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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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2005-09, Vol.39 (3), p.746-751
Hauptverfasser: Uran, Steinar, Landmark, Kristin, Normann, Per Trygve, Hals, Petter-Arnt, Toft, Kim Gunnar, Skotland, Tore
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container_title Journal of pharmaceutical and biomedical analysis
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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
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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. 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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. 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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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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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