Pesticide biosensors: trends and progresses.


Journal

Analytical and bioanalytical chemistry
ISSN: 1618-2650
Titre abrégé: Anal Bioanal Chem
Pays: Germany
ID NLM: 101134327

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 13 06 2023
accepted: 10 08 2023
revised: 08 08 2023
medline: 9 10 2023
pubmed: 5 9 2023
entrez: 5 9 2023
Statut: ppublish

Résumé

Pesticides, chemical substances extensively employed in agriculture to optimize crop yields, pose potential risks to human and environmental health. Consequently, regulatory frameworks are in place to restrict pesticide residue concentrations in water intended for human consumption. These regulations are implemented to safeguard consumer safety and mitigate any adverse effects on the environment and public health. Although gas chromatography- and liquid chromatography-mass spectrometry (GC-MS and LC-MS) are highly efficient techniques for pesticide quantification, their use is not suitable for real-time monitoring due to the need for sophisticated laboratory pretreatment of samples prior to analysis. Since they would enable analyte detection with selectivity and sensitivity without sample pretreatment, biosensors appear as a promising alternative. These consist of a bioreceptor allowing for specific recognition of the target and of a detection platform, which translates the biological interaction into a measurable signal. As early detection systems remain urgently needed to promptly alert and act in case of pollution, we review here the biosensors described in the literature for pesticide detection to advance their development for use in the field.

Identifiants

pubmed: 37668672
doi: 10.1007/s00216-023-04911-4
pii: 10.1007/s00216-023-04911-4
doi:

Substances chimiques

Pesticides 0
Pesticide Residues 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

5899-5924

Subventions

Organisme : Région Nouvelle Aquitaine
ID : CONV-2019-0227
Organisme : Communauté d'agglomération de Pau Béarn Pyrénées
ID : OPE-2020-0032
Organisme : Agence Nationale pour la Recherche
ID : OPE-2018-0020

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.

