Novel core etching technique of gold nanoparticles for colorimetric dopamine detection
This study develops a novel and high performance colorimetric probe for dopamine (DA) detection. Aqueous-phase gold nanoparticles (AuNPs) extracted with 4-(dimethylamino)pyridine (DMAP) from toluene solvent are used as the reaction probes. The original AuNPs of diameter around 13 nm separate into 2-...
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description | This study develops a novel and high performance colorimetric probe for dopamine (DA) detection. Aqueous-phase gold nanoparticles (AuNPs) extracted with 4-(dimethylamino)pyridine (DMAP) from toluene solvent are used as the reaction probes. The original AuNPs of diameter around 13 nm separate into 2-5 nm sizes when dopamine (DA) is added, resulting in the color change of the AuNP solution from red to blackish green. Transmission electron microscopy (TEM) observations and dynamic light scattering (DLS) tests show that the AuNPs break into their smaller sizes right after addition of DA. The results confirm that the DMAP capped AuNPs are etched by the DA molecules due to the strong affinity between DA and AuNPs, thus causing a blue shift in the absorption spectrum. The concentration of DA is quantitatively monitored by using a UV-Vis spectrometer with a limit of detection (LOD) as low as 5 nM. In addition, the results also show that the methods developed appear to have no significant problems in detecting DA in the sample even with the presence of (10 mM) common interferents such as ascorbic acid (AA), homovanillic acid (HVA), catechol (CA) and glutathione (GSH). The developed AuNP etching protocol for dopamine detection provides a novel and versatile approach for rapid biosensing applications. |
doi_str_mv | 10.1039/c2an35586h |
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Aqueous-phase gold nanoparticles (AuNPs) extracted with 4-(dimethylamino)pyridine (DMAP) from toluene solvent are used as the reaction probes. The original AuNPs of diameter around 13 nm separate into 2-5 nm sizes when dopamine (DA) is added, resulting in the color change of the AuNP solution from red to blackish green. Transmission electron microscopy (TEM) observations and dynamic light scattering (DLS) tests show that the AuNPs break into their smaller sizes right after addition of DA. The results confirm that the DMAP capped AuNPs are etched by the DA molecules due to the strong affinity between DA and AuNPs, thus causing a blue shift in the absorption spectrum. The concentration of DA is quantitatively monitored by using a UV-Vis spectrometer with a limit of detection (LOD) as low as 5 nM. In addition, the results also show that the methods developed appear to have no significant problems in detecting DA in the sample even with the presence of (10 mM) common interferents such as ascorbic acid (AA), homovanillic acid (HVA), catechol (CA) and glutathione (GSH). The developed AuNP etching protocol for dopamine detection provides a novel and versatile approach for rapid biosensing applications.</description><identifier>ISSN: 0003-2654</identifier><identifier>EISSN: 1364-5528</identifier><identifier>DOI: 10.1039/c2an35586h</identifier><identifier>PMID: 23016153</identifier><identifier>CODEN: ANALAO</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Analytical chemistry ; Ascorbic Acid - chemistry ; Biological and medical sciences ; Biosensors ; Biotechnology ; Catechols - chemistry ; Chemistry ; Cyclic N-Oxides - chemistry ; Dopamine - analysis ; Electrochemical Techniques ; Exact sciences and technology ; Fundamental and applied biological sciences. Psychology ; General, instrumentation ; Glutathione - chemistry ; Gold - chemistry ; Homovanillic Acid - chemistry ; Metal Nanoparticles - chemistry ; Methods. Procedures. 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Aqueous-phase gold nanoparticles (AuNPs) extracted with 4-(dimethylamino)pyridine (DMAP) from toluene solvent are used as the reaction probes. The original AuNPs of diameter around 13 nm separate into 2-5 nm sizes when dopamine (DA) is added, resulting in the color change of the AuNP solution from red to blackish green. Transmission electron microscopy (TEM) observations and dynamic light scattering (DLS) tests show that the AuNPs break into their smaller sizes right after addition of DA. The results confirm that the DMAP capped AuNPs are etched by the DA molecules due to the strong affinity between DA and AuNPs, thus causing a blue shift in the absorption spectrum. The concentration of DA is quantitatively monitored by using a UV-Vis spectrometer with a limit of detection (LOD) as low as 5 nM. In addition, the results also show that the methods developed appear to have no significant problems in detecting DA in the sample even with the presence of (10 mM) common interferents such as ascorbic acid (AA), homovanillic acid (HVA), catechol (CA) and glutathione (GSH). The developed AuNP etching protocol for dopamine detection provides a novel and versatile approach for rapid biosensing applications.