental Health, Technological University Dublin, D07 H6K8 Dublin, Ireland.ORCID 0000-0002-4953-1131

Funding

Irish research council (IRC) post graduate scholarship GOIPG/2021/978
6 · The paper itself

Abstract

Driven by their exceptional optical characteristics, robust chemical stability, and facile bioconjugation, gold nanoparticles (AuNPs) have emerged as a preferred material for detection and biosensing applications in scientific research. This study involves the development of a simple, rapid, and cost-effective colorimetric immuno-sensing probe to detect aflatoxin B1 and zearalenone using AuNP antibody (AuNP-mAb) conjugates. Anti-toxin antibodies were attached to the AuNPs by using the physical adsorption method. The colorimetric immunosensor developed operates on the principle that the optical properties of the AuNP are very sensitive to aggregation, which can be induced by a critical high salt concentration. Although the presence of antibodies on the AuNP surface inhibits the aggregation, these antibodies bind to the toxin with higher affinity, which leads to exposure of the surface of AuNPs and aggregation in a salt environment. The aggregation triggers a noticeable but variable alteration in color from red to purple and blueish gray, as a result of a red shift in the surface plasmon resonance band of the AuNPs. The extent of the shift is dependent on the toxin exposure dose and can be quantified using a calibration curve through UV-Visible-NIR spectroscopy. The limit of detection using this assay was determined to be as low as 0.15 ng/mL for both zearalenone and aflatoxin B1. The specificity of the prepared immunoprobe was analyzed for a particular mycotoxin in the presence of other mycotoxins. The developed immunoprobe was evaluated for real-world applicability using artificially spiked samples. This colorimetric immunoprobe based on localized surface plasmon resonance (LSPR) has a reduced detection limit compared to other immunoassays, a rapid readout, low cost, and facile fabrication.

Indexed as

Aflatoxin B1Biosensing TechniquesColorimetryGoldMetal NanoparticlesMycotoxinsAntibodiesImmunoassayLimit of DetectionSurface Plasmon ResonanceZearalenoneAflatoxin B1AntibodiesGoldMycotoxinsZearalenoneaflatoxin B1bioconjugatescolorimetric sensorlocalized surface plasmon resonancezearalenone

Identifiers

PMID39451705
PMCPMC11506043

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.