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An electrochemiluminescence sensor based on CdSe@CdS-functionalized MoS2 and a GOD-labeled DNA probe for the sensitive detection of Hg(ii)
In this study, a novel electrochemiluminescence (ECL) biosensor based on a CdSe@CdS quantum dot (QD)-functionalized MoS2-modified electrode was developed for the sensitive detection of mercury ions. Polycationic poly(diallyldimethylammonium chloride) (PDDA) and negatively charged QDs were adsorbed o...
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Published in: | Analytical methods 2020-01, Vol.12 (4), p.491-498 |
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description | In this study, a novel electrochemiluminescence (ECL) biosensor based on a CdSe@CdS quantum dot (QD)-functionalized MoS2-modified electrode was developed for the sensitive detection of mercury ions. Polycationic poly(diallyldimethylammonium chloride) (PDDA) and negatively charged QDs were adsorbed on the surface of MoS2, in sequence, to form the QD–PDDA–MoS2 composites, which were employed as matrices for immobilizing thymine-rich DNA sequences (DNA1). The gold nanoparticles (AuNPs) were combined with another type of thymine-rich DNA sequences (DNA2) and glucose oxidase (GOD) to prepare the GOD–AuNP–DNA2 conjugates. The composites were characterized via UV-visible absorption spectroscopy, fluorescence and transmission electron microscopy. A thymine–Hg2+–thymine complex was formed through Hg2+ mismatching with DNA1 and DNA2. GOD was, therefore, modified onto the electrode surface. GOD catalyzed the reduction of dissolved oxygen by glucose to produce hydrogen peroxide, which was a co-reactant of the QDs. The electrochemiluminescence signal of the biosensor increased linearly with the increase in the Hg2+ concentration over the range from 1.0 × 10−12 to 1.0 × 10−6 M with a detection limit of 1 × 10−13 M. The reproducibility, stability and specificity of the biosensor was also studied. The biosensor was used to determine Hg2+ in a real water sample and satisfactory results were obtained. |
doi_str_mv | 10.1039/c9ay02524c |
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Polycationic poly(diallyldimethylammonium chloride) (PDDA) and negatively charged QDs were adsorbed on the surface of MoS2, in sequence, to form the QD–PDDA–MoS2 composites, which were employed as matrices for immobilizing thymine-rich DNA sequences (DNA1). The gold nanoparticles (AuNPs) were combined with another type of thymine-rich DNA sequences (DNA2) and glucose oxidase (GOD) to prepare the GOD–AuNP–DNA2 conjugates. The composites were characterized via UV-visible absorption spectroscopy, fluorescence and transmission electron microscopy. A thymine–Hg2+–thymine complex was formed through Hg2+ mismatching with DNA1 and DNA2. GOD was, therefore, modified onto the electrode surface. GOD catalyzed the reduction of dissolved oxygen by glucose to produce hydrogen peroxide, which was a co-reactant of the QDs. The electrochemiluminescence signal of the biosensor increased linearly with the increase in the Hg2+ concentration over the range from 1.0 × 10−12 to 1.0 × 10−6 M with a detection limit of 1 × 10−13 M. The reproducibility, stability and specificity of the biosensor was also studied. The biosensor was used to determine Hg2+ in a real water sample and satisfactory results were obtained.</description><identifier>ISSN: 1759-9660</identifier><identifier>EISSN: 1759-9679</identifier><identifier>DOI: 10.1039/c9ay02524c</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Absorption spectroscopy ; Biosensors ; Cadmium selenides ; Cadmium sulfide ; Composite materials ; Deoxyribonucleic acid ; Dissolved oxygen ; DNA ; Electrochemiluminescence ; Electrodes ; Fluorescence ; Gene sequencing ; Glucose oxidase ; Gold ; Hydrogen peroxide ; Mercury ; Mercury (metal) ; Mercury compounds ; Molybdenum disulfide ; Nanoparticles ; Nucleotide sequence ; Quantum dots ; Thymine ; Transmission electron microscopy ; Water analysis ; Water sampling</subject><ispartof>Analytical methods, 2020-01, Vol.12 (4), p.491-498</ispartof><rights>Copyright Royal Society of Chemistry 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Zhang-Jin, He</creatorcontrib><creatorcontrib>Tian-Fang, Kang</creatorcontrib><creatorcontrib>Li-Ping, Lu</creatorcontrib><creatorcontrib>Shui-Yuan, Cheng</creatorcontrib><title>An electrochemiluminescence sensor based on CdSe@CdS-functionalized MoS2 and a GOD-labeled DNA probe for the sensitive detection of Hg(ii)</title><title>Analytical methods</title><description>In this study, a novel electrochemiluminescence (ECL) biosensor based on a CdSe@CdS quantum dot (QD)-functionalized MoS2-modified electrode was developed for the sensitive detection of mercury ions. Polycationic poly(diallyldimethylammonium chloride) (PDDA) and negatively charged QDs were adsorbed on the surface of MoS2, in sequence, to form the QD–PDDA–MoS2 composites, which were employed as matrices for immobilizing thymine-rich DNA