Références

Cooper J, Dobson H. The benefits of pesticides to mankind and the environment. Crop Prot. 2007;26:1337–48. https://doi.org/10.1016/j.cropro.2007.03.022 .
Koutros S, Lynch CF, Ma X, Lee WJ, Hoppin JA, Christensen CH, Andreotti G, Freeman LB, Rusiecki JA, Hou L, Sandler DP, Alavanja MCR. Heterocyclic aromatic amine pesticide use and human cancer risk: results from the U.S. Agricultural Health Study. Int J Cancer. 2009;124:1206–12. https://doi.org/10.1002/ijc.24020 .
pubmed: 19058219 pmcid: 2904521
Amr S, Dawson R, Saleh DA, Magder LS, St George DM, El-Daly M, Squibb K, Mikhail NN, Abdel-Hamid M, Khaled H, Loffredo CA. Pesticides, gene polymorphisms, and bladder cancer among Egyptian agricultural workers. Arch Environ Occup Health. 2015;70:19–26. https://doi.org/10.1080/19338244.2013.853646 .
pubmed: 24219772 pmcid: 4018465
Alavanja MCR, Dosemeci M, Samanic C, Lubin J, Lynch CF, Knott C, Barker J, Hoppin JA, Sandler DP, Coble J, Thomas K, Blair A. Pesticides and lung cancer risk in the agricultural health study cohort. Am J Epidemiol. 2004;160:876–85. https://doi.org/10.1093/aje/kwh290 .
pubmed: 15496540
Beane Freeman LE, Bonner MR, Blair A, Hoppin JA, Sandler DP, Lubin JH, Dosemeci M, Lynch CF, Knott C, Alavanja MCR. Cancer incidence among male pesticide applicators in the Agricultural health study cohort exposed to diazinon. Am J Epidemiol. 2005;162:1070–9. https://doi.org/10.1093/aje/kwi321 .
pubmed: 16236997
Kole RK, Banerjee H, Bhattacharyya A. Monitoring of market fish samples for endosulfan and hexachlorocyclohexane residues in and around calcutta. Bull Environ Contam Toxicol. 2001;67:554–9. https://doi.org/10.1007/s001280159 .
pubmed: 11779071
USGS Scientific Investigations Report 2009–5132: trends in pesticide concentrations in corn-belt streams, 1996–2006. https://pubs.usgs.gov/sir/2009/5132/ . Accessed 22 Oct 2021
(2023) S-métolachlore : vers l’interdiction des principaux usages pour préserver la qualité des eaux souterraines. In: Anses - Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail. https://www.anses.fr/fr/content/s-metolachlor-preserver-qualite-eaux . Accessed 18 Apr 2023
Vainio H, Heseltine E, Shuker L, McGregor D, Partensky C. Meeting report: Occupational exposures in insecticide application and some pesticides. Eur J Cancer Oncol. 1991;27:284–9. https://doi.org/10.1016/0277-5379(91)90517-H .
Lamy D. Barbezieux-Saint-Hilaire?: un chantier école pour prendre soin de l’eau potable. Sud Ouest.  2021. https://www.sudouest.fr/charente/barbezieux-saint-hilaire/barbezieux-saint-hilaire-un-chantier-ecole-pour-prendre-soin-de-l-eau-potable-6561742.php .
Haib J, Hofer I, Renaud J-M. Analysis of multiple pesticide residues in tobacco using pressurized liquid extraction, automated solid-phase extraction clean-up and gas chromatography–tandem mass spectrometry. J Chromatogr A. 2003;1020:173–87. https://doi.org/10.1016/j.chroma.2003.08.049 .
pubmed: 14661742
Lesueur C, Knittl P, Gartner M, Mentler A, Fuerhacker M. Analysis of 140 pesticides from conventional farming foodstuff samples after extraction with the modified QuECheRS method. Food Control. 2008;19:906–14. https://doi.org/10.1016/j.foodcont.2007.09.002 .
Gamón M, Lleó C, Ten A, Mocholí F. Multiresidue determination of pesticides in fruit and vegetables by gas chromatography/tandem mass spectrometry. J AOAC Int. 2001;84:1209–16. https://doi.org/10.1093/jaoac/84.4.1209 .
pubmed: 11501925
Pang G-F, Liu Y-M, Fan C-L, Zhang J-J, Cao Y-Z, Li X-M, Li Z-Y, Wu Y-P, Guo T-T. Simultaneous determination of 405 pesticide residues in grain by accelerated solvent extraction then gas chromatography-mass spectrometry or liquid chromatography-tandem mass spectrometry. Anal Bioanal Chem. 2006;384:1366–408. https://doi.org/10.1007/s00216-005-0237-9 .
pubmed: 16520938
Lehotay SJ, de Kok A, Hiemstra M, van Bodegraven P. Validation of a fast and easy method for the determination of residues from 229 pesticides in fruits and vegetables using gas and liquid chromatography and mass spectrometric detection. J AOAC Int. 2005;88:595–614. https://doi.org/10.1093/jaoac/88.2.595 .
pubmed: 15859089
Baruah S, Dutta J. Nanotechnology applications in pollution sensing and degradation in agriculture: a review. Environ Chem Lett. 2009;7:191–204. https://doi.org/10.1007/s10311-009-0228-8 .
Verma ML. Nanobiotechnology advances in enzymatic biosensors for the agri-food industry. Environ Chem Lett. 2017;15:555–60. https://doi.org/10.1007/s10311-017-0640-4 .
Verdian A. Apta-nanosensors for detection and quantitative determination of acetamiprid – a pesticide residue in food and environment. Talanta. 2018;176:456–64. https://doi.org/10.1016/j.talanta.2017.08.070 .
pubmed: 28917776
Hara TO, Singh B. Electrochemical biosensors for detection of pesticides and heavy metal toxicants in water: recent trends and progress. ACS EST Water. 2021;1:462–78. https://doi.org/10.1021/acsestwater.0c00125 .
Gong Z, Huang Y, Hu X, Zhang J, Chen Q, Chen H. Recent progress in electrochemical nano-biosensors for detection of pesticides and mycotoxins in foods. Biosensors. 2023;13:140. https://doi.org/10.3390/bios13010140 .
pubmed: 36671974 pmcid: 9856537
Electrochemical biosensors for detection of pesticides and heavy metal toxicants in water: recent trends and progress. https://pubs.acs.org/doi/epdf/10.1021/acsestwater.0c00125 . Accessed 26 Jul 2023
Ba Hashwan SS, Khir MHBM, Al-Douri Y, Ahmed AY. Recent progress in the development of biosensors for chemicals and pesticides detection. IEEE Access. 2020;8:82514–27. https://doi.org/10.1109/ACCESS.2020.2991380 .
Sharma SK, Sehgal N, Kumar A. Biomolecules for development of biosensors and their applications. Curr Appl Phys. 2003;3:307–16. https://doi.org/10.1016/S1567-1739(02)00219-5 .
Patel H, Rawtani D, Agrawal YK. A newly emerging trend of chitosan-based sensing platform for the organophosphate pesticide detection using acetylcholinesterase- a review. Trends Food Sci Technol. 2019;85:78–91. https://doi.org/10.1016/j.tifs.2019.01.007 .
