超高效液相色谱-串联质谱法同时测定土壤中13种硝基咪唑类抗生素的含量  被引量:4

Simultaneous Determination of Residues of 13Nitroimidazole Antibiotics in Soil by Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry

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作  者:唐会鑫 谷悦 郭二菱 郭爱静[2] 王可 杨莉丽[1] TANG Huixin;GU Yue;GUO Erling;GUO Aijing;WANG Ke;YANG Lili(College of Chemistry and Materials Science,Hebei Normal University,Shijiazhuang050024,China;Shijiazhuang Technology Innovation Center for Chemical Poison Detection and Risk Early Warning,Shijiazhuang Center for Disease Control and Prevention,Shijiazhuang050011,China)

机构地区:[1]河北师范大学化学与材料科学学院,石家庄050024 [2]石家庄市疾病预防控制中心,石家庄市化学毒物检测及风险预警技术创新中心,石家庄050011

出  处:《理化检验(化学分册)》2023年第5期606-611,共6页Physical Testing and Chemical Analysis(Part B:Chemical Analysis)

基  金:河北省省级科技计划资助(223777116D)。

摘  要:取5.00 g土壤样品,加入4 mL水,涡旋混匀后加入10 mL乙腈提取剂,涡旋提取3 min。加入1 g氯化钠,在室温下离心10 min,分取7.5 mL上清液,加入0.3 g无水硫酸镁,涡旋30 s后在25℃下离心5 min。分取5 mL上清液,于35℃氮吹至干。用1 mL甲醇复溶,过0.22μm滤膜,滤液中13种硝基咪唑类抗生素在Phenomenex Kinetex F5 100?色谱柱上用不同体积比0.1%(体积分数,下同)甲酸溶液和甲醇的混合溶液进行梯度洗脱分离,以喷射流电喷雾离子源正离子(AJS ESI+)模式电离,以多反应监测(MRM)模式检测,以基质匹配法定量。结果显示,各抗生素的质量浓度均在0.5~100.0μg·L^(-1)与对应的峰面积呈线性关系,测定下限(10S/N)为0.01~0.07μg·kg^(-1)。按标准加入法进行回收试验,回收率为71.5%~116%,测定值的相对标准偏差(n=5)为1.1%~7.8%。方法用于20份实际样品的分析,仅在一份样品中检出了迪美唑,检出量为8.39μg·kg^(-1)。An aliquot(5.00g)of soil sample was taken,and mixed with 4mL of water by vortex.The extractant(10mL of acetonitrile)was added,and the mixture was vortexed for 3min.After adding 1g of sodium chloride,the mixture was centrifuged for 10min at room temperature,and 7.5mL of the supernatant was taken,and mixed with 0.3g of anhydrous magnesium sulfate.The mixture was vortexed for 30sand centrifugated for 5min at 25℃.An aliquot(5mL)of the supernatant was taken and blown to dryness by nitrogen at 35℃.The residue was redissolved by 1mL of methanol,and the mixed solution was passed through a 0.22μm filtration membrane.Thirteen nitroimidazole antibiotics in the filtrate were separated on Phenomenex Kinetex F5100Åcolumn with mixed solutions composed of methanol and 0.1%(volume fraction)formic acid solution at different volume ratios by gradient elution,and ionized by AJS ESI+mode,detected by MRM mode,quantified by matrix matched method.As shown by the results,linear relationships between values of the mass concentration and the peak area of each antibiotic were kept in the same range of 0.5-100.0μg·L^(-1),with lower limits of determination(10S/N)in the range of 0.01-0.07μg·kg^(-1).Test for recovery was made by standard addition method,giving recoveries in the range of 71.5%-116%,and RSDs(n=5)of the determined values ranged from 1.1%to 7.8%.The proposed method was applied to the analysis of 20actual samples,dimetridazole was detected in 1sample with detection amount of 8.39μg·kg^(-1).

关 键 词:超高效液相色谱-串联质谱法(UHPLC-MS/MS) 硝基咪唑类抗生素 残留量 土壤 

分 类 号:O657.53[理学—分析化学]

 

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