A respiration–metabolism chamber system and a GC–MS method developed for studying exhalation of perfluorobutane in rats after intravenous injection of the ultrasound contrast agent Sonazoid
Sonazoid™ is a new contrast agent for ultrasound imaging comprising an aqueous suspension of lipid-stabilised perfluorobutane (PFB) gas microbubbles. A respiration–metabolism chamber system was developed to collect exhaled air following intravenous administration of Sonazoid™ to rats. Analysis of PF...
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creator | Uran, Steinar Landmark, Kristin Normann, Per Trygve Hals, Petter-Arnt Toft, Kim Gunnar Skotland, Tore |
description | Sonazoid™ is a new contrast agent for ultrasound imaging comprising an aqueous suspension of lipid-stabilised perfluorobutane (PFB) gas microbubbles. A respiration–metabolism chamber system was developed to collect exhaled air following intravenous administration of Sonazoid™ to rats. Analysis of PFB in the exhaled rat air was performed using a modified version of an earlier published method for blood samples, i.e. an automatic headspace gas chromatographic mass spectrometric (GC–MS) method using electron impact ionisation. The calibration standards were PFB diluted in air (2.5–1800
pg/ml). Perfluoropentane (PFP) was used as an internal standard and the MS detector was set to single ion monitoring of the base fragment ions of PFB (
m/
z 69 and 119) and PFP (
m/
z 69). The calibration curve, made by plotting the peak area ratios of PFB (
m/
z 69) to PFP (
m/
z 69) against the theoretical concentration of PFB, was fitted to a linear equation with weighting 1/
y
2 and found to be reproducible. The lower limit of quantification (LLOQ) was 2.5
pg PFB/ml. The between-day variation of the method was below 2.6% relative standard deviation (R.S.D.) and the within-day variation of the method was below 6.4% R.S.D. The accuracy of the method was evaluated and showed a relative error less than 5.2%. PFB was found to be stable for 14 days when stored in Tedlar sample bags at room temperature. An even lower detection limit may be obtained by using the more time-consuming process of solid-phase micro extraction; thus, by concentrating PFB on carboxen–PDMS fibres an LLOQ of 0.5
pg PFB/ml was obtained. When five rats were given an i.v. bolus injection of Sonazoid™ at a dose of 8
μl microbubbles/kg a mean recovery of 96% (range, 81–110%) was found during 24
h; more than 50% was exhaled during the first 30
min after injection. |
doi_str_mv | 10.1016/j.jpba.2005.04.038 |
format | Article |
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pg/ml). Perfluoropentane (PFP) was used as an internal standard and the MS detector was set to single ion monitoring of the base fragment ions of PFB (
m/
z 69 and 119) and PFP (
m/
z 69). The calibration curve, made by plotting the peak area ratios of PFB (
m/
z 69) to PFP (
m/
z 69) against the theoretical concentration of PFB, was fitted to a linear equation with weighting 1/
y
2 and found to be reproducible. The lower limit of quantification (LLOQ) was 2.5
pg PFB/ml. The between-day variation of the method was below 2.6% relative standard deviation (R.S.D.) and the within-day variation of the method was below 6.4% R.S.D. The accuracy of the method was evaluated and showed a relative error less than 5.2%. PFB was found to be stable for 14 days when stored in Tedlar sample bags at room temperature. An even lower detection limit may be obtained by using the more time-consuming process of solid-phase micro extraction; thus, by concentrating PFB on carboxen–PDMS fibres an LLOQ of 0.5
pg PFB/ml was obtained. When five rats were given an i.v. bolus injection of Sonazoid™ at a dose of 8
μl microbubbles/kg a mean recovery of 96% (range, 81–110%) was found during 24
h; more than 50% was exhaled during the first 30
