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Toxins (Basel)
2015 Dec 30;81:. doi: 10.3390/toxins8010011.
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Determination of Gonyautoxin-4 in Echinoderms and Gastropod Matrices by Conversion to Neosaxitoxin Using 2-Mercaptoethanol and Post-Column Oxidation Liquid Chromatography with Fluorescence Detection.
Silva M
,
Rey V
,
Botana A
,
Vasconcelos V
,
Botana L
.
Abstract
Paralytic Shellfish Toxin blooms are common worldwide, which makes their monitoring crucial in the prevention of poisoning incidents. These toxins can be monitored by a variety of techniques, including mouse bioassay, receptor binding assay, and liquid chromatography with either mass spectrometric or pre- or post-column fluorescence detection. The post-column oxidation liquid chromatography with fluorescence detection method, used routinely in our laboratory, has been shown to be a reliable method for monitoring paralytic shellfish toxins in mussel, scallop, oyster and clam species. However, due to its high sensitivity to naturally fluorescent matrix interferences, when working with unconventional matrices, there may be problems in identifying toxins because of naturally fluorescent interferences that co-elute with the toxin peaks. This can lead to erroneous identification. In this study, in order to overcome this challenge in echinoderm and gastropod matrices, we optimized the conversion of Gonyautoxins 1 and 4 to Neosaxitoxin with 2-mercaptoethanol. We present a new and less time-consuming method with a good recovery (82.2%, RSD 1.1%, n = 3), requiring only a single reaction step.
Figure 1. Paralytic Shellfish Toxins (PSTs) elution pattern in mussel matrix spiked with standards.
Figure 2. 4 nmol of GTX1, 4 incubated with 1 M 2-ME in 0.1 M phosphate buffer, pH 7.4 during 30 min in water bath: (a) before incubation; (b) after incubation.
Figure 3. (a) Sample 477 (S. haemostoma) before transformation; (b) sample 477 (S. haemostoma) after transformation.
Figure 4. (a) Sample 454 (Cerithium vulgatum) before transformation; (b) sample 454 (Cerithium vulgatum) after transformation.
Baker,
GTX(4) imposters: characterization of fluorescent compounds synthesized by Pseudomonas stutzeri SF/PS and Pseudomonas/Alteromonas PTB-1, symbionts of saxitoxin-producing Alexandrium spp.
2003, Pubmed
Baker,
GTX(4) imposters: characterization of fluorescent compounds synthesized by Pseudomonas stutzeri SF/PS and Pseudomonas/Alteromonas PTB-1, symbionts of saxitoxin-producing Alexandrium spp.
2003,
Pubmed
DeGrasse,
Pre- versus post-column oxidation liquid chromatography fluorescence detection of paralytic shellfish toxins.
2011,
Pubmed
Lawrence,
Quantitative determination of paralytic shellfish poisoning toxins in shellfish using prechromatographic oxidation and liquid chromatography with fluorescence detection: collaborative study.
2005,
Pubmed
Li,
Analysis of paralytic shellfish toxins and their metabolites in shellfish from the North Yellow Sea of China.
2012,
Pubmed
Rey,
Influence of different shellfish matrices on the separation of PSP toxins using a postcolumn oxidation liquid chromatography method.
2015,
Pubmed
Rodrigues,
Paralytic shellfish poisoning due to ingestion of Gymnodinium catenatum contaminated cockles--application of the AOAC HPLC official method.
2012,
Pubmed
Rourke,
Rapid postcolumn methodology for determination of paralytic shellfish toxins in shellfish tissue.
2008,
Pubmed
Sato,
Identification of thioether intermediates in the reductive transformation of gonyautoxins into saxitoxins by thiols.
2000,
Pubmed
Shimizu,
Transformation of paralytic shellfish toxins as demonstrated in scallop homogenates.
1981,
Pubmed
Silva,
New invertebrate vectors for PST, spirolides and okadaic acid in the North Atlantic.
2013,
Pubmed
,
Echinobase
Vale,
In vitro and in vivo evaluation of paralytic shellfish poisoning toxin potency and the influence of the pH of extraction.
2008,
Pubmed
van de Riet,
Liquid chromatography post-column oxidation (PCOX) method for the determination of paralytic shellfish toxins in mussels, clams, oysters, and scallops: collaborative study.
2011,
Pubmed