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中国精品科技期刊2020
张飞,王远,马小宁,等. 超高效液相色谱-串联质谱法检测卤肉中36种兽药残留[J]. 食品工业科技,2023,44(13):340−348. doi: 10.13386/j.issn1002-0306.2022080155.
引用本文: 张飞,王远,马小宁,等. 超高效液相色谱-串联质谱法检测卤肉中36种兽药残留[J]. 食品工业科技,2023,44(13):340−348. doi: 10.13386/j.issn1002-0306.2022080155.
ZHANG Fei, WANG Yuan, MA Xiaoning, et al. Determination of 36 Veterinary Drug Residues in Cooked Meat by Ultra Performance Liquid Chromatography-tandem Mass Spectrometry[J]. Science and Technology of Food Industry, 2023, 44(13): 340−348. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022080155.
Citation: ZHANG Fei, WANG Yuan, MA Xiaoning, et al. Determination of 36 Veterinary Drug Residues in Cooked Meat by Ultra Performance Liquid Chromatography-tandem Mass Spectrometry[J]. Science and Technology of Food Industry, 2023, 44(13): 340−348. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022080155.

超高效液相色谱-串联质谱法检测卤肉中36种兽药残留

Determination of 36 Veterinary Drug Residues in Cooked Meat by Ultra Performance Liquid Chromatography-tandem Mass Spectrometry

  • 摘要: 建立了卤肉中金刚烷胺、磺胺类、喹诺酮类及氯霉素类等36种兽药残留的检测方法。卤肉样品通过乙腈-水溶液(V:V=8:2)提取,PRiME HLB固相萃取柱净化,配有电喷雾离子源(ESI±)的超高效液相色谱-串联质谱(UPLC-MS/MS),在正负离子多反应监测(MRM)模式下同时测定,基质匹配标准曲线定量。结果表明,所研究的36种兽药在0.5~20.0 ng/mL浓度范围内均呈良好线性关系(R2>0.999)。本方法中36种药物的检出限均为0.10 μg/kg,定量限均为0.33 μg/kg,在高中低3个不同浓度(0.5,1.0和5.0 μg/kg)36种兽药的添加回收率为70.8%~106.9%,相对标准偏差(RSD, n=6)0.2%~6.2%。该研究建立的方法操作简单、准确性高、回收率和重现性好,可同时对卤肉中的36种兽药残留进行测定。

     

    Abstract: A method was developed for the determination of amantadine sulfonamides, quinolones and chloramphenicols in cooked meat. The samples were extracted with acetonitrile-water mixtures (V:V=8:2), purified with PRiME HLB solid phase extraction column. 36 veterinary drugs were determined by ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) with an electrospray ion source (ESI±) in positive and negative ion switching scanning mode. The results showed that the 36 veterinary drugs showed a good linear relationship in the concentration range of 0.5~20.0 ng/mL (R2>0.999). The limits of detection were 0.10 μg/kg and the limits of quantitation were 0.33 μg/kg. The average recovery was 70.8%~106.9% in the range of high, medium and low concentrations (0.5, 1.0 and 5.0 μg/kg). The relative standard deviations (RSD, n=6) was 0.2%~6.2%. The method is simple, sensitive and accurate, and could be used for the determination of 36 veterinary drug residues in cooked meat.

     

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