min after injection.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2005.04.038</identifier><identifier>PMID: 15964732</identifier><identifier>CODEN: JPBADA</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analysis ; Analytical, structural and metabolic biochemistry ; Animals ; Biological and medical sciences ; Calibration ; Chemistry, Pharmaceutical - methods ; Contrast agent ; Contrast Media - pharmacology ; Electrons ; Exhalation ; Ferric Compounds - pharmacology ; Fluorocarbons - analysis ; Fluorocarbons - pharmacokinetics ; Fluorocarbons - pharmacology ; Fundamental and applied biological sciences. Psychology ; Gas Chromatography-Mass Spectrometry - methods ; GC–MS ; General pharmacology ; Headspace ; Injections, Intravenous ; Ions ; Iron - pharmacology ; Male ; Mass Spectrometry ; Medical sciences ; Oxides - pharmacology ; Oxygen Consumption ; Perfluorobutane ; Pharmacology. Drug treatments ; Quality Control ; Rats ; Rats, Sprague-Dawley ; Reproducibility of Results ; Time Factors ; Ultrasound</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2005-09, Vol.39 (3), p.746-751</ispartof><rights>2005 Elsevier B.V.</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-4d9f505a510bbf5576374886a7f6216b413fdfba9f404f253fa66b957dbb4eec3</citedby><cites>FETCH-LOGICAL-c415t-4d9f505a510bbf5576374886a7f6216b413fdfba9f404f253fa66b957dbb4eec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpba.2005.04.038$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17518819$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15964732$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uran, Steinar</creatorcontrib><creatorcontrib>Landmark, Kristin</creatorcontrib><creatorcontrib>Normann, Per Trygve</creatorcontrib><creatorcontrib>Hals, Petter-Arnt</creatorcontrib><creatorcontrib>Toft, Kim Gunnar</creatorcontrib><creatorcontrib>Skotland, Tore</creatorcontrib><title>A respiration–metabolism chamber system and a GC–MS method developed for studying exhalation of perfluorobutane in rats after intravenous injection of the ultrasound contrast agent Sonazoid</title><title>Journal of pharmaceutical and biomedical analysis</title><addtitle>J Pharm Biomed Anal</addtitle><description>Sonazoid™ is a new contrast agent for ultrasound imaging comprising an aqueous suspension of lipid-stabilised perfluorobutane (PFB) gas microbubbles. A respiration–metabolism chamber system was developed to collect exhaled air following intravenous administration of Sonazoid™ to rats. Analysis of PFB in the exhaled rat air was performed using a modified version of an earlier published method for blood samples, i.e. an automatic headspace gas chromatographic mass spectrometric (GC–MS) method using electron impact ionisation. The calibration standards were PFB diluted in air (2.5–1800
pg/ml). Perfluoropentane (PFP) was used as an internal standard and the MS detector was set to single ion monitoring of the base fragment ions of PFB (
m/
z 69 and 119) and PFP (
m/
z 69). The calibration curve, made by plotting the peak area ratios of PFB (
m/
z 69) to PFP (
m/
z 69) against the theoretical concentration of PFB, was fitted to a linear equation with weighting 1/
y
2 and found to be reproducible. The lower limit of quantification (LLOQ) was 2.5
pg PFB/ml. The between-day variation of the method was below 2.6% relative standard deviation (R.S.D.) and the within-day variation of the method was below 6.4% R.S.D. The accuracy of the method was evaluated and showed a relative error less than 5.2%. PFB was found to be stable for 14 days when stored in Tedlar sample bags at room temperature. An even lower detection limit may be obtained by using the more time-consuming process of solid-phase micro extraction; thus, by concentrating PFB on carboxen–PDMS fibres an LLOQ of 0.5
pg PFB/ml was obtained. When five rats were given an i.v. bolus injection of Sonazoid™ at a dose of 8
μl microbubbles/kg a mean recovery of 96% (range, 81–110%) was found during 24
h; more than 50% was exhaled during the first 30