Yan X, Li H, Su X. Review of optical sensors for pesticides. TrAC, Trends Anal Chem. 2018;103:1–20. https://doi.org/10.1016/j.trac.2018.03.004 .
Dalefield R. Veterinary toxicology for Australia and New Zealand. Elsevier. 2017;628. 
Simonian AL, Efremenko EN, Wild JR. Discriminative detection of neurotoxins in multi-component samples. Anal Chim Acta. 2001;444:179–86. https://doi.org/10.1016/S0003-2670(01)01099-6 .
Arduini F, Cinti S, Caratelli V, Amendola L, Palleschi G, Moscone D. Origami multiple paper-based electrochemical biosensors for pesticide detection. Biosens Bioelectron. 2019;126:346–54. https://doi.org/10.1016/j.bios.2018.10.014 .
pubmed: 30466052
de Lima F, Lucca BG, Barbosa AMJ, Ferreira VS, Moccelini SK, Franzoi AC, Vieira IC. Biosensor based on pequi polyphenol oxidase immobilized on chitosan crosslinked with cyanuric chloride for thiodicarb determination. Enzyme Microb Technol. 2010;47:153–8. https://doi.org/10.1016/j.enzmictec.2010.05.006 .
Kim G-Y, Kang M-S, Shim J, Moon S-H. Substrate-bound tyrosinase electrode using gold nanoparticles anchored to pyrroloquinoline quinone for a pesticide biosensor. Sens Actuators B Chem. 2008;133:1–4. https://doi.org/10.1016/j.snb.2008.01.055 .
Garcı́a Sánchez F, NavasDı́az A, Ramos Peinado MC, Belledone C. Free and sol–gel immobilized alkaline phosphatase-based biosensor for the determination of pesticides and inorganic compounds. Anal Chim Acta. 2003;484:45–51. https://doi.org/10.1016/S0003-2670(03)00310-6 .
Mazzei F, Botrè F, Montilla S, Pilloton R, Podestà E, Botrè C. Alkaline phosphatase inhibition based electrochemical sensors for the detection of pesticides. J Electroanal Chem. 2004;574:95–100. https://doi.org/10.1016/j.jelechem.2004.08.004 .
Moccelini SK, Vieira IC, de Lima F, Lucca BG, Barbosa AMJ, Ferreira VS. Determination of thiodicarb using a biosensor based on alfalfa sprout peroxidase immobilized in self-assembled monolayers. Talanta. 2010;82:164–70. https://doi.org/10.1016/j.talanta.2010.04.015 .
pubmed: 20685452
Mazzei F, Botrè F, Botrè C. Acid phosphatase/glucose oxidase-based biosensors for the determination of pesticides. Anal Chim Acta. 1996;336:67–75. https://doi.org/10.1016/S0003-2670(96)00378-9 .
Vaghela C, Kulkarni M, Haram S, Aiyer R, Karve M. A novel inhibition based biosensor using urease nanoconjugate entrapped biocomposite membrane for potentiometric glyphosate detection. Int J Biol Macromol. 2018;108:32–40. https://doi.org/10.1016/j.ijbiomac.2017.11.136 .
pubmed: 29174355
Berkal MA, Palas Q, Ricard E, Lartigau-Dagron C, Ronga L, Toulmé J-J, Parat C, Nardin C. Glyphosate-exonuclease interactions: reduced enzymatic activity as a route to glyphosate biosensing. Macromol Biosci. 2023: e2200508. https://doi.org/10.1002/mabi.202200508
Chauhan N, Pundir CS. An amperometric biosensor based on acetylcholinesterase immobilized onto iron oxide nanoparticles/multi-walled carbon nanotubes modified gold electrode for measurement of organophosphorus insecticides. Anal Chim Acta. 2011;701:66–74. https://doi.org/10.1016/j.aca.2011.06.014 .
pubmed: 21763810
Ma L, Zhou L, He Y, Wang L, Huang Z, Jiang Y, Gao J. Mesoporous bimetallic PtPd nanoflowers as a platform to enhance electrocatalytic activity of acetylcholinesterase for organophosphate pesticide detection. Electroanalysis. 2018;30:1801–10. https://doi.org/10.1002/elan.201700845 .
Gai P, Zhang S, Yu W, Li H, Li F. Light-driven self-powered biosensor for ultrasensitive organophosphate pesticide detection via integration of the conjugated polymer-sensitized CdS and enzyme inhibition strategy. J Mater Chem B. 2018;6:6842–7. https://doi.org/10.1039/C8TB02286K .
pubmed: 32254700
El-Moghazy AY, Amaly N, Istamboulie G, Nitin N, Sun G. A signal-on electrochemical aptasensor based on silanized cellulose nanofibers for rapid point-of-use detection of ochratoxin A. Microchim Acta. 2020;187:535. https://doi.org/10.1007/s00604-020-04509-y .
Long Q, Li H, Zhang Y, Yao S. Upconversion nanoparticle-based fluorescence resonance energy transfer assay for organophosphorus pesticides. Biosens Bioelectron. 2015;68:168–74. https://doi.org/10.1016/j.bios.2014.12.046 .
pubmed: 25569873
Luo D, Huang X, Liu B, Zou W, Wu Y. Facile colorimetric nanozyme sheet for the rapid detection of glyphosate in agricultural products based on inhibiting peroxidase-like catalytic activity of porous Co
pubmed: 33721998
Ma L, Zhou L, He Y, Wang L, Huang Z, Jiang Y, Gao J. Hierarchical nanocomposites with an N-doped carbon shell and bimetal core: Novel enzyme nanocarriers for electrochemical pesticide detection. Biosens Bioelectron. 2018;121:166–73. https://doi.org/10.1016/j.bios.2018.08.038 .
pubmed: 30218924
Goyal MR, Malik JA, Pandiselvam R. Enzyme Inactivation in Food Processing: Technologies, Materials, and Applications. CRC Press.  2023;568.
Wu J, Yang Q, Li Q, Li H, Li F. Two-dimensional MnO2 nanozyme-mediated homogeneous electrochemical detection of organophosphate pesticides without the interference of H2O2 and color. Anal Chem. 2021;93:4084–91. https://doi.org/10.1021/acs.analchem.0c05257 .
pubmed: 33588528
Borah H, Gogoi S, Kalita S, Puzari P. A broad spectrum amperometric pesticide biosensor based on glutathione S-transferase immobilized on graphene oxide-gelatin matrix. J Electroanal Chem. 2018;828:116–23. https://doi.org/10.1016/j.jelechem.2018.09.047 .
Zhao F, Yao Y, Li X, Lan L, Jiang C, Ping J. Metallic transition metal dichalcogenide nanosheets as an effective and biocompatible transducer for electrochemical detection of pesticide. Anal Chem. 2018;90:11658–64. https://doi.org/10.1021/acs.analchem.8b03250 .
pubmed: 30156095
Han Z, Chi C, Bai B, Liu G, Rao Q, Peng S, Liu H, Zhao Z, Zhang D, Wu A. Chromogenic platform based on recombinant Drosophila melanogaster acetylcholinesterase for visible unidirectional assay of organophosphate and carbamate insecticide residues. Anal Chim Acta. 2012;720:126–33. https://doi.org/10.1016/j.aca.2012.01.041 .
