Tunable nanogap devices for ultra-sensitive electrochemical impedance biosensing

A wealth of research has been available discussing nanogap devices for detecting very small quantities of biomolecules by observing their electrical behavior generally performed in dry conditions. We report that a gold nanogapped electrode with tunable gap length for ultra-sensitive detection of str...

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Veröffentlicht in:Analytica chimica acta 2016-01, Vol.905, p.58-65
Hauptverfasser: Lu, Yong, Guo, Zheng, Song, Jing-Jing, Huang, Qin-An, Zhu, Si-Wei, Huang, Xing-Jiu, Wei, Yan
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container_start_page 58
container_title Analytica chimica acta
container_volume 905
creator Lu, Yong
Guo, Zheng
Song, Jing-Jing
Huang, Qin-An
Zhu, Si-Wei
Huang, Xing-Jiu
Wei, Yan
description A wealth of research has been available discussing nanogap devices for detecting very small quantities of biomolecules by observing their electrical behavior generally performed in dry conditions. We report that a gold nanogapped electrode with tunable gap length for ultra-sensitive detection of streptavidin based on electrochemical impedance technique. The gold nanogap is fabricated using simple monolayer film deposition and in-situ growth of gold nanoparticles in a traditional interdigitated array (IDA) microelectrode. The electrochemical impedance biosensor with a 25-nm nanogap is found to be ultra-sensitive to the specific binding of streptavidin to biotin. The binding of the streptavidin hinder the electron transfer between two electrodes, resulting in a large increase in electron-transfer resistance (Ret) for operating the impedance. A linear relation between the relative Ret and the logarithmic value of streptavidin concentration is observed in the concentration range from 1 pM (picomolar) to 100 nM (nanomolar). The lowest detectable concentration actually measured reaches 1 pM. We believe that such an electrochemical impedance nanogap biosensor provides a useful approach towards biomolecular detection that could be extended to a number of other systems. [Display omitted] •A tunable gold nanogap device was used as to electrochemical impedance biosensor.•Linear range from 1 pM to 100 nM with LOD of 1 pM for streptavidin detection was obtained.•The nanogap devices exhibit a satisfactory precision, stability, and reproducibility.•The combination of electrochemical impedance technique and nanogap devices was achieved.
doi_str_mv 10.1016/j.aca.2015.11.036
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We report that a gold nanogapped electrode with tunable gap length for ultra-sensitive detection of streptavidin based on electrochemical impedance technique. The gold nanogap is fabricated using simple monolayer film deposition and in-situ growth of gold nanoparticles in a traditional interdigitated array (IDA) microelectrode. The electrochemical impedance biosensor with a 25-nm nanogap is found to be ultra-sensitive to the specific binding of streptavidin to biotin. The binding of the streptavidin hinder the electron transfer between two electrodes, resulting in a large increase in electron-transfer resistance (Ret) for operating the impedance. A linear relation between the relative Ret and the logarithmic value of streptavidin concentration is observed in the concentration range from 1 pM (picomolar) to 100 nM (nanomolar). The lowest detectable concentration actually measured reaches 1 pM. We believe that such an electrochemical impedance nanogap biosensor provides a useful approach towards biomolecular detection that could be extended to a number of other systems. [Display omitted] •A tunable gold nanogap device was used as to electrochemical impedance biosensor.•Linear range from 1 pM to 100 nM with LOD of 1 pM for streptavidin detection was obtained.•The nanogap devices exhibit a satisfactory precision, stability, and reproducibility.•The combination of electrochemical impedance technique and nanogap devices was achieved.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2015.11.036</identifier><identifier>PMID: 26755137</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Biosensing Techniques ; Biotin - metabolism ; Electric Impedance ; Electrochemical impedance ; Electron-transfer resistance ; Equipment Design ; Nanotechnology ; Protein Binding ; Streptavidin ; Streptavidin - metabolism ; Tunable nanogap devices ; Ultra-sensitive</subject><ispartof>Analytica chimica acta, 2016-01, Vol.905, p.58-65</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. 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We believe that such an electrochemical impedance nanogap biosensor provides a useful approach towards biomolecular detection that could be extended to a number of other systems. [Display omitted] •A tunable gold nanogap device was used as to electrochemical impedance biosensor.