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Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis

Liquid chromatography/tandem mass spectrometry (LC–MS/MS) is widely used to determine vitamin D(3) metabolites in biological samples. The ionization efficiencies of these metabolites, however, are poor under electrospray ionization conditions. Moreover, the chromatographic separation of multiple vit...

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Autores principales: Alexandridou, Anastasia, Volmer, Dietrich A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823060/
https://www.ncbi.nlm.nih.gov/pubmed/36342509
http://dx.doi.org/10.1007/s00216-022-04409-5
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author Alexandridou, Anastasia
Volmer, Dietrich A.
author_facet Alexandridou, Anastasia
Volmer, Dietrich A.
author_sort Alexandridou, Anastasia
collection PubMed
description Liquid chromatography/tandem mass spectrometry (LC–MS/MS) is widely used to determine vitamin D(3) metabolites in biological samples. The ionization efficiencies of these metabolites, however, are poor under electrospray ionization conditions. Moreover, the chromatographic separation of multiple vitamin D metabolites and their epimers can be challenging. For these reasons, chemical derivatization reagents are often used to improve sensitivity and selectivity of analysis. While the derivatization schemes have been proven to be very effective, one missing aspect is the investigation of the stability of the chemical derivatization products in stored sample extracts. In this study, we investigated the long-term stability of several vitamin D(3) metabolites after 1 and 3 months of storage at − 20 °C. Five vitamin D(3) metabolites were examined after derivatization with seven different derivatization reagents. Generally, Amplifex products were the most stable in the long term in our study with 11–20% degraded after 1 month of storage and 14–35% after 3 months. The stabilities for some of the metabolites′ 4-[2-(6,7-dimethoxy-4-methyl-3-oxo-3,4-dihydroquinoxalyl)ethyl]-1,2,4-triazoline-3,5-dione (DMEQ-TAD), 2-fluoro-1-methylpyridinium p-toluenesulfonate (FMP-TS), isonicotinoyl chloride (INC) and 4-phenyl-1,2,4-triazoline-3,5-dione acetylated (PTAD-Ac) products were also acceptable after 1 month of storage. Other derivatized metabolites, however, degraded extensively already after 1 month of storage, such as 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) (54–72% degradation) and 2-nitrosopyridine (PyrNO) (32–100% degradation). Importantly, for every metabolite, there was an optimum derivatization reagent that met the criteria of stability proposed by international regulatory bodies after 1 month of storage. Some derivatives were stable for even up to 3 months of storage, with degradation of less than 15%. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-022-04409-5.
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spelling pubmed-98230602023-01-08 Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis Alexandridou, Anastasia Volmer, Dietrich A. Anal Bioanal Chem Research Paper Liquid chromatography/tandem mass spectrometry (LC–MS/MS) is widely used to determine vitamin D(3) metabolites in biological samples. The ionization efficiencies of these metabolites, however, are poor under electrospray ionization conditions. Moreover, the chromatographic separation of multiple vitamin D metabolites and their epimers can be challenging. For these reasons, chemical derivatization reagents are often used to improve sensitivity and selectivity of analysis. While the derivatization schemes have been proven to be very effective, one missing aspect is the investigation of the stability of the chemical derivatization products in stored sample extracts. In this study, we investigated the long-term stability of several vitamin D(3) metabolites after 1 and 3 months of storage at − 20 °C. Five vitamin D(3) metabolites were examined after derivatization with seven different derivatization reagents. Generally, Amplifex products were the most stable in the long term in our study with 11–20% degraded after 1 month of storage and 14–35% after 3 months. The stabilities for some of the metabolites′ 4-[2-(6,7-dimethoxy-4-methyl-3-oxo-3,4-dihydroquinoxalyl)ethyl]-1,2,4-triazoline-3,5-dione (DMEQ-TAD), 2-fluoro-1-methylpyridinium p-toluenesulfonate (FMP-TS), isonicotinoyl chloride (INC) and 4-phenyl-1,2,4-triazoline-3,5-dione acetylated (PTAD-Ac) products were also acceptable after 1 month of storage. Other derivatized metabolites, however, degraded extensively already after 1 month of storage, such as 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) (54–72% degradation) and 2-nitrosopyridine (PyrNO) (32–100% degradation). Importantly, for every metabolite, there was an optimum derivatization reagent that met the criteria of stability proposed by international regulatory bodies after 1 month of storage. Some derivatives were stable for even up to 3 months of storage, with degradation of less than 15%. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00216-022-04409-5. Springer Berlin Heidelberg 2022-11-07 2023 /pmc/articles/PMC9823060/ /pubmed/36342509 http://dx.doi.org/10.1007/s00216-022-04409-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Paper
Alexandridou, Anastasia
Volmer, Dietrich A.
Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis
title Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis
title_full Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis
title_fullStr Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis
title_full_unstemmed Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis
title_short Stability of sample extracts of vitamin D(3) metabolites after chemical derivatization for LC–MS/MS analysis
title_sort stability of sample extracts of vitamin d(3) metabolites after chemical derivatization for lc–ms/ms analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9823060/
https://www.ncbi.nlm.nih.gov/pubmed/36342509
http://dx.doi.org/10.1007/s00216-022-04409-5
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