Amplified cathodic electrochemiluminescence of luminol based on Pd and Pt nanoparticles and glucose oxidase decorated graphene as trace label for ultrasensitive detection of protein

An ultrasensitive electrochemiluminescence (ECL) immunosensor was constructed for ultrasensitive detection of carcinoembryonic antigen (CEA) based on an amplified cathodic ECL of luminol at low potential. Firstly, Au nanoparticles (AuNPs) were electrodeposited onto single walled carbon nanotube–grap...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Talanta (Oxford) 2013-09, Vol.113, p.106-112
Hauptverfasser: Cao, Yaling, Yuan, Ruo, Chai, Yaqin, Liu, Huijing, Liao, Yuhong, Zhuo, Ying
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 112
container_issue
container_start_page 106
container_title Talanta (Oxford)
container_volume 113
creator Cao, Yaling
Yuan, Ruo
Chai, Yaqin
Liu, Huijing
Liao, Yuhong
Zhuo, Ying
description An ultrasensitive electrochemiluminescence (ECL) immunosensor was constructed for ultrasensitive detection of carcinoembryonic antigen (CEA) based on an amplified cathodic ECL of luminol at low potential. Firstly, Au nanoparticles (AuNPs) were electrodeposited onto single walled carbon nanotube–graphene composites (CNTs–Gra) coated glass carbon electrode (GCE) with enhanced surface area and good biocompatibility to capture primary antibody (Ab1) and then bind the antigen analytes. Secondly, Pd and Pt nanoparticles (Pd&PtNPs) decorated reduced graphene oxide (Pd&PtNPs@rGO) and glucose oxidase (GOD) labeled secondary antibody (Pd&PtNPs@ rGO–GOD–Ab2) could be captured onto the electrode surface by a sandwich immunoassay protocol to generate amplified cathodic ECL signals of luminol in the presence of glucose. The Pd&PtNPs@rGO composites and loaded GOD promoted luminol cathodic ECL response by efficiently catalyzing glucose to in-situ produce amount of hydrogen peroxide (H2O2) working as a coreactant of luminol. Then in turn Pd&PtNPs catalyzed H2O2 to generate various reactive oxygen species (ROSs), which accelerated the cathodic ECL reaction of luminol, enhanced the cathodic ECL intensity of luminol and improved the sensitivity of the immunosensor. The as-proposed ECL immunosensor exhibited sensitive response on the detection of CEA ranging from 0.0001ngmL−1 to 160ngmL−1 with a detection limit of 0.03pgmL−1 (S/N=3). Moreover, the stability, specificity, lifetime and reproducibility tests demonstrated the feasibility of the developed immunoassay, which can be further extended to the detection of other disease biomarkers. •An ECL immunosensor was constructed based on an amplified cathodic ECL of luminol.•AuNPs deposited on CNTs–Gra improved biocompatible surface area and electron transfer rate.•Pd&PtNPs@rGO enhanced the loading amount of GOD and amplified the cathodic ECL of luminol.•The proposed immunosensor had excellent performance for the detection of CEA.
