• EI
  • Scopus
  • 中国科技期刊卓越行动计划项目资助期刊
  • 北大核心期刊
  • DOAJ
  • EBSCO
  • 中国核心学术期刊RCCSE A+
  • 中国精品科技期刊
  • JST China
  • FSTA
  • 中国农林核心期刊
  • 中国科技核心期刊CSTPCD
  • CA
  • WJCI
  • 食品科学与工程领域高质量科技期刊分级目录第一方阵T1
中国精品科技期刊2020

UPLC-MS/MS检测原料奶中脱呋喃甲酰基头孢噻呋残留方法的建立

赵静, 刘鹏, 钱镭

赵静, 刘鹏, 钱镭. UPLC-MS/MS检测原料奶中脱呋喃甲酰基头孢噻呋残留方法的建立[J]. 食品工业科技, 2014, (16): 92-95. DOI: 10.13386/j.issn1002-0306.2014.16.011
引用本文: 赵静, 刘鹏, 钱镭. UPLC-MS/MS检测原料奶中脱呋喃甲酰基头孢噻呋残留方法的建立[J]. 食品工业科技, 2014, (16): 92-95. DOI: 10.13386/j.issn1002-0306.2014.16.011
ZHAO Jing, LIU Peng, QIAN Lei. Establishment on UPLC-MS/MS detection methods for desfuroylceftiofur in raw milk[J]. Science and Technology of Food Industry, 2014, (16): 92-95. DOI: 10.13386/j.issn1002-0306.2014.16.011
Citation: ZHAO Jing, LIU Peng, QIAN Lei. Establishment on UPLC-MS/MS detection methods for desfuroylceftiofur in raw milk[J]. Science and Technology of Food Industry, 2014, (16): 92-95. DOI: 10.13386/j.issn1002-0306.2014.16.011

UPLC-MS/MS检测原料奶中脱呋喃甲酰基头孢噻呋残留方法的建立

详细信息
    作者简介:

    赵静 (1989-) , 女, 在读硕士研究生, 研究方向:乳品质量与安全。;

  • 中图分类号: O657.63;TS252.7

Establishment on UPLC-MS/MS detection methods for desfuroylceftiofur in raw milk

  • 摘要: 目的:建立超高压液相色谱-串联质谱法(UPLC-MS/MS)测定原料奶中脱呋喃甲酰基头孢噻呋来间接衡量头孢噻呋残留的方法。方法:利用T3色谱柱,以含有0.02%的甲酸水-乙腈溶液为流动相进行梯度洗脱,采用二硫赤藓糖醇将原料奶中头孢噻呋分解为脱呋喃甲酰头孢噻呋(DFC),由碘乙酰胺衍生化为稳定的DFC乙酰胺形式(DCA),样品再经HLB固相萃取柱富集净化后,进行UPLC-MS/MS检测。结果:m/z 430.12>125.79为定量离子对,m/z 430.12>241.04为定性离子对,回收率在98.6%102.2%,精密度(RSD)为2.51%3.87%,最低检出限为0.45ng/mL。结论:该方法可用于原料奶中脱呋喃甲酰基头孢噻呋残留的测定。 
    Abstract: Objective:A ultra-high pressure liquid chromatograph-tandem mass spectrometry (UPLC-MS/MS) was established for determination of desfuroylceftiofur residues in raw milk. Methods:T3 column was used with a mixed solution of 0.02% formic acid-acetonitrile as mobile phase. The cefliofur in bovine raw milk was decomposed by dithioerythritol to produce desfuroylceftiofur (DFC) , which was further stabilized by derivatization to desfuroylceftiofur acetamide (DCA) using iodoacetamide, then the samples were concentrated and purified by HLB SPE cartridge and determined by UPLC-MS/MS.Results:The quantitative ion was m/z 430.12>125.79.The qualitative ion was m/z 430.12>241.04. The recovery were 98.6%~102.2%, the relative standard deviations (RSD) were 2.51%~3.87%, the minimum detectable values were 0.45ng/mL. Conclusion:This method could be used for the routine analysis of desfuroylceftiofur residues in raw milk.
  • [1] 王慧, 陈小军, 刘伟, 等.动物专用头孢噻呋[J].动物医学进展, 2009, 30 (1) :104-108.
    [2] 刘世娟.HPLC-MS/MS检测肌肉组织中多头孢菌素残留方法的建立[D].合肥:安徽农业大学, 2012.
    [3] 昌莉丽, 张春辉, 肖传斌, 等.RP-HPLC法测定头孢噻呋混悬注射液含量[J].西北农业学报, 2010 (6) :44-47.
    [4] 王金涛.畜禽专用抗菌剂头孢噻呋[J].养殖技术顾问, 2011 (5) :209.
    [5] 严凤, 顾欣, 李丹妮, 等.奶牛乳房内灌注头孢噻呋钠的消除动力学研究[J].中国兽药杂志, 2011, 45 (9) :26-28.
    [6] 中华人名共和国农业部235号公告.《动物性食品中兽药最高残留限量》[S].北京:农业部, 2002.
    [7]

    Kress C, Seidler C, Kerp B, et al.Experiences with an identification and quantification program for inhibitor-positive milk samples[J].Analytica Chimica Acta, 2007, 586 (1) :275-279.

