食品科学 ›› 2014, Vol. 35 ›› Issue (4): 116-121.doi: 10.7506/spkx1002-6630-201404024

• 分析检测 • 上一篇    下一篇

超高压液相色谱-高分辨质谱快速筛查和确证食用贝类中多种原多甲藻酸贝类毒素

韩 深,刘 鑫,李建辉,王珮玥,古 瑾,张朝晖*   

  1. 北京出入境检验检疫局检验检疫技术中心,北京 100026
  • 收稿日期:2013-03-25 修回日期:2014-01-22 出版日期:2014-02-25 发布日期:2014-03-17
  • 通讯作者: 张朝晖 E-mail:zhangzhh@bjciq.gov.cn
  • 基金资助:

    国家质检总局科技计划项目(2011IK193;2012IK145);国家质检总局质检行业公益性科研专项(201210029)

Rapid Profiling and Confirmation of Azaspiracids in Edible Shellfishes by Ultra High Performance Liquid Chromatography-High Resolution Mass Spectrometry

HAN Shen, LIU Xin, LI Jian-hui, WANG Pei-yue, GU Jin, ZHANG Zhao-hui*   

  1. Testing Center, Beijing Entry-Exit Inspection and Quarantine Bureau, Beijing 100026, China
  • Received:2013-03-25 Revised:2014-01-22 Online:2014-02-25 Published:2014-03-17
  • Contact: ZHANG Zhao-hui E-mail:zhangzhh@bjciq.gov.cn

摘要:

建立超高压液相色谱-高分辨质谱快速筛查和确证贻贝、牡蛎、蚌类、扇贝等食用贝类及其制品中3 种天然形式的原多甲藻酸贝类毒素的检测方法。样品中的原多甲藻酸采用乙腈-水体系均质提取,应用改进型QuEChERS技术净化,在乙腈-水(含5 mmol/L醋酸铵和0.1%甲酸)体系经Acquity HSS T3柱(150 mm×2.1 mm,1.8 μm)梯度洗脱,实现了3 种原多甲藻酸贝类毒素的基线分离。该方法基于电喷雾正离子模式,采用高分辨质谱一级全扫描和数据依赖扫描,对食用贝类及其制品样品中的原多甲藻酸贝类毒素进行检测。3 种贝类毒素的定量限均为10 μg/kg(RSN>10);在10~500 μg/L范围内线性关系良好,相关系数(R2)均大于0.99。应用该方法对国内外多个地区的贝类产品进行了筛查及确证,其中部分样品检出原多甲藻酸贝类毒素。该方法灵敏度高,重复性好,操作简便、快捷,适用于食用贝类及其制品中多种原多甲藻酸贝类毒素的筛查分析。

关键词: 原多甲藻酸贝类毒素, 超高压液相色谱-高分辨质谱, QuEChERS

Abstract:

An ultra high performance liquid chromatography-high resolution mass spectrometric method (UHPLC-LTQ/
Orbitrap) was developed for the rapid profiling and confirmation of 3 natural azaspiracids (AZAs) (AZA-1, AZA-2 and
AZA-3) in edible shellfishes including mussels, oysters, clams and scallops as well as related products. Samples were
homogeneously extracted with acetonitrile-water. The diluted supernatants were then purified with a modified QuEChERS
method. The separation was performed on an Acquity HSS T3 column (150 mm × 2.1 mm, 1.8 μm) by gradient elution with
acetonitrile in water containing 5 mmol/L ammonium acetate and 0.1% formic acid. The high-resolution mass spectrometry
was carried out by means of electrospray ionization in positive ion mode (ESI+). The AZAs were detected by high-resolution
MS under full scan and data-dependent scan modes, respectively. The limits of quantification (LOQ, RSN > 10) were 10 μg/kg
for all the 3 AZA s. The calibration curves showed good linearity within the concentration range of 10 μg/L to 500 μg/L with
correlation coefficients (R2) more than 0.99. Shellfish samples from home and abroad were profiled and confirmed by the
established method. AZA s were found in some samples. Therefore this method is easy, sensitive, reproducible and efficient,
and can be applied to profile and confirm AZA s in edible shellfishes and related products.

Key words: azaspiracids shellfish toxins, high performance liquid chromatography-high resolution mass spectrometry, QuEChERS

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