Determination of Quinolones Residues in Animal-originated Foodstuffs by Ultrafiltration Tube Cleaning and High Performance Liquid Chromatography-Tandem Mass Spectrometry
|更新时间:
|
Determination of Quinolones Residues in Animal-originated Foodstuffs by Ultrafiltration Tube Cleaning and High Performance Liquid Chromatography-Tandem Mass Spectrometry
Vol. 35, Issue 1, Pages: 42-47(2016)
作者机构:
威海出入境检验检疫局
作者简介:
基金信息:
DOI:
CLC:
扫 描 看 全 文
Determination of Quinolones Residues in Animal-originated Foodstuffs by Ultrafiltration Tube Cleaning and High Performance Liquid Chromatography-Tandem Mass Spectrometry. [J]. 35(1):42-47(2016)
DOI:
Determination of Quinolones Residues in Animal-originated Foodstuffs by Ultrafiltration Tube Cleaning and High Performance Liquid Chromatography-Tandem Mass Spectrometry. [J]. 35(1):42-47(2016)DOI:
Determination of Quinolones Residues in Animal-originated Foodstuffs by Ultrafiltration Tube Cleaning and High Performance Liquid Chromatography-Tandem Mass Spectrometry
A new method was established for the simultaneous determination of 10 quinolone(QN) residues in animal-originated foodstuffs by ultrafiltration tube cleaning with high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS).After extraction with acetonitrile (containing 1%acetic acid),the extract was purified with 50 mL Millipore ultrafiltration tube (Molecular Weight Cut-Off,MWCO:3 kD),and then the centrifugal liquid was evaporated to dryness under a stream of nitrogen,and redissolved.The analytes were separated on a Waters Xbridge C18 column using 0.1%formic acid-acetonitrile as mobile phase.The identification and quantification of 10 quinolone residues were carried out under positive electrospray ionization (ESI+) in multiple reaction monitoring (MRM) mode,the quantification analysis was performed by the external standard method.The calibration curves showed good linearities in the range of 5.0-100 μg/kg for all QNs.The limits of detection for all QNs were in the range of 0.15-0.75 μg/kg,and the limits of quantitation were 0.49-2.59 μg/kg.The recoveries of these analytes varied from 71.4%to 85.9%at spiked levels of 5.0,10,50 μg/kg,with relative standard deviations of 3.9%-10.7%.This method was simple,rapid,sensitive and reproducible,and could be applied in the determination of 10 quinolone residues in anima-originated foodstuffs.
关键词
超滤管高效液相色谱-串联质谱动物源食品喹诺酮类药物
Keywords
ultrafiltration tubehigh performance liquid chromatography-tandem mass spectrometry(HPLC-MS/MS)animal-originated foodstuffsquinolones
Detection of Seven Quinolones in Honey by High Performance Liquid Chromatography with Effervescent Assisted Liquid Phase Microextraction
Determination of Acetylgestagens in Ovine Milk by High Performance Liquid Chromatography-Tandem Mass Spectrometry
Determination of Biotin in Infant Formula Milk Powder by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Immunoaffinity Purification Column
Determination of Perchlorate in Fruits by Solid Phase Extraction/18O Labeled Perchlorate Dilution High Performance Liquid Chromatography-Tandem Mass Spectrometry
Determination of 16 Perfluoroalkyl Acids in Textiles by HPLC-MS/MS
Related Author
No data
Related Institution
Institute of Agricultural Quality Standards and Testing Technology,Tianjin Academy of Agricultural Sciences
Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry,College of Animal Science and Veterinary Medicine,Tianjin Agricultural University