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A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker

In this study, a new strategy for the simultaneous quantization of five serotonin 5-hydroxytryptamine receptor antagonists—ondansetron, azasetron, ramosetron, granisetron, and tropisetron—either in infusion samples or in injection dosage form was first established based on high-performance liquid ch...

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Autores principales: Chen, Fuchao, Fang, Baoxia, Li, Peng, Wang, Sicen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257339/
https://www.ncbi.nlm.nih.gov/pubmed/34257662
http://dx.doi.org/10.1155/2021/5533646
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author Chen, Fuchao
Fang, Baoxia
Li, Peng
Wang, Sicen
author_facet Chen, Fuchao
Fang, Baoxia
Li, Peng
Wang, Sicen
author_sort Chen, Fuchao
collection PubMed
description In this study, a new strategy for the simultaneous quantization of five serotonin 5-hydroxytryptamine receptor antagonists—ondansetron, azasetron, ramosetron, granisetron, and tropisetron—either in infusion samples or in injection dosage form was first established based on high-performance liquid chromatography combined with a quantitative analysis of multiple components by a single marker. The quantitative analysis of multicomponents by a single marker method was conducted with ondansetron as an internal reference substance and performed using relative retention time and ultraviolet spectral similarity as the double indicator. The quantitative analysis of the 5-HT(3) receptor antagonists was calculated and investigated based on the relative correction factors. Chromatographic separation was achieved using a C(18) column (150 mm × 4.6 mm, 5.0 μm), and the mobile phase was composed of acetonitrile-0.05 mol·L(−1) potassium dihydrogen phosphate (pH 4.0) (25 : 75) at a flow rate of 1.0 mL·min(−1) and detection wavelengths of 307 nm (ondansetron, azasetron, ramosetron), 302 nm (granisetron), and 285 nm (tropisetron). In addition, the accuracy of the quantitative analysis of multicomponents by a single marker method was compared with an external standard method, and no significant difference was observed between the two methods. The established method is rapid, is easy, and does not require many reference substances, and it can been successfully applied as part of the quality control of the five 5-HT(3) receptor antagonists in their injection dosage form and infusion sample drugs in hospitals.
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spelling pubmed-82573392021-07-12 A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker Chen, Fuchao Fang, Baoxia Li, Peng Wang, Sicen Int J Anal Chem Research Article In this study, a new strategy for the simultaneous quantization of five serotonin 5-hydroxytryptamine receptor antagonists—ondansetron, azasetron, ramosetron, granisetron, and tropisetron—either in infusion samples or in injection dosage form was first established based on high-performance liquid chromatography combined with a quantitative analysis of multiple components by a single marker. The quantitative analysis of multicomponents by a single marker method was conducted with ondansetron as an internal reference substance and performed using relative retention time and ultraviolet spectral similarity as the double indicator. The quantitative analysis of the 5-HT(3) receptor antagonists was calculated and investigated based on the relative correction factors. Chromatographic separation was achieved using a C(18) column (150 mm × 4.6 mm, 5.0 μm), and the mobile phase was composed of acetonitrile-0.05 mol·L(−1) potassium dihydrogen phosphate (pH 4.0) (25 : 75) at a flow rate of 1.0 mL·min(−1) and detection wavelengths of 307 nm (ondansetron, azasetron, ramosetron), 302 nm (granisetron), and 285 nm (tropisetron). In addition, the accuracy of the quantitative analysis of multicomponents by a single marker method was compared with an external standard method, and no significant difference was observed between the two methods. The established method is rapid, is easy, and does not require many reference substances, and it can been successfully applied as part of the quality control of the five 5-HT(3) receptor antagonists in their injection dosage form and infusion sample drugs in hospitals. Hindawi 2021-06-26 /pmc/articles/PMC8257339/ /pubmed/34257662 http://dx.doi.org/10.1155/2021/5533646 Text en Copyright © 2021 Fuchao Chen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chen, Fuchao
Fang, Baoxia
Li, Peng
Wang, Sicen
A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker
title A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker
title_full A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker
title_fullStr A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker
title_full_unstemmed A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker
title_short A Fast and Validated HPLC Method for the Simultaneous Analysis of Five 5-HT(3) Receptor Antagonists via the Quantitative Analysis of Multicomponents by a Single Marker
title_sort fast and validated hplc method for the simultaneous analysis of five 5-ht(3) receptor antagonists via the quantitative analysis of multicomponents by a single marker
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8257339/
https://www.ncbi.nlm.nih.gov/pubmed/34257662
http://dx.doi.org/10.1155/2021/5533646
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