Quantitative determination of paralytic shellfish toxins in cultured toxic algae by LC-MS/MS

被引:36
作者
Watanabe, Ryuichi [1 ]
Matsushima, Ryoji [1 ]
Harada, Tomoko [1 ]
Oikawa, Hiroshi [2 ]
Murata, Masakazu [1 ]
Suzuki, Toshiyuki [1 ]
机构
[1] Natl Res Inst Fisheries Sci, Res Ctr Biochem & Food Technol, Yokohama, Kanagawa 2368648, Japan
[2] Natl Res Inst Fisheries & Environm Inland Sea, Hiroshima 7390452, Japan
来源
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT | 2013年 / 30卷 / 08期
关键词
Alexandrium; Anabaena; cyanobacteria; dinoflagellates; HILIC; LC-MS; paralytic shellfish toxins; saxitoxins; LIQUID-CHROMATOGRAPHY; MASS-SPECTROMETRY; POISONING TOXINS; PRECHROMATOGRAPHIC OXIDATION; FLUORESCENCE; SAXITOXIN; ANALOGS;
D O I
10.1080/19440049.2013.793456
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We developed a sample preparation and LC-MS/MS method for the determination of saxitoxins in toxic algae. Paralytic shellfish toxins (PSTs) were successfully separated by gradient elution on an amide column with the hydrophilic interaction mode and quantified with multiple reaction monitoring (MRM) detection in the positive ion mode. This method showed good performance in the summed LODs and LOQs for all 12 toxins, 25 and 84nM, respectively. Next, extracts of cultured strains of a toxic dinoflagellate Alexandrium tamarense and a freshwater cyanobacteria Anabaena circinalis were treated in a short column of basic alumina and the toxic fractions were analysed by our LC-MS/MS method and by HPLC with fluorescence detection. Comparison of the results obtained by the two methods demonstrated that approximately equivalent results were obtained for both the dinoflagellate and the cyanobacteria. In addition, the retention time of the toxins showed acceptable shifts. Therefore, the clean-up of the toxic algal extracts by using the basic alumina column controlled unwanted chromatographic behaviour and variable ionisation efficiency during MS detection. LC-MS/MS for saxitoxins has great potential as a rapid analytical method for determining all primary saxitoxins in cultured algae.
引用
收藏
页码:1351 / 1357
页数:7
相关论文
共 20 条
  • [1] *AOAC INT, 1995, 97422 AOAC INT, P21
  • [2] AOAC Official Methods of Analysis of AOAC international, 2012, 201102 AOAC INT
  • [3] AOAC Official Methods of Analysis of AOAC international, 2006, 200506 AOAC INT, P79
  • [4] Hydrophilic interaction liquid chromatography-mass spectrometry for the analysis of paralytic shellfish poisoning (PSP) toxins
    Dell'Aversano, C
    Hess, P
    Quilliam, MA
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2005, 1081 (02) : 190 - 201
  • [5] Analysis of cyanobacterial toxins by hydrophilic interaction liquid chromatography-mass spectrometry
    Dell'Aversano, C
    Eaglesham, GK
    Quilliam, MA
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2004, 1028 (01) : 155 - 164
  • [6] Application of a new zwitterionic hydrophillic interaction chromatography column for determination of paralytic shellfish poisoning toxins
    Diener, Marc
    Erler, Katrin
    Christian, Bernd
    Luckas, Bernd
    [J]. JOURNAL OF SEPARATION SCIENCE, 2007, 30 (12) : 1821 - 1826
  • [7] Paralytic shellfish poisoning: Seafood safety and human health perspectives
    Etheridge, Stacey M.
    [J]. TOXICON, 2010, 56 (02) : 108 - 122
  • [8] GOTO H, 1998, HARMFUL ALGAE, P216
  • [9] Verification and quantification of saxitoxin from algal samples using fast and validated hydrophilic interaction liquid chromatography-tandem mass spectrometry method
    Halme, Mia
    Rapinoja, Marja-Leena
    Karjalainen, Maaret
    Vanninen, Paula
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2012, 880 : 50 - 57
  • [10] Detection and confirmation of saxitoxin analogues in freshwater benthic Lyngbya wollei algae collected in the St. Lawrence River (Canada) by liquid chromatography-tandem mass spectrometry
    Lajeunesse, Andre
    Segura, Pedro A.
    Gelinas, Malorie
    Hudon, Christiane
    Thomas, Krista
    Quilliam, Michael A.
    Gagnon, Christian
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2012, 1219 : 93 - 103