sequences (DNA1). The gold nanoparticles (AuNPs) were combined with another type of thymine-rich DNA sequences (DNA2) and glucose oxidase (GOD) to prepare the GOD–AuNP–DNA2 conjugates. The composites were characterized via UV-visible absorption spectroscopy, fluorescence and transmission electron microscopy. A thymine–Hg2+–thymine complex was formed through Hg2+ mismatching with DNA1 and DNA2. GOD was, therefore, modified onto the electrode surface. GOD catalyzed the reduction of dissolved oxygen by glucose to produce hydrogen peroxide, which was a co-reactant of the QDs. The electrochemiluminescence signal of the biosensor increased linearly with the increase in the Hg2+ concentration over the range from 1.0 × 10−12 to 1.0 × 10−6 M with a detection limit of 1 × 10−13 M. The reproducibility, stability and specificity of the biosensor was also studied. The biosensor was used to determine Hg2+ in a real water sample and satisfactory results were obtained.</description><subject>Absorption spectroscopy</subject><subject>Biosensors</subject><subject>Cadmium selenides</subject><subject>Cadmium sulfide</subject><subject>Composite materials</subject><subject>Deoxyribonucleic acid</subject><subject>Dissolved oxygen</subject><subject>DNA</subject><subject>Electrochemiluminescence</subject><subject>Electrodes</subject><subject>Fluorescence</subject><subject>Gene sequencing</subject><subject>Glucose oxidase</subject><subject>Gold</subject><subject>Hydrogen peroxide</subject><subject>Mercury</subject><subject>Mercury (metal)</subject><subject>Mercury compounds</subject><subject>Molybdenum disulfide</subject><subject>Nanoparticles</subject><subject>Nucleotide sequence</subject><subject>Quantum dots</subject><subject>Thymine</subject><subject>Transmission electron microscopy</subject><subject>Water analysis</subject><subject>Water sampling</subject><issn>1759-9660</issn><issn>1759-9679</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNo9z81KAzEQB_AgCtbqxScIeNHDaj42u5ubpdVWqPaw3ks2O2lTtolusoI-gk9tsOIcZgb-8GMGoUtKbinh8k5L9UmYYLk-QiNaCpnJopTH_3tBTtFZCDtCCskLOkLfE4ehAx17r7ewt92wtw6CBqcBB3DB97hRAVrsHZ62NdynlpnB6Wi9U539StGzrxlWrsUKz1ezrFNNIls8e5ngt943gE1S4vYA2mg_ALcQ4ZfA3uDF5tram3N0YlQX4OJvjlH9-PA6XWTL1fxpOllmG8ZIzHIp2kYRYQzLRUVpwyvCVEtBKp6XXGpRGKlTyTxlpWgqootcqsKwpgQ-RlcHNV32PkCI650f-vRJWDOeV4xRIQn_Ac33Y5c</recordid><startdate>20200128</startdate><enddate>20200128</enddate><creator>Zhang-Jin, He</creator><creator>Tian-Fang, Kang</creator><creator>Li-Ping, Lu</creator><creator>Shui-Yuan, Cheng</creator><general>Royal Society of Chemistry</general><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SE</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>H8G</scope><scope>JG9</scope><scope>L7M</scope><scope>P64</scope></search><sort><creationdate>20200128</creationdate><title>An electrochemiluminescence sensor based on CdSe@CdS-functionalized MoS2 and a GOD-labeled DNA probe for the sensitive detection of Hg(ii)</title><author>Zhang-Jin, He ; 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Polycationic poly(diallyldimethylammonium chloride) (PDDA) and negatively charged QDs were adsorbed on the surface of MoS2, in sequence, to form the QD–PDDA–MoS2 composites, which were employed as matrices for immobilizing thymine-rich DNA sequences (DNA1). The gold nanoparticles (AuNPs) were combined with another type of thymine-rich DNA sequences (DNA2) and glucose oxidase (GOD) to prepare the GOD–AuNP–DNA2 conjugates. The composites were characterized via UV-visible absorption spectroscopy, fluorescence and transmission electron microscopy. A thymine–Hg2+–thymine complex was formed through Hg2+ mismatching with DNA1 and DNA2. GOD was, therefore, modified onto the electrode surface. GOD catalyzed the reduction of dissolved oxygen by glucose to produce hydrogen peroxide, which was a co-reactant of the QDs. The electrochemiluminescence signal of the biosensor increased linearly with the increase in the Hg2+ concentration over the range from 1.0 × 10−12 to 1.0 × 10−6 M with a detection limit of 1 × 10−13 M. The reproducibility, stability and specificity of the biosensor was also studied. The biosensor was used to determine Hg2+ in a real water sample and satisfactory results were obtained.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c9ay02524c</doi><tpages>8</tpages></addata></record> |
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subjects | Absorption spectroscopy Biosensors Cadmium selenides Cadmium sulfide Composite materials Deoxyribonucleic acid Dissolved oxygen DNA Electrochemiluminescence Electrodes Fluorescence Gene sequencing Glucose oxidase Gold Hydrogen peroxide Mercury Mercury (metal) Mercury compounds Molybdenum disulfide Nanoparticles Nucleotide sequence Quantum dots Thymine Transmission electron microscopy Water analysis Water sampling |
title | An electrochemiluminescence sensor based on CdSe@CdS-functionalized MoS2 and a GOD-labeled DNA probe for the sensitive detection of Hg(ii) |
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