•Linear range from 1 pM to 100 nM with LOD of 1 pM for streptavidin detection was obtained.•The nanogap devices exhibit a satisfactory precision, stability, and reproducibility.•The combination of electrochemical impedance technique and nanogap devices was achieved.</description><subject>Biosensing Techniques</subject><subject>Biotin - metabolism</subject><subject>Electric Impedance</subject><subject>Electrochemical impedance</subject><subject>Electron-transfer resistance</subject><subject>Equipment Design</subject><subject>Nanotechnology</subject><subject>Protein Binding</subject><subject>Streptavidin</subject><subject>Streptavidin - metabolism</subject><subject>Tunable nanogap devices</subject><subject>Ultra-sensitive</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwAWxQlmwSPHYdJ2KFEC-pEizK2nKccXGVR7GTSvw9Li0sWY1mdO6V5hByCTQDCvnNOtNGZ4yCyAAyyvMjMoVC8nTO2fyYTCmlPGW5pBNyFsI6rgzo_JRM4k0I4HJK3pZjp6sGk053_Upvkhq3zmBIbO-TsRm8TgN2wQ1uiwk2aAbfmw9sndFN4toN1rozmFSu_8G61Tk5sboJeHGYM_L--LC8f04Xr08v93eL1HDBh1SDzEsrJBpdc7RoS-BlXktLRcUtlzmtbQESCsYiBcCEBRSMFWUpBZvnfEau970b33-OGAbVumCwaXSH_RhU7KdFznlUMCOwR43vQ_Bo1ca7VvsvBVTtRKq1iiLVTqQCUFFkzFwd6seqxfov8WsuArd7AOOTW4deBeMwuqidj5ZU3bt_6r8B4QuDFg</recordid><startdate>20160128</startdate><enddate>20160128</enddate><creator>Lu, Yong</creator><creator>Guo, Zheng</creator><creator>Song, Jing-Jing</creator><creator>Huang, Qin-An</creator><creator>Zhu, Si-Wei</creator><creator>Huang, Xing-Jiu</creator><creator>Wei, Yan</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160128</creationdate><title>Tunable nanogap devices for ultra-sensitive electrochemical impedance biosensing</title><author>Lu, Yong ; Guo, Zheng ; Song, Jing-Jing ; Huang, Qin-An ; Zhu, Si-Wei ; Huang, Xing-Jiu ; Wei, Yan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-a1769f57ecad3efef91396d7f05b3f3760df8171822f571125f1e522899752463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biosensing Techniques</topic><topic>Biotin - metabolism</topic><topic>Electric Impedance</topic><topic>Electrochemical impedance</topic><topic>Electron-transfer resistance</topic><topic>Equipment Design</topic><topic>Nanotechnology</topic><topic>Protein Binding</topic><topic>Streptavidin</topic><topic>Streptavidin - metabolism</topic><topic>Tunable nanogap devices</topic><topic>Ultra-sensitive</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Yong</creatorcontrib><creatorcontrib>Guo, Zheng</creatorcontrib><creatorcontrib>Song, Jing-Jing</creatorcontrib><creatorcontrib>Huang, Qin-An</creatorcontrib><creatorcontrib>Zhu, Si-Wei</creatorcontrib><creatorcontrib>Huang, Xing-Jiu</creatorcontrib><creatorcontrib>Wei, Yan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Yong</au><au>Guo, Zheng</au><au>Song, Jing-Jing</au><au>Huang, Qin-An</au><au>Zhu, Si-Wei</au><au>Huang, Xing-Jiu</au><au>Wei, Yan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tunable nanogap devices for ultra-sensitive electrochemical impedance biosensing</atitle><jtitle>Analytica chimica acta</jtitle><addtitle>Anal Chim Acta</addtitle><date>2016-01-28</date><risdate>2016</risdate><volume>905</volume><spage>58</spage><epage>65</epage><pages>58-65</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><abstract>A wealth of research has been available discussing nanogap devices for detecting very small quantities of biomolecules by observing their electrical behavior generally performed in dry conditions. 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We believe that such an electrochemical impedance nanogap biosensor provides a useful approach towards biomolecular detection that could be extended to a number of other systems. [Display omitted] •A tunable gold nanogap device was used as to electrochemical impedance biosensor.•Linear range from 1 pM to 100 nM with LOD of 1 pM for streptavidin detection was obtained.•The nanogap devices exhibit a satisfactory precision, stability, and reproducibility.•The combination of electrochemical impedance technique and nanogap devices was achieved.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26755137</pmid><doi>10.1016/j.aca.2015.11.036</doi><tpages>8</tpages></addata></record>
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subjects Biosensing Techniques
Biotin - metabolism
Electric Impedance
Electrochemical impedance
Electron-transfer resistance
Equipment Design
Nanotechnology
Protein Binding
Streptavidin
Streptavidin - metabolism
Tunable nanogap devices
Ultra-sensitive
title Tunable nanogap devices for ultra-sensitive electrochemical impedance biosensing
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