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Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking
Quetiapine is an atypical antipsychotic drug that can be used to treat mental disorders, including schizophrenia, bipolar disorder and Alzheimer’s disease. Quetiapine is mainly converted into the active metabolites of norquetiapine and 7-hydroxyquetiapine by the liver enzymes CYP3A4 and CYP2D6. In t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taiwan Food and Drug Administration
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931024/ https://www.ncbi.nlm.nih.gov/pubmed/35649137 http://dx.doi.org/10.38212/2224-6614.3378 |
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author | Liu, Tai-Ling Fang, Li-Shan Liou, Jing-Ru Dai, Jia-Shan Chen, Yen-Ling |
author_facet | Liu, Tai-Ling Fang, Li-Shan Liou, Jing-Ru Dai, Jia-Shan Chen, Yen-Ling |
author_sort | Liu, Tai-Ling |
collection | PubMed |
description | Quetiapine is an atypical antipsychotic drug that can be used to treat mental disorders, including schizophrenia, bipolar disorder and Alzheimer’s disease. Quetiapine is mainly converted into the active metabolites of norquetiapine and 7-hydroxyquetiapine by the liver enzymes CYP3A4 and CYP2D6. In this study, liquid-liquid extraction (LLE) was used as a sample pretreatment method to eliminate interferences in plasma. tert-Butyl methyl ether was chosen as the extraction solvent. Field-enhanced sample injection (FESS), an online preconcentration technique, was used to analyze quetiapine and its metabolites norquetiapine and 7-hydroxyquetiapine in plasma. The optimal separation condition was 120 mM phosphate (pH 4.0) containing 0.005% (w/v) polyvinyl pyrrolidone and 40% (v/v) methanol. The methanol plug was 0.3 psi for 6 s, the sample was electrokinetic injection by 10 kV for 60 s at positive polarity, and the separation voltage was set at 26 kV. In this experiment, quetiapine, norquetiapine and 7-hydroxyquetiapine were successfully extracted from plasma by the LLE method and stacking and separated by FESS within 15 min. The limits of detection (S/N = 3) of quetiapine, norquetiapine and 7-hydroxyquetiapine were 0.25 ng/mL, 0.50 ng/mL and 1.00 ng/mL, respectively. The linear ranges of quetiapine, norquetiapine and 7-hydroxyquetiapine were 3–120 ng/mL and the correlation coefficients were 0.999. Compared with that of the traditional capillary zone electrophoresis method, the sensitivity enrichment of analytes was 463-835-fold. The optimal experimental conditions were successfully applied to the analysis of plasma samples from patients taking quetiapine for the treatment of schizophrenia. |
format | Online Article Text |
id | pubmed-9931024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taiwan Food and Drug Administration |
record_format | MEDLINE/PubMed |
spelling | pubmed-99310242023-02-16 Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking Liu, Tai-Ling Fang, Li-Shan Liou, Jing-Ru Dai, Jia-Shan Chen, Yen-Ling J Food Drug Anal Original Article Quetiapine is an atypical antipsychotic drug that can be used to treat mental disorders, including schizophrenia, bipolar disorder and Alzheimer’s disease. Quetiapine is mainly converted into the active metabolites of norquetiapine and 7-hydroxyquetiapine by the liver enzymes CYP3A4 and CYP2D6. In this study, liquid-liquid extraction (LLE) was used as a sample pretreatment method to eliminate interferences in plasma. tert-Butyl methyl ether was chosen as the extraction solvent. Field-enhanced sample injection (FESS), an online preconcentration technique, was used to analyze quetiapine and its metabolites norquetiapine and 7-hydroxyquetiapine in plasma. The optimal separation condition was 120 mM phosphate (pH 4.0) containing 0.005% (w/v) polyvinyl pyrrolidone and 40% (v/v) methanol. The methanol plug was 0.3 psi for 6 s, the sample was electrokinetic injection by 10 kV for 60 s at positive polarity, and the separation voltage was set at 26 kV. In this experiment, quetiapine, norquetiapine and 7-hydroxyquetiapine were successfully extracted from plasma by the LLE method and stacking and separated by FESS within 15 min. The limits of detection (S/N = 3) of quetiapine, norquetiapine and 7-hydroxyquetiapine were 0.25 ng/mL, 0.50 ng/mL and 1.00 ng/mL, respectively. The linear ranges of quetiapine, norquetiapine and 7-hydroxyquetiapine were 3–120 ng/mL and the correlation coefficients were 0.999. Compared with that of the traditional capillary zone electrophoresis method, the sensitivity enrichment of analytes was 463-835-fold. The optimal experimental conditions were successfully applied to the analysis of plasma samples from patients taking quetiapine for the treatment of schizophrenia. Taiwan Food and Drug Administration 2021-12-15 /pmc/articles/PMC9931024/ /pubmed/35649137 http://dx.doi.org/10.38212/2224-6614.3378 Text en © 2021 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Original Article Liu, Tai-Ling Fang, Li-Shan Liou, Jing-Ru Dai, Jia-Shan Chen, Yen-Ling Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking |
title | Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking |
title_full | Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking |
title_fullStr | Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking |
title_full_unstemmed | Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking |
title_short | Determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking |
title_sort | determination of quetiapine and its metabolites in plasma by field-enhanced sample stacking |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931024/ https://www.ncbi.nlm.nih.gov/pubmed/35649137 http://dx.doi.org/10.38212/2224-6614.3378 |
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