Carson M C
U.S. Food and Drug Administration, Division of Veterinary Medical Research, Beltsville, MD 20705.
J AOAC Int. 1993 Mar-Apr;76(2):329-34.
A method was developed for the determination of 7 tetracyclines in milk. Raw milk samples are defatted, acidified, and centrifuged to remove proteins, and the tetracyclines are specifically absorbed from the milk by chelation with metal ions bound to small Chelating Sepharose Fast Flow columns. The tetracyclines are removed from these columns with EDTA-containing buffer, and the extracts are further cleaned up by centrifugal ultrafiltration. Finally, the extracts are concentrated and analyzed simultaneously by on-line concentration. This method has limits of detection for individual tetracyclines of < 5 ng/mL and was validated with fortified milk samples at 15, 30, and 60 ng/mL. Recoveries exceeded 60% for all tetracyclines at all levels, with good precision. The method was also tested on milk from cows dosed with each of the tetracyclines. Advantages of this method over existing methods include its sensitivity, minimal use of organic solvents, and speed; with an autosampler, at least 14 samples can be processed and analyzed in 1 day.
开发了一种测定牛奶中7种四环素的方法。将生牛奶样品脱脂、酸化并离心以去除蛋白质,通过与结合在小螯合琼脂糖快速流动柱上的金属离子螯合,从牛奶中特异性吸收四环素。用含EDTA的缓冲液从这些柱上洗脱四环素,提取物通过离心超滤进一步净化。最后,提取物浓缩并通过在线浓缩同时进行分析。该方法对单个四环素的检测限<5 ng/mL,并用添加了15、30和60 ng/mL四环素的强化牛奶样品进行了验证。所有水平的所有四环素回收率均超过60%,精密度良好。该方法还在分别用每种四环素处理过的奶牛的牛奶上进行了测试。该方法相对于现有方法的优点包括其灵敏度、有机溶剂使用量最少以及速度快;使用自动进样器,一天内至少可处理和分析14个样品。