Yuning Zhao , Xiaojing Cui , Yilong Wang , Zhendong Wang , Xiaofei Li , Ying Wang , Huaixia Yang , Yanju Liu , Mingsan Miao
{"title":"集成 MoS2/CuS-Au 和 SI-RAFT 的增强型电化学传感器,用于 cTnI 检测中的双重信号放大。","authors":"Yuning Zhao , Xiaojing Cui , Yilong Wang , Zhendong Wang , Xiaofei Li , Ying Wang , Huaixia Yang , Yanju Liu , Mingsan Miao","doi":"10.1016/j.bioelechem.2024.108862","DOIUrl":null,"url":null,"abstract":"<div><div>Cardiac troponin I (cTnI) is known to be among the prominent diagnostic bio-marker for acute myocardial infarction (AMI). In this paper, we proposed an electrochemical aptasensor with nanomaterial MoS<sub>2</sub>/CuS-Au as the substrate material and perillaldehyde (PA) as the surface-initiated reversible addition fragmentation chain transfer (SI-RAFT) polymerization monomer by mediating the in-situ deposition of silver metal on the electrode surface for ultrasensitive detection of cTnI. The substrate material MoS<sub>2</sub>/CuS-Au not only accelerated the rate transfer between electron, but also provided more active sites for aptamers introduction. The perillaldehyde (PA) monomers were modified onto the electrode by surface-initiated reversible addition fragmentation chain transfer polymerization (SI-RAFT), and the signal was amplified in one step by reducing silver ions to metallic silver deposited in situ on the upper of the electrode surface. Under optimum reaction conditions, this aptasensor achieved a detection limit down to 10.83 fg·mL<sup>−1</sup>. The proposed aptasensor without additional natural enzymes or biological tags, had a promising potential for use in the diagnosis of early acute myocardial infarction (AMI).</div></div>","PeriodicalId":252,"journal":{"name":"Bioelectrochemistry","volume":"163 ","pages":"Article 108862"},"PeriodicalIF":4.8000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhanced electrochemical aptasensor integrating MoS2/CuS-Au and SI-RAFT for dual signal amplification in cTnI detection\",\"authors\":\"Yuning Zhao , Xiaojing Cui , Yilong Wang , Zhendong Wang , Xiaofei Li , Ying Wang , Huaixia Yang , Yanju Liu , Mingsan Miao\",\"doi\":\"10.1016/j.bioelechem.2024.108862\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cardiac troponin I (cTnI) is known to be among the prominent diagnostic bio-marker for acute myocardial infarction (AMI). In this paper, we proposed an electrochemical aptasensor with nanomaterial MoS<sub>2</sub>/CuS-Au as the substrate material and perillaldehyde (PA) as the surface-initiated reversible addition fragmentation chain transfer (SI-RAFT) polymerization monomer by mediating the in-situ deposition of silver metal on the electrode surface for ultrasensitive detection of cTnI. The substrate material MoS<sub>2</sub>/CuS-Au not only accelerated the rate transfer between electron, but also provided more active sites for aptamers introduction. The perillaldehyde (PA) monomers were modified onto the electrode by surface-initiated reversible addition fragmentation chain transfer polymerization (SI-RAFT), and the signal was amplified in one step by reducing silver ions to metallic silver deposited in situ on the upper of the electrode surface. Under optimum reaction conditions, this aptasensor achieved a detection limit down to 10.83 fg·mL<sup>−1</sup>. The proposed aptasensor without additional natural enzymes or biological tags, had a promising potential for use in the diagnosis of early acute myocardial infarction (AMI).</div></div>\",\"PeriodicalId\":252,\"journal\":{\"name\":\"Bioelectrochemistry\",\"volume\":\"163 \",\"pages\":\"Article 108862\"},\"PeriodicalIF\":4.8000,\"publicationDate\":\"2024-12-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioelectrochemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S156753942400224X\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioelectrochemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S156753942400224X","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Enhanced electrochemical aptasensor integrating MoS2/CuS-Au and SI-RAFT for dual signal amplification in cTnI detection
Cardiac troponin I (cTnI) is known to be among the prominent diagnostic bio-marker for acute myocardial infarction (AMI). In this paper, we proposed an electrochemical aptasensor with nanomaterial MoS2/CuS-Au as the substrate material and perillaldehyde (PA) as the surface-initiated reversible addition fragmentation chain transfer (SI-RAFT) polymerization monomer by mediating the in-situ deposition of silver metal on the electrode surface for ultrasensitive detection of cTnI. The substrate material MoS2/CuS-Au not only accelerated the rate transfer between electron, but also provided more active sites for aptamers introduction. The perillaldehyde (PA) monomers were modified onto the electrode by surface-initiated reversible addition fragmentation chain transfer polymerization (SI-RAFT), and the signal was amplified in one step by reducing silver ions to metallic silver deposited in situ on the upper of the electrode surface. Under optimum reaction conditions, this aptasensor achieved a detection limit down to 10.83 fg·mL−1. The proposed aptasensor without additional natural enzymes or biological tags, had a promising potential for use in the diagnosis of early acute myocardial infarction (AMI).
期刊介绍:
An International Journal Devoted to Electrochemical Aspects of Biology and Biological Aspects of Electrochemistry
Bioelectrochemistry is an international journal devoted to electrochemical principles in biology and biological aspects of electrochemistry. It publishes experimental and theoretical papers dealing with the electrochemical aspects of:
• Electrified interfaces (electric double layers, adsorption, electron transfer, protein electrochemistry, basic principles of biosensors, biosensor interfaces and bio-nanosensor design and construction.
• Electric and magnetic field effects (field-dependent processes, field interactions with molecules, intramolecular field effects, sensory systems for electric and magnetic fields, molecular and cellular mechanisms)
• Bioenergetics and signal transduction (energy conversion, photosynthetic and visual membranes)
• Biomembranes and model membranes (thermodynamics and mechanics, membrane transport, electroporation, fusion and insertion)
• Electrochemical applications in medicine and biotechnology (drug delivery and gene transfer to cells and tissues, iontophoresis, skin electroporation, injury and repair).
• Organization and use of arrays in-vitro and in-vivo, including as part of feedback control.
• Electrochemical interrogation of biofilms as generated by microorganisms and tissue reaction associated with medical implants.