{"title":"A Dual-Mode Electrochemical Aptasensor for Ultrasensitive Detecting Acetamiprid Based on Hollow Porous Fe2O3 Cubes","authors":"Jing Cheng, Hanbiao Liu, Jianhui Liu, Jiangle Yi, Changli Zhou, Dong Tian, Fangquan Xia","doi":"10.1002/slct.202404077","DOIUrl":null,"url":null,"abstract":"<p>Acetamiprid, a widely utilized pesticide, poses risks to human health due to the bioaccumulation of its residues. Detecting pesticide residues is crucial for effective pesticide management. To enhance the sensitivity and accuracy of pesticide detection, researchers have developed dual-mode sensors that allow for mutual validation of the two signals. In this paper, a dual-mode electrochemical sensor for detecting acetamiprid was constructed using H<sub>2</sub>O<sub>2</sub> and methylene blue (MB) as probes. The electrochemical signal of MB was measured using square wave voltammetry (SWV) mode, followed by the detection of the reduction signal of H<sub>2</sub>O<sub>2</sub> in amperometric i-t curve (i-t) mode. The two signals complemented each other, thereby reducing errors and enhancing measurement accuracy. Additionally, hollow porous Fe<sub>2</sub>O<sub>3</sub> cubes were synthesized to catalyze the reduction of H<sub>2</sub>O<sub>2</sub> to enhance mass transfer rates. The detection limit in SWV mode was 0.034 pM (S/N = 3), with a linear equation represented as Δ<i>I</i> = 5.39lgc-33.80 (<i>R</i><sup>2 </sup>= 0.99) within the concentration range of 0.1 pM to 0 .1µM. The detection limit in i-t mode was 0.38 nM (S/N = 3), with a linear equation expressed as Δ<i>I</i> = -7.26lgc-77.20 (<i>R</i><sup>2 </sup>= 0.99) within the concentration range of 0.1 nM to 0.1 µM. This dual-mode electrochemical sensor offers a promising approach for detecting pesticide residues.</p>","PeriodicalId":146,"journal":{"name":"ChemistrySelect","volume":"9 44","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2024-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistrySelect","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/slct.202404077","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Acetamiprid, a widely utilized pesticide, poses risks to human health due to the bioaccumulation of its residues. Detecting pesticide residues is crucial for effective pesticide management. To enhance the sensitivity and accuracy of pesticide detection, researchers have developed dual-mode sensors that allow for mutual validation of the two signals. In this paper, a dual-mode electrochemical sensor for detecting acetamiprid was constructed using H2O2 and methylene blue (MB) as probes. The electrochemical signal of MB was measured using square wave voltammetry (SWV) mode, followed by the detection of the reduction signal of H2O2 in amperometric i-t curve (i-t) mode. The two signals complemented each other, thereby reducing errors and enhancing measurement accuracy. Additionally, hollow porous Fe2O3 cubes were synthesized to catalyze the reduction of H2O2 to enhance mass transfer rates. The detection limit in SWV mode was 0.034 pM (S/N = 3), with a linear equation represented as ΔI = 5.39lgc-33.80 (R2 = 0.99) within the concentration range of 0.1 pM to 0 .1µM. The detection limit in i-t mode was 0.38 nM (S/N = 3), with a linear equation expressed as ΔI = -7.26lgc-77.20 (R2 = 0.99) within the concentration range of 0.1 nM to 0.1 µM. This dual-mode electrochemical sensor offers a promising approach for detecting pesticide residues.
期刊介绍:
ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.