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...
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Veröffentlicht in: | Analytical & bioanalytical chemistry (Print) 2011-11, Vol.401 (9), p.2723-2732 |
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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 |
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-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 & 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&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 & 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. 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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 & 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> |
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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 |
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