Study on the detection limits of a new argon gas cluster ion beam secondary ion mass spectrometry apparatus using lipid compound samples
RATIONALE Ar gas cluster ion beam secondary ion mass spectrometry (Ar‐GCIB SIMS) has been developed as one of the most powerful tools used for analyzing complex biological materials because of its distinctively high secondary ion yield of large organic molecules. However, for the practical analysis...
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Veröffentlicht in: | Rapid communications in mass spectrometry 2014-04, Vol.28 (8), p.917-920 |
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creator | Fujii, Makiko Nakagawa, Shunichirou Matsuda, Kazuhiro Man, Naoki Seki, Toshio Aoki, Takaaki Matsuo, Jiro |
description | RATIONALE
Ar gas cluster ion beam secondary ion mass spectrometry (Ar‐GCIB SIMS) has been developed as one of the most powerful tools used for analyzing complex biological materials because of its distinctively high secondary ion yield of large organic molecules. However, for the practical analysis of minor components in complex biological materials, the sensitivity of the technique is still insufficient.
METHODS
The detection limits of our original Ar‐GCIB SIMS apparatus were investigated by measuring lipid compound samples in positive ion mode. The samples were mixtures of 1,2‐distearoyl‐sn‐glycero‐3‐phosphocholine (C44H88NO8P, DSPC) and 1,2‐dipalmitoyl‐sn‐glycero‐3‐phosphocholine (C40H80NO8P, DPPC). The primary ions were accelerated with 10 keV and the mean cluster size was 1500. The secondary [M+H]+ ions emitted from the sample were analyzed using an orthogonal acceleration time‐of‐flight mass spectrometer (oa‐TOF‐MS). In addition, the isotope abundance ratio and the ratio of the [M+H]+ ion signal to the fragment ion signal acquired with Ar‐GCIB SIMS were compared with those obtained with conventional Bi cluster SIMS.
RESULTS
Secondary [M+H]+ ions and some characteristic fragment ions were clearly observed with high quantitative accuracy in the mass spectra acquired with Ar‐GCIB SIMS. The results were clearly better than those obtained with conventional Bi cluster SIMS.
CONCLUSIONS
The detection limit of Ar‐GCIB SIMS was found to be below 0.1% and was much lower than that of conventional Bi cluster SIMS because of the high [M+H]+ ion yield and the low background. The results suggested that the new Ar‐GCIB SIMS apparatus has the capability to acquire valuable information on complex biological materials. Copyright © 2014 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/rcm.6867 |
format | Article |
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Ar gas cluster ion beam secondary ion mass spectrometry (Ar‐GCIB SIMS) has been developed as one of the most powerful tools used for analyzing complex biological materials because of its distinctively high secondary ion yield of large organic molecules. However, for the practical analysis of minor components in complex biological materials, the sensitivity of the technique is still insufficient.
METHODS
The detection limits of our original Ar‐GCIB SIMS apparatus were investigated by measuring lipid compound samples in positive ion mode. The samples were mixtures of 1,2‐distearoyl‐sn‐glycero‐3‐phosphocholine (C44H88NO8P, DSPC) and 1,2‐dipalmitoyl‐sn‐glycero‐3‐phosphocholine (C40H80NO8P, DPPC). The primary ions were accelerated with 10 keV and the mean cluster size was 1500. The secondary [M+H]+ ions emitted from the sample were analyzed using an orthogonal acceleration time‐of‐flight mass spectrometer (oa‐TOF‐MS). In addition, the isotope abundance ratio and the ratio of the [M+H]+ ion signal to the fragment ion signal acquired with Ar‐GCIB SIMS were compared with those obtained with conventional Bi cluster SIMS.
RESULTS
Secondary [M+H]+ ions and some characteristic fragment ions were clearly observed with high quantitative accuracy in the mass spectra acquired with Ar‐GCIB SIMS. The results were clearly better than those obtained with conventional Bi cluster SIMS.
