Zhao Funian, Zhang Xuezhu, Gan Yiru
Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China.
J Chromatogr A. 2004 Nov 5;1055(1-2):109-14. doi: 10.1016/j.chroma.2004.08.131.
A method has been developed to analyze residual tetracyclines (TCs) (oxytetracycline (OTC), tetracycline (TC), chlortetracycline (CTC), methacycline (MTC), doxycycline (DC)) in ovine milk, using high-performance liquid chromatography (HPLC) with a coulometric electrode array system. The samples were pretreated, using liquid-liquid extraction based on hexane. The chromatography was performed, using a C18 column (150 mm x 4 mm i.d. and 5 microm) with a mobile phase: sodium phosphate monobasic dihydrate (pH 2.2, 0.05 M)-acetonitrile (78:22, v/v). The flow rate of mobile phase was kept constantly at 1ml/min. The residues were monitored by an ESA electrochemical detector. Potentials of four electrodes in series were set at 400, 660, 680 and 700 mV, respectively. The first electrode was set to remove those interfering substances that may co-elute with TCs and the other three electrodes were used for quantification. The maximal potential of our detection was 700 mV. Calibration curve showed good linearity and the detection limit of TCs was 12.5, 20, 25, 10 and 25 ng/ml, respectively. Optimization of the pH of the mobile phase, the proportion of acetonitrile and the pH of the pretreatment were also performed. Recoveries of TCs from spiked samples were more than 88% and the relative standard deviations were less than 4.3%. This method was reliable, sensitive, economical and suited for routine monitoring of TC residues in ovine dairy milk.
已开发出一种使用带库仑电极阵列系统的高效液相色谱法(HPLC)分析羊奶中残留四环素(TCs)(土霉素(OTC)、四环素(TC)、金霉素(CTC)、甲烯土霉素(MTC)、强力霉素(DC))的方法。样品采用基于己烷的液液萃取进行预处理。色谱分析使用C18柱(150 mm×4 mm内径,5微米),流动相为:磷酸二氢钠一水合物(pH 2.2,0.05 M)-乙腈(78:22,v/v)。流动相流速保持恒定在1ml/min。残留物通过ESA电化学检测器进行监测。串联的四个电极的电位分别设置为400、660、680和700 mV。第一个电极用于去除可能与TCs共洗脱的干扰物质,其他三个电极用于定量分析。我们检测的最大电位为700 mV。校准曲线显示出良好的线性,TCs的检测限分别为12.5、20、25、10和25 ng/ml。还对流动相的pH值、乙腈比例和预处理的pH值进行了优化。加标样品中TCs的回收率超过88%,相对标准偏差小于4.3%。该方法可靠、灵敏、经济,适用于羊奶中TCs残留的常规监测。