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出 处:《齐齐哈尔医学院学报》2011年第4期514-518,共5页Journal of Qiqihar Medical University
摘 要:采用液相色谱-串联质谱仪,建立了牛奶和奶粉中乙酰丙嗪cetopromaizine、氯丙嗪chlor-promazin、氟哌啶醇haloperidol、丙酰二甲氨基丙吩噻嗪propionylpromazine、甲苯噻嗪xylazine、阿扎哌隆azaperone及其代谢物阿扎哌醇azaperol和咔唑心安carazolol残留量的液相色谱-串联质谱测定方法。结果表明八种镇定剂在牛奶中添加水平0.10~0.50μg/kg到0.80~4.00μg/kg,其回收率在86.29%~92.49%之间,相对标准偏差在8.99%~20.56%之间;在奶粉中添加水平0.80~2.00μg/kg到2.0~8.00μg/kg,其回收率在81.59%~97.49%之间,相对标准偏差在1.76%~16.70%之间。八种镇定剂在确定的添加范围内线性关系良好。八种镇定剂在牛奶中的方法检出限为0.1~0.5μg/kg,在奶粉中的方法检出限为0.8~4.0μg/kg。LC-MS-MS method was established for the determination of cetopromaizine chlorpromazin,haloperidol,propionylpromazine,xylazine,azaperone,azaperol and carazolol residues in bovine milk and milk powder.The result showed that the average spiked recoveries of eight tranquillizers at the spiked level 0.10~0.50 μg/kg to 0.80~4.00 μg/kg were from 86.29%~92.49% with relative standard deviations(RSDS) of 8.99%~20.56% for bovine milk and at the spiked level 0.80~2.00 μg/kg to 2.0~8.00 μg/kg were from81.59%~97.49% with relative standard deviations(RSDS) of 1.76%~16.70% for milk powder.The result showed a good linea relationship.The limits of determination of method for eight tranguillizers were from 0.10 μg/kg to 0.50 μg/kg for bovine milk and 0.8 μg/kg to 4.0 μg/kg for milk powder.
关 键 词:液相色谱-串联质谱 牛奶 奶粉 乙酰丙嗪 氯丙嗪 氟哌啶醇 丙酰二甲氨基丙吩噻嗪 甲苯噻嗪 阿扎哌隆 阿扎哌醇 咔唑心安 残留量
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