Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry

An ultra performance liquid chromatography – electrospray ionization triple-quadruple tandem mass spectrometric(UPLC–ESI MS /MS) method was developed for determining Quinololine antibiotics (Carbadox,, Quinocetone, Mequindox, Olaquindox, Cyadox, Tilmicosin, Tylosin, quinoxaline-2-carboxylic acid, 3-...

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Main Authors: Zha Yu-bing, Yang Chun-liang, Lv Yi-zhi, Ye Jian-zhi, Zeng Shao-dong, Wang Xiao-fang, Deng Xiao-hong, Ma Hui-fang, Pan Xiaowei, Lin Li-yun
Format: Article
Language:English
Published: EDP Sciences 2020-01-01
Series:E3S Web of Conferences
Online Access:https://www.e3s-conferences.org/articles/e3sconf/pdf/2020/73/e3sconf_acic2020_01033.pdf
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spelling doaj-bcee7b6fca5c440c83865da39ee1a3762021-04-02T19:03:13ZengEDP SciencesE3S Web of Conferences2267-12422020-01-012130103310.1051/e3sconf/202021301033e3sconf_acic2020_01033Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass SpectrometryZha Yu-bing0Yang Chun-liangLv Yi-zhi1Ye Jian-zhiZeng Shao-dongWang Xiao-fang2Deng Xiao-hong3Ma Hui-fangPan XiaoweiLin Li-yunAgriculture Products Processing Research Institute of South ChinaAgricultural technology extension CenterAgriculture Products Processing Research Institute of South ChinaAgricultural technology extension CenterAn ultra performance liquid chromatography – electrospray ionization triple-quadruple tandem mass spectrometric(UPLC–ESI MS /MS) method was developed for determining Quinololine antibiotics (Carbadox,, Quinocetone, Mequindox, Olaquindox, Cyadox, Tilmicosin, Tylosin, quinoxaline-2-carboxylic acid, 3-methylquinoxaline-2-carboxylic acid) and aminoglycoside antibiotics(Tilmicosin, Tylosin) residues in Penaeus. vannamei, Samples were extracted with acidified acetonitrile, then cleaned up with hexane. The separation of targets was carried out on a Waters BEH C18 column using acetonitrile and 0. 1% fomicacid as mobile phase. Analyte identification and quantification were performed by MS/MS under multiple-reaction monitering(MRM) mode with the external standard method. The results showed that there were good linear relationships between peak area and concentrations of nine targets in the range of 2.5 ~ 50 μg/L, with correlation coefficients more than 0. 999 and The limits of detection(LOD) were in the range of 0. 1 ~ 0.9 μg/kg. the recoveries ranged from 80.2% ~ 94.0%, with RSDs of 1.7%~8.4%. The method is simple, accurate and precise, and It could satisfy the requirement of mass and fast analysis in the laborator.https://www.e3s-conferences.org/articles/e3sconf/pdf/2020/73/e3sconf_acic2020_01033.pdf
collection DOAJ
language English
format Article
sources DOAJ
author Zha Yu-bing
Yang Chun-liang
Lv Yi-zhi
Ye Jian-zhi
Zeng Shao-dong
Wang Xiao-fang
Deng Xiao-hong
Ma Hui-fang
Pan Xiaowei
Lin Li-yun
spellingShingle Zha Yu-bing
Yang Chun-liang
Lv Yi-zhi
Ye Jian-zhi
Zeng Shao-dong
Wang Xiao-fang
Deng Xiao-hong
Ma Hui-fang
Pan Xiaowei
Lin Li-yun
Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
E3S Web of Conferences
author_facet Zha Yu-bing
Yang Chun-liang
Lv Yi-zhi
Ye Jian-zhi
Zeng Shao-dong
Wang Xiao-fang
Deng Xiao-hong
Ma Hui-fang
Pan Xiaowei
Lin Li-yun
author_sort Zha Yu-bing
title Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
title_short Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
title_full Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
title_fullStr Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
title_full_unstemmed Determination of Residues of two Aminoglycoside antibiotics and five Quinololine antibiotics and Their Metabolites in Penaeus vannamei by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
title_sort determination of residues of two aminoglycoside antibiotics and five quinololine antibiotics and their metabolites in penaeus vannamei by ultra high performance liquid chromatography tandem mass spectrometry
publisher EDP Sciences
series E3S Web of Conferences
issn 2267-1242
publishDate 2020-01-01
description An ultra performance liquid chromatography – electrospray ionization triple-quadruple tandem mass spectrometric(UPLC–ESI MS /MS) method was developed for determining Quinololine antibiotics (Carbadox,, Quinocetone, Mequindox, Olaquindox, Cyadox, Tilmicosin, Tylosin, quinoxaline-2-carboxylic acid, 3-methylquinoxaline-2-carboxylic acid) and aminoglycoside antibiotics(Tilmicosin, Tylosin) residues in Penaeus. vannamei, Samples were extracted with acidified acetonitrile, then cleaned up with hexane. The separation of targets was carried out on a Waters BEH C18 column using acetonitrile and 0. 1% fomicacid as mobile phase. Analyte identification and quantification were performed by MS/MS under multiple-reaction monitering(MRM) mode with the external standard method. The results showed that there were good linear relationships between peak area and concentrations of nine targets in the range of 2.5 ~ 50 μg/L, with correlation coefficients more than 0. 999 and The limits of detection(LOD) were in the range of 0. 1 ~ 0.9 μg/kg. the recoveries ranged from 80.2% ~ 94.0%, with RSDs of 1.7%~8.4%. The method is simple, accurate and precise, and It could satisfy the requirement of mass and fast analysis in the laborator.
url https://www.e3s-conferences.org/articles/e3sconf/pdf/2020/73/e3sconf_acic2020_01033.pdf
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