doi_str_mv 10.1016/j.talanta.2013.03.018
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1356394483</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0039914013001677</els_id><sourcerecordid>1356394483</sourcerecordid><originalsourceid>FETCH-LOGICAL-c525t-74698e920d9763d067e18b3105854275fd042e234a23f3206973d98ddc467e663</originalsourceid><addsrcrecordid>eNqFkd1u1DAQhS0EokvhEQBfcpNlHCdOcoWqqvxIlagEvba89mTXKydebKeCB-P9mO0u3CJZsjz6zpzxHMZeC1gLEOr9fl1MMHMx6xqEXAMd0T9hK9F3spJtJ5-yFYAcqkE0cMFe5LwHgFqCfM4uatlBrySs2O-r6RD86NFxa8ouOm85BrQlRbvDyYdl8jNmi7NFHkf--I6Bb0wmSZz5neNmdvyu8NnM8WBS8TZgfixuw2JjJt1P74jnDm1MppBwm8xhhzNyk3lJhnoHs8HAx5j4EqiScc6--IejqNA4nqzI_pBiQT-_ZM9GEzK-Ot-X7P7jzffrz9Xt109frq9uK9vWbam6Rg09DjW4oVPSgepQ9BspoO3bpu7a0UFTYy0bU8tR1qCGTrqhd842hColL9m7U1_y_bFgLnrytItAi8e4ZC1kq-TQNL0ktD2hNsWcE476kPxk0i8tQB8T03t9TkwfE9NAR_Ske3O2WDYTun-qvxER8PYEjCZqs00-6_tv1EFRnCDpX0R8OBFIq3jwmHS2_hiY84lWp130_xniDyeMtlw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1356394483</pqid></control><display><type>article</type><title>Amplified cathodic electrochemiluminescence of luminol based on Pd and Pt nanoparticles and glucose oxidase decorated graphene as trace label for ultrasensitive detection of protein</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Cao, Yaling ; Yuan, Ruo ; Chai, Yaqin ; Liu, Huijing ; Liao, Yuhong ; Zhuo, Ying</creator><creatorcontrib>Cao, Yaling ; Yuan, Ruo ; Chai, Yaqin ; Liu, Huijing ; Liao, Yuhong ; Zhuo, Ying</creatorcontrib><description><![CDATA[An ultrasensitive electrochemiluminescence (ECL) immunosensor was constructed for ultrasensitive detection of carcinoembryonic antigen (CEA) based on an amplified cathodic ECL of luminol at low potential. Firstly, Au nanoparticles (AuNPs) were electrodeposited onto single walled carbon nanotube–graphene composites (CNTs–Gra) coated glass carbon electrode (GCE) with enhanced surface area and good biocompatibility to capture primary antibody (Ab1) and then bind the antigen analytes. Secondly, Pd and Pt nanoparticles (Pd&PtNPs) decorated reduced graphene oxide (Pd&PtNPs@rGO) and glucose oxidase (GOD) labeled secondary antibody (Pd&PtNPs@ rGO–GOD–Ab2) could be captured onto the electrode surface by a sandwich immunoassay protocol to generate amplified cathodic ECL signals of luminol in the presence of glucose. The Pd&PtNPs@rGO composites and loaded GOD promoted luminol cathodic ECL response by efficiently catalyzing glucose to in-situ produce amount of hydrogen peroxide (H2O2) working as a coreactant of luminol. Then in turn Pd&PtNPs catalyzed H2O2 to generate various reactive oxygen species (ROSs), which accelerated the cathodic ECL reaction of luminol, enhanced the cathodic ECL intensity of luminol and improved the sensitivity of the immunosensor. The as-proposed ECL immunosensor exhibited sensitive response on the detection of CEA ranging from 0.0001ngmL−1 to 160ngmL−1 with a detection limit of 0.03pgmL−1 (S/N=3). Moreover, the stability, specificity, lifetime and reproducibility tests demonstrated the feasibility of the developed immunoassay, which can be further extended to the detection of other disease biomarkers. •An ECL immunosensor was constructed based on an amplified cathodic ECL of luminol.•AuNPs deposited on CNTs–Gra improved biocompatible surface area and electron transfer rate.•Pd&PtNPs@rGO enhanced the loading amount of GOD and amplified the cathodic ECL of luminol.•The proposed immunosensor had excellent performance for the detection of CEA.]]></description><identifier>ISSN: 0039-9140</identifier><identifier>EISSN: 1873-3573</identifier><identifier>DOI: 10.1016/j.talanta.2013.03.018</identifier><identifier>PMID: 23708630</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>antibodies ; Antibodies - chemistry ; Antibodies - immunology ; antigens ; biocompatibility ; biomarkers ; Carcinoembryonic Antigen - analysis ; Carcinoembryonic Antigen - immunology ; detection limit ; Electrochemical Techniques ; Electrochemiluminescence ; Electrodes ; glass ; glucose ; Glucose oxidase ; Glucose Oxidase - chemistry ; gold ; Graphene ; graphene oxide ; Graphite - chemistry ; Hydrogen peroxide ; immunoassays ; immunosensors ; Luminescent Agents - chemistry ; Luminescent Measurements ; Luminol ; Luminol - chemistry ; Metal Nanoparticles - chemistry ; Nanocomposites - chemistry ; nanogold ; Nanoparticles ; Palladium - chemistry ; Platinum - chemistry ; reactive oxygen species ; surface area</subject><ispartof>Talanta (Oxford), 2013-09, Vol.113, p.106-112</ispartof><rights>2013 Elsevier B.V.