min after injection.</description><subject>Analysis</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Calibration</subject><subject>Chemistry, Pharmaceutical - methods</subject><subject>Contrast agent</subject><subject>Contrast Media - pharmacology</subject><subject>Electrons</subject><subject>Exhalation</subject><subject>Ferric Compounds - pharmacology</subject><subject>Fluorocarbons - analysis</subject><subject>Fluorocarbons - pharmacokinetics</subject><subject>Fluorocarbons - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gas Chromatography-Mass Spectrometry - methods</subject><subject>GC–MS</subject><subject>General pharmacology</subject><subject>Headspace</subject><subject>Injections, Intravenous</subject><subject>Ions</subject><subject>Iron - pharmacology</subject><subject>Male</subject><subject>Mass Spectrometry</subject><subject>Medical sciences</subject><subject>Oxides - pharmacology</subject><subject>Oxygen Consumption</subject><subject>Perfluorobutane</subject><subject>Pharmacology. Drug treatments</subject><subject>Quality Control</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reproducibility of Results</subject><subject>Time Factors</subject><subject>Ultrasound</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtuFDEQhlsIRIbABVggb2DXjd1t90NiE40gQQpiEZDYWX6UMx51243tHjGsuAMn4iqcJB5mUHawsiV_9VeVv6J4TnBFMGlfb6vtLEVVY8wqTCvc9A-KFem7pqxb-uVhscJdQ8oO9-yseBLjFmeQDPRxcUbY0NKuqVfFrwsUIM42iGS9-_3j5wRJSD_aOCG1EZOEgOI-JpiQcBoJdLnO0IcblLmN10jDDkY_g0bGZzItem_dLYJvGzH-iUTeoBmCGRcfvFyScICsQ7lfRMKkHG9dCmIHzi8x37eg_palDaBlzI_RL7m38gcwJiRuwSV045347q1-WjwyYozw7HSeF5_fvf20viqvP16-X19cl4oSlkqqB8MwE4xgKQ1jXdt0tO9b0Zm2Jq2kpDHaSDEYiqmpWWNE28qBdVpKCqCa8-LVMXcO_usCMfHJRgXjmDfKo_O2z_ENrf8LZgV1l1VksD6CKvgYAxg-BzuJsOcE84NhvuUHw_xgmGPKs-Fc9OKUvsgJ9H3JSWkGXp4AEZUYTRBO2XjPdYz0PRky9-bIQf60nYXAo7LgFGgbsgOuvf3XHHdyJMvt</recordid><startdate>20050915</startdate><enddate>20050915</enddate><creator>Uran, Steinar</creator><creator>Landmark, Kristin</creator><creator>Normann, Per Trygve</creator><creator>Hals, Petter-Arnt</creator><creator>Toft, Kim Gunnar</creator><creator>Skotland, Tore</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20050915</creationdate><title>A respiration–metabolism chamber system and a GC–MS method developed for studying exhalation of perfluorobutane in rats after intravenous injection of the ultrasound contrast agent Sonazoid</title><author>Uran, Steinar ; Landmark, Kristin ; Normann, Per Trygve ; Hals, Petter-Arnt ; Toft, Kim Gunnar ; Skotland, Tore</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-4d9f505a510bbf5576374886a7f6216b413fdfba9f404f253fa66b957dbb4eec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Analysis</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calibration</topic><topic>Chemistry, Pharmaceutical - methods</topic><topic>Contrast agent</topic><topic>Contrast Media - pharmacology</topic><topic>Electrons</topic><topic>Exhalation</topic><topic>Ferric Compounds - pharmacology</topic><topic>Fluorocarbons - analysis</topic><topic>Fluorocarbons - pharmacokinetics</topic><topic>Fluorocarbons - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gas Chromatography-Mass Spectrometry - methods</topic><topic>GC–MS</topic><topic>General pharmacology</topic><topic>Headspace</topic><topic>Injections, Intravenous</topic><topic>Ions</topic><topic>Iron - pharmacology</topic><topic>Male</topic><topic>Mass Spectrometry</topic><topic>Medical sciences</topic><topic>Oxides - pharmacology</topic><topic>Oxygen Consumption</topic><topic>Perfluorobutane</topic><topic>Pharmacology. Drug treatments</topic><topic>Quality Control</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reproducibility of Results</topic><topic>Time Factors</topic><topic>Ultrasound</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uran, Steinar</creatorcontrib><creatorcontrib>Landmark, Kristin</creatorcontrib><creatorcontrib>Normann, Per