Tan H S, Ramachandran P, Cacini W
Division of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati Medical Center, OH 45267-0004, USA.
J Pharm Biomed Anal. 1996 Nov;15(2):259-65. doi: 10.1016/0731-7085(96)01829-8.
A method for the assay of mixtures of amprolium and ethopabate in chicken feed was developed utilizing reversed-phase high-performance liquid chromatography (HPLC) after sample clean-up of a methanolic extract by solid-phase extraction using CN cartridges. HPLC was done with benzocaine as internal standard on a C-8 column with methanol-water 40:60, containing octanesulfonic acid, triethylamine and acetic acid, as mobile phase. Eluate was monitored at 274 nm. Baseline separation was achieved with retention times of approximately 7.5, 9.4, and 10.4 min, for amprolium, benzocaine, and ethopabate respectively. Feed constituents did not give peaks after 6.5 min. Peak area ratios were linear over 10-180 ng of amprolium, and 2-18 ng of ethopabate injected. Limits of quantitation at AUFS 0.05 were 0.5 and 0.3 ng respectively. Recovery studies from spiked feed (n = 9), covering +/- 30% of usual doses in feed, gave percent recoveries (+/- SD) of 99.4 +/- 1.4% for amprolium and 100.5 +/- 2.6% for ethopabate. Applying the method to two different batches of commercial feed gave results which were comparable to those obtained by the AOAC spectrofluorometric methods.
建立了一种测定鸡饲料中氨丙啉和乙氧酰胺苯甲酯混合物的方法,该方法是利用反相高效液相色谱法(HPLC),先用CN柱对甲醇提取物进行固相萃取以净化样品。HPLC以苯佐卡因作为内标,在C-8柱上进行,流动相为甲醇-水(40:60),其中含有辛烷磺酸、三乙胺和乙酸。在274 nm处监测洗脱液。氨丙啉、苯佐卡因和乙氧酰胺苯甲酯的保留时间分别约为7.5、9.4和10.4分钟,实现了基线分离。饲料成分在6.5分钟后没有出现峰。注入10 - 180 ng氨丙啉和2 - 18 ng乙氧酰胺苯甲酯时,峰面积比呈线性关系。在AUFS 0.05时的定量限分别为0.5 ng和0.3 ng。对添加了药物的饲料进行回收率研究(n = 9),添加量覆盖饲料中常用剂量的±30%,氨丙啉的回收率(±标准差)为99.4 ± 1.4%,乙氧酰胺苯甲酯的回收率为100.5 ± 2.6%。将该方法应用于两批不同的商业饲料,所得结果与AOAC荧光分光光度法的结果相当。