Tunable multiplexed fluorescence biosensing platform for simultaneous and selective detection of paraquat and carbendazim pesticides

•BPNSs as a single acceptor paired with tunable multicolor UCNPs as donors.•A novel multiplexed FRET sensor was developed for paraquat and carbendazim detection.•The detection limits of paraquat and carbendazim were 0.18 ng/mL and 0.45 ng/mL.•This work offers a universal biosensing platform in advan...

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Published inFood chemistry Vol. 388; p. 132950
Main Authors Wang, Li, Haruna, Suleiman A., Ahmad, Waqas, Wu, Jizhong, Chen, Quansheng, Ouyang, Qin
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 15.09.2022
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Abstract •BPNSs as a single acceptor paired with tunable multicolor UCNPs as donors.•A novel multiplexed FRET sensor was developed for paraquat and carbendazim detection.•The detection limits of paraquat and carbendazim were 0.18 ng/mL and 0.45 ng/mL.•This work offers a universal biosensing platform in advancing multiplexed analysis. The monitoring of multiple pesticides commonly used in food is a prerequisite for public health safety. Herein, a multiplexed biosensor based on fluorescence resonance energy transfer (FRET) from multicolor upconversion nanoparticles (UCNPs)to single black phosphorus nanosheets (BPNSs) was successfully developed for simultaneous and selective detection of paraquat and carbendazim pesticides. Due to the strong π-π stacking interactions, aptamers functionalized UCNPs may adsorb on the BPNSs surface, allowing strong upconversion fluorescence quenching. In the presence of paraquat and carbendazim, the aptamers preferentially integrated with their corresponding targets and altered the aptamer’s conformation, restoring the fluorescence. An excellent linear correlation was observed from 1.0 to 1.0 × 105 ng/mL, with a limit of detection of 0.18 ng/mL for paraquat and 0.45 ng/mL for carbendazim. The developed aptasensor was further validated by commercial enzyme-linked immunoassays without significant differences in practical detection. Additionally, this work offers new insights into monitoring multiple targets simultaneously.
AbstractList The monitoring of multiple pesticides commonly used in food is a prerequisite for public health safety. Herein, a multiplexed biosensor based on fluorescence resonance energy transfer (FRET) from multicolor upconversion nanoparticles (UCNPs)to single black phosphorus nanosheets (BPNSs) was successfully developed for simultaneous and selective detection of paraquat and carbendazim pesticides. Due to the strong π-π stacking interactions, aptamers functionalized UCNPs may adsorb on the BPNSs surface, allowing strong upconversion fluorescence quenching. In the presence of paraquat and carbendazim, the aptamers preferentially integrated with their corresponding targets and altered the aptamer's conformation, restoring the fluorescence. An excellent linear correlation was observed from 1.0 to 1.0 × 10  ng/mL, with a limit of detection of 0.18 ng/mL for paraquat and 0.45 ng/mL for carbendazim. The developed aptasensor was further validated by commercial enzyme-linked immunoassays without significant differences in practical detection. Additionally, this work offers new insights into monitoring multiple targets simultaneously.
•BPNSs as a single acceptor paired with tunable multicolor UCNPs as donors.•A novel multiplexed FRET sensor was developed for paraquat and carbendazim detection.•The detection limits of paraquat and carbendazim were 0.18 ng/mL and 0.45 ng/mL.•This work offers a universal biosensing platform in advancing multiplexed analysis. The monitoring of multiple pesticides commonly used in food is a prerequisite for public health safety. Herein, a multiplexed biosensor based on fluorescence resonance energy transfer (FRET) from multicolor upconversion nanoparticles (UCNPs)to single black phosphorus nanosheets (BPNSs) was successfully developed for simultaneous and selective detection of paraquat and carbendazim pesticides. Due to the strong π-π stacking interactions, aptamers functionalized UCNPs may adsorb on the BPNSs surface, allowing strong upconversion fluorescence quenching. In the presence of paraquat and carbendazim, the aptamers preferentially integrated with their corresponding targets and altered the aptamer’s conformation, restoring the fluorescence. An excellent linear correlation was observed from 1.0 to 1.0 × 105 ng/mL, with a limit of detection of 0.18 ng/mL for paraquat and 0.45 ng/mL for carbendazim. The developed aptasensor was further validated by commercial enzyme-linked immunoassays without significant differences in practical detection. Additionally, this work offers new insights into monitoring multiple targets simultaneously.
ArticleNumber 132950
Author Ouyang, Qin
Wang, Li
Ahmad, Waqas
Wu, Jizhong
Haruna, Suleiman A.
Chen, Quansheng
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Keywords Black phosphorus nanosheets
Aptamer
Fluorescence resonance energy transfer
Pesticides
Upconversion nanoparticles
Language English
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Snippet •BPNSs as a single acceptor paired with tunable multicolor UCNPs as donors.•A novel multiplexed FRET sensor was developed for paraquat and carbendazim...
The monitoring of multiple pesticides commonly used in food is a prerequisite for public health safety. Herein, a multiplexed biosensor based on fluorescence...
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SubjectTerms Aptamer
Aptamers, Nucleotide
Benzimidazoles
Biosensing Techniques
Black phosphorus nanosheets
Carbamates
Fluorescence Resonance Energy Transfer
Limit of Detection
Paraquat
Pesticides
Upconversion nanoparticles
Title Tunable multiplexed fluorescence biosensing platform for simultaneous and selective detection of paraquat and carbendazim pesticides
URI https://dx.doi.org/10.1016/j.foodchem.2022.132950
https://www.ncbi.nlm.nih.gov/pubmed/35483279
https://search.proquest.com/docview/2658229931
Volume 388
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