Department of Physical and Analytical Chemistry, EPS of Linares, University of Jaén, Linares, Jaén, Spain.
J Agric Food Chem. 2011 May 11;59(9):5125-32. doi: 10.1021/jf200364w. Epub 2011 Apr 15.
This paper reports a systematic approach to the development of a method that combines continuous solid-phase extraction and gas chromatography-mass spectrometry for the simultaneous determination of 20 pharmacologically active substances including antibacterials (chloramphenicol, florfenicol, pyrimethamine, thiamphenicol), nonsteroideal anti-inflammatories (diclofenac, flunixin, ibuprofen, ketoprofen, naproxen, mefenamic acid, niflumic acid, phenylbutazone), antiseptic (triclosan), antiepileptic (carbamazepine), lipid regulator (clofibric acid), β-blockers (metoprolol, propranolol), and hormones (17α-ethinylestradiol, estrone, 17β-estradiol) in milk samples. The sample preparation procedure involves deproteination of the milk, followed by sample enrichment and cleanup by continuous solid-phase extraction. The proposed method provides a linear response over the range of 0.6-5000 ng/kg and features limits of detection from 0.2 to 1.2 ng/kg depending on the particular analyte. The method was successfully applied to the determination of pharmacologically active substance residues in food samples including whole, raw, half-skim, skim, and powdered milk from different sources (cow, goat, and human breast).
本文报道了一种系统的方法开发,该方法结合连续固相萃取和气相色谱-质谱法,用于同时测定 20 种药理活性物质,包括抗菌药物(氯霉素、氟苯尼考、乙胺嘧啶、硫胺酚)、非甾体抗炎药(双氯芬酸、氟尼辛、布洛芬、酮洛芬、萘普生、甲芬那酸、尼氟酸、保泰松)、防腐剂(三氯生)、抗癫痫药(卡马西平)、调脂药(氯贝特酸)、β-受体阻滞剂(美托洛尔、普萘洛尔)和激素(17α-乙炔基雌二醇、雌酮、17β-雌二醇)在牛奶样品中的含量。样品制备过程包括牛奶的去蛋白处理,然后通过连续固相萃取进行样品富集和净化。该方法在 0.6-5000ng/kg 范围内呈线性响应,特定分析物的检测限从 0.2 到 1.2ng/kg 不等。该方法成功应用于不同来源(牛、山羊和人乳)的全脂、生乳、半脱脂、脱脂和奶粉等食品样品中药理活性物质残留的测定。