    [8] 于洁.兽用抗微生物药物残留质谱筛选方法研究[D].武汉:华中农业大学, 2012.
    [9] 李铁柱, 孙永海, 郗伟东.受体分析结合酶联免疫检测牛乳中的头孢噻呋残留[J].高等学校化学学报, 2008, 29 (3) :473-476.
    [10] Biland觩ic'N, Kolanovic'B S, Varenina I, et al.Veterinary drug residues determination in raw milk in Croatia[J].Food Control, 2011, 22 (12) :1941-1948.
    [11] 程瑶, 商军, 曹建东.紫外分光光度法快速测定盐酸头孢噻呋注射液的含量[J].上海畜牧兽医通讯, 2011 (5) :10-11.
    [12] Grzelak E M, Malinowska I, Choma I M.Determination of cefacetrile and cefuroxime residues in milk by thin-layer chromatography[J].Journal of Liquid Chromatography&Related Technologies誖, 2009, 32 (14) :2043-2049.
    [13]

    Nogueira D R, Silva L M, Arend M Z, et al.Development and validation of an HPLC method for determination of ceftiofur sodium[J].Chromatographia, 2007, 65 (7-8) :401-406.

    [14]

    Zheng M M, Ruan G D, Feng Y Q.Hybrid organic-inorganic silica monolith with hydrophobic/strong cation-exchange functional groups as a sorbent for micro-solid phase extraction[J].Journal of Chromatography A, 2009, 1216 (45) :7739-7746.

    [15]

    Kantiani L, FarréM, BarcelóD.Analytical methodologies for the detection ofβ-lactam antibiotics in milk and feed samples[J].TrAC Trends in Analytical Chemistry, 2009, 28 (6) :729-744.

    [16]

    Junza A, Amatya R, Barrón D, et al.Comparative study of the LC-MS/MS and UPLC-MS/MS for the multi-residue analysis of quinolones, penicillins and cephalosporins in cow milk, and validation according to the regulation 2002/657/EC[J].Journal of Chromatography B, 2011, 879 (25) :2601-2610.

    [17] Martos P A, Jayasundara F, Dolbeer J, et al.Multiclass, Multiresidue Drug Analysis, Including Aminoglycosides, in Animal Tissue Using Liquid Chromatography Coupled to Tandem Mass Spectrometry覮[J].Journal of Agricultural and Food Chemistry, 2010, 58 (10) :5932-5944.
    [18]

    Turnipseed S B, Storey J M, Clark S B, et al.Analysis of Veterinary Drugs and Metabolites in Milk Using Quadrupole Time-of-Flight Liquid Chromatography-Mass Spectrometry[J].Journal of Agricultural and Food Chemistry, 2011, 59 (14) :7569-7581.

    [19]

    Kantiani L, FarréM, i Freixiedas J M G, et al.Determination of antibacterials in animal feed by pressurized liquid extraction followed by online purification and liquid chromatographyelectrospray tandem mass spectrometry[J].Analytical and Bioanalytical Chemistry, 2010, 398 (3) :1195-1205.

    [20]

    Becker M, Zittlau E, Petz M.Quantitative determination of ceftiofur-related residues in bovine raw milk by LC-MS/MS with electrospray ionization[J].European Food Research and Technology, 2003, 217 (5) :449-456.

    [21]

    Tang Y Y, Lu H F, Lin H Y, et al.Multiclass analysis of23 veterinary drugs in milk by ultraperformance liquid chromatography-electrospray tandem mass spectrometry[J].Journal of Chromatography B, 2012, 881:12-19.

    [22]

    Becker M, Zittlau E, Petz M.Residue analysis of 15 penicillins and cephalosporins in bovine muscle, kidney and milk by liquid chromatography-tandem mass spectrometry[J].Analytica Chimica Acta, 2004, 520 (1) :19-32.

    [23] TSQ Quantum液质联用仪使用手册[M].上海:赛默飞世尔科技 (上海) 有限公司, 2007.
计量
  • 文章访问数:  88
  • HTML全文浏览量:  3
  • PDF下载量:  125
  • 被引次数: 0
出版历程
  • 收稿日期:  2013-12-04

目录

    /

    返回文章
    返回