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作 者:刘思洁[1] 方赤光[1] 张博[1] 李青[1] 张丽薇[1]
机构地区:[1]吉林省卫生监测检验中心理化检验所,长春130062
出 处:《中国媒介生物学及控制杂志》2007年第5期379-381,共3页Chinese Journal of Vector Biology and Control
摘 要:目的建立高效液相色谱法(HPLC)同时测定毒饵中杀鼠灵、溴敌隆、大隆3种抗凝血灭鼠剂的含量。方法在C18色谱柱,以甲醇+0.1%乙酸(90+10)为流动相,检测波长为265nm,柱温为室温下进行检测。结果3种灭鼠剂在5.0~300.0μg/ml浓度之间呈现良好的线性关系,杀鼠灵:Y=2.58×10^7x-1.23×10^5,r=0.9996;溴敌隆:Y=2.09×10^7x+1.56×10^5,r=0.9995;大隆:Y=1.79×10^7x+1.02×10^5,r=0.9992;相对标准偏差为1.03%~2.16%,回收率在93.7%~98.8%之间。结论HPLC法操作简便、准确、快速,可同时对这3种抗凝血灭鼠剂含量进行检测。Objective To establish a high performance liquid chromatography method for determination of the concentration of warfarin, bromadiolone, brodifacoum in the poison bait. Methods Warfarin, bromadiolone and brodifacoum were separated on a C18 column using methanol (50%): 0.1% aceticacid (50%) as the mobile phase at a flow rate of 1.0 ml/min, and detection wave 265 nm. Results The linear range were 5.0μg/ml to 300.0 μg/ml, warfarin Y=2.58×10^7x-1.23×10^5,r=0.9996;bromadiolone Y=2.09×10^7x+1.56×10^5,r=0.9995;brodifacoum Y=1.79×10^7x+1.02×10^5,r=0.9992; the relative standard deviation were 1.03% to 2.16% and the rate of recovery were 93.7% to 98.8% . Conclusion The method established in the present paper is simple, precise, fast and suitable for determination the concentration of warfarin, bromadiolone, brodifacoum in poison bait.
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