CONCLUSIONS
The detection limit of Ar‐GCIB SIMS was found to be below 0.1% and was much lower than that of conventional Bi cluster SIMS because of the high [M+H]+ ion yield and the low background. The results suggested that the new Ar‐GCIB SIMS apparatus has the capability to acquire valuable information on complex biological materials. Copyright © 2014 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.6867</identifier><identifier>PMID: 24623696</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>1,2-Dipalmitoylphosphatidylcholine - analysis ; 1,2-Dipalmitoylphosphatidylcholine - chemistry ; Argon - chemistry ; Biological materials ; Clusters ; Fragmentation ; Ion beams ; Ions - analysis ; Ions - chemistry ; Limit of Detection ; Lipids ; Mass spectrometers ; Mass spectroscopy ; Models, Chemical ; Secondary ion mass spectrometry ; Spectrometry, Mass, Secondary Ion - methods</subject><ispartof>Rapid communications in mass spectrometry, 2014-04, Vol.28 (8), p.917-920</ispartof><rights>Copyright © 2014 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4867-7a86ed1aba6c483691a1784571223e40a81ff45cb7c1b0b2fd485d7e3df068b63</citedby><cites>FETCH-LOGICAL-c4867-7a86ed1aba6c483691a1784571223e40a81ff45cb7c1b0b2fd485d7e3df068b63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Frcm.6867$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Frcm.6867$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24623696$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujii, Makiko</creatorcontrib><creatorcontrib>Nakagawa, Shunichirou</creatorcontrib><creatorcontrib>Matsuda, Kazuhiro</creatorcontrib><creatorcontrib>Man, Naoki</creatorcontrib><creatorcontrib>Seki, Toshio</creatorcontrib><creatorcontrib>Aoki, Takaaki</creatorcontrib><creatorcontrib>Matsuo, Jiro</creatorcontrib><title>Study on the detection limits of a new argon gas cluster ion beam secondary ion mass spectrometry apparatus using lipid compound samples</title><title>Rapid communications in mass spectrometry</title><addtitle>Rapid Commun. Mass Spectrom</addtitle><description>RATIONALE
Ar gas cluster ion beam secondary ion mass spectrometry (Ar‐GCIB SIMS) has been developed as one of the most powerful tools used for analyzing complex biological materials because of its distinctively high secondary ion yield of large organic molecules. However, for the practical analysis of minor components in complex biological materials, the sensitivity of the technique is still insufficient.
METHODS
The detection limits of our original Ar‐GCIB SIMS apparatus were investigated by measuring lipid compound samples in positive ion mode. The samples were mixtures of 1,2‐distearoyl‐sn‐glycero‐3‐phosphocholine (C44H88NO8P, DSPC) and 1,2‐dipalmitoyl‐sn‐glycero‐3‐phosphocholine (C40H80NO8P, DPPC). The primary ions were accelerated with 10 keV and the mean cluster size was 1500. The secondary [M+H]+ ions emitted from the sample were analyzed using an orthogonal acceleration time‐of‐flight mass spectrometer (oa‐TOF‐MS). In addition, the isotope abundance ratio and the ratio of the [M+H]+ ion signal to the fragment ion signal acquired with Ar‐GCIB SIMS were compared with those obtained with conventional Bi cluster SIMS.
RESULTS
Secondary [M+H]+ ions and some characteristic fragment ions were clearly observed with high quantitative accuracy in the mass spectra acquired with Ar‐GCIB SIMS. The results were clearly better than those obtained with conventional Bi cluster SIMS.
CONCLUSIONS
The detection limit of Ar‐GCIB SIMS was found to be below 0.1% and was much lower than that of conventional Bi cluster SIMS because of the high [M+H]+ ion yield and the low background. The results suggested that the new Ar‐GCIB SIMS apparatus has the capability to acquire valuable information on complex biological materials. Copyright © 2014 John Wiley & Sons, Ltd.</description><subject>1,2-Dipalmitoylphosphatidylcholine - analysis</subject><subject>1,2-Dipalmitoylphosphatidylcholine - chemistry</subject><subject>Argon - chemistry</subject><subject>Biological materials</subject><subject>Clusters</subject><subject>Fragmentation</subject><subject>Ion beams</subject><subject>Ions - analysis</subject><subject>Ions - chemistry</subject><subject>Limit of Detection</subject><subject>Lipids</subject><subject>Mass spectrometers</subject><subject>Mass spectroscopy</subject><subject>Models, Chemical</subject><subject>Secondary ion mass spectrometry</subject><subject>Spectrometry, Mass, Secondary Ion - methods</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkd2K1DAYhoMo7uwqeAUS8MSTrkmaJu2hzOoorD-siuBJSJOvY9emqfladucOvGwz7riCIHgU8ubhgTcvIY84O-WMiWfJhVNVK32HrDhrdMFEye-SFWsqXkje1EfkGPGSMc4rwe6TIyGVKFWjVuTHh3nxOxpHOn8F6mEGN_f5NvShn5HGjlo6whW1aZvTrUXqhgVnSHRPtWADRXBx9DbtfkXBIlKcsibFAHNO7TTZZOcF6YL9uM3qqffUxTDFZfQUbZgGwAfkXmcHhIeH84R8evni4_pVcf5u83r9_LxwMhcstK0VeG5bq3KQO3DLdS0rzYUoQTJb866TlWu14y1rRedlXXkNpe-YqltVnpCnN94pxe8L4GxCjw6GwY4QFzS8KjnjpdTsP1CmdVMJ0WT0yV_oZVzSmIvsKaUaxrT8I3QpIibozJT6kH_OcGb2Q5o8pNkPmdHHB-HSBvC34O_lMlDcAFf9ALt_iszF-s1BeOD7vN71LW_TN5NfdWU-v90YLTYX788qab6UPwF3CLcH</recordid><startdate>20140430</startdate><enddate>20140430</enddate><creator>Fujii, Makiko</creator><creator>Nakagawa, Shunichirou</creator><creator>Matsuda, Kazuhiro</creator><creator>Man, Naoki</creator><creator>Seki, Toshio</creator><creator>Aoki, Takaaki</creator><creator>Matsuo, Jiro</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>JQ2</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20140430</creationdate><title>Study