Cargando…

Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors

During the analysis of benziamidazole-class irreversible proton pump inhibitors, an unusual mass spectral response with the mass-to-charge ratio at [M+10](+) intrigued us, as it couldn't be assigned to any literature known relevant structure, intermediate or adduct ion. Moreover, this mysteriou...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Dong, Wang, Chunyu, Fan, Yanxia, Gu, Jingkai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334273/
https://www.ncbi.nlm.nih.gov/pubmed/37440908
http://dx.doi.org/10.1016/j.jpha.2023.04.011
_version_ 1785070825089531904
author Sun, Dong
Wang, Chunyu
Fan, Yanxia
Gu, Jingkai
author_facet Sun, Dong
Wang, Chunyu
Fan, Yanxia
Gu, Jingkai
author_sort Sun, Dong
collection PubMed
description During the analysis of benziamidazole-class irreversible proton pump inhibitors, an unusual mass spectral response with the mass-to-charge ratio at [M+10](+) intrigued us, as it couldn't be assigned to any literature known relevant structure, intermediate or adduct ion. Moreover, this mysterious mass pattern of [M+10](+) has been gradually observed by series of marketed proton pump inhibitors, viz. omeprazole, pantoprazole, lansoprazole and rabeprazole. All the previous attempts to isolate the corresponding component were unsuccessful. The investigation of present work addresses this kind of signal to a pyridinium thiocyanate mass spectral intermediate (10), which is the common fragment ion of series of labile aggregates. The origin of such aggregates can be traced to the reactive intermediates formed by acid-promoted degradation. These reactive intermediates tend to react with each other and give raise series of complicated aggregates systematically in a water/acetonitrile solution by electrospray ionization. The structure of the corresponding pyridinium thiocyanate species of omeprazole (10a) has been eventually characterized with the help of synthetic specimen (10a′). Our structural proposal as well as its origin was supported by in situ nuclear magnetic resonance, chemical derivatization and colorimetric experiments.
format Online
Article
Text
id pubmed-10334273
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Xi'an Jiaotong University
record_format MEDLINE/PubMed
spelling pubmed-103342732023-07-12 Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors Sun, Dong Wang, Chunyu Fan, Yanxia Gu, Jingkai J Pharm Anal Original Article During the analysis of benziamidazole-class irreversible proton pump inhibitors, an unusual mass spectral response with the mass-to-charge ratio at [M+10](+) intrigued us, as it couldn't be assigned to any literature known relevant structure, intermediate or adduct ion. Moreover, this mysterious mass pattern of [M+10](+) has been gradually observed by series of marketed proton pump inhibitors, viz. omeprazole, pantoprazole, lansoprazole and rabeprazole. All the previous attempts to isolate the corresponding component were unsuccessful. The investigation of present work addresses this kind of signal to a pyridinium thiocyanate mass spectral intermediate (10), which is the common fragment ion of series of labile aggregates. The origin of such aggregates can be traced to the reactive intermediates formed by acid-promoted degradation. These reactive intermediates tend to react with each other and give raise series of complicated aggregates systematically in a water/acetonitrile solution by electrospray ionization. The structure of the corresponding pyridinium thiocyanate species of omeprazole (10a) has been eventually characterized with the help of synthetic specimen (10a′). Our structural proposal as well as its origin was supported by in situ nuclear magnetic resonance, chemical derivatization and colorimetric experiments. Xi'an Jiaotong University 2023-06 2023-04-21 /pmc/articles/PMC10334273/ /pubmed/37440908 http://dx.doi.org/10.1016/j.jpha.2023.04.011 Text en © 2023 The Authors 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/).
spellingShingle Original Article
Sun, Dong
Wang, Chunyu
Fan, Yanxia
Gu, Jingkai
Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors
title Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors
title_full Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors
title_fullStr Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors
title_full_unstemmed Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors
title_short Identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors
title_sort identification, structure elucidation and origin of a common pyridinium-thiocyanate intermediate in electrospray mass spectrometry among the benziamidazole-class proton pump inhibitors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334273/
https://www.ncbi.nlm.nih.gov/pubmed/37440908
http://dx.doi.org/10.1016/j.jpha.2023.04.011
work_keys_str_mv AT sundong identificationstructureelucidationandoriginofacommonpyridiniumthiocyanateintermediateinelectrospraymassspectrometryamongthebenziamidazoleclassprotonpumpinhibitors
AT wangchunyu identificationstructureelucidationandoriginofacommonpyridiniumthiocyanateintermediateinelectrospraymassspectrometryamongthebenziamidazoleclassprotonpumpinhibitors
AT fanyanxia identificationstructureelucidationandoriginofacommonpyridiniumthiocyanateintermediateinelectrospraymassspectrometryamongthebenziamidazoleclassprotonpumpinhibitors
AT gujingkai identificationstructureelucidationandoriginofacommonpyridiniumthiocyanateintermediateinelectrospraymassspectrometryamongthebenziamidazoleclassprotonpumpinhibitors