[Determination of amantadine, rimantadine and dimethylamantadine residues in poultry by ultra-performance liquid chromatography-tandem mass spectrometry].

Jian Ma, Yanhong Chen, Ming Zhang, Yuankun Zhao
{"title":"[Determination of amantadine, rimantadine and dimethylamantadine residues in poultry by ultra-performance liquid chromatography-tandem mass spectrometry].","authors":"Jian Ma,&nbsp;Yanhong Chen,&nbsp;Ming Zhang,&nbsp;Yuankun Zhao","doi":"10.19813/j.cnki.weishengyanjiu.2023.02.018","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To establish a method for determination of amantadine, rimantadine and dimethylamantadine residues in poultry matrix by ultra-performance liquid chromatography-tandem mass spectrometry.</p><p><strong>Methods: </strong>Poultry samples were extracted with acid acetonitrile, salting out, and then the organic phase was cleaned up by C_(18) and PSA. A Waters ACQUITYTM UPLC HSS T3 column(100 mm×2.1 mm, 1.7 mm)was used for liquid chromatography separation, ESI positive ion scan was used with multiple reaction monitoring(MRM) mode and quantified by matrix-matched external standard method.</p><p><strong>Results: </strong>At the spiked level of 0.5, 1.0 and 5.0 μg/kg, the recoveries of each compound were in the range of 81.3%-91.1% with the relative standard deviations of 6.5%-11.3%. The qualitative limits of detections were 0.06-0.2 μg/kg and the quantitative limits were 0.2-0.5 μg/kg for the 3 target compounds. The established method was applied to the detection of the 3 target compounds in 30 poultry samples, and none of the target compounds exceeded the residue limits.</p><p><strong>Conclusion: </strong>The method is simple, rapid, high sensitivity and good stability, with a wide variety and a certain development. It can be used for the daily monitoring of the veterinary drug residues in poultry.</p>","PeriodicalId":23789,"journal":{"name":"Wei sheng yan jiu = Journal of hygiene research","volume":"52 2","pages":"286-291"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Wei sheng yan jiu = Journal of hygiene research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19813/j.cnki.weishengyanjiu.2023.02.018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To establish a method for determination of amantadine, rimantadine and dimethylamantadine residues in poultry matrix by ultra-performance liquid chromatography-tandem mass spectrometry.

Methods: Poultry samples were extracted with acid acetonitrile, salting out, and then the organic phase was cleaned up by C_(18) and PSA. A Waters ACQUITYTM UPLC HSS T3 column(100 mm×2.1 mm, 1.7 mm)was used for liquid chromatography separation, ESI positive ion scan was used with multiple reaction monitoring(MRM) mode and quantified by matrix-matched external standard method.

Results: At the spiked level of 0.5, 1.0 and 5.0 μg/kg, the recoveries of each compound were in the range of 81.3%-91.1% with the relative standard deviations of 6.5%-11.3%. The qualitative limits of detections were 0.06-0.2 μg/kg and the quantitative limits were 0.2-0.5 μg/kg for the 3 target compounds. The established method was applied to the detection of the 3 target compounds in 30 poultry samples, and none of the target compounds exceeded the residue limits.

Conclusion: The method is simple, rapid, high sensitivity and good stability, with a wide variety and a certain development. It can be used for the daily monitoring of the veterinary drug residues in poultry.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[超高效液相色谱-串联质谱法测定家禽中金刚烷胺、金刚乙胺和二甲金刚烷胺残留]。
目的:建立超高效液相色谱-串联质谱法测定家禽基质中金刚烷胺、金刚乙胺和二甲金刚烷胺残留量的方法。方法:用酸性乙腈提取家禽样品,盐析后用c18和PSA对有机相进行净化。采用Waters ACQUITYTM UPLC HSS T3色谱柱(100 mm×2.1 mm, 1.7 mm)进行液相色谱分离,ESI正离子扫描采用多反应监测(MRM)模式,基质匹配外标法定量。结果:在加标水平为0.5、1.0、5.0 μg/kg时,各化合物的加标回收率为81.3% ~ 91.1%,相对标准偏差为6.5% ~ 11.3%。3种目标化合物的检出定性限为0.06 ~ 0.2 μg/kg,定量限为0.2 ~ 0.5 μg/kg。将所建立的方法应用于30份家禽样品中3种目标化合物的检测,结果表明3种目标化合物均未超过残留限量。结论:该方法简便、快速、灵敏度高、稳定性好,品种广泛,具有一定的发展前景。可用于家禽体内兽药残留的日常监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Status of dietary energy and consumption of food among Chinese diabetics aged 45 years and above in 2015]. [Contamination and dietary exposure assessment of 2-chloropropanol esters in vegetable oils available on Zhejiang market during 2016-2020]. [Effect of different delivery modes on the level of protein, glucose and blood lipids in cord artery and vein blood]. [Secular trend in overweight and obesity among Chinese children and adolescents of 7-18 years old during 2000-2019]. [Rapid confirmation method of food poisoning caused by Bacillus cereus cereulide in rice and flour products].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1