pubmed: 22365130
Matějovský L, Pitschmann V. New carrier made from glass nanofibres for the colorimetric biosensor of cholinesterase inhibitors. Biosensors. 2018;8:51. https://doi.org/10.3390/bios8020051 .
pubmed: 29848955 pmcid: 6023030
Li H, Zhao S, Wang Z, Li F. Controllable preparation of 2D V2O5 peroxidase-mimetic nanozyme to develop portable paper-based analytical device for intelligent pesticide assay. Small. 2023;19:2206465. https://doi.org/10.1002/smll.202206465 .
Gai P, Pu L, Wang C, Zhu D, Li F. CeO2@NC nanozyme with robust dephosphorylation ability of phosphotriester: a simple colorimetric assay for rapid and selective detection of paraoxon. Biosens Bioelectron. 2023;220:114841. https://doi.org/10.1016/j.bios.2022.114841 .
pubmed: 36323162
Liu G, Guo W, Song D. A multianalyte electrochemical immunosensor based on patterned carbon nanotubes modified substrates for detection of pesticides. Biosens Bioelectron. 2014;52:360–6. https://doi.org/10.1016/j.bios.2013.09.009 .
pubmed: 24084164
Li S, Li MQ, Jia Fu W, Xue Qin R, Xi N. Acetylcholinesterase based rGO-TEPA-copper nanowires biosensor for detecting malathion. Int J Electrochem. 2020: Sci 505–514. https://doi.org/10.20964/2020.01.75
Cheng Y, Lai O-M, Tan C-P, Panpipat W, Cheong L-Z, Shen C. Proline-modified UIO-66 as nanocarriers to enhance Candida rugosa lipase catalytic activity and stability for electrochemical detection of nitrofen. ACS Appl Mater Interfaces. 2021;13:4146–55. https://doi.org/10.1021/acsami.0c17134 .
pubmed: 33440928
Yang G, He Y, Zhao J, Chen S, Yuan R. Ratiometric electrochemiluminescence biosensor based on Ir nanorods and CdS quantum dots for the detection of organophosphorus pesticides. Sensors and Actuators B: Chemical. 2021;341:130008. https://doi.org/10.1016/j.snb.2021.130008 .
Li X, Gao X, Gai P, Liu X, Li F. Degradable metal-organic framework/methylene blue composites-based homogeneous electrochemical strategy for pesticide assay. Sensors Actuators B Chem. 2020;323:128701. https://doi.org/10.1016/j.snb.2020.128701 .
Key Lab of Modern Precision Agriculture System Integration Research and Key Lab of Agricultural Information Acquisition Technology Ministry of Education, China Agricultural University, Beijing 100083 P.R. China, Wang H. A sensitive acetylcholinesterase biosensor based on screen printed electrode modified with Fe3O4 nanoparticle and graphene for chlorpyrifos determination. Int J Electrochem Sci. 2016: 10906–10918. https://doi.org/10.20964/2016.12.90 .
Chen D, Jiayun F, Zengning L, Yemin G, Xia S, Xiangyou W, Zhiqiang W. A simple acetylcholinesterase biosensor based on ionic liquid/multiwalled carbon nanotubes-modified screen- printed electrode for rapid detecting chlorpyrifos. Int J Electrochem Sci. 2017:9465–9477. https://doi.org/10.20964/2017.10.12 .
Jiang B, Lu M, Xu M. Amperometric sensing of organophosphorus pesticides based on covalently attached multilayer assemblies of diazo-resin, Prussian blue single-walled carbon nanotubes, and acetylcholinesterase. RevRoumChim. 2019;64:763–74. https://doi.org/10.33224/rrch/2019.64.9.3 .
Cui H-F, Zhang T-T, Lv Q-Y, Song X, Zhai X-J, Wang G-G. An acetylcholinesterase biosensor based on doping Au nanorod@SiO2 nanoparticles into TiO2-chitosan hydrogel for detection of organophosphate pesticides. Biosens Bioelectron. 2019;141:111452. https://doi.org/10.1016/j.bios.2019.111452 .
pubmed: 31252259
Bilal S, Mudassir Hassan M, FayyazurRehman M, Nasir M, Jamil Sami A, Hayat A. An insect acetylcholinesterase biosensor utilizing WO3/g-C3N4 nanocomposite modified pencil graphite electrode for phosmet detection in stored grains. Food Chem. 2021;346:128894. https://doi.org/10.1016/j.foodchem.2020.128894 .
pubmed: 33422918
Zhao G, Zhou B, Wang X, Shen J, Zhao B. Detection of organophosphorus pesticides by nanogold/mercaptomethamidophos multi-residue electrochemical biosensor. Food Chem. 2021;354:129511. https://doi.org/10.1016/j.foodchem.2021.129511 .
pubmed: 33735695
Jia L, Zhou Y, Wu K, Feng Q, Wang C, He P. Acetylcholinesterase modified AuNPs-MoS2-rGO/PI flexible film biosensor: towards efficient fabrication and application in paraoxon detection. Bioelectrochemistry. 2020;131:107392. https://doi.org/10.1016/j.bioelechem.2019.107392 .
pubmed: 31707277
Chen G, Jin M, Ma J, Yan M, Cui X, Wang Y, Zhang X, Li H, Zheng W, Zhang Y, Abd El-Aty AM, Hacımüftüoğlu A, Wang J. Competitive bio-barcode immunoassay for highly sensitive detection of parathion based on bimetallic nanozyme catalysis. J Agric Food Chem. 2020;68:660–8. https://doi.org/10.1021/acs.jafc.9b06125 .
pubmed: 31804828
Korram J, Dewangan L, Karbhal I, Nagwanshi R, Vaishanav SK, Ghosh KK, Satnami ML. CdTe QD-based inhibition and reactivation assay of acetylcholinesterase for the detection of organophosphorus pesticides. RSC Adv. 2020;10:24190–202. https://doi.org/10.1039/d0ra03055d .
pubmed: 35516221 pmcid: 9055098
Apilux A, Siangproh W, Insin N, Chailapakul O, Prachayasittikul V. Paper-based thioglycolic acid (TGA)-capped CdTe QD device for rapid screening of organophosphorus and carbamate insecticides. Anal Methods. 2017;9:519–27. https://doi.org/10.1039/C6AY02883G .
Sharma D, Wangoo N, Sharma RK. Sensing platform for pico-molar level detection of ethyl parathion using Au–Ag nanoclusters based enzymatic strategy. Talanta. 2021;221:121267. https://doi.org/10.1016/j.talanta.2020.121267 .
pubmed: 33076046
Luo Q, Yu F, Yang F, Yang C, Qiu P, Wang X. A 3D-printed self-propelled, highly sensitive mini-motor for underwater pesticide detection. Talanta. 2018;183:297–303. https://doi.org/10.1016/j.talanta.2018.02.059 .
pubmed: 29567179
Chang J, Yu L, Hou T, Hu R, Li F. Direct and specific detection of glyphosate using a phosphatase-like nanozyme-mediated chemiluminescence strategy. Anal Chem. 2023;95:4479–85. https://doi.org/10.1021/acs.analchem.2c05198 .
pubmed: 36802539
Kröger S, Setford SJ, Turner APF. Immunosensor for 2,4-dichlorophenoxyacetic acid in aqueous/organic solvent soil extracts. Anal Chem. 1998;70:5047–53. https://doi.org/10.1021/ac9805100 .
