Size characterization and quantification of silver nanoparticles by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry

A method for determining the size of silver nanoparticles and their quantification by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (ICP-MS) is proposed and was tested in consumer products. Experimental conditions were studied in detail to avoid a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Analytical & bioanalytical chemistry (Print) 2011-11, Vol.401 (9), p.2723-2732
Hauptverfasser: Bolea, E., Jiménez-Lamana, J., Laborda, F., Castillo, J. R.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2732
container_issue 9
container_start_page 2723
container_title Analytical & bioanalytical chemistry (Print)
container_volume 401
creator Bolea, E.
Jiménez-Lamana, J.
Laborda, F.
Castillo, J. R.
description A method for determining the size of silver nanoparticles and their quantification by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (ICP-MS) is proposed and was tested in consumer products. Experimental conditions were studied in detail to avoid aggregation processes or alteration of the original size distributions. Additionally, losses from sorption processes onto the channel membrane were minimized for correct quantification of the nanoparticles. Mobile phase composition, injection/focusing, and fractionation conditions were evaluated in terms of their influence on both separation resolution and recovery. The ionic strength, pH, and the presence of ionic and nonionic surfactants had a strong influence on both separation and recovery of the nanoparticles. In general, better results were obtained under those conditions that favored charge repulsions with the membrane. Recovery values of 83 ± 8% and 93 ± 4% with respect to the content of silver nanoparticles were achieved for the consumer products studied. Silver nanoparticle standards were used for size calibration of the channel. The results were compared with those obtained by photon correlation spectroscopy and images taken by transmission electron microscopy. The quantification of silver nanoparticles was performed by direct injection of ionic silver standard solutions into the ICP-MS system, integration of the corresponding peaks, and interpolation of the fractogram area. A limit of detection of 5.6 μg L -1 silver, which corresponds to a number concentration of 1×10 12 L -1 for nanoparticles of 10 nm, was achieved for an injection volume of 20 μL.
doi_str_mv 10.1007/s00216-011-5201-2
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_901304160</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A394663561</galeid><sourcerecordid>A394663561</sourcerecordid><originalsourceid>FETCH-LOGICAL-c581t-a3fcc5d996ec619eb713a62a1b13c93140afd113ecdcaf102f79c11ae84249f03</originalsourceid><addsrcrecordid>eNqNks1u1TAQhSMEoqXwAGyQNwg2KR4ncZJlVZUfqRILYB3NdcatK8dO7aRV-kA8J45yuexK5YVHM98cjzUny94CPwXO60-RcwEy5wB5JTjk4ll2DBKaXMiKPz_EpTjKXsV4wzlUDciX2ZGAuuJNI46z3z_MAzF1jQHVRME84GS8Y-h6djujm4w2akt5zaKxdxSYQ-dHDJNRliLbLQzjMgw0BaOYtv6eaUO2z7dw1U3tm4by82ipZ_dmumbG9XOq3ZFdDoXRYhyQDRgjiyOpKfhVeHmdvdBoI73Z3yfZr88XP8-_5pffv3w7P7vMVfrZlGOhlar6tpWkJLS0q6FAKRB2UKi2gJKj7gEKUr1CDVzoulUASE0pylbz4iT7sOmOwd_OFKduMFGRtejIz7FrORS8BLmSHx8loS7LWgjZiKehUMv6CSjUkPZWiuL_KG9EckfZ1Ak93dArtNQZp_2U1pJOT4NR3pE2KX9WtKWURSUhNcDWoIKPMZDuxmAGDEtS7VbrdZv1umS9brVet47-bj_PvBuoP3T89VoC3u8BjAptcoZTJv7jyrqooJKJExsXU8ldUehu_BxcWvsjr_8BivPz6g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1082216487</pqid></control><display><type>article</type><title>Size characterization and quantification of silver nanoparticles by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry</title><source>SpringerLink Journals - AutoHoldings</source><creator>Bolea, E. ; Jiménez-Lamana, J. ; Laborda, F. ; Castillo, J. R.</creator><creatorcontrib>Bolea, E. ; Jiménez-Lamana, J. ; Laborda, F. ; Castillo, J. R.