李 强,韵小娟,王 娇,李庆霞,符 雨.液相色谱-串联质谱法检测中兽药中非法添加氟喹诺酮类药物含量的不确定度评估[J].食品安全质量检测学报,2019,10(11):3356-3361
液相色谱-串联质谱法检测中兽药中非法添加氟喹诺酮类药物含量的不确定度评估
Uncertainty evaluation of fluoroquinolones illegally added in veterinary herbal medicine by liquid chromatography-tandem mass spectrometry
投稿时间:2019-04-18  修订日期:2019-05-30
DOI:
中文关键词:  液相色谱-串联质谱法  中兽药  氟喹诺酮类  不确定度  评估
英文关键词:liquid chromatography-tandem mass spectrometry  veterinary herbal medicine  fluoroquinolones  uncertainty  evaluation
基金项目:2019年海南省自然科学基金青年基金项目(819QN393)
作者单位
李 强 海南省动物疫病预防控制中心 
韵小娟 海南省动物疫病预防控制中心 
王 娇 海南省动物疫病预防控制中心 
李庆霞 海南省动物疫病预防控制中心 
符 雨 海南省动物疫病预防控制中心 
AuthorInstitution
LI Qiang Hainan Animal Disease Prevention and Control Center 
YUN Xiao-Juan Hainan Animal Disease Prevention and Control Center 
WANG Jiao Hainan Animal Disease Prevention and Control Center 
LI Qing-Xia Hainan Animal Disease Prevention and Control Center 
FU Yu Hainan Animal Disease Prevention and Control Center 
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中文摘要:
      目的 评估液相色谱-串联质谱法检测中兽药中非法添加氟喹诺酮类药物含量的不确定度。方法 建立液相色谱-串联质谱法检测中兽药(肥猪散、健胃散、银翘散)中非法添加氟喹诺酮类药物的含量测定方法, 根据JJF1059.1-2012《测量不确定度评定与表示》的相关规定, 对该方法的不确定度进行评定。结果 中兽药中氟喹诺酮类药物含量分别为C(Enro)=100.90 mg/kg、C(Cip)=100.34 mg/kg、C(Norf)=100.21 mg/kg、C(Oflo)=100.61 mg/kg时, 95%置信水平下, 取k=2, 不确定度评估结果分别表示为X(Enro)=(100.90±6.957) mg/kg; X(Cip)=(100.34±7.067) mg/kg; X(Norf)=(100.21±6.898) mg/kg; X(Oflo)=(100.61±6.957) mg/kg。结论 评定结果表明, 影响检测结果的主要因素为液相色谱-串联质谱仪的灵敏度、天平的精密度、操作的规范性。
英文摘要:
      Objective To evaluate the uncertainty of determination of fluoroquinolones illegally added in veterinary medicine by liquid chromatography-tandem mass spectrometry (LC-MS/MS). Methods A method for the determination of fluoroquinolones illegally added in veterinary herbal medicine (feizhu powder, Jianwei powder, Yinqiao powder) by liquid chromatography-tandem mass spectrometry was established. According to the relevant provisions of JJF1059.1-2012 Measurement uncertainty evaluation and representation, the uncertainty of the method was evaluated. Results The content of fluoroquinolones in veterinary medicine was C(Enro)=100.90 mg/kg, C(Cip)=100.34 mg/kg, C(Norf)=100.21 mg/kg, C(Oflo)=100.61 mg/kg, respectively, when 95% confidence level, k=2, and the evaluation results were X(Enro)=(100.90±6.957) mg/kg, X(Cip)=(100.34±7.067) mg/kg, X(Norf)= (100.21±6.898) mg/kg, X(Oflo)=(100.61±6.957) mg/kg, respectively. Conclusion The main sources of uncertainty are the sensitivity of the liquid chromatography-tandem mass spectrometer, the precision of the balance, and the standard of operation.
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