</description><subject>Analytical chemistry</subject><subject>Ascorbic Acid - chemistry</subject><subject>Biological and medical sciences</subject><subject>Biosensors</subject><subject>Biotechnology</subject><subject>Catechols - chemistry</subject><subject>Chemistry</subject><subject>Cyclic N-Oxides - chemistry</subject><subject>Dopamine - analysis</subject><subject>Electrochemical Techniques</subject><subject>Exact sciences and technology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General, instrumentation</subject><subject>Glutathione - chemistry</subject><subject>Gold - chemistry</subject><subject>Homovanillic Acid - chemistry</subject><subject>Metal Nanoparticles - chemistry</subject><subject>Methods. Procedures. 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Psychology</topic><topic>General, instrumentation</topic><topic>Glutathione - chemistry</topic><topic>Gold - chemistry</topic><topic>Homovanillic Acid - chemistry</topic><topic>Metal Nanoparticles - chemistry</topic><topic>Methods. Procedures. Technologies</topic><topic>Spectrometric and optical methods</topic><topic>Spectrophotometry, Ultraviolet</topic><topic>Toluene - chemistry</topic><topic>Various methods and equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>LEE, Ho-Cheng</creatorcontrib><creatorcontrib>CHEN, Tzu-Heng</creatorcontrib><creatorcontrib>TSENG, Wei-Lung</creatorcontrib><creatorcontrib>LIN, Che-Hsin</creatorcontrib><collection>Pascal-Francis</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>Analyst (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>LEE, Ho-Cheng</au><au>CHEN, Tzu-Heng</au><au>TSENG, Wei-Lung</au><au>LIN, Che-Hsin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel core etching technique of gold nanoparticles for colorimetric dopamine detection</atitle><jtitle>Analyst (London)</jtitle><addtitle>Analyst</addtitle><date>2012-11-21</date><risdate>2012</risdate><volume>137</volume><issue>22</issue><spage>5352</spage><epage>5357</epage><pages>5352-5357</pages><issn>0003-2654</issn><eissn>1364-5528</eissn><coden>ANALAO</coden><abstract>This study develops a novel and high performance colorimetric probe for dopamine (DA) detection. Aqueous-phase gold nanoparticles (AuNPs) extracted with 4-(dimethylamino)pyridine (DMAP) from toluene solvent are used as the reaction probes. The original AuNPs of diameter around 13 nm separate into 2-5 nm sizes when dopamine (DA) is added, resulting in the color change of the AuNP solution from red to blackish green. Transmission electron microscopy (TEM) observations and dynamic light scattering (DLS) tests show that the AuNPs break into their smaller sizes right after addition of DA. The results confirm that the DMAP capped AuNPs are etched by the DA molecules due to the strong affinity between DA and AuNPs, thus causing a blue shift in the absorption spectrum. The concentration of DA is quantitatively monitored by using a UV-Vis spectrometer with a limit of detection (LOD) as low as 5 nM. In addition, the results also show that the methods developed appear to have no significant problems in detecting DA in the sample even with the presence of (10 mM) common interferents such as ascorbic acid (AA), homovanillic acid (HVA), catechol (CA) and glutathione (GSH). The developed AuNP etching protocol for dopamine detection provides a novel and versatile approach for rapid biosensing applications.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><pmid>23016153</pmid><doi>10.1039/c2an35586h</doi><tpages>6</tpages></addata></record> |
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subjects | Analytical chemistry Ascorbic Acid - chemistry Biological and medical sciences Biosensors Biotechnology Catechols - chemistry Chemistry Cyclic N-Oxides - chemistry Dopamine - analysis Electrochemical Techniques Exact sciences and technology Fundamental and applied biological sciences. Psychology General, instrumentation Glutathione - chemistry Gold - chemistry Homovanillic Acid - chemistry Metal Nanoparticles - chemistry Methods. Procedures. Technologies Spectrometric and optical methods Spectrophotometry, Ultraviolet Toluene - chemistry Various methods and equipments |
title | Novel core etching technique of gold nanoparticles for colorimetric dopamine detection |
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