固相萃取-液相色谱-串联质谱法测定贝类中的脂溶性贝类毒素
作者:
作者单位:

(1.珠海市疾病预防控制中心,广东 珠海 519060;2.广东省疾病预防控制中心,广东 广州 511430)

作者简介:

陈剑刚 男 主任技师 研究方向为食品违禁药物风险监测检验与环境职业有机物分析 E-mail:davidchenjg@sina.com

通讯作者:

中图分类号:

基金项目:

珠海市科技计划项目(2013D0401990022)


Determination of lipophilic marine toxins in shellfish by high performance liquid chromatography-tandem mass spectrometry with solid phase extraction
Author:
Affiliation:

(Zhuhai Center for Disease Control and Prevention,Guangdong Zhuhai 519000,China)

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    建立了测定贝类中大田软海绵酸(OA)、鳍藻毒素(DTX1、DTX2)、紫贻贝毒素(YTX)、原多甲藻酸贝毒素(AZA1)、螺环内酯毒素(SPX1)6种脂溶性贝类毒素的固相萃取-高效液相色谱-串联质谱方法。方法 匀浆贝类组织,用80%甲醇提取,StrataTM-X固相萃取小柱净化,0.3%氨水甲醇溶液洗脱,离心超滤管离心纯化。采用XTerra MS C18柱(150 mm×2.1 mm,35 μm)分离,以含6.7 mmol/L氨水的90%乙腈-水溶液为流动相进行梯度洗脱,选择多反应监测模式检测,正、负离子切换扫描,基质标准校正外标法定量。结果 6种脂溶性贝类毒素的定量限为0.2~1.0 μg/kg,在相应浓度范围内线性良好,相关系数均>0.995;低、中、高3个添加水平的平均加标回收率在78.8%~116%之间;相对标准偏差(RSD)为3.8%~14.5%。应用建立的方法对多份贝类样品进行分析,均未检出目标组分。结论 方法选择性、灵敏性和准确度高,适用于贝类产品中脂溶性贝类毒素的确证及定量分析。

    Abstract:

    A solid-phase extraction coupled to high performance liquid chromatography-tandem mass spectrometry(LC-MS/MS)was developed for determination of six lipophilic marine toxins, including OA, DTX2,YTX,DTX1, AZA1 and SPX1 in shellfish.Methods Homogenised tissues were extracted twice with 80% methanol in water, and resulting extracts were cleaned-upon StrataTM-X solid phase extraction column and eluted with MeOH solutions containing 0.3% NH4OH,followed by filtering through a ultra-filter centrifuge tube. The target components were separated and gradient eluted on a XTerraMS C18 column using mobile phases of MeCN/water and water, both phase containing 6.7mmol/L NH4OH, and simultaneously quantified by switching alternatively between positive ions and negative ions under multiple reactions monitoring mode. The matrix-matched external standard calibration were carried out for the quantitative analysis. Results The limits of quantification ranged from 0.2 to 1.0 μg/kg for six marine lipophilic toxins. The calibration curves were linear in the respective concentration ranges, with the correlation coefficients >0.995. The average recoveries for toxins at three concentration levels were 78.8%-116%, and their relative standard deviation varied between 3.8% and 14.5%.The method was applied to analyze several shellfish samples, but no one was positive. Conclusion The method developed was selective, sensitive and accurate, and was suitable for analysis and confirmation of marine lipophilic toxins in shellfish.

    参考文献
    相似文献
    引证文献
引用本文

陈剑刚,朱炳辉,梁素丹,张瑰,吴西梅.固相萃取-液相色谱-串联质谱法测定贝类中的脂溶性贝类毒素[J].中国食品卫生杂志,2015,27(6):624-629.

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2015-06-08
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2015-12-14
  • 出版日期:
文章二维码
《中国食品卫生杂志》邮寄地址与联系方式变更通知
关闭