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作 者:张海超 贾海涛 张婧雯 王敬 艾连峰 霍惠玲 李研东 Zhang Haichao;Jia Haitao;Zhang Jingwen;Wang Jing;Ai Lianfeng;Huo Huiling;Li Yandong(Shijiazhuang Customs Technology Center,Hebei Shijiazhuang 050011;Hebei Provincial Veterinary Drug Inspection Institute,Hebei Shijiazhuang 050050)
机构地区:[1]石家庄海关技术中心,河北石家庄050011 [2]河北省兽药监察所,河北石家庄050050
出 处:《现代畜牧兽医》2021年第10期20-24,共5页Modern Journal of Animal Husbandry and Veterinary Medicine
基 金:河北省科技计划项目(19226614D);河北省科技计划项目(19225503D);总署科技计划项目(2019HK112)。
摘 要:试验建立了固相萃取/液相色谱-串联质谱法测定兽药制剂中8种硝基咪唑类药物的方法。样品采用乙腈提取,SCX固相萃取柱净化,经Waters BEH C18(100 mm×2.1 mm,1.7μm)色谱柱分离,以0.1%甲酸水和乙腈为流动相进行梯度洗脱,质谱采用正离子模式扫描,MRM模式进行分析。8种硝基咪唑类化合物在10~500μg/L范围内线性关系较好,相关系数大于0.9999。方法检出限为0.02 mg/kg,定量限为0.05 mg/kg。待测物在0.05、0.10、0.50 mg/kg 3个浓度水平下平均回收率在84.1%~101.6%之间,相对标准偏差在2.74%~11.60%之间。该方法可用于兽药制剂中硝基咪唑类药物的测定。A method was developed for the detection of eight nitroimidazoles in veterinary drug preparations by solid phase extraction purification with liquid chromatography tandem mass spectrometry(LC-MS/MS).The samples were extracted with acetonitrile,SCX solid phase extraction column was purified,separated by Waters BEH C18(100 mm×2.1 mm,1.7μm)chromatographic column,and gradient elution was carried out with 0.1% formic acid water and acetonitrile as mobile phases.The mass spectrometer was operated using positive under multiple reaction monitoring(MRM)mode.The results showed that there was good linear relationship(10~500μg/L)for the eight nitroimidazoles with the correlation coefficient more than 0.9999.The limit of detection(LOD)and limit of quantization(LOQ)were0.02 mg/kg and 0.05 mg/kg for the eight nitroimidazoles.The average recoveries was in the range of 84.1%~101.6%,the relative standard deviation was between 2.74% and 11.60% with the concentration levels at 0.05,0.10,and 0.50 mg/kg for the analytes.The proposed method can be applied to determination of nitroimidazoles in veterinary drug preparations.
关 键 词:液相色谱-串联质谱 固相萃取 SCX 硝基咪唑 兽药制剂
分 类 号:S859[农业科学—临床兽医学]
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