Trygve</creatorcontrib><creatorcontrib>Hals, Petter-Arnt</creatorcontrib><creatorcontrib>Toft, Kim Gunnar</creatorcontrib><creatorcontrib>Skotland, Tore</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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uran, Steinar</au><au>Landmark, Kristin</au><au>Normann, Per Trygve</au><au>Hals, Petter-Arnt</au><au>Toft, Kim Gunnar</au><au>Skotland, Tore</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A respiration–metabolism chamber system and a GC–MS method developed for studying exhalation of perfluorobutane in rats after intravenous injection of the ultrasound contrast agent Sonazoid</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2005-09-15</date><risdate>2005</risdate><volume>39</volume><issue>3</issue><spage>746</spage><epage>751</epage><pages>746-751</pages><issn>0731-7085</issn><eissn>1873-264X</eissn><coden>JPBADA</coden><abstract>Sonazoid™ is a new contrast agent for ultrasound imaging comprising an aqueous suspension of lipid-stabilised perfluorobutane (PFB) gas microbubbles. A respiration–metabolism chamber system was developed to collect exhaled air following intravenous administration of Sonazoid™ to rats. Analysis of PFB in the exhaled rat air was performed using a modified version of an earlier published method for blood samples, i.e. an automatic headspace gas chromatographic mass spectrometric (GC–MS) method using electron impact ionisation. The calibration standards were PFB diluted in air (2.5–1800
pg/ml). Perfluoropentane (PFP) was used as an internal standard and the MS detector was set to single ion monitoring of the base fragment ions of PFB (
m/
z 69 and 119) and PFP (
m/
z 69). The calibration curve, made by plotting the peak area ratios of PFB (
m/
z 69) to PFP (
m/
z 69) against the theoretical concentration of PFB, was fitted to a linear equation with weighting 1/
y
2 and found to be reproducible. The lower limit of quantification (LLOQ) was 2.5
pg PFB/ml. The between-day variation of the method was below 2.6% relative standard deviation (R.S.D.) and the within-day variation of the method was below 6.4% R.S.D. The accuracy of the method was evaluated and showed a relative error less than 5.2%. PFB was found to be stable for 14 days when stored in Tedlar sample bags at room temperature. An even lower detection limit may be obtained by using the more time-consuming process of solid-phase micro extraction; thus, by concentrating PFB on carboxen–PDMS fibres an LLOQ of 0.5
pg PFB/ml was obtained. When five rats were given an i.v. bolus injection of Sonazoid™ at a dose of 8
μl microbubbles/kg a mean recovery of 96% (range, 81–110%) was found during 24
h; more than 50% was exhaled during the first 30
min after injection.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15964732</pmid><doi>10.1016/j.jpba.2005.04.038</doi><tpages>6</tpages></addata></record> |
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source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Analysis Analytical, structural and metabolic biochemistry Animals Biological and medical sciences Calibration Chemistry, Pharmaceutical - methods Contrast agent Contrast Media - pharmacology Electrons Exhalation Ferric Compounds - pharmacology Fluorocarbons - analysis Fluorocarbons - pharmacokinetics Fluorocarbons - pharmacology Fundamental and applied biological sciences. Psychology Gas Chromatography-Mass Spectrometry - methods GC–MS General pharmacology Headspace Injections, Intravenous Ions Iron - pharmacology Male Mass Spectrometry Medical sciences Oxides - pharmacology Oxygen Consumption Perfluorobutane Pharmacology. Drug treatments Quality Control Rats Rats, Sprague-Dawley Reproducibility of Results Time Factors Ultrasound |
title | A respiration–metabolism chamber system and a GC–MS method developed for studying exhalation of perfluorobutane in rats after intravenous injection of the ultrasound contrast agent Sonazoid |
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