</creatorcontrib><description>A method for determining the size of silver nanoparticles and their quantification by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (ICP-MS) is proposed and was tested in consumer products. Experimental conditions were studied in detail to avoid aggregation processes or alteration of the original size distributions. Additionally, losses from sorption processes onto the channel membrane were minimized for correct quantification of the nanoparticles. Mobile phase composition, injection/focusing, and fractionation conditions were evaluated in terms of their influence on both separation resolution and recovery. The ionic strength, pH, and the presence of ionic and nonionic surfactants had a strong influence on both separation and recovery of the nanoparticles. In general, better results were obtained under those conditions that favored charge repulsions with the membrane. Recovery values of 83 ± 8% and 93 ± 4% with respect to the content of silver nanoparticles were achieved for the consumer products studied. Silver nanoparticle standards were used for size calibration of the channel. The results were compared with those obtained by photon correlation spectroscopy and images taken by transmission electron microscopy. The quantification of silver nanoparticles was performed by direct injection of ionic silver standard solutions into the ICP-MS system, integration of the corresponding peaks, and interpolation of the fractogram area. A limit of detection of 5.6 μg L -1 silver, which corresponds to a number concentration of 1×10 12 L -1 for nanoparticles of 10 nm, was achieved for an injection volume of 20 μL.</description><identifier>ISSN: 1618-2642</identifier><identifier>EISSN: 1618-2650</identifier><identifier>DOI: 10.1007/s00216-011-5201-2</identifier><identifier>PMID: 21750882</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Analytical Chemistry ; Biochemistry ; Channels ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Chromatographic methods and physical methods associated with chromatography ; Exact sciences and technology ; Food Science ; Fractionation ; Laboratory Medicine ; Mass spectrometry ; Monitoring/Environmental Analysis ; Nanoparticles ; Original Paper ; Other chromatographic methods ; Recovery ; Separation ; Silver ; Spectrometric and optical methods ; Surface active agents</subject><ispartof>Analytical &amp; bioanalytical chemistry (Print), 2011-11, Vol.401 (9), p.2723-2732</ispartof><rights>Springer-Verlag 2011</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2011 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c581t-a3fcc5d996ec619eb713a62a1b13c93140afd113ecdcaf102f79c11ae84249f03</citedby><cites>FETCH-LOGICAL-c581t-a3fcc5d996ec619eb713a62a1b13c93140afd113ecdcaf102f79c11ae84249f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00216-011-5201-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00216-011-5201-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,23909,23910,25118,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=24735156$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21750882$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bolea, E.</creatorcontrib><creatorcontrib>Jiménez-Lamana, J.</creatorcontrib><creatorcontrib>Laborda, F.</creatorcontrib><creatorcontrib>Castillo, J. R.</creatorcontrib><title>Size characterization and quantification of silver nanoparticles by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry</title><title>Analytical &amp; bioanalytical chemistry (Print)</title><addtitle>Anal Bioanal Chem</addtitle><addtitle>Anal Bioanal Chem</addtitle><description>A method for determining the size of silver nanoparticles and their quantification by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (ICP-MS) is proposed and was tested in consumer products. Experimental conditions were studied in detail to avoid aggregation processes or alteration of the original size distributions. Additionally, losses from sorption processes onto the channel membrane were minimized for correct quantification of the nanoparticles. Mobile phase composition, injection/focusing, and fractionation conditions were evaluated in terms of their influence on both separation resolution and recovery. The