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分散固相萃取结合UPLC-MS/MS测定柑桔中青霉素G及其代谢物残留
引用本文:周杰,赵静,董超,张耀海,赵其阳,焦必宁. 分散固相萃取结合UPLC-MS/MS测定柑桔中青霉素G及其代谢物残留[J]. 分析测试学报, 2019, 38(4): 442-448
作者姓名:周杰  赵静  董超  张耀海  赵其阳  焦必宁
作者单位:中国农业科学院/西南大学柑桔研究所,农业农村部柑桔产品质量安全风险评估实验室(重庆),农业农村部柑桔及苗木质量监督检验测试中心,重庆400712;中国农业科学院/西南大学柑桔研究所,农业农村部柑桔产品质量安全风险评估实验室(重庆),农业农村部柑桔及苗木质量监督检验测试中心,重庆400712;中国农业科学院/西南大学柑桔研究所,农业农村部柑桔产品质量安全风险评估实验室(重庆),农业农村部柑桔及苗木质量监督检验测试中心,重庆400712;中国农业科学院/西南大学柑桔研究所,农业农村部柑桔产品质量安全风险评估实验室(重庆),农业农村部柑桔及苗木质量监督检验测试中心,重庆400712;中国农业科学院/西南大学柑桔研究所,农业农村部柑桔产品质量安全风险评估实验室(重庆),农业农村部柑桔及苗木质量监督检验测试中心,重庆400712;中国农业科学院/西南大学柑桔研究所,农业农村部柑桔产品质量安全风险评估实验室(重庆),农业农村部柑桔及苗木质量监督检验测试中心,重庆400712
基金项目:国家现代农业(柑桔)产业技术体系建设专项(CARS-26);国家柑桔及热带作物产品质量安全风险评估专项(GJFP2018004);2017年农业行业标准制订项目(181721301092371115);中央高校基本科研业务费专项资金(SWU116078)
摘    要:建立了分散固相萃取结合超高效液相色谱-串联质谱(DSPE/UPLC-MS/MS)快速检测柑桔中青霉素G及其代谢物青霉二酸和去羧青霉噻唑酸的分析方法。样品经80%乙腈提取,十八烷基键合硅胶吸附剂(C18)净化。目标残留物经Acquity UPLC~?HSS T3色谱柱分离,以乙腈-0.1%甲酸溶液为流动相进行梯度洗脱,采用正离子多反应监测模式(MRM)检测,基质匹配标准曲线法定量。结果表明,3种目标分析物可在5 min内实现有效快速分离;在5~2 000μg/L质量浓度范围内线性关系良好(r^2≥0.998 1),方法检出限(LOD)为0.5~1μg/kg,定量下限(LOQ)为5~10μg/kg。在3个不同加标水平下,柑桔果肉、果皮和全果中的平均回收率为76.7%~107%,相对标准偏差(RSD)为1.3%~9.6%。该方法快速、简便、灵敏、准确,适用于柑桔中青霉素G及其两种代谢物残留的测定。

关 键 词:分散固相萃取  青霉素G  代谢物  超高效液相色谱-串联质谱(UPLC-MS/MS)  柑桔

Determination of Penicillin G and Its Metabolite Residues in Citrus by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry with Dispersive Solid-phase Extraction
ZHOU Jie,ZHAO Jing,DONG Chao,ZHANG Yao-hai,ZHAO Qi-yang,JIAO Bi-ning. Determination of Penicillin G and Its Metabolite Residues in Citrus by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry with Dispersive Solid-phase Extraction[J]. Journal of Instrumental Analysis, 2019, 38(4): 442-448
Authors:ZHOU Jie  ZHAO Jing  DONG Chao  ZHANG Yao-hai  ZHAO Qi-yang  JIAO Bi-ning
Affiliation:(Quality Supervision and Testing Center for Citrus and Seedling,Laboratory of Risk Assessment for Citrus Quality and Safety,Ministry of Agriculture and Rural Affairs,Citrus Research Institute,Southwest University/Chinese Academy of Agricultural Sciences,Chongqing 400712,China)
Abstract:A rapid method was developed for the determination of penicillin G and its two metabolites (penillic acid and penilloic acid ) residues in citrus by dispersive solid-phase extraction/ultra-high performance liquid chromatography-tandem mass spectrometry (DSPE/UPLC-MS/MS ).The citrus samples were extracted with 80 % acetonitrile,then purified with C 18 .The analytes were separated on an Acquity UPLC^■ HSS T3 column with acetonitrile and 0.1 % formic acid solution as mobile phases by gradient elution,and finally detected by tandem mass spectrometry in positive ESI mode (ESI +).Identification and quantitation were performed by UPLC-MS/MS under multi-reaction monitoring (MRM ) mode and matrix-matched standard curve method,respectively.Results showed that three analytes could realize an effective and rapid separation within 5 min.There were good linear relationships for the analytes in the concentration range of 5-2 000 μg/L with their correlation coefficients ( r 2 ) not less than 0.998 1.The limits of detection (LOD ) and limits of quantitation (LOQ ) of the method were in the ranges of 0.5-1 μg/kg and 5-10 μg/kg,respectively.The spiked recoveries for penicillin G and its metabolites in blank citrus samples were in the range of 76.7 %-107 %,with relative standard deviations (RSD ) of 1.3 %-9.6 %.The method is rapid,simple,sensitive and accurate,and is suitable for the determination of penicillin G and its two metabolite residues in citrus.
Keywords:dispersive solid-phase extraction  penicillin G  metabolites  ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS )  citrus
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