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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,...

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Autores principales: Yang, Shupeng, Shi, Weimin, Hu, Dingfei, Zhang, Suxia, Zhang, Huiyan, Wang, Zhanhui, Cheng, Linli, Sun, Feifei, Shen, Jianzhong, Cao, Xingyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
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.
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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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