A Rapid Gas Chromatographic Method Quantitating Clozapine in Human Plasma or Serum for the Purpose of Therapeutic Monitoring
A gas chromatographic method using nitrogen-phosphorus detection was developed to quantitate clozapine in plasma or serum. Methyl clonazepam was used as an internal standard. Sample preparation included a single-step extraction with ethyl acetate, which was injected directly onto a wide-bore capilla...
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Veröffentlicht in: | Journal of analytical toxicology 1995-11, Vol.19 (7), p.537-541 |
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creator | Jennison, Thomas A. Brown, Paul Crossett, Jonathan Kushnir, Mark Urry, Francis M. |
description | A gas chromatographic method using nitrogen-phosphorus detection was developed to quantitate clozapine in plasma or serum. Methyl clonazepam was used as an internal standard. Sample preparation included a single-step extraction with ethyl acetate, which was injected directly onto a wide-bore capillary column. Within-run and total precision, measured as percent coefficient of variation, were determined at low, therapeutic, and high clozapine plasma concentrations. The within-run precision for the low, therapeutic, and high clozapine plasma samples was 5.2, 2.7, and 2.4%, respectively. The total precision for the low, therapeutic, and high clozapine plasma samples was 10.0, 2.6, and 2.0%, respectively. Analytical accuracy was evaluated by comparing quantitative results with those obtained from a reference laboratory. Those samples containing therapeutic or high concentrations agreed within 3%; the sample containing a subtherapeutic concentration differed by 11.9%. The limit of quantitation was determined to be 35 ng/mL, and the upper limit of linearity was 3000 ng/mL. No significant interferences were detected after testing more than two dozen drugs and metabolites. |
doi_str_mv | 10.1093/jat/19.7.537 |
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Methyl clonazepam was used as an internal standard. Sample preparation included a single-step extraction with ethyl acetate, which was injected directly onto a wide-bore capillary column. Within-run and total precision, measured as percent coefficient of variation, were determined at low, therapeutic, and high clozapine plasma concentrations. The within-run precision for the low, therapeutic, and high clozapine plasma samples was 5.2, 2.7, and 2.4%, respectively. The total precision for the low, therapeutic, and high clozapine plasma samples was 10.0, 2.6, and 2.0%, respectively. Analytical accuracy was evaluated by comparing quantitative results with those obtained from a reference laboratory. Those samples containing therapeutic or high concentrations agreed within 3%; the sample containing a subtherapeutic concentration differed by 11.9%. The limit of quantitation was determined to be 35 ng/mL, and the upper limit of linearity was 3000 ng/mL. No significant interferences were detected after testing more than two dozen drugs and metabolites.</description><identifier>ISSN: 0146-4760</identifier><identifier>EISSN: 1945-2403</identifier><identifier>DOI: 10.1093/jat/19.7.537</identifier><identifier>PMID: 8577174</identifier><identifier>CODEN: JATOD3</identifier><language>eng</language><publisher>Niles, IL: Oxford University Press</publisher><subject>Analysis ; Antipsychotic Agents - blood ; Antipsychotic Agents - therapeutic use ; Biological and medical sciences ; Chromatography, Gas - methods ; clonazepam ; Clonazepam - blood ; Clozapine ; Clozapine - blood ; Clozapine - therapeutic use ; Drug Interactions ; Drug Monitoring ; Drugs ; Ethyl acetate ; General pharmacology ; Humans ; Medical sciences ; Metabolites ; Methylation ; Pharmacology. Drug treatments ; Quantitation ; Reference Standards ; Reproducibility of Results</subject><ispartof>Journal of analytical toxicology, 1995-11, Vol.19 (7), p.537-541</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-9a289e97fce22f8367661545fbb55342f64342b08884ff37d4ee9cb0e8f95a6b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2898472$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8577174$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jennison, Thomas A.