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In Vitro and in Vivo Metabolite Profiling of Valnemulin Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight Hybrid Mass Spectrometry
[Image: see text] Valnemulin, a semisynthetic pleuromutilin derivative related to tiamulin, is broadly used to treat bacterial diseases of animals. Despite its widespread use, metabolism in animals has not yet been fully investigated. To better understand valnemulin biotransformation, in this study,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166035/ https://www.ncbi.nlm.nih.gov/pubmed/25156794 http://dx.doi.org/10.1021/jf5012402 |
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author | Yang, Shupeng Shi, Weimin Hu, Dingfei Zhang, Suxia Zhang, Huiyan Wang, Zhanhui Cheng, Linli Sun, Feifei Shen, Jianzhong Cao, Xingyuan |
author_facet | Yang, Shupeng Shi, Weimin Hu, Dingfei Zhang, Suxia Zhang, Huiyan Wang, Zhanhui Cheng, Linli Sun, Feifei Shen, Jianzhong Cao, Xingyuan |
author_sort | Yang, Shupeng |
collection | PubMed |
description | [Image: see text] Valnemulin, a semisynthetic pleuromutilin derivative related to tiamulin, is broadly used to treat bacterial diseases of animals. Despite its widespread use, metabolism in animals has not yet been fully investigated. To better understand valnemulin biotransformation, in this study, metabolites of valnemulinin in in vitro and in vivo rats, chickens, swines, goats, and cows were identified and elucidated using ultraperformance liquid chromatography–quadrupole/time-of-flight hybrid mass spectrometry (UPLC-Q/TOF-MS). As a result, there were totally 7 metabolites of valnemulin identified in vitro and 75, 61, and 74 metabolites detected in in vivo rats, chickens, and swines, respectively, and the majority of metabolites were reported for the first time. The main metabolic pathways of valnemulin were found to be hydroxylation in the mutilin part (the ring system) and the side chain, oxidization on the sulfur of the side chain to form S-oxides, hydrolysis of the amido bond, and acetylization in the amido of the side chain. In addition, hydroxylation in the mutilin part was proposed to be the primary metabolic route. Furthermore, the results revealed that 2β-hydroxyvalnemulin (V1) and 8α-hydroxyvalnemulin (V2) were the major metabolites for rats and swines and S-oxides (V6) in chickens. |
format | Online Article Text |
id | pubmed-4166035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-41660352015-08-26 In Vitro and in Vivo Metabolite Profiling of Valnemulin Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight Hybrid Mass Spectrometry Yang, Shupeng Shi, Weimin Hu, Dingfei Zhang, Suxia Zhang, Huiyan Wang, Zhanhui Cheng, Linli Sun, Feifei Shen, Jianzhong Cao, Xingyuan J Agric Food Chem [Image: see text] Valnemulin, a semisynthetic pleuromutilin derivative related to tiamulin, is broadly used to treat bacterial diseases of animals. Despite its widespread use, metabolism in animals has not yet been fully investigated. To better understand valnemulin biotransformation, in this study, metabolites of valnemulinin in in vitro and in vivo rats, chickens, swines, goats, and cows were identified and elucidated using ultraperformance liquid chromatography–quadrupole/time-of-flight hybrid mass spectrometry (UPLC-Q/TOF-MS). As a result, there were totally 7 metabolites of valnemulin identified in vitro and 75, 61, and 74 metabolites detected in in vivo rats, chickens, and swines, respectively, and the majority of metabolites were reported for the first time. The main metabolic pathways of valnemulin were found to be hydroxylation in the mutilin part (the ring system) and the side chain, oxidization on the sulfur of the side chain to form S-oxides, hydrolysis of the amido bond, and acetylization in the amido of the side chain. In addition, hydroxylation in the mutilin part was proposed to be the primary metabolic route. Furthermore, the results revealed that 2β-hydroxyvalnemulin (V1) and 8α-hydroxyvalnemulin (V2) were the major metabolites for rats and swines and S-oxides (V6) in chickens. American Chemical Society 2014-08-26 2014-09-17 /pmc/articles/PMC4166035/ /pubmed/25156794 http://dx.doi.org/10.1021/jf5012402 Text en Copyright © 2014 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Yang, Shupeng Shi, Weimin Hu, Dingfei Zhang, Suxia Zhang, Huiyan Wang, Zhanhui Cheng, Linli Sun, Feifei Shen, Jianzhong Cao, Xingyuan In Vitro and in Vivo Metabolite Profiling of Valnemulin Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight Hybrid Mass Spectrometry |
title | In Vitro
and in Vivo Metabolite Profiling of Valnemulin
Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight
Hybrid Mass Spectrometry |
title_full | In Vitro
and in Vivo Metabolite Profiling of Valnemulin
Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight
Hybrid Mass Spectrometry |
title_fullStr | In Vitro
and in Vivo Metabolite Profiling of Valnemulin
Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight
Hybrid Mass Spectrometry |
title_full_unstemmed | In Vitro
and in Vivo Metabolite Profiling of Valnemulin
Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight
Hybrid Mass Spectrometry |
title_short | In Vitro
and in Vivo Metabolite Profiling of Valnemulin
Using Ultraperformance Liquid Chromatography–Quadrupole/Time-of-Flight
Hybrid Mass Spectrometry |
title_sort | in vitro
and in vivo metabolite profiling of valnemulin
using ultraperformance liquid chromatography–quadrupole/time-of-flight
hybrid mass spectrometry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166035/ https://www.ncbi.nlm.nih.gov/pubmed/25156794 http://dx.doi.org/10.1021/jf5012402 |
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