pubmed: 9852786
Skládal P, Kaláb T. A multichannel immunochemical sensor for determination of 2,4-dichlorophenoxyacetic acid. Anal Chim Acta. 1995;316:73–8. https://doi.org/10.1016/0003-2670(95)00342-W .
Kaláb T, Skládal P. A disposable amperometric immunosensor for 2,4-dichlorophenoxyacetic acid. Anal Chim Acta. 1995;304:361–8. https://doi.org/10.1016/0003-2670(94)00641-X .
Bier FF, Ehrentreich-Förster E, Dölling R, Eremenko AV, Scheller FW. A redox-label immunosensor on basis of a bi-enzyme electrode. Anal Chim Acta. 1997;344:119–24. https://doi.org/10.1016/S0003-2670(97)00050-0 .
Audrey S, Beatriz P-S, Jean-Louis M. Biosensors for pesticide detection: new trends. Am J Anal Chem. 2012:2012. https://doi.org/10.4236/ajac.2012.33030 .
Reynoso EC, Torres E, Bettazzi F, Palchetti I. Trends and perspectives in immunosensors for determination of currently-used pesticides: the case of glyphosate, organophosphates, and neonicotinoids. Biosensors. 2019;9:20. https://doi.org/10.3390/bios9010020 .
pubmed: 30720729 pmcid: 6468886
Hongsibsong S, Wipasa J, Pattarawarapan M, Chantara S, Stuetz W, Nosten F, Prapamontol T. Development and application of an indirect competitive enzyme-linked immunosorbent assay for the detection of p, p ′-DDE in human milk and comparison of the results against GC-ECD. J Agric Food Chem. 2012;60:16–22. https://doi.org/10.1021/jf203440b .
pubmed: 22122759
Liu J, Song S, Wu A, Kuang H, Liu L, Xiao J, Xu C. Development of immunochromatographic strips for the detection of dicofol. Analyst. 2021;146:2240–7. https://doi.org/10.1039/D0AN02238A .
pubmed: 33596275
Qiu X, Zhu T, Yao B, Hu J, Hu S. Contribution of dicofol to the current DDT pollution in China. Environ Sci Technol. 2005;39:4385–90. https://doi.org/10.1021/es050342a .
pubmed: 16047771
Lee HU, Shin HY, Lee JY, Song YS, Park C, Kim SW. Quantitative detection of glyphosate by simultaneous analysis of uv spectroscopy and fluorescence using DNA-labeled gold nanoparticles. J Agric Food Chem. 2010;58:12096–100. https://doi.org/10.1021/jf102784t .
pubmed: 21047070
Guo Y, Liu R, Liu Y, Xiang D, Liu Y, Gui W, Li M, Zhu G. A non-competitive surface plasmon resonance immunosensor for rapid detection of triazophos residue in environmental and agricultural samples. Sci Total Environ. 2018;613–614:783–91. https://doi.org/10.1016/j.scitotenv.2017.09.157 .
pubmed: 28946376
Mehta J, Vinayak P, Tuteja SK, Chhabra VA, Bhardwaj N, Paul AK, Kim K-H, Deep A. Graphene modified screen printed immunosensor for highly sensitive detection of parathion. Biosens Bioelectron. 2016;83:339–46. https://doi.org/10.1016/j.bios.2016.04.058 .
pubmed: 27135939
González-Martínez MÁ, Brun EM, Puchades R, Maquieira Á, Ramsey K, Rubio F. Glyphosate immunosensor. Application for Water and Soil Analysis. Anal Chem. 2005;77:4219–27. https://doi.org/10.1021/ac048431d .
pubmed: 15987130
European Parliament COUNCIL DIRECTIVE 98/83/EC, Official Journal. Council Directive 98/83/EC on the quality of water intended for human consumption.  2015. Accessed 14 Nov 2022. https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:01998L0083-20151027&from=EN .
Koukouvinos G, Τsialla Z, Petrou PS, Misiakos K, Goustouridis D, Ucles Moreno A, Fernandez-Alba AR, Raptis I, Kakabakos SE. Fast simultaneous detection of three pesticides by a white light reflectance spectroscopy sensing platform. Sens Actuators B Chem. 2017;238:1214–23. https://doi.org/10.1016/j.snb.2016.09.035 .
Riedel T, Majek P, Rodriguez-Emmenegger C, Brynda E. Surface plasmon resonance: advances of label-free approaches in the analysis of biological samples. Bioanalysis. 2014;6:3325–36. https://doi.org/10.4155/bio.14.246 .
pubmed: 25534789
Scarano S, Mascini M, Turner APF, Minunni M. Surface plasmon resonance imaging for affinity-based biosensors. Biosens Bioelectron. 2010;25:957–66. https://doi.org/10.1016/j.bios.2009.08.039 .
pubmed: 19765967
Gouzy M-F, Keß M, Krämer PM. A SPR-based immunosensor for the detection of isoproturon. Biosens Bioelectron. 2009;24:1563–8. https://doi.org/10.1016/j.bios.2008.08.005 .
pubmed: 18799300
Yakes BJ, Kanyuck KM, DeGrasse SL. First report of a direct surface plasmon resonance immunosensor for a small molecule seafood toxin. Anal Chem. 2014;86:9251–5. https://doi.org/10.1021/ac502271y .
pubmed: 25117539
Munoz EM, Lorenzo-Abalde S, González-Fernández Á, Quintela O, Lopez-Rivadulla M, Riguera R. Direct surface plasmon resonance immunosensor for in situ detection of benzoylecgonine, the major cocaine metabolite. Biosens Bioelectron. 2011;26:4423–8. https://doi.org/10.1016/j.bios.2011.04.056 .
pubmed: 21664118
Wijaya IPM, Ju Nie T, Gandhi S, Boro R, Palaniappan A, Wei Hau G, Rodriguez I, Raman Suri C, Mhaisalkar SG. Femtomolar detection of 2,4-dichlorophenoxyacetic acid herbicides via competitive immunoassays using microfluidic based carbon nanotube liquid gated transistor. Lab Chip. 2010;10:634–8. https://doi.org/10.1039/B918566F .
pubmed: 20162239
Sharma P, Gandhi S, Chopra A, Sekar N, Raman Suri C. Fluoroimmunoassay based on suppression of fluorescence self-quenching for ultra-sensitive detection of herbicide diuron. Anal Chim Acta. 2010;676:87–92. https://doi.org/10.1016/j.aca.2010.07.042 .
pubmed: 20800747
Jiao Y, Jia H, Guo Y, Zhang H, Wang Z, Sun X, Zhao J. An ultrasensitive aptasensor for chlorpyrifos based on ordered mesoporous carbon/ferrocene hybrid multiwalled carbon nanotubes. RSC Adv. 2016;6:58541–8. https://doi.org/10.1039/c6ra07735h .
Talan A, Mishra A, Eremin SA, Narang J, Kumar A, Gandhi S. Ultrasensitive electrochemical immuno-sensing platform based on gold nanoparticles triggering chlorpyrifos detection in fruits and vegetables. Biosens Bioelectron. 2018;105:14–21. https://doi.org/10.1016/j.bios.2018.01.013 .
pubmed: 29346076
Bettazzi F, Romero Natale A, Torres E, Palchetti I. Glyphosate determination by coupling an immuno-magnetic assay with electrochemical sensors. Sensors. 2018;18:2965. https://doi.org/10.3390/s18092965 .
