Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometry

ObjectiveTo develop a method for the determination of nosiheptide residue in food animal tissues (porcine muscle, porcine liver, porcine kidney, chicken muscle, chicken liver and chicken kidney) with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS).MethodsAfter extracted...

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Main Authors: NIE Chen, HAN Jingjing, ZHAO Sa, YANG Fan, HE Jingcheng, WANG Peifeng, LI Mingzhe, LIN Chao, ZHANG Hongwei
Format: Article
Language:zho
Published: The Editorial Office of Chinese Journal of Food Hygiene 2022-07-01
Series:Zhongguo shipin weisheng zazhi
Subjects:
Online Access:http://www.zgspws.com/zgspwszz/article/abstract/202204019?st=article_issue
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author NIE Chen
HAN Jingjing
ZHAO Sa
YANG Fan
HE Jingcheng
WANG Peifeng
LI Mingzhe
LIN Chao
ZHANG Hongwei
author_facet NIE Chen
HAN Jingjing
ZHAO Sa
YANG Fan
HE Jingcheng
WANG Peifeng
LI Mingzhe
LIN Chao
ZHANG Hongwei
author_sort NIE Chen
collection DOAJ
description ObjectiveTo develop a method for the determination of nosiheptide residue in food animal tissues (porcine muscle, porcine liver, porcine kidney, chicken muscle, chicken liver and chicken kidney) with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS).MethodsAfter extracted by 0.1% acidic acetonitrile, the nosiheptide extract was cleaned up by Captiva ND cartridge and determined by HPLC-MS/MS in negative electrospray ionization mode. Quantification was performed using corresponding matrix-matched calibration curves.ResultsNosiheptide in corresponding matrix showed good linear relationships (r>0.99) in the calibration range of 2~200 μg/L, and the limit of detection (LOD) and limit of quantification (LOQ) of the method were 2.0 and 7.0 μg/kg, respectively. The recoveries of the method ranged from 76.27% to 92.31% at the spiking level of 3.5, 7.0 and 70 μg/kg with relative standard deviations of 2.15%~8.03%.ConclusionThe proposed method is simple, rapid, accurate as well as reproducible and can be applied to monitor and determine nosiheptide residue in food animal tissues.
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spelling doaj.art-cdd76db37636453db2489e8cc0b762a02022-12-27T09:24:57ZzhoThe Editorial Office of Chinese Journal of Food HygieneZhongguo shipin weisheng zazhi1004-84562022-07-0134475576010.13590/j.cjfh.2022.04.0191004-8456(2022)04-0755-06Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometryNIE Chen0HAN Jingjing1ZHAO Sa2YANG Fan3HE Jingcheng4WANG Peifeng5LI Mingzhe6LIN Chao7ZHANG Hongwei8Qingdao Customs Technology Center, Shandong Qingdao 266002, ChinaQingdao Customs Technology Center, Shandong Qingdao 266002, ChinaQingdao Customs Technology Center, Shandong Qingdao 266002, ChinaSchool of Food Science and Engineering, Ocean University of China, Shandong Qingdao 266002, ChinaQingdao Customs Technology Center, Shandong Qingdao 266002, ChinaQingdao Customs Technology Center, Shandong Qingdao 266002, ChinaQingdao Customs Technology Center, Shandong Qingdao 266002, ChinaQingdao Customs Technology Center, Shandong Qingdao 266002, ChinaQingdao Customs Technology Center, Shandong Qingdao 266002, ChinaObjectiveTo develop a method for the determination of nosiheptide residue in food animal tissues (porcine muscle, porcine liver, porcine kidney, chicken muscle, chicken liver and chicken kidney) with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS).MethodsAfter extracted by 0.1% acidic acetonitrile, the nosiheptide extract was cleaned up by Captiva ND cartridge and determined by HPLC-MS/MS in negative electrospray ionization mode. Quantification was performed using corresponding matrix-matched calibration curves.ResultsNosiheptide in corresponding matrix showed good linear relationships (r>0.99) in the calibration range of 2~200 μg/L, and the limit of detection (LOD) and limit of quantification (LOQ) of the method were 2.0 and 7.0 μg/kg, respectively. The recoveries of the method ranged from 76.27% to 92.31% at the spiking level of 3.5, 7.0 and 70 μg/kg with relative standard deviations of 2.15%~8.03%.ConclusionThe proposed method is simple, rapid, accurate as well as reproducible and can be applied to monitor and determine nosiheptide residue in food animal tissues.http://www.zgspws.com/zgspwszz/article/abstract/202204019?st=article_issuehigh performance liquid chromatography-tandem mass spectrometrynosiheptidefood animal tissues
spellingShingle NIE Chen
HAN Jingjing
ZHAO Sa
YANG Fan
HE Jingcheng
WANG Peifeng
LI Mingzhe
LIN Chao
ZHANG Hongwei
Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometry
Zhongguo shipin weisheng zazhi
high performance liquid chromatography-tandem mass spectrometry
nosiheptide
food animal tissues
title Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometry
title_full Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometry
title_fullStr Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometry
title_full_unstemmed Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometry
title_short Determination of nosiheptide residue in food animal tissues by high performance liquid chromatography-tandem mass spectrometry
title_sort determination of nosiheptide residue in food animal tissues by high performance liquid chromatography tandem mass spectrometry
topic high performance liquid chromatography-tandem mass spectrometry
nosiheptide
food animal tissues
url http://www.zgspws.com/zgspwszz/article/abstract/202204019?st=article_issue
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