陈 梦,范 蕾,蒋凯亚,姜 川,陈卫平,王伟影.高效液相色谱法测定牛奶中四环素类兽药残留量的不确定度评定[J].食品安全质量检测学报,2020,11(15):5088-5093
高效液相色谱法测定牛奶中四环素类兽药残留量的不确定度评定
Uncertainty evaluation for the determination of tetracycline drug residues in milk by high performance liquid chromatography
投稿时间:2020-04-14  修订日期:2020-07-27
DOI:
中文关键词:  四环素类  不确定度  高效液相色谱法  牛奶
英文关键词:tetracycline drug residues  uncertainty  high performance liquid chromatography  milk
基金项目:
作者单位
陈 梦 丽水市食品药品与质量技术检验检测院 
范 蕾 丽水市食品药品与质量技术检验检测院 
蒋凯亚 丽水市农业农村局 
姜 川 丽水市食品药品与质量技术检验检测院 
陈卫平 丽水市食品药品与质量技术检验检测院 
王伟影 丽水市食品药品与质量技术检验检测院 
AuthorInstitution
CHEN Meng Lishui Institute for Food and Drug & Quality and Technical Inspection 
FAN Lei Lishui Institute for Food and Drug & Quality and Technical Inspection 
JIANG Kai-Ya Lishui agricultural and rural Bureau 
JIANG Chuan Lishui Institute for Food and Drug & Quality and Technical Inspection 
CHEN Wei-Ping Lishui Institute for Food and Drug & Quality and Technical Inspection 
WANG Wei-Ying Lishui Institute for Food and Drug & Quality and Technical Inspection 
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中文摘要:
      目的 评定高效液相色谱法测定牛奶中四环素类兽药残留量的不确定度。方法 依据GB/T 21317-2007《动物源性食品中四环素类兽药残留量检测方法 液相色谱-质谱/质谱法与高效液相色谱法》, 建立相关数学模型, 对高效液相色谱法实验过程中的不确定度来源进行分析与评定。结果 当高效液相色谱法测定牛奶中土霉素、四环素、金霉素、强力霉素的残留量分别为0.939、0.825、0.838、0.900 mg/kg时, 扩展不确定度分别为0.078、0.073、0.081、0.078 mg/kg (k=2)。结论 检测结果的不确定度主要受标准溶液配制、工作曲线拟合、样品回收率影响。
英文摘要:
      Objective To evaluate the uncertainty of the determination of tetracycline drug residues in milk by high performance liquid chromatography. Methods According to GB/T 21317-2007 Determination of tetracycline residues in food of animal origin by high performance liquid chromatography-tandem mass spectrometry method and high performance liquid chromatography method, relevant mathematical models were established to analyze and evaluate the sources of uncertainty in the high performance liquid chromatography experiment. Results When the content of oxytetracycline, tetracycline, aureomycin, deoxytetracycline in milk was 0.939, 0.825, 0.838, 0.900 mg/kg by high performance liquid chromatography, its extended relative uncertainty was 0.078, 0.073, 0.081, 0.078 mg/kg (k=2), respectively. Conclusion The uncertainty of detection results is mainly affected by standard solution preparation, working curve fitting and sample recovery rate.
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