</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-74698e920d9763d067e18b3105854275fd042e234a23f3206973d98ddc467e663</citedby><cites>FETCH-LOGICAL-c525t-74698e920d9763d067e18b3105854275fd042e234a23f3206973d98ddc467e663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.talanta.2013.03.018$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23708630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Yaling</creatorcontrib><creatorcontrib>Yuan, Ruo</creatorcontrib><creatorcontrib>Chai, Yaqin</creatorcontrib><creatorcontrib>Liu, Huijing</creatorcontrib><creatorcontrib>Liao, Yuhong</creatorcontrib><creatorcontrib>Zhuo, Ying</creatorcontrib><title>Amplified cathodic electrochemiluminescence of luminol based on Pd and Pt nanoparticles and glucose oxidase decorated graphene as trace label for ultrasensitive detection of protein</title><title>Talanta (Oxford)</title><addtitle>Talanta</addtitle><description><![CDATA[An ultrasensitive electrochemiluminescence (ECL) immunosensor was constructed for ultrasensitive detection of carcinoembryonic antigen (CEA) based on an amplified cathodic ECL of luminol at low potential. Firstly, Au nanoparticles (AuNPs) were electrodeposited onto single walled carbon nanotube–graphene composites (CNTs–Gra) coated glass carbon electrode (GCE) with enhanced surface area and good biocompatibility to capture primary antibody (Ab1) and then bind the antigen analytes. Secondly, Pd and Pt nanoparticles (Pd&PtNPs) decorated reduced graphene oxide (Pd&PtNPs@rGO) and glucose oxidase (GOD) labeled secondary antibody (Pd&PtNPs@ rGO–GOD–Ab2) could be captured onto the electrode surface by a sandwich immunoassay protocol to generate amplified cathodic ECL signals of luminol in the presence of glucose. The Pd&PtNPs@rGO composites and loaded GOD promoted luminol cathodic ECL response by efficiently catalyzing glucose to in-situ produce amount of hydrogen peroxide (H2O2) working as a coreactant of luminol. Then in turn Pd&PtNPs catalyzed H2O2 to generate various reactive oxygen species (ROSs), which accelerated the cathodic ECL reaction of luminol, enhanced the cathodic ECL intensity of luminol and improved the sensitivity of the immunosensor. The as-proposed ECL immunosensor exhibited sensitive response on the detection of CEA ranging from 0.0001ngmL−1 to 160ngmL−1 with a detection limit of 0.03pgmL−1 (S/N=3). Moreover, the stability, specificity, lifetime and reproducibility tests demonstrated the feasibility of the developed immunoassay, which can be further extended to the detection of other disease biomarkers. •An ECL immunosensor was constructed based on an amplified cathodic ECL of luminol.•AuNPs deposited on CNTs–Gra improved biocompatible surface area and electron transfer rate.•Pd&PtNPs@rGO enhanced the loading amount of GOD and amplified the cathodic ECL of luminol.•The proposed immunosensor had excellent performance for the detection of CEA.]]></description><subject>antibodies</subject><subject>Antibodies - chemistry</subject><subject>Antibodies - immunology</subject><subject>antigens</subject><subject>biocompatibility</subject><subject>biomarkers</subject><subject>Carcinoembryonic Antigen - analysis</subject><subject>Carcinoembryonic Antigen - immunology</subject><subject>detection limit</subject><subject>Electrochemical Techniques</subject><subject>Electrochemiluminescence</subject><subject>Electrodes</subject><subject>glass</subject><subject>glucose</subject><subject>Glucose oxidase</subject><subject>Glucose Oxidase - chemistry</subject><subject>gold</subject><subject>Graphene</subject><subject>graphene