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
Hauptverfasser: Jennison, Thomas A., Brown, Paul, Crossett, Jonathan, Kushnir, Mark, Urry, Francis M.
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container_end_page 541
container_issue 7
container_start_page 537
container_title Journal of analytical toxicology
container_volume 19
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.
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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. 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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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