</creatorcontrib><creatorcontrib>Brown, Paul</creatorcontrib><creatorcontrib>Crossett, Jonathan</creatorcontrib><creatorcontrib>Kushnir, Mark</creatorcontrib><creatorcontrib>Urry, Francis M.</creatorcontrib><title>A Rapid Gas Chromatographic Method Quantitating Clozapine in Human Plasma or Serum for the Purpose of Therapeutic Monitoring</title><title>Journal of analytical toxicology</title><addtitle>Journal of Analytical Toxicology</addtitle><description>A gas chromatographic method using nitrogen-phosphorus detection was developed to quantitate clozapine in plasma or serum. Methyl clonazepam was used as an internal standard. Sample preparation included a single-step extraction with ethyl acetate, which was injected directly onto a wide-bore capillary column. Within-run and total precision, measured as percent coefficient of variation, were determined at low, therapeutic, and high clozapine plasma concentrations. The within-run precision for the low, therapeutic, and high clozapine plasma samples was 5.2, 2.7, and 2.4%, respectively. The total precision for the low, therapeutic, and high clozapine plasma samples was 10.0, 2.6, and 2.0%, respectively. Analytical accuracy was evaluated by comparing quantitative results with those obtained from a reference laboratory. Those samples containing therapeutic or high concentrations agreed within 3%; the sample containing a subtherapeutic concentration differed by 11.9%. The limit of quantitation was determined to be 35 ng/mL, and the upper limit of linearity was 3000 ng/mL. No significant interferences were detected after testing more than two dozen drugs and metabolites.</description><subject>Analysis</subject><subject>Antipsychotic Agents - blood</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Chromatography, Gas - methods</subject><subject>clonazepam</subject><subject>Clonazepam - blood</subject><subject>Clozapine</subject><subject>Clozapine - blood</subject><subject>Clozapine - therapeutic use</subject><subject>Drug Interactions</subject><subject>Drug Monitoring</subject><subject>Drugs</subject><subject>Ethyl acetate</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Metabolites</subject><subject>Methylation</subject><subject>Pharmacology. Drug treatments</subject><subject>Quantitation</subject><subject>Reference Standards</subject><subject>Reproducibility of Results</subject><issn>0146-4760</issn><issn>1945-2403</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90c1rFDEYBvAgSl2rN69CDlJ6cLb5TuZYFtsVK9a6guwlZGaTTurMZEwyoOIfb3SXPXpJAs8vz-F9AXiJ0RKjml48mHyB66VcciofgQWuGa8IQ_QxWCDMRMWkQE_Bs5QeEMJCCXoCThSXEku2AL8v4Z2Z_A5emwRXXQyDyeE-mqnzLfxgcxd28NNsxuyzyX68h6s-_CofRgv9CNfzYEZ425s0GBgi_GzjPEBXXrmz8HaOU0gWBgc3nS2dds5_W8Poc4il7Dl44kyf7IvDfQq-XL3drNbVzcfrd6vLm6plWOaqNkTVtpautYQ4RYUUAnPGXdNwThlxgpWzQUop5hyVO2Zt3TbIKldzIxp6Cs72vVMM32ebsh58am3fm9GGOWksEWGSqwLP_w_LvBkXDIlC3-xpG0NK0To9RT-Y-LOgf06XvWhca6nLXgp_dWiem8HujviwiJK_PuQmtaZ30YytT0dWBqCYJIVVe-ZTtj-OsYnftJBUcr3-utUbQt7fse1Wr-kftqelWw</recordid><startdate>19951101</startdate><enddate>19951101</enddate><creator>Jennison, Thomas A.</creator><creator>Brown, Paul</creator><creator>Crossett, Jonathan</creator><creator>Kushnir, Mark</creator><creator>Urry, Francis M.