oxide</subject><subject>Graphite - chemistry</subject><subject>Hydrogen peroxide</subject><subject>immunoassays</subject><subject>immunosensors</subject><subject>Luminescent Agents - chemistry</subject><subject>Luminescent Measurements</subject><subject>Luminol</subject><subject>Luminol - chemistry</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Nanocomposites - chemistry</subject><subject>nanogold</subject><subject>Nanoparticles</subject><subject>Palladium - chemistry</subject><subject>Platinum - chemistry</subject><subject>reactive oxygen species</subject><subject>surface area</subject><issn>0039-9140</issn><issn>1873-3573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd1u1DAQhS0EokvhEQBfcpNlHCdOcoWqqvxIlagEvba89mTXKydebKeCB-P9mO0u3CJZsjz6zpzxHMZeC1gLEOr9fl1MMHMx6xqEXAMd0T9hK9F3spJtJ5-yFYAcqkE0cMFe5LwHgFqCfM4uatlBrySs2O-r6RD86NFxa8ouOm85BrQlRbvDyYdl8jNmi7NFHkf--I6Bb0wmSZz5neNmdvyu8NnM8WBS8TZgfixuw2JjJt1P74jnDm1MppBwm8xhhzNyk3lJhnoHs8HAx5j4EqiScc6--IejqNA4nqzI_pBiQT-_ZM9GEzK-Ot-X7P7jzffrz9Xt109frq9uK9vWbam6Rg09DjW4oVPSgepQ9BspoO3bpu7a0UFTYy0bU8tR1qCGTrqhd842hColL9m7U1_y_bFgLnrytItAi8e4ZC1kq-TQNL0ktD2hNsWcE476kPxk0i8tQB8T03t9TkwfE9NAR_Ske3O2WDYTun-qvxER8PYEjCZqs00-6_tv1EFRnCDpX0R8OBFIq3jwmHS2_hiY84lWp130_xniDyeMtlw</recordid><startdate>20130915</startdate><enddate>20130915</enddate><creator>Cao, Yaling</creator><creator>Yuan, Ruo</creator><creator>Chai, Yaqin</creator><creator>Liu, Huijing</creator><creator>Liao, Yuhong</creator><creator>Zhuo, Ying</creator><general>Elsevier B.V</general><scope>FBQ</scope><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>20130915</creationdate><title>Amplified cathodic electrochemiluminescence of luminol based on Pd and Pt nanoparticles and glucose oxidase decorated graphene as trace label for ultrasensitive detection of protein</title><author>Cao, Yaling ; Yuan, Ruo ; Chai, Yaqin ; Liu, Huijing ; Liao, Yuhong ; Zhuo, Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-74698e920d9763d067e18b3105854275fd042e234a23f3206973d98ddc467e663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>antibodies</topic><topic>Antibodies - chemistry</topic><topic>Antibodies - immunology</topic><topic>antigens</topic><topic>biocompatibility</topic><topic>biomarkers</topic><topic>Carcinoembryonic Antigen - analysis</topic><topic>Carcinoembryonic Antigen - immunology</topic><topic>detection limit</topic><topic>Electrochemical Techniques</topic><topic>Electrochemiluminescence</topic><topic>Electrodes</topic><topic>glass</topic><topic>glucose</topic><topic>Glucose oxidase</topic><topic>Glucose Oxidase - chemistry</topic><topic>gold</topic><topic>Graphene</topic><topic>graphene oxide</topic><topic>Graphite - chemistry</topic><topic>Hydrogen peroxide</topic><topic>immunoassays</topic><topic>immunosensors</topic><topic>Luminescent Agents - chemistry</topic><topic>Luminescent Measurements</topic><topic>Luminol</topic><topic>Luminol - chemistry</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Nanocomposites - chemistry</topic><topic>nanogold</topic><topic>Nanoparticles</topic><topic>Palladium - chemistry</topic><topic>Platinum - chemistry</topic><topic>reactive oxygen species</topic><topic>surface area</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Yaling</creatorcontrib><creatorcontrib>Yuan, Ruo</creatorcontrib><creatorcontrib>Chai, Yaqin</creatorcontrib><creatorcontrib>Liu, Huijing</creatorcontrib><creatorcontrib>Liao, Yuhong</creatorcontrib><creatorcontrib>Zhuo, Ying</creatorcontrib><collection>AGRIS</collection><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>Talanta (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Yaling</au><au>Yuan, Ruo</au><au>Chai, Yaqin</au><au>Liu, Huijing</au><au>Liao, Yuhong</au><au>Zhuo, Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amplified cathodic electrochemiluminescence of luminol based on Pd and Pt nanoparticles and glucose oxidase decorated graphene as trace label for ultrasensitive detection of protein</atitle><jtitle>Talanta (Oxford)</jtitle><addtitle>Talanta</addtitle><date>2013-09-15</date><risdate>2013</risdate><volume>113</volume><spage>106</spage><epage>112</epage><pages>106-112</pages><issn>0039-9140</issn><eissn>1873-3573</eissn><abstract><![CDATA[An ultrasensitive electrochemiluminescence (ECL) immunosensor was constructed for ultrasensitive detection of carcinoembryonic antigen (CEA) based on an amplified cathodic ECL of luminol at low potential. Firstly, Au nanoparticles (AuNPs) were electrodeposited onto single walled carbon nanotube–graphene composites (CNTs–Gra) coated glass carbon electrode (GCE) with enhanced surface area and good biocompatibility to capture primary antibody (Ab1) and then bind the antigen analytes. Secondly, Pd and Pt nanoparticles (Pd&PtNPs) decorated reduced graphene oxide (Pd&PtNPs@rGO) and glucose oxidase (GOD) labeled secondary antibody (Pd&PtNPs@ rGO–GOD–Ab2) could be captured onto the electrode surface by a sandwich immunoassay protocol to generate amplified cathodic ECL signals of luminol in the presence of glucose. The Pd&PtNPs@rGO composites and loaded GOD promoted luminol cathodic ECL response by efficiently catalyzing glucose to in-situ produce amount of hydrogen peroxide (H2O2) working as a coreactant of luminol. Then in turn Pd&PtNPs catalyzed H2O2 to generate various reactive oxygen species (ROSs), which accelerated the cathodic ECL reaction of luminol, enhanced the cathodic ECL intensity of luminol and improved the sensitivity of the immunosensor. The as-proposed ECL immunosensor exhibited sensitive response on the detection of CEA ranging from 0.0001ngmL−1 to 160ngmL−1 with a detection limit of 0.03pgmL−1 (S/N=3). Moreover, the stability, specificity, lifetime and reproducibility tests demonstrated the feasibility of the developed immunoassay, which can be further extended to the detection of other disease biomarkers. •An ECL immunosensor was constructed based on an amplified cathodic ECL of luminol.•AuNPs deposited on CNTs–Gra improved biocompatible surface area and electron transfer rate.•Pd&PtNPs@rGO enhanced the loading amount of GOD and amplified the cathodic ECL of luminol.•The proposed immunosensor had excellent performance for the detection of CEA.]]></abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23708630</pmid><doi>10.1016/j.talanta.2013.03.018</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0039-9140
ispartof Talanta (Oxford), 2013-09, Vol.113, p.106-112
issn 0039-9140
1873-3573
language eng
recordid cdi_proquest_miscellaneous_1356394483
source MEDLINE; Elsevier ScienceDirect Journals
subjects antibodies
Antibodies - chemistry
Antibodies - immunology
antigens
biocompatibility
biomarkers
Carcinoembryonic Antigen - analysis
Carcinoembryonic Antigen - immunology
detection limit
Electrochemical Techniques
Electrochemiluminescence
Electrodes
glass
glucose
Glucose oxidase
Glucose Oxidase - chemistry
gold
Graphene
graphene oxide
Graphite - chemistry
Hydrogen peroxide
immunoassays
immunosensors
Luminescent Agents - chemistry
Luminescent Measurements
Luminol
Luminol - chemistry
Metal Nanoparticles - chemistry
Nanocomposites - chemistry
nanogold
Nanoparticles
Palladium - chemistry
Platinum - chemistry
reactive oxygen species
surface area
title Amplified cathodic electrochemiluminescence of luminol based on Pd and Pt nanoparticles and glucose oxidase decorated graphene as trace label for ultrasensitive detection of protein
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T23%3A13%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amplified%20cathodic%20electrochemiluminescence%20of%20luminol%20based%20on%20Pd%20and%20Pt%20nanoparticles%20and%20glucose%20oxidase%20decorated%20graphene%20as%20trace%20label%20for%20ultrasensitive%20detection%20of%20protein&rft.jtitle=Talanta%20(Oxford)&rft.au=Cao,%20Yaling&rft.date=2013-09-15&rft.volume=113&rft.spage=106&rft.epage=112&rft.pages=106-112&rft.issn=0039-9140&rft.eissn=1873-3573&rft_id=info:doi/10.1016/j.talanta.2013.03.018&rft_dat=%3Cproquest_cross%3E1356394483%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1356394483&rft_id=info:pmid/23708630&rft_els_id=S0039914013001677&rfr_iscdi=true