Competitive fluorescent immunosensor based on catalytic hairpin self-assembly for multiresidue detection of organophosphate pesticides in agricultural products

•Dual signal amplification was achieved by combining immunoassay and nucleic acid amplification.•The method could occur at a constant temperature without enzyme catalysis.•The detection limit was as low as 0.012, 0.0057, and 0.0074 ng/mL.•Signals were detected through different fluorescent groups mo...

Full description

Saved in:
Bibliographic Details
Published inFood chemistry Vol. 413; p. 135607
Main Authors Wang, Yuanshang, Abd El-Aty, A.M., Wang, Shanshan, Cui, Xueyan, Zhao, Jing, Lei, Xingmei, Xu, Lingyuan, She, Yongxin, Jin, Fen, Eun, Jong-Bang, Shim, Jae-Han, Wang, Jing, Jin, Maojun, Hammock, Bruce D.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.07.2023
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•Dual signal amplification was achieved by combining immunoassay and nucleic acid amplification.•The method could occur at a constant temperature without enzyme catalysis.•The detection limit was as low as 0.012, 0.0057, and 0.0074 ng/mL.•Signals were detected through different fluorescent groups modified on DNA strands.•The designed sensor leads to a new direction for trace analysis of multiple pesticide residues. Simple and rapid multiresidue trace detection of organophosphate pesticides (OPs) is extremely important for various reasons, including food safety, environmental monitoring, and national health. Here, a catalytic hairpin self-assembly (CHA)-based competitive fluorescent immunosensor was developed to detect OPs in agricultural products, involving enabled dual signal amplification followed by a CHA reaction. The developed method could detect 0.01–50 ng/mL triazophos, parathion, and chlorpyrifos, with limits of detection (LODs) of 0.012, 0.0057, and 0.0074 ng/mL, respectively. The spiked recoveries of samples measured using this assay ranged from 82.8 % to 110.6 %, with CV values ranging between 5.5 % and 18.5 %. This finding suggests that the CHA-based competitive fluorescent immunosensor is a reliable and accurate method for detecting OPs in agricultural products. The results correlated well with those obtained from the liquid chromatography-tandem mass spectrometry (LC–MS/MS) method, indicating that the CHA-based biosensor is able to accurately detect OPs and can be used as a reliable alternative to the LC–MS/MS method. Additionally, the CHA-based biosensor is simpler and faster than LC–MS/MS, which makes it a more practical and cost-effective option for the detection of OPs. In summary, the CHA-based competitive fluorescent immunosensor can be considered a promising approach for trace analysis and multiresidue determination of pesticides, which can open up new horizons in the fields of food safety, environmental monitoring, and national health.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0308-8146
1873-7072
1873-7072
DOI:10.1016/j.foodchem.2023.135607