Xuwei Guo, Youzhi Su, Jun Liu, Yanmei Li, Fang Li, Hongqin Lei
{"title":"多孔过滤净化结合高效液相色谱-串联质谱法同时测定畜禽肉中的农药、兽药、霉菌毒素和持久性有机污染物","authors":"Xuwei Guo, Youzhi Su, Jun Liu, Yanmei Li, Fang Li, Hongqin Lei","doi":"10.1007/s12161-024-02615-8","DOIUrl":null,"url":null,"abstract":"<div><p>A method for the determination of 106 pesticides, 74 veterinary drugs, 10 mycotoxins, and 18 persistent organic pollutants in livestock and poultry meat was developed and validated in the present study. The meat was extracted with acetonitrile under citric acid caching and purified using the multi-plug filtration clean-up (m-PFC) column. The components were separated using liquid chromatography on a C<sub>18</sub> column and then eluted using a gradient of the aqueous solutions of acetonitrile and 0.1% formic acid (containing 2 mmol/L ammonium acetate) as the mobile phase. The mass spectrometry analysis was performed next using two electrospraying scan modes—the positive ion mode and the negative ion mode, and multiple reaction monitoring (MRM) modes. The results revealed that all 208 target analytes exhibited good linearity in their respective linear ranges, with the correlation coefficient of each analyte above 0.9953 and the corresponding limits of quantification (LOQs) in the range of 0.1–9.8 µg/kg. The average recovery values of 189 targets at three different spiked levels of low, medium, and high ranged from 70.1 to 120.0%, and the corresponding values of relative standard deviation (RSD) ranged from 1.3 to 15.0%, respectively. The remaining 19 targets exhibited the average recovery values [at three different spiked levels of low, medium, and high] ranging from 18.6 to 58.9%, with the corresponding RSD values ranging from 1.5 to 11.3%. The developed method was applied to 132 batches of livestock and poultry meat, and nine pesticides and seven veterinary drugs were detected in the concentration range of 0.1–24.8 µg/kg. These results suggested that the developed method is simple, reliable, reproducible, and suitable for the determination of pesticides, veterinary drugs, mycotoxins, and persistent organic pollutants in livestock and poultry meat.</p></div>","PeriodicalId":561,"journal":{"name":"Food Analytical Methods","volume":"17 7","pages":"957 - 996"},"PeriodicalIF":2.6000,"publicationDate":"2024-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multi-plug Filtration Purification Combined with High-Performance Liquid Chromatography-Tandem Mass Spectrometry for the Simultaneous Determination of Pesticides, Veterinary Drugs, Mycotoxins, and Persistent Organic Pollutants in Livestock and Poultry Meat\",\"authors\":\"Xuwei Guo, Youzhi Su, Jun Liu, Yanmei Li, Fang Li, Hongqin Lei\",\"doi\":\"10.1007/s12161-024-02615-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A method for the determination of 106 pesticides, 74 veterinary drugs, 10 mycotoxins, and 18 persistent organic pollutants in livestock and poultry meat was developed and validated in the present study. The meat was extracted with acetonitrile under citric acid caching and purified using the multi-plug filtration clean-up (m-PFC) column. The components were separated using liquid chromatography on a C<sub>18</sub> column and then eluted using a gradient of the aqueous solutions of acetonitrile and 0.1% formic acid (containing 2 mmol/L ammonium acetate) as the mobile phase. The mass spectrometry analysis was performed next using two electrospraying scan modes—the positive ion mode and the negative ion mode, and multiple reaction monitoring (MRM) modes. The results revealed that all 208 target analytes exhibited good linearity in their respective linear ranges, with the correlation coefficient of each analyte above 0.9953 and the corresponding limits of quantification (LOQs) in the range of 0.1–9.8 µg/kg. The average recovery values of 189 targets at three different spiked levels of low, medium, and high ranged from 70.1 to 120.0%, and the corresponding values of relative standard deviation (RSD) ranged from 1.3 to 15.0%, respectively. The remaining 19 targets exhibited the average recovery values [at three different spiked levels of low, medium, and high] ranging from 18.6 to 58.9%, with the corresponding RSD values ranging from 1.5 to 11.3%. The developed method was applied to 132 batches of livestock and poultry meat, and nine pesticides and seven veterinary drugs were detected in the concentration range of 0.1–24.8 µg/kg. These results suggested that the developed method is simple, reliable, reproducible, and suitable for the determination of pesticides, veterinary drugs, mycotoxins, and persistent organic pollutants in livestock and poultry meat.</p></div>\",\"PeriodicalId\":561,\"journal\":{\"name\":\"Food Analytical Methods\",\"volume\":\"17 7\",\"pages\":\"957 - 996\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-03-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Food Analytical Methods\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12161-024-02615-8\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"FOOD SCIENCE & TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food Analytical Methods","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s12161-024-02615-8","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
Multi-plug Filtration Purification Combined with High-Performance Liquid Chromatography-Tandem Mass Spectrometry for the Simultaneous Determination of Pesticides, Veterinary Drugs, Mycotoxins, and Persistent Organic Pollutants in Livestock and Poultry Meat
A method for the determination of 106 pesticides, 74 veterinary drugs, 10 mycotoxins, and 18 persistent organic pollutants in livestock and poultry meat was developed and validated in the present study. The meat was extracted with acetonitrile under citric acid caching and purified using the multi-plug filtration clean-up (m-PFC) column. The components were separated using liquid chromatography on a C18 column and then eluted using a gradient of the aqueous solutions of acetonitrile and 0.1% formic acid (containing 2 mmol/L ammonium acetate) as the mobile phase. The mass spectrometry analysis was performed next using two electrospraying scan modes—the positive ion mode and the negative ion mode, and multiple reaction monitoring (MRM) modes. The results revealed that all 208 target analytes exhibited good linearity in their respective linear ranges, with the correlation coefficient of each analyte above 0.9953 and the corresponding limits of quantification (LOQs) in the range of 0.1–9.8 µg/kg. The average recovery values of 189 targets at three different spiked levels of low, medium, and high ranged from 70.1 to 120.0%, and the corresponding values of relative standard deviation (RSD) ranged from 1.3 to 15.0%, respectively. The remaining 19 targets exhibited the average recovery values [at three different spiked levels of low, medium, and high] ranging from 18.6 to 58.9%, with the corresponding RSD values ranging from 1.5 to 11.3%. The developed method was applied to 132 batches of livestock and poultry meat, and nine pesticides and seven veterinary drugs were detected in the concentration range of 0.1–24.8 µg/kg. These results suggested that the developed method is simple, reliable, reproducible, and suitable for the determination of pesticides, veterinary drugs, mycotoxins, and persistent organic pollutants in livestock and poultry meat.
期刊介绍:
Food Analytical Methods publishes original articles, review articles, and notes on novel and/or state-of-the-art analytical methods or issues to be solved, as well as significant improvements or interesting applications to existing methods. These include analytical technology and methodology for food microbial contaminants, food chemistry and toxicology, food quality, food authenticity and food traceability. The journal covers fundamental and specific aspects of the development, optimization, and practical implementation in routine laboratories, and validation of food analytical methods for the monitoring of food safety and quality.