Evaluation of a method for assaying sulfonamide antimicrobial residues in cheese:: Hot-water extraction and liquid chromatography-tandem mass spectrometry

被引:26
作者
Berardi, Giorgio [1 ]
Bogialli, Sara [1 ]
Curini, Roberta [1 ]
Di Corcia, Antonio [1 ]
Lagana, Aldo [1 ]
机构
[1] Univ Roma La Sapienza, Dipartimento Chim, I-00185 Rome, Italy
关键词
sulfonamide antimicrobials; matrix solid-phase dispersion; heated water as extractant; LC-MS/; MS;
D O I
10.1021/jf060545y
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Several sulfonamide antimicrobials (SAAs) are largely used in veterinary medicine. A rapid, specific, and sensitive procedure for determining 12 SAAs in cheese is presented. The method is based on the matrix solid-phase dispersion technique followed by liquid chromatography (LC)-tandem mass spectrometry (MS) equipped with an electrospray ion source. Target compounds were extracted from Mozzarella, Asiago, Parmigiano, Emmenthal, and Camembert cheese samples by 6 mL of water modified with 10% methanol and heated at 120 degrees C. The addition of methanol to hot water served to improve remarkably extraction yields of the most lipophilic SAAs, that is, sulfadimethoxine and sulfaquinoxaline. After acidification and filtration, 100 mu L of the aqueous extract was injected in the LC column. MS data acquisition was performed in the multireaction monitoring mode, selecting two precursor-to-product ion transitions for each target compound. Methanol-modified hot water appeared to be an efficient extractant, because absolute recovery ranged between 67 and 88%. Using sulfamoxole as surrogate analyte, recovery of the 12 analytes spiked in the five types of cheese considered at the 50 ng/g level ranged between 75 and 105% with RSD not higher than 11%. Statistical analysis of the mean recovery data showed that the extraction efficiency was not affected by the type of cheese analyzed. This result indicates this method could be applied to other cheese types not considered here. The accuracy of the method was determined at three spike levels, that is, 20, 50, and 100 ng/g, and varied between 73 and 102% with relative standard deviastions ranging between 4 and 12%. On the basis of a signal-to-noise ratio of 10, limits of quantification were estimated to be < 1 ng/g.
引用
收藏
页码:4537 / 4543
页数:7
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