{"title":"An in situ-boosted electrochemiluminescence biosensor for serotonin detection sensitized with Co3O4 nanoplates and self-feedback DNA recycling","authors":"Yongguang Gao , Qiumei Feng , Xiangmin Miao , Yufei Fu","doi":"10.1016/j.bios.2025.117464","DOIUrl":null,"url":null,"abstract":"<div><div>Here, we described an in situ-boosted electrochemiluminescence (ECL) biosensor for serotonin detection sensitized with the catalysis of Co<sub>3</sub>O<sub>4</sub> nanoplates and self-feedback DNA recycling (SFDR). Specifically, aptamer:S duplex was attached onto the surface of magnetic beads via amide bond. When serotonin presented, it competitively combined with aptamer from aptamer:S duplex. Then, the released S strands reacted with hairpin DNA (H) containing the silenced Mg<sup>2+</sup>-assisted DNAzyme site in the loop part that immobilized on CdS quantum dots (CdS QDs) modified electrode. The activating Mg<sup>2+</sup>-assisted DNAzyme cut off H and re-liberated S strands. Therefore, the Mg<sup>2+</sup>-DNAzyme-aided recycle happened to produce numerous residual single-stranded DNA segments and then reacted with Co<sub>3</sub>O<sub>4</sub>-modified P strands on the electrode surface. Such results directly introduced Co<sub>3</sub>O<sub>4</sub> nanoplates close to CdS QDs, resulting in the reduction of H<sub>2</sub>O<sub>2</sub> to •OH and the increase of ECL emission of CdS QDs in CdS QDs-H<sub>2</sub>O<sub>2</sub> system. Based on such signal amplification strategy, a low detection limit of 1.5 pM was obtained for serotonin detection. This approach enabled the proposed ECL biosensor promising for the future application in the trace detection of serotonin.</div></div>","PeriodicalId":259,"journal":{"name":"Biosensors and Bioelectronics","volume":"281 ","pages":"Article 117464"},"PeriodicalIF":10.7000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biosensors and Bioelectronics","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0956566325003380","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Here, we described an in situ-boosted electrochemiluminescence (ECL) biosensor for serotonin detection sensitized with the catalysis of Co3O4 nanoplates and self-feedback DNA recycling (SFDR). Specifically, aptamer:S duplex was attached onto the surface of magnetic beads via amide bond. When serotonin presented, it competitively combined with aptamer from aptamer:S duplex. Then, the released S strands reacted with hairpin DNA (H) containing the silenced Mg2+-assisted DNAzyme site in the loop part that immobilized on CdS quantum dots (CdS QDs) modified electrode. The activating Mg2+-assisted DNAzyme cut off H and re-liberated S strands. Therefore, the Mg2+-DNAzyme-aided recycle happened to produce numerous residual single-stranded DNA segments and then reacted with Co3O4-modified P strands on the electrode surface. Such results directly introduced Co3O4 nanoplates close to CdS QDs, resulting in the reduction of H2O2 to •OH and the increase of ECL emission of CdS QDs in CdS QDs-H2O2 system. Based on such signal amplification strategy, a low detection limit of 1.5 pM was obtained for serotonin detection. This approach enabled the proposed ECL biosensor promising for the future application in the trace detection of serotonin.
期刊介绍:
Biosensors & Bioelectronics, along with its open access companion journal Biosensors & Bioelectronics: X, is the leading international publication in the field of biosensors and bioelectronics. It covers research, design, development, and application of biosensors, which are analytical devices incorporating biological materials with physicochemical transducers. These devices, including sensors, DNA chips, electronic noses, and lab-on-a-chip, produce digital signals proportional to specific analytes. Examples include immunosensors and enzyme-based biosensors, applied in various fields such as medicine, environmental monitoring, and food industry. The journal also focuses on molecular and supramolecular structures for enhancing device performance.