pubmed: 30200562 pmcid: 6164882
Jiao S, Liu P, Liu Y, Zou R, Zhao Y, Liu Y, Zhu G, Guo Y. Binding properties of broad-specific monoclonal antibodies against three organophosphorus pesticides by a direct surface plasmon resonance immunosensor. Anal Bioanal Chem. 2018;410:7263–73. https://doi.org/10.1007/s00216-018-1337-7 .
pubmed: 30209512
Cheng N, Shi Q, Zhu C, Li S, Lin Y, Du D. Pt-Ni(OH)2 nanosheets amplified two-way lateral flow immunoassays with smartphone readout for quantification of pesticides. Biosens Bioelectron. 2019;142:111498. https://doi.org/10.1016/j.bios.2019.111498 .
pubmed: 31319328
Hou L, Zhang X, Kong M, Jiang G, Sun Y, Mo W, Lin T, Ye F, Zhao S. A competitive immunoassay for electrochemical impedimetric determination of chlorpyrifos using a nanogold-modified glassy carbon electrode based on enzymatic biocatalytic precipitation. Mikrochim Acta. 2020;187:204. https://doi.org/10.1007/s00604-020-4175-1 .
pubmed: 32146610
Kaur N, Bhatnagar A, Bhalla A, Prabhakar N. Determination of an organophosphate pesticide using antibody immobilised hybrid nanocomposites. Int J Environ Anal Chem. 2021;101:1485–98. https://doi.org/10.1080/03067319.2019.1685665 .
Valera E, García-Febrero R, Pividori I, Sánchez-Baeza F, Marco M-P. Coulombimetric immunosensor for paraquat based on electrochemical nanoprobes. Sens Actuators B Chem. 2014;194:353–60. https://doi.org/10.1016/j.snb.2013.12.029 .
Cui L, Wu J, Ju H. Label-free signal-on aptasensor for sensitive electrochemical detection of arsenite. Biosens Bioelectron. 2016;79:861–5. https://doi.org/10.1016/j.bios.2016.01.010 .
pubmed: 26785310
Verdian-Doghaei A, Housaindokht MR, Abnous Kh. A fluorescent aptasensor for potassium ion detection-based triple-helix molecular switch. Anal Biochem. 2014;466:72–5. https://doi.org/10.1016/j.ab.2014.08.014 .
pubmed: 25173515
Ran G, Wu F, Ni X, Li X, Li X, Liu D, Sun J, Xie C, Yao D, Bai W. A novel label-free electrochemical aptasensor with one-step assembly process for rapid detection of lead (II) ions. Sens Actuators B Chem. 2020;320:128326. https://doi.org/10.1016/j.snb.2020.128326 .
Xiao Y, Lubin AA, Heeger AJ, Plaxco KW. Label-free electronic detection of thrombin in blood serum by using an aptamer-based sensor. Angew Chem. 2005;117:5592–5. https://doi.org/10.1002/ange.200500989 .
Huizenga DE, Szostak JW. A DNA aptamer that binds adenosine and ATP. Biochemistry. 1995;34:656–65.
pubmed: 7819261
Qi X, Yan X, Zhao L, Huang Y, Wang S, Liang X. A facile label-free electrochemical aptasensor constructed with nanotetrahedron and aptamer-triplex for sensitive detection of small molecule: Saxitoxin. J Electroanal Chem. 2020;858:113805. https://doi.org/10.1016/j.jelechem.2019.113805 .
Li W, Luo Y, Gao T, Yang L, Wang J, Pei R. in vitro selection of DNA aptamers for a small-molecule porphyrin by gold nanoparticle-based SELEX. J Mol Evol. 2019;87:231–9. https://doi.org/10.1007/s00239-019-09905-4 .
pubmed: 31432230
Kaur H. Aptamer conjugated quantum dots for imaging cellular uptake in cancer cells. J Nanosci Nanotechnol. 2019;19:3798–803. https://doi.org/10.1166/jnn.2019.16735 .
pubmed: 30764936
Wang Q, Luo B, Yang X, Wang K, Liu L, Du S, Li Z. Elucidation of the effect of aptamer immobilization strategies on the interaction between cell and its aptamer using atomic force spectroscopy. J Mol Recognit. 2016;29:151–8. https://doi.org/10.1002/jmr.2514 .
pubmed: 26530526
Zhang Y, Lai BS, Juhas M. Recent advances in aptamer discovery and applications. Molecules. 2019;24:941. https://doi.org/10.3390/molecules24050941 .
pubmed: 30866536 pmcid: 6429292
McKeague M, DeRosa MC. Challenges and opportunities for small molecule aptamer development. J Nucleic Acids. 2012;2012:e748913. https://doi.org/10.1155/2012/748913 .
Stoltenburg R, Reinemann C, Strehlitz B. FluMag-SELEX as an advantageous method for DNA aptamer selection. Anal Bioanal Chem. 2005;383:83–91. https://doi.org/10.1007/s00216-005-3388-9 .
pubmed: 16052344
Spiga FM, Maietta P, Guiducci C. More DNA–aptamers for small drugs: a capture–SELEX coupled with surface plasmon resonance and high-throughput sequencing. ACS Comb Sci. 2015;17:326–33. https://doi.org/10.1021/acscombsci.5b00023 .
pubmed: 25875077
Xie M, Zhao F, Zhang Y, Xiong Y, Han S. Recent advances in aptamer-based optical and electrochemical biosensors for detection of pesticides and veterinary drugs. Food Control. 2022;131:108399. https://doi.org/10.1016/j.foodcont.2021.108399 .
Bala R, Kumar M, Bansal K, Sharma RK, Wangoo N. Ultrasensitive aptamer biosensor for malathion detection based on cationic polymer and gold nanoparticles. Biosens Bioelectron. 2016;85:445–9. https://doi.org/10.1016/j.bios.2016.05.042 .
pubmed: 27208476
Bai W, Zhu C, Liu J, Yan M, Yang S, Chen A. Gold nanoparticle–based colorimetric aptasensor for rapid detection of six organophosphorous pesticides. Environ Toxicol Chem. 2015;34:2244–9. https://doi.org/10.1002/etc.3088 .
pubmed: 26031388
Yang K-A, Pei R, Stojanovic MN. In vitro selection and amplification protocols for isolation of aptameric sensors for small molecules. Methods. 2016;106:58–65. https://doi.org/10.1016/j.ymeth.2016.04.032 .
pubmed: 27155227 pmcid: 4981533
Wang H-B, Li Y, Bai H-Y, Liu Y-M. DNA-templated Au nanoclusters and MnO2 sheets: a label-free and universal fluorescence biosensing platform. Sens Actuators B Chem. 2018;259:204–10. https://doi.org/10.1016/j.snb.2017.12.048 .
Xiong Z, Wang Q, Xie Y, Li N, Yun W, Yang L. Simultaneous detection of aflatoxin B1 and ochratoxin A in food samples by dual DNA tweezers nanomachine. Food Chem. 2021;338:128122. https://doi.org/10.1016/j.foodchem.2020.128122 .
pubmed: 33091999
Li Y, Zhang N, Wang H, Zhao Q. Fluorescence anisotropy-based signal-off and signal-on aptamer assays using lissamine rhodamine b as a label for ochratoxin A. J Agric Food Chem. 2020;68:4277–83. https://doi.org/10.1021/acs.jafc.0c00549 .
pubmed: 32182058
