食品科学 ›› 2023, Vol. 44 ›› Issue (8): 324-329.doi: 10.7506/spkx1002-6630-20220818-218

• 安全检测 • 上一篇    下一篇

QuEChERS-超高压液相色谱-串联质谱法同时测定水产品中的6 种丁香酚类麻醉剂

林晨, 吴敏, 王凯, 曾三妹, 吴佳雯, 钟莉萍, 凌淞江   

  1. (1.中国药科大学基础医学与临床药学学院,江苏 南京 211198;2.厦门海关技术中心,福建 厦门 361006;3.集美大学水产学院,福建 厦门 361021)
  • 出版日期:2023-04-25 发布日期:2023-05-06
  • 基金资助:
    “十三五”国家重点研发计划重点专项(2017YFC1601606);福建省社会发展引导性(重点)项目(2018Y0075)

Simultaneous Determination of Eugenol and Its Five Derivatives in Aquatic Products by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry Combined with Quick, Easy, Cheap, Effective, Rugged and Safe Extraction

LIN Chen, WU Min, WANG Kai, ZENG Sanmei, WU Jiawen, ZHONG Liping, LING Songjiang   

  1. (1. School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing 211198, China; 2. Technical Center, Xiamen Customs, Xiamen 361006, China; 3. Fisheries College, Jimei University, Xiamen 361021, China)
  • Online:2023-04-25 Published:2023-05-06

摘要: 建立了同时测定水产品中的丁香酚、异丁香酚、甲基丁香酚、甲基异丁香酚、乙酸丁香酚酯、乙酰基异丁香酚残留量的超高压液相色谱-串联质谱法。样品用乙腈提取,经50 mg乙二胺-N-丙基硅烷、100 mg C18、150 mg MgSO4净化,采用Kinetex C18(2.1 mm×100 mm,2.6 μm)色谱柱分离,以甲醇-水作为流动相进行梯度洗脱,电喷雾离子源正负快速切换,多反应监测模式检测,内标法定量。丁香酚和异丁香酚的线性范围为2~100 ng/mL,其他4 种丁香酚类药物的线性范围为1~100 ng/mL,线性相关系数均不低于0.999。丁香酚类药物检出限(信噪比为3)为0.5~1.5 µg/kg,定量限为2.0~5.0 µg/kg。6 种丁香酚类麻醉剂的方法回收率为67.0%~106.4%,相对标准偏差为1.2%~15.7%。该方法能实现对水产品中丁香酚类麻醉剂的准确、快速检测,测定结果可靠。

关键词: QuEChERS;超高压液相色谱-串联质谱;丁香酚类麻醉剂;水产品;内标法

Abstract: An ultra-high performance liquid chromatography-tandem mass spectrometric (UPLC-MS/MS) method was developed for the simultaneous determination of eugenol and its five derivatives including isoeugenol, methyl eugenol, methyl isoeugenol, acetyl eugenol and acetylisoeugenol in aquatic products. The samples were extracted with acetonitrile, and then the extracted supernatant was cleaned up with 50 mg of primary secondary amine (PSA) and 100 mg of C18 and 150 mg of MgSO4. Separation of the targets was performed on a Kinetex C18 (2.1 mm × 100 mm, 2.6 μm) chromatographic column by gradient elution using a mobile phase of water and methanol. The six eugenol derivatives were detected using an electrospray ionization (ESI) source with fast switching between the positive and negative ionization modes in the multiple reaction monitoring (MRM) mode, and quantified by the internal standard method using eugenol-D3 as the internal standard (IS). The calibration curves showed a good linearity in the range of 2–100 ng/mL for eugenol and isoeugenol, and 1–100 ng/mL for four other eugenol derivatives with correlation coefficient (r) ≥ 0.999. The average recoveries of spiked samples were between 67.0% and 106.4% with relative standard deviations (RSDs) of 1.2%–15.7%. The limits of detection (LOD, RSN = 3) and quantitation (LOQ) were 0.5–1.5 and 2.0–5.0 μg/kg, respectively. The method is an accurate, rapid and reliable assay for the detection of eugenol and its derivatives in aquatic products.

Key words: Quick, Easy, Cheap, Effective, Rugged and Safe; ultra-high performance liquid chromatography-tandem mass spectrometry; eugenol derivatives; aquatic products; internal standard method

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