ionic strength, pH, and the presence of ionic and nonionic surfactants had a strong influence on both separation and recovery of the nanoparticles. In general, better results were obtained under those conditions that favored charge repulsions with the membrane. Recovery values of 83 ± 8% and 93 ± 4% with respect to the content of silver nanoparticles were achieved for the consumer products studied. Silver nanoparticle standards were used for size calibration of the channel. The results were compared with those obtained by photon correlation spectroscopy and images taken by transmission electron microscopy. The quantification of silver nanoparticles was performed by direct injection of ionic silver standard solutions into the ICP-MS system, integration of the corresponding peaks, and interpolation of the fractogram area. A limit of detection of 5.6 μg L -1 silver, which corresponds to a number concentration of 1×10 12 L -1 for nanoparticles of 10 nm, was achieved for an injection volume of 20 μL.</description><subject>Analytical Chemistry</subject><subject>Biochemistry</subject><subject>Channels</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Exact sciences and technology</subject><subject>Food Science</subject><subject>Fractionation</subject><subject>Laboratory Medicine</subject><subject>Mass spectrometry</subject><subject>Monitoring/Environmental Analysis</subject><subject>Nanoparticles</subject><subject>Original Paper</subject><subject>Other chromatographic methods</subject><subject>Recovery</subject><subject>Separation</subject><subject>Silver</subject><subject>Spectrometric and optical methods</subject><subject>Surface active agents</subject><issn>1618-2642</issn><issn>1618-2650</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqNks1u1TAQhSMEoqXwAGyQNwg2KR4ncZJlVZUfqRILYB3NdcatK8dO7aRV-kA8J45yuexK5YVHM98cjzUny94CPwXO60-RcwEy5wB5JTjk4ll2DBKaXMiKPz_EpTjKXsV4wzlUDciX2ZGAuuJNI46z3z_MAzF1jQHVRME84GS8Y-h6djujm4w2akt5zaKxdxSYQ-dHDJNRliLbLQzjMgw0BaOYtv6eaUO2z7dw1U3tm4by82ipZ_dmumbG9XOq3ZFdDoXRYhyQDRgjiyOpKfhVeHmdvdBoI73Z3yfZr88XP8-_5pffv3w7P7vMVfrZlGOhlar6tpWkJLS0q6FAKRB2UKi2gJKj7gEKUr1CDVzoulUASE0pylbz4iT7sOmOwd_OFKduMFGRtejIz7FrORS8BLmSHx8loS7LWgjZiKehUMv6CSjUkPZWiuL_KG9EckfZ1Ak93dArtNQZp_2U1pJOT4NR3pE2KX9WtKWURSUhNcDWoIKPMZDuxmAGDEtS7VbrdZv1umS9brVet47-bj_PvBuoP3T89VoC3u8BjAptcoZTJv7jyrqooJKJExsXU8ldUehu_BxcWvsjr_8BivPz6g</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Bolea, E.</creator><creator>Jiménez-Lamana, J.</creator><creator>Laborda, F.</creator><creator>Castillo, J. R.</creator><general>Springer-Verlag</general><general>Springer</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QH</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20111101</creationdate><title>Size characterization and quantification of silver nanoparticles by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry</title><author>Bolea, E. ; Jiménez-Lamana, J. ; Laborda, F. ; Castillo, J. R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c581t-a3fcc5d996ec619eb713a62a1b13c93140afd113ecdcaf102f79c11ae84249f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Analytical Chemistry</topic><topic>Biochemistry</topic><topic>Channels</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Exact sciences and technology</topic><topic>Food Science</topic><topic>Fractionation</topic><topic>Laboratory Medicine</topic><topic>Mass spectrometry</topic><topic>Monitoring/Environmental Analysis</topic><topic>Nanoparticles</topic><topic>Original Paper</topic><topic>Other chromatographic methods</topic><topic>Recovery</topic><topic>Separation</topic><topic>Silver</topic><topic>Spectrometric and optical methods</topic><topic>Surface active agents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bolea, E.</creatorcontrib><creatorcontrib>Jiménez-Lamana, J.</creatorcontrib><creatorcontrib>Laborda, F.</creatorcontrib><creatorcontrib>Castillo, J. R.</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 3: Aquatic Pollution &amp; Environmental Quality</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical &amp; bioanalytical chemistry (Print)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bolea, E.