Essam M. Dief , Wenxian Tang , Liam R. Carroll , Tony Breton , J. Justin Gooding
{"title":"基于配体的电化学传感器的制备:芳基重氮直接接枝方法。","authors":"Essam M. Dief , Wenxian Tang , Liam R. Carroll , Tony Breton , J. Justin Gooding","doi":"10.1039/d5cc00857c","DOIUrl":null,"url":null,"abstract":"<div><div>Electrochemical aptamer-based (EAB) sensors represent a promising platform for continuous monitoring of a wide range of biomarkers due to the unique properties of aptamers, such as high affinity, target binding reversibility and ease of designing them for a desired target analyte. Currently, the performance of EAB sensors is limited by the instability of the molecule/electrode link that is mostly based on the gold–sulphur semi-covalent bonds that can be chemically and electrochemically unstable during operation of an EAB sensor. In this work, we introduce, for the first time, an aryl diazonium salt-derived covalent surface chemistry that enables the direct grafting of aptamers on gold electrodes, in a single step, by the spontaneous reduction of an <em>in situ</em> diazotized aryl-aminated aptamer derivative. This method allows for more robust attachment of aptamers on gold electrodes <em>via</em> the formation of a more stable interfacial gold–carbon bond. The fabricated sensor shows a capability to continuously monitor the antibiotic vancomycin target in phosphate-buffered saline (PBS) solution for over 48 hours. This work opens new avenues to overcome the instability related to thiol–gold chemistry for the development of EAB sensors in wearable devices.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 42","pages":"Pages 7648-7651"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation of electrochemical aptamer-based sensors: a direct aryl diazonium grafting approach†\",\"authors\":\"Essam M. Dief , Wenxian Tang , Liam R. Carroll , Tony Breton , J. Justin Gooding\",\"doi\":\"10.1039/d5cc00857c\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Electrochemical aptamer-based (EAB) sensors represent a promising platform for continuous monitoring of a wide range of biomarkers due to the unique properties of aptamers, such as high affinity, target binding reversibility and ease of designing them for a desired target analyte. Currently, the performance of EAB sensors is limited by the instability of the molecule/electrode link that is mostly based on the gold–sulphur semi-covalent bonds that can be chemically and electrochemically unstable during operation of an EAB sensor. In this work, we introduce, for the first time, an aryl diazonium salt-derived covalent surface chemistry that enables the direct grafting of aptamers on gold electrodes, in a single step, by the spontaneous reduction of an <em>in situ</em> diazotized aryl-aminated aptamer derivative. This method allows for more robust attachment of aptamers on gold electrodes <em>via</em> the formation of a more stable interfacial gold–carbon bond. The fabricated sensor shows a capability to continuously monitor the antibiotic vancomycin target in phosphate-buffered saline (PBS) solution for over 48 hours. This work opens new avenues to overcome the instability related to thiol–gold chemistry for the development of EAB sensors in wearable devices.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 42\",\"pages\":\"Pages 7648-7651\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734525008353\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734525008353","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Preparation of electrochemical aptamer-based sensors: a direct aryl diazonium grafting approach†
Electrochemical aptamer-based (EAB) sensors represent a promising platform for continuous monitoring of a wide range of biomarkers due to the unique properties of aptamers, such as high affinity, target binding reversibility and ease of designing them for a desired target analyte. Currently, the performance of EAB sensors is limited by the instability of the molecule/electrode link that is mostly based on the gold–sulphur semi-covalent bonds that can be chemically and electrochemically unstable during operation of an EAB sensor. In this work, we introduce, for the first time, an aryl diazonium salt-derived covalent surface chemistry that enables the direct grafting of aptamers on gold electrodes, in a single step, by the spontaneous reduction of an in situ diazotized aryl-aminated aptamer derivative. This method allows for more robust attachment of aptamers on gold electrodes via the formation of a more stable interfacial gold–carbon bond. The fabricated sensor shows a capability to continuously monitor the antibiotic vancomycin target in phosphate-buffered saline (PBS) solution for over 48 hours. This work opens new avenues to overcome the instability related to thiol–gold chemistry for the development of EAB sensors in wearable devices.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.