Turberg M P, Macy T D, Lewis J J, Coleman M R
Lilly Research Laboratories, Eli Lilly and Co., Greenfield, IN 46140, USA.
J AOAC Int. 1995 Nov-Dec;78(6):1394-402.
A liquid chromatographic (LC) method is described for determination of ractopamine hydrochloride (LY031537) in swine and turkey tissues. Liver, kidney, muscle, and fat samples were homogenized in methanol. An aliquot of the extract was evaporated, diluted with water, and buffered to pH 10.5 +/- 0.5 with sodium carbonate to convert ractopamine hydrochloride to a free base. The free base was extracted from the buffered sample with ethyl acetate. The extract was further purified on a Bond Elut acid-washed silica solid-phase extraction cartridge. After converting the free base back to the salt form with pH 4.5 buffer, analytical separation and quantitation of ractopamine hydrochloride was performed on an IBM C18 column with coulometric detection at +600 mV. The limit of detection of the method was approximately 0.5 ppb as determined in swine liver. Overall recovery levels ranged between 75 and 100% for samples of liver, kidney, muscle, and fat fortified at 1 to 100 ppb. The coefficients of variation ranged from 2 to 18% for samples fortified at 1 to 100 ppb.
描述了一种用于测定猪和火鸡组织中盐酸莱克多巴胺(LY031537)的液相色谱(LC)方法。将肝脏、肾脏、肌肉和脂肪样品在甲醇中匀浆。取一部分提取物蒸发,用水稀释,并用碳酸钠缓冲至pH 10.5±0.5,将盐酸莱克多巴胺转化为游离碱。用乙酸乙酯从缓冲后的样品中萃取游离碱。提取物在Bond Elut酸洗硅胶固相萃取柱上进一步纯化。用pH 4.5缓冲液将游离碱转化回盐形式后,在IBM C18柱上进行分析分离,采用库仑检测法在+600 mV下对盐酸莱克多巴胺进行定量。该方法在猪肝中的检测限约为0.5 ppb。对于添加浓度为1至100 ppb的肝脏、肾脏、肌肉和脂肪样品,总体回收率在75%至100%之间。对于添加浓度为1至100 ppb的样品,变异系数在2%至18%之间。