</creator><general>Oxford University Press</general><general>Preston</general><scope>BSCLL</scope><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>19951101</creationdate><title>A Rapid Gas Chromatographic Method Quantitating Clozapine in Human Plasma or Serum for the Purpose of Therapeutic Monitoring</title><author>Jennison, Thomas A. ; Brown, Paul ; Crossett, Jonathan ; Kushnir, Mark ; Urry, Francis M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-9a289e97fce22f8367661545fbb55342f64342b08884ff37d4ee9cb0e8f95a6b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Analysis</topic><topic>Antipsychotic Agents - blood</topic><topic>Antipsychotic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Chromatography, Gas - methods</topic><topic>clonazepam</topic><topic>Clonazepam - blood</topic><topic>Clozapine</topic><topic>Clozapine - blood</topic><topic>Clozapine - therapeutic use</topic><topic>Drug Interactions</topic><topic>Drug Monitoring</topic><topic>Drugs</topic><topic>Ethyl acetate</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Metabolites</topic><topic>Methylation</topic><topic>Pharmacology. Drug treatments</topic><topic>Quantitation</topic><topic>Reference Standards</topic><topic>Reproducibility of Results</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jennison, Thomas A.</creatorcontrib><creatorcontrib>Brown, Paul</creatorcontrib><creatorcontrib>Crossett, Jonathan</creatorcontrib><creatorcontrib>Kushnir, Mark</creatorcontrib><creatorcontrib>Urry, Francis M.</creatorcontrib><collection>Istex</collection><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>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Journal of analytical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jennison, Thomas A.</au><au>Brown, Paul</au><au>Crossett, Jonathan</au><au>Kushnir, Mark</au><au>Urry, Francis M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Rapid Gas Chromatographic Method Quantitating Clozapine in Human Plasma or Serum for the Purpose of Therapeutic Monitoring</atitle><jtitle>Journal of analytical toxicology</jtitle><addtitle>Journal of Analytical Toxicology</addtitle><date>1995-11-01</date><risdate>1995</risdate><volume>19</volume><issue>7</issue><spage>537</spage><epage>541</epage><pages>537-541</pages><issn>0146-4760</issn><eissn>1945-2403</eissn><coden>JATOD3</coden><abstract>A gas chromatographic method using nitrogen-phosphorus detection was developed to quantitate clozapine in plasma or serum. Methyl clonazepam was used as an internal standard. Sample preparation included a single-step extraction with ethyl acetate, which was injected directly onto a wide-bore capillary column. Within-run and total precision, measured as percent coefficient of variation, were determined at low, therapeutic, and high clozapine plasma concentrations. The within-run precision for the low, therapeutic, and high clozapine plasma samples was 5.2, 2.7, and 2.4%, respectively. The total precision for the low, therapeutic, and high clozapine plasma samples was 10.0, 2.6, and 2.0%, respectively. Analytical accuracy was evaluated by comparing quantitative results with those obtained from a reference laboratory. Those samples containing therapeutic or high concentrations agreed within 3%; the sample containing a subtherapeutic concentration differed by 11.9%. The limit of quantitation was determined to be 35 ng/mL, and the upper limit of linearity was 3000 ng/mL. No significant interferences were detected after testing more than two dozen drugs and metabolites.</abstract><cop>Niles, IL</cop><pub>Oxford University Press</pub><pmid>8577174</pmid><doi>10.1093/jat/19.7.537</doi><tpages>5</tpages></addata></record> |
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source | Oxford University Press Journals Digital Archive legacy; MEDLINE; Alma/SFX Local Collection |
subjects | Analysis Antipsychotic Agents - blood Antipsychotic Agents - therapeutic use Biological and medical sciences Chromatography, Gas - methods clonazepam Clonazepam - blood Clozapine Clozapine - blood Clozapine - therapeutic use Drug Interactions Drug Monitoring Drugs Ethyl acetate General pharmacology Humans Medical sciences Metabolites Methylation Pharmacology. Drug treatments Quantitation Reference Standards Reproducibility of Results |
title | A Rapid Gas Chromatographic Method Quantitating Clozapine in Human Plasma or Serum for the Purpose of Therapeutic Monitoring |
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