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作 者:杨志凌[1] 陈杖榴[1] 方炳虎[1] 曾振灵[1] 丁焕中[1]
机构地区:[1]华南农业大学广东省兽药研制与安全评价重点实验室,广东广州510642
出 处:《色谱》2003年第3期245-247,共3页Chinese Journal of Chromatography
基 金:国家自然科学基金资助项目(批准号:30130140).
摘 要:建立了猪组织中克伦特罗的高效液相色谱 电化学检测方法。色谱柱为DiscoveryC18柱(5μm,4 6mmi.d.×250mm);流动相为1.7mmol/L氯化锂 甲酸 甲醇(体积比为65∶1∶34)混合溶液,流速为1 0mL/min;柱温为40 0℃;电化学检测器工作电位为1 25V。猪组织中克伦特罗含量为0 5~500ng/g时,克伦特罗的含量与其峰面积之间存在良好的线性关系(r>0 99),在组织中按0 5,50,500ng/g3个添加水平做克伦特罗的回收率试验,其回收率为75 8%~87 1%(n=4)。该方法重现性好,灵敏度高,简便,可用于猪的肌肉、肺脏、肝脏、肾脏及脂肪组织中克伦特罗残留的检测。A convenient and reliable high performance liquid chromatographic method (HPLC)with electrochemical detection was developed for the deterimination of clenbuterol in pig tissues. The tissue samples were homogenized and the drug was extracted by liquidliquid partitioning with an organic solution. Separation conditions are as follows: a Discovery C18 column (5 μm ,46 mm i.d.×250 mm), 1.7 mmol/L LiClformic acidmethanol (65∶1∶34, v/v) solution as mobile phase, flow rate 10 mL/min and column temperature 400 ℃. The working potential of the electrochemical detector was 125 V. The calibration curves were linear (r>099) for clenbuterol concentrations of 05-500 ng/g in pig tissues. The recoveries ranged from 758% to 871% at three spike levels of 05, 50 and 500 ng/g. The limit of quantitation (LOQ) was 05 ng/g in pig tissues such as muscle, lung, liver, kidney and adipose. The method showed good reproducibility, high sensitivity, and fast speed.
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