Simultaneous determination of aminoglycoside antibiotics in milk by liquid chromatography with tandem mass spectrometry

被引:9
|
作者
Kajita, Hiroko [1 ]
Akutsu, Chizuko [1 ]
Hatakeyama, Eriko [1 ]
Komukai, Takashi [1 ]
机构
[1] Res Inst Environm Sci & Publ Hlth Iwate Prefectur, Morioka, Iwate 0200852, Japan
来源
关键词
aminoglycoside antibiotic; milk; simultaneous determination; LC/MS/MS; cation-exchange cartridge column;
D O I
10.3358/shokueishi.49.189
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
A multiresidue method was developed for determination of nine aminoglycoside antibiotics (streptomycin, dihydrostreptomycin, spectinomycin, neomycin, kanamycin, gentamicin, destomycin A, apramycin, and tobramycin) in milk by LC/MS/MS. The drugs were extracted with 0.01 mol/L potassium dihydrogen phosphate containing 2% trichloroacetic acid, and the extracted solution was cleaned on cation-exchange cartridge columns (Oasis WCX and Oasis MCX). LC separation was performed on a TSK-gel VMpak25 column (50 mm x 2.0 mm i.d.) using gradient elution with 0.1% formic acid and acetonitrile containing 0.1% formic acid as the mobile phase. Recoveries of the drugs spiked at 0.01 or 0.1 mu g/g in milk ranged from 66.1 to 110.8%, with a coefficient of variation of less than 17.1%. Limits of quantification of the drugs in milk were 0.001 similar to 0.01 mu g/g. This method was used for analysis of milk from a lactating cow treated for clinical mastitis with two intramammary infusions of kanamycin (KM). Milk samples were analyzed during the withdrawal times at 12-hour intervals. KM concentrations were lower than the Japanese provisional MRLs (0.4 mu g/g) at 60 hours after infusion, and subsequently fell to 0.0 1 mu g/g.
引用
收藏
页码:189 / 195
页数:7
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