Zhu X, Xu H, Li W, Dong Y, Chi Y. A novel hybrid platform of g-C3N4 nanosheets /nucleic-acid-stabilized silver nanoclusters for sensing protein. Anal Chim Acta. 2019;1091:112–8. https://doi.org/10.1016/j.aca.2019.09.030 .
pubmed: 31679564
Yin N, Yuan S, Zhang M, Wang J, Li Y, Peng Y, Bai J, Ning B, Liang J, Gao Z. An aptamer-based fluorometric zearalenone assay using a lighting-up silver nanocluster probe and catalyzed by a hairpin assembly. Microchim Acta. 2019;186:765. https://doi.org/10.1007/s00604-019-3984-6 .
Su L, Wang S, Wang L, Yan Z, Yi H, Zhang D, Shen G, Ma Y. Fluorescent aptasensor for carbendazim detection in aqueous samples based on gold nanoparticles quenching Rhodamine B. Spectrochim Acta A Mol Biomol Spectrosc. 2020;225:117511. https://doi.org/10.1016/j.saa.2019.117511 .
pubmed: 31513979
Zhu K, Lv T, Qin T, Huang Y, Wang L, Liu B. A flavonoid-based fluorescent probe enables the accurate quantification of human serum albumin by minimizing the interference from blood lipids. Chem Commun. 2019;55:13983–6. https://doi.org/10.1039/C9CC08015E .
Wang W, Vellaisamy K, Li G, Wu C, Ko C-N, Leung C-H, Ma D-L. Development of a long-lived luminescence probe for visualizing β-galactosidase in ovarian carcinoma cells. Anal Chem. 2017;89:11679–84. https://doi.org/10.1021/acs.analchem.7b03114 .
pubmed: 28969424
Ko C-N, Yang C, Lin S, Li S, Dong Z, Liu J, Lee SM-Y, Leung C-H, Ma D-L. A long-lived phosphorescence iridium(III) complex as a switch on-off-on probe for live zebrafish monitoring of endogenous sulfide generation. Biosens Bioelectron. 2017;94:575–83. https://doi.org/10.1016/j.bios.2017.03.050 .
pubmed: 28364704
Li G, Adam Henry S, Liu H, Kang T-S, Nao S-C, Zhao Y, Wu C, Jin J, Zhang J-T, Leung C-H, Chan PWH, Ma D-L. A robust photoluminescence screening assay identifies uracil-DNA glycosylase inhibitors against prostate cancer. Chem Sci. 2020;11:1750–60. https://doi.org/10.1039/C9SC05623H .
pubmed: 34123270 pmcid: 8148385
Lagarto J, Dyer BT, Talbot C, Sikkel MB, Peters NS, French PMW, Lyon AR, Dunsby C. Application of time-resolved autofluorescence to label-free in vivo optical mapping of changes in tissue matrix and metabolism associated with myocardial infarction and heart failure. Biomed Opt Express BOE. 2015;6:324–46. https://doi.org/10.1364/BOE.6.000324 .
pubmed: 25780727
Ma D-L, Wang M, He B, Yang C, Wang W, Leung C-H. A Luminescent cocaine detection platform using a split g-quadruplex-selective iridium(III) complex and a three-way DNA junction architecture. ACS Appl Mater Interfaces. 2015;7:19060–7. https://doi.org/10.1021/acsami.5b05861 .
pubmed: 26284502
Chen F, Li G, Liu H, Leung C-H, Ma D-L. G-quadruplex-based detection of glyphosate in complex biological systems by a time-resolved luminescent assay. Sens Actuators B Chem. 2020;320:128393. https://doi.org/10.1016/j.snb.2020.128393 .
Wang R-H, Zhu C-L, Wang L-L, Xu L-Z, Wang W-L, Yang C, Zhang Y. Dual-modal aptasensor for the detection of isocarbophos in vegetables. Talanta. 2019;205:120094. https://doi.org/10.1016/j.talanta.2019.06.094 .
pubmed: 31450466
Hossain MK, Kitahama Y, Huang GG, Han X, Ozaki Y. Surface-enhanced Raman scattering: realization of localized surface plasmon resonance using unique substrates and methods. Anal Bioanal Chem. 2009;394:1747–60. https://doi.org/10.1007/s00216-009-2762-4 .
pubmed: 19384546
Yu J, Ma Y, Yang C, Zhang H, Liu L, Su J, Gao Y. SERS-active composite based on rGO and Au/Ag core-shell nanorods for analytical applications. Sens Actuators B Chem. 2018;254:182–8. https://doi.org/10.1016/j.snb.2017.07.034 .
Liu Y, Li R, Zhou N, Li M, Huang C, Mao H. Recyclable 3D SERS devices based on ZnO nanorod-grafted nanowire forests for biochemical sensing. Appl Surface Sci. 2022;582:152336. https://doi.org/10.1016/j.apsusc.2021.152336 .
Song D, Yang R, Long F, Zhu A. Applications of magnetic nanoparticles in surface-enhanced Raman scattering (SERS) detection of environmental pollutants. J Environ Sci. 2019;80:14–34. https://doi.org/10.1016/j.jes.2018.07.004 .
Botta R, Eiamchai P, Horprathum M, Limwichean S, Chananonnawathorn C, Patthanasettakul V, Maezono R, Jomphoak A, Nuntawong N. 3D structured laser engraves decorated with gold nanoparticle SERS chips for paraquat herbicide detection in environments. Sens Actuators B Chem. 2020;304:127327. https://doi.org/10.1016/j.snb.2019.127327 .
Pang S, Yang T, He L. Review of surface enhanced Raman spectroscopic (SERS) detection of synthetic chemical pesticides. TrAC, Trends Anal Chem. 2016;85:73–82. https://doi.org/10.1016/j.trac.2016.06.017 .
Bernat A, Samiwala M, Albo J, Jiang X, Rao Q. Challenges in SERS-based pesticide detection and plausible solutions. J Agric Food Chem. 2019;67:12341–7. https://doi.org/10.1021/acs.jafc.9b05077 .
pubmed: 31635458
Albarghouthi N, Eisnor MM, Pye CC, Brosseau CL. Electrochemical surface-enhanced raman spectroscopy (EC-SERS) and computational study of atrazine: toward point-of-need detection of prevalent herbicides. J Phys Chem C. 2022;126:9836–42. https://doi.org/10.1021/acs.jpcc.2c02337 .
Kamkrua N, Ngernsutivorakul T, Limwichean S, Eiamchai P, Chananonnawathorn C, Pattanasetthakul V, Ricco R, Choowongkomon K, Horprathum M, Nuntawong N, Bora T, Botta R. Au Nanoparticle-based surface-enhanced raman spectroscopy aptasensors for paraquat herbicide detection. ACS Appl Nano Mater. 2023;6:1072–82. https://doi.org/10.1021/acsanm.2c04556 .
Yuan R, Li H-K, He H. Recent advances in metal/covalent organic framework-based electrochemical aptasensors for biosensing applications. Dalton Trans. 2021;50:14091–104. https://doi.org/10.1039/D1DT02360H .
pubmed: 34609402
Nutiu R, Li Y. In vitro selection of structure-switching signaling aptamers. Angew Chem Int Ed. 2005;44:1061–5.
Madianos L, Skotadis E, Tsekenis G, Patsiouras L, Tsigkourakos M, Tsoukalas D. Ιmpedimetric nanoparticle aptasensor for selective and label free pesticide detection. Microelectron Eng. 2018;189:39–45. https://doi.org/10.1016/j.mee.2017.12.016 .
