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引用本文:赵超群,刘柱,李樱红,陈万勤,罗金文.UHPLC-MS/MS同时测定牛奶中5种头孢类药物残留[J].中国现代应用药学,2020,37(11):1350-1354.
ZHAO Chaoqun,LIU Zhu,LI Yinghong,CHEN Wanqin,LUO Jinwen.Simultaneous Determination of Five Cephalosporins Residues in Milk by UHPLC-MS/MS[J].Chin J Mod Appl Pharm(中国现代应用药学),2020,37(11):1350-1354.
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UHPLC-MS/MS同时测定牛奶中5种头孢类药物残留
赵超群, 刘柱, 李樱红, 陈万勤, 罗金文
浙江省食品药品检验研究院, 杭州 310052
摘要:
目的 建立采用UHPLC-MS/MS同时测定牛奶中5种头孢菌素类药物残留的方法。方法 牛奶样品(约5 g)加10 mL Na2EDTA-McIlvaine提取液提取后,涡旋离心,取中层清液,加入0.1 mol·L-1 NaOH溶液调节pH至8.5,取上清液过HLB固相萃取柱富集并净化。富集浓缩后以Waters ACQUITY UPLC BEH(2.1 mm×50 mm,1.7 μm)色谱柱为分离柱,以0.1%甲酸溶液和乙腈为流动相进行梯度洗脱。采用电喷雾正离子源,以多反应监测模式进行质谱检测。结果 牛奶中5种头孢菌素类药物在1~20倍定量限浓度范围内有良好的线性关系,所得回收率为88.1%~114%,重复性试验RSD(n=6)均<6.55%,检出限为0.7~1.6 μg·kg-1结论 本方法专属性好、灵敏度高、准确性好,可多组分同时测定牛奶中的头孢类药物残留。
关键词:  超高效液相色谱-串联质谱法  固相萃取  牛奶  头孢菌素类药物残留
DOI:10.13748/j.cnki.issn1007-7693.2020.11.013
分类号:R917
基金项目:浙江省食品药品监管系统科技计划项目(2018008);浙江省基础公益研究计划项目(LGC19C200001)
Simultaneous Determination of Five Cephalosporins Residues in Milk by UHPLC-MS/MS
ZHAO Chaoqun, LIU Zhu, LI Yinghong, CHEN Wanqin, LUO Jinwen
Zhejiang Institute for Food and Drug Control, Hangzhou 310052, China
Abstract:
OBJECTIVE To establish a method for simultaneous determination of 5 cephalosporins residues in milk by UHPLC-MS/MS. METHODS Milk samples(about 5 g) were extracted by 10 mL Na2EDTA-McIlvaine, centrifuged by a vortex, then get the middle-level clear liquid, the pH was adjusted to 8.5 by adding 0.1 mol·L-1 NaOH solution, the supernatant were enriched and purified by HLB solid phase extraction column. The separation and analysis was performed on a Waters ACQUITY UPLC BEH(2.1 mm×50 mm, 1.7 μm) after enrichment and concentration. The mobile phase consisted of 0.1% formic acid and acetonitrile(gradient elution). Electrospray positive ion source was used for mass spectrometry detection by multiple reaction monitoring mode. RESULTS The five cephalosporins residues in milk had a good linear relationship within the quantitative limit of 20 times. The recoveries were 88.1%-114%, the RSD of repeatability test(n=6) was <6.55%, and the detection limit was 0.7-1.6 μg·kg-1. CONCLUSION The method has good specificity, sensitivity and accuracy, and can be used for the simultaneous determination of cephalosporins residues in milk.
Key words:  UHPLC-MS/MS  solid phase extraction  milk  cephalosporins residues
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