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中国精品科技期刊2020
王东鹏,叶诚. 增强型固相萃取净化-高效液相色谱-串联质谱法测定鲈鱼中18种磺胺类药物的残留量[J]. 食品工业科技,2022,43(14):371−377. doi: 10.13386/j.issn1002-0306.2021110162.
引用本文: 王东鹏,叶诚. 增强型固相萃取净化-高效液相色谱-串联质谱法测定鲈鱼中18种磺胺类药物的残留量[J]. 食品工业科技,2022,43(14):371−377. doi: 10.13386/j.issn1002-0306.2021110162.
WANG Dongpeng, YE Cheng. Determination of 18 Sulfonamide Drugs Residues in Lateolabrax japonicus by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Enhanced Solid Phase Extraction[J]. Science and Technology of Food Industry, 2022, 43(14): 371−377. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021110162.
Citation: WANG Dongpeng, YE Cheng. Determination of 18 Sulfonamide Drugs Residues in Lateolabrax japonicus by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Enhanced Solid Phase Extraction[J]. Science and Technology of Food Industry, 2022, 43(14): 371−377. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2021110162.

增强型固相萃取净化-高效液相色谱-串联质谱法测定鲈鱼中18种磺胺类药物的残留量

Determination of 18 Sulfonamide Drugs Residues in Lateolabrax japonicus by High Performance Liquid Chromatography-Tandem Mass Spectrometry with Enhanced Solid Phase Extraction

  • 摘要: 建立了增强型脂质去除固相萃取净化高效液相色谱串联质谱法同时检测鲈鱼中18种磺胺类药物残留的分析方法。鱼肉样品经1%甲酸乙腈提取,增强型脂质去除固相萃取柱进行净化,用CNW Athena C18-WP色谱柱(2.1 mm×100 mm,3 μm)进行分离,以甲醇和0.1%甲酸水溶液为流动相梯度洗脱,ESI正离子模式扫描,采用多反应监测模式测定,内标法定量。结果表明:18种磺胺类药物在5~200 ng/mL范围内具有良好的线性关系(r≥0.9962),方法的检出限和定量限分别为0.11~0.47和0.37~1.57 μg/kg。在3个不同浓度添加水平下,样品回收率在73.30%~116.9%之间,相对标准偏差为0.29%~7.74%(n=6)。该方法操作简单,准确快速,灵敏度高,可用于鲈鱼中多种磺胺类药物残留的检测。

     

    Abstract: A high-performance liquid chromatography-tandem mass spectrometry method was developed for simultaneous determination of 18 sulfonamide drugs residues in fish. The samples were extracted by 1% formic acid acetonitrile and the extracts were purified on enhanced solid-phase extraction column. The 18 sulfonamide drugs were analyzed by CNW Athena C18-WP column (2.1 mm×100 mm, 3 μm) using methanol and 0.1% formic acid as the mobile phases, the sample was analyzed under the multiple reaction monitoring mode with positive electrospray ionization(ESI+) and quantify by internal standard. The results showed that good linearities were obtained for the 18 sulfonamides in 5~200 ng/mL (r≥0.9962). The limits of detection and quantification for sulfonamides were 0.11~0.47 and 0.37~1.57 μg/kg, respectively. The recoveries at three concentrations ranged from 73.30%~116.9%, with the RSD from 0.29%~7.74% (n=6). The method was simple, accurate, rapid, and highly sensitive. The method was successfully used for measurement of multiple sulfanilamide drugs residues in fish.

     

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