Madianos L, Tsekenis G, Skotadis E, Patsiouras L, Tsoukalas D. A highly sensitive impedimetric aptasensor for the selective detection of acetamiprid and atrazine based on microwires formed by platinum nanoparticles. Biosens Bioelectron. 2018;101:268–74. https://doi.org/10.1016/j.bios.2017.10.034 .
pubmed: 29096365
Fan L, Zhang C, Liang G, Yan W, Guo Y, Bi Y, Dong C. Highly sensitive photoelectrochemical aptasensor based on MoS2 quantum dots/TiO2 nanotubes for detection of atrazine. Sens Actuators B Chem. 2021;334:129652. https://doi.org/10.1016/j.snb.2021.129652 .
Li S, Li J, Luo J, Xu Z, Ma X. A microfluidic chip containing a molecularly imprinted polymer and a DNA aptamer for voltammetric determination of carbofuran. Microchim Acta. 2018;185:295. https://doi.org/10.1007/s00604-018-2835-1 .
Xu G, Huo D, Hou C, Zhao Y, Bao J, Yang M, Fa H. A regenerative and selective electrochemical aptasensor based on copper oxide nanoflowers-single walled carbon nanotubes nanocomposite for chlorpyrifos detection. Talanta. 2018;178:1046–52. https://doi.org/10.1016/j.talanta.2017.08.086 .
pubmed: 29136795
Zhu Q-Q, Li H-K, Sun X-L, Han Z-Y, Sun J, He H. Rational incorporation of covalent organic framework/carbon nanotube (COF/CNT) composites for electrochemical aptasensing of ultra-trace atrazine. J Mater Chem C. 2021;9:8043–50. https://doi.org/10.1039/D1TC01506K .
Sun C, Liu M, Sun H, Lu H, Zhao G. Immobilization-free photoelectrochemical aptasensor for environmental pollutants: design, fabrication and mechanism. Biosens Bioelectron. 2019;140:111352. https://doi.org/10.1016/j.bios.2019.111352 .
pubmed: 31163397
Fan L, Zhang C, Yan W, Guo Y, Shuang S, Dong C, Bi Y. Design of a facile and label-free electrochemical aptasensor for detection of atrazine. Talanta. 2019;201:156–64. https://doi.org/10.1016/j.talanta.2019.03.114 .
pubmed: 31122406
Wang Y, Sun H, Liu M, Lu H, Zhao G. A novel self-powered aptasensor for environmental pollutants detection based on simple and efficient enzymatic biofuel cell. Sens Actuators B Chem. 2020;305:127468. https://doi.org/10.1016/j.snb.2019.127468 .
Sun H, Sun C, Ding X, Lu H, Liu M, Zhao G. In situ monitoring of the selective adsorption mechanism of small environmental pollutant molecules on aptasensor interface by attenuated total reflection surface enhanced infrared absorption spectroscopy (ATR–SEIRAS). J Hazard Mater. 2021;403:123953. https://doi.org/10.1016/j.jhazmat.2020.123953 .
pubmed: 33264997
Romero-Reyes MA, Heemstra JM. Sequestration and removal of multiple small-molecule contaminants using an optimized aptamer-based ultrafiltration system. Bioconjugate Chem. 2021;32:2043–51. https://doi.org/10.1021/acs.bioconjchem.1c00344 .
 Yao Z, Yao Z, Jia X, Ren S, Yang S, Gao Z. Suspension array platform based on aptamer for high-throughput detection of five environmental hormones. Research Square. 2021. https://doi.org/10.21203/rs.3.rs-1089406/v1 .
Wei X, Sun Y, Liu C, Li Z, Zou X, Zhang D, Zhang W, Shi J, Huang X, Li Y. A nitrile-mediated SERS aptasensor coupled with magnetic separation for optical interference-free detection of atrazine. Sens Actuators B Chem. 2021;329:129075. https://doi.org/10.1016/j.snb.2020.129075 .
Abnous K, Danesh NM, Ramezani M, Emrani AS, Taghdisi SM. A novel colorimetric sandwich aptasensor based on an indirect competitive enzyme-free method for ultrasensitive detection of chloramphenicol. Biosens Bioelectron. 2016;78:80–6. https://doi.org/10.1016/j.bios.2015.11.028 .
pubmed: 26599477
Weerathunge P, Behera BK, Zihara S, Singh M, Prasad SN, Hashmi S, Mariathomas PRD, Bansal V, Ramanathan R. Dynamic interactions between peroxidase-mimic silver nanozymes and chlorpyrifos-specific aptamers enable highly-specific pesticide sensing in river water. Anal Chim Acta. 2019;1083:157–65. https://doi.org/10.1016/j.aca.2019.07.066 .
pubmed: 31493806
Cheng N, Song Y, Fu Q, Du D, Luo Y, Wang Y, Xu W, Lin Y. Aptasensor based on fluorophore-quencher nano-pair and smartphone spectrum reader for on-site quantification of multi-pesticides. Biosens Bioelectron. 2018;117:75–83. https://doi.org/10.1016/j.bios.2018.06.002 .
pubmed: 29886189 pmcid: 8672368
Rong Y, Li H, Ouyang Q, Ali S, Chen Q. Rapid and sensitive detection of diazinon in food based on the FRET between rare-earth doped upconversion nanoparticles and graphene oxide. Spectrochim Acta A Mol Biomol Spectrosc. 2020;239:118500. https://doi.org/10.1016/j.saa.2020.118500 .
pubmed: 32470816
Liu Q, Zhang R, Yu B, Liang A, Jiang Z. A highly sensitive gold nanosol SERS aptamer assay for glyphosate with a new COF nanocatalytic reaction of glycol-Au(III). Sens Actuators B Chem. 2021;344:130288. https://doi.org/10.1016/j.snb.2021.130288 .
Jiang M, Chen C, He J, Zhang H, Xu Z. Fluorescence assay for three organophosphorus pesticides in agricultural products based on magnetic-assisted fluorescence labeling aptamer probe. Food Chem. 2020;307:125534-.
Li X, Tang X, Chen X, Qu B, Lu L. Label-free and enzyme-free fluorescent isocarbophos aptasensor based on MWCNTs and G-quadruplex. Talanta. 2018;188:232–7. https://doi.org/10.1016/j.talanta.2018.05.092 .
pubmed: 30029369
Liu D-L, Li Y, Sun R, Xu J-Y, Chen Y, Sun C-Y. Colorimetric detection of organophosphorus pesticides based on the broad-spectrum aptamer. J Nanosci Nanotechnol. 2020;20:2114–21. https://doi.org/10.1166/jnn.2020.17358 .
pubmed: 31492219
Abnous K, Danesh NM, Ramezani M, Alibolandi M, Emrani AS, Lavaee P, Taghdisi SM. A colorimetric gold nanoparticle aggregation assay for malathion based on target-induced hairpin structure assembly of complementary strands of aptamer. Microchim Acta. 2018;185:216. https://doi.org/10.1007/s00604-018-2752-3 .

Auteurs

Mohamed Amine Berkal (MA)

Universite de Pau Et Des Pays de L'Adour, E2S UPPA, CNRS, IPREM, Pau, France.

Corinne Nardin (C)

Universite de Pau Et Des Pays de L'Adour, E2S UPPA, CNRS, IPREM, Pau, France. corinne.nardin@univ-pau.fr.

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