on the detection limits of a new argon gas cluster ion beam secondary ion mass spectrometry apparatus using lipid compound samples</title><author>Fujii, Makiko ; Nakagawa, Shunichirou ; Matsuda, Kazuhiro ; Man, Naoki ; Seki, Toshio ; Aoki, Takaaki ; Matsuo, Jiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4867-7a86ed1aba6c483691a1784571223e40a81ff45cb7c1b0b2fd485d7e3df068b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>1,2-Dipalmitoylphosphatidylcholine - analysis</topic><topic>1,2-Dipalmitoylphosphatidylcholine - chemistry</topic><topic>Argon - chemistry</topic><topic>Biological materials</topic><topic>Clusters</topic><topic>Fragmentation</topic><topic>Ion beams</topic><topic>Ions - analysis</topic><topic>Ions - chemistry</topic><topic>Limit of Detection</topic><topic>Lipids</topic><topic>Mass spectrometers</topic><topic>Mass spectroscopy</topic><topic>Models, Chemical</topic><topic>Secondary ion mass spectrometry</topic><topic>Spectrometry, Mass, Secondary Ion - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujii, Makiko</creatorcontrib><creatorcontrib>Nakagawa, Shunichirou</creatorcontrib><creatorcontrib>Matsuda, Kazuhiro</creatorcontrib><creatorcontrib>Man, Naoki</creatorcontrib><creatorcontrib>Seki, Toshio</creatorcontrib><creatorcontrib>Aoki, Takaaki</creatorcontrib><creatorcontrib>Matsuo, Jiro</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>ProQuest Computer Science Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Rapid communications in mass spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujii, Makiko</au><au>Nakagawa, Shunichirou</au><au>Matsuda, Kazuhiro</au><au>Man, Naoki</au><au>Seki, Toshio</au><au>Aoki, Takaaki</au><au>Matsuo, Jiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study on the detection limits of a new argon gas cluster ion beam secondary ion mass spectrometry apparatus using lipid compound samples</atitle><jtitle>Rapid communications in mass spectrometry</jtitle><addtitle>Rapid Commun. Mass Spectrom</addtitle><date>2014-04-30</date><risdate>2014</risdate><volume>28</volume><issue>8</issue><spage>917</spage><epage>920</epage><pages>917-920</pages><issn>0951-4198</issn><eissn>1097-0231</eissn><abstract>RATIONALE
Ar gas cluster ion beam secondary ion mass spectrometry (Ar‐GCIB SIMS) has been developed as one of the most powerful tools used for analyzing complex biological materials because of its distinctively high secondary ion yield of large organic molecules. However, for the practical analysis of minor components in complex biological materials, the sensitivity of the technique is still insufficient.
METHODS
The detection limits of our original Ar‐GCIB SIMS apparatus were investigated by measuring lipid compound samples in positive ion mode. The samples were mixtures of 1,2‐distearoyl‐sn‐glycero‐3‐phosphocholine (C44H88NO8P, DSPC) and 1,2‐dipalmitoyl‐sn‐glycero‐3‐phosphocholine (C40H80NO8P, DPPC). The primary ions were accelerated with 10 keV and the mean cluster size was 1500. The secondary [M+H]+ ions emitted from the sample were analyzed using an orthogonal acceleration time‐of‐flight mass spectrometer (oa‐TOF‐MS). In addition, the isotope abundance ratio and the ratio of the [M+H]+ ion signal to the fragment ion signal acquired with Ar‐GCIB SIMS were compared with those obtained with conventional Bi cluster SIMS.
RESULTS
Secondary [M+H]+ ions and some characteristic fragment ions were clearly observed with high quantitative accuracy in the mass spectra acquired with Ar‐GCIB SIMS. The results were clearly better than those obtained with conventional Bi cluster SIMS.
CONCLUSIONS
The detection limit of Ar‐GCIB SIMS was found to be below 0.1% and was much lower than that of conventional Bi cluster SIMS because of the high [M+H]+ ion yield and the low background. The results suggested that the new Ar‐GCIB SIMS apparatus has the capability to acquire valuable information on complex biological materials. Copyright © 2014 John Wiley & Sons, Ltd.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24623696</pmid><doi>10.1002/rcm.6867</doi><tpages>4</tpages></addata></record> |
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subjects | 1,2-Dipalmitoylphosphatidylcholine - analysis 1,2-Dipalmitoylphosphatidylcholine - chemistry Argon - chemistry Biological materials Clusters Fragmentation Ion beams Ions - analysis Ions - chemistry Limit of Detection Lipids Mass spectrometers Mass spectroscopy Models, Chemical Secondary ion mass spectrometry Spectrometry, Mass, Secondary Ion - methods |
title | Study on the detection limits of a new argon gas cluster ion beam secondary ion mass spectrometry apparatus using lipid compound samples |
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