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 in | Food chemistry Vol. 388; p. 132950 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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. |
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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 |
Author_xml | – sequence: 1 givenname: Li surname: Wang fullname: Wang, Li – sequence: 2 givenname: Suleiman A. surname: Haruna fullname: Haruna, Suleiman A. – sequence: 3 givenname: Waqas surname: Ahmad fullname: Ahmad, Waqas – sequence: 4 givenname: Jizhong surname: Wu fullname: Wu, Jizhong – sequence: 5 givenname: Quansheng surname: Chen fullname: Chen, Quansheng email: qschen@ujs.edu.cn – sequence: 6 givenname: Qin surname: Ouyang fullname: Ouyang, Qin email: oyqyf@ujs.edu.cn |
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Keywords | Black phosphorus nanosheets Aptamer Fluorescence resonance energy transfer Pesticides Upconversion nanoparticles |
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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 |
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