</au><au>Jiménez-Lamana, J.</au><au>Laborda, F.</au><au>Castillo, J. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Size characterization and quantification of silver nanoparticles by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry</atitle><jtitle>Analytical &amp; bioanalytical chemistry (Print)</jtitle><stitle>Anal Bioanal Chem</stitle><addtitle>Anal Bioanal Chem</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>401</volume><issue>9</issue><spage>2723</spage><epage>2732</epage><pages>2723-2732</pages><issn>1618-2642</issn><eissn>1618-2650</eissn><abstract>A method for determining the size of silver nanoparticles and their quantification by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry (ICP-MS) is proposed and was tested in consumer products. Experimental conditions were studied in detail to avoid aggregation processes or alteration of the original size distributions. Additionally, losses from sorption processes onto the channel membrane were minimized for correct quantification of the nanoparticles. Mobile phase composition, injection/focusing, and fractionation conditions were evaluated in terms of their influence on both separation resolution and recovery. The ionic strength, pH, and the presence of ionic and nonionic surfactants had a strong influence on both separation and recovery of the nanoparticles. In general, better results were obtained under those conditions that favored charge repulsions with the membrane. Recovery values of 83 ± 8% and 93 ± 4% with respect to the content of silver nanoparticles were achieved for the consumer products studied. Silver nanoparticle standards were used for size calibration of the channel. The results were compared with those obtained by photon correlation spectroscopy and images taken by transmission electron microscopy. The quantification of silver nanoparticles was performed by direct injection of ionic silver standard solutions into the ICP-MS system, integration of the corresponding peaks, and interpolation of the fractogram area. A limit of detection of 5.6 μg L -1 silver, which corresponds to a number concentration of 1×10 12 L -1 for nanoparticles of 10 nm, was achieved for an injection volume of 20 μL.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>21750882</pmid><doi>10.1007/s00216-011-5201-2</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1618-2642
ispartof Analytical & bioanalytical chemistry (Print), 2011-11, Vol.401 (9), p.2723-2732
issn 1618-2642
1618-2650
language eng
recordid cdi_proquest_miscellaneous_901304160
source SpringerLink Journals - AutoHoldings
subjects Analytical Chemistry
Biochemistry
Channels
Characterization and Evaluation of Materials
Chemistry
Chemistry and Materials Science
Chromatographic methods and physical methods associated with chromatography
Exact sciences and technology
Food Science
Fractionation
Laboratory Medicine
Mass spectrometry
Monitoring/Environmental Analysis
Nanoparticles
Original Paper
Other chromatographic methods
Recovery
Separation
Silver
Spectrometric and optical methods
Surface active agents
title Size characterization and quantification of silver nanoparticles by asymmetric flow field-flow fractionation coupled with inductively coupled plasma mass spectrometry
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T14%3A34%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Size%20characterization%20and%20quantification%20of%20silver%20nanoparticles%20by%20asymmetric%20flow%20field-flow%20fractionation%20coupled%20with%20inductively%20coupled%20plasma%20mass%20spectrometry&rft.jtitle=Analytical%20&%20bioanalytical%20chemistry%20(Print)&rft.au=Bolea,%20E.&rft.date=2011-11-01&rft.volume=401&rft.issue=9&rft.spage=2723&rft.epage=2732&rft.pages=2723-2732&rft.issn=1618-2642&rft.eissn=1618-2650&rft_id=info:doi/10.1007/s00216-011-5201-2&rft_dat=%3Cgale_proqu%3EA394663561%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1082216487&rft_id=info:pmid/21750882&rft_galeid=A394663561&rfr_iscdi=true