1987
DOI: 10.1271/bbb1961.51.877
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Fluorometric determination of diarrhetic shellfish toxins by high-performance liquid chromatography.

Abstract: Two principal toxins of diarrhetic shellfish poisoning, okadaic acid and dinophysistoxin-1, were esterified with 9-anthryldiazomethane in methanol. After cleaning with a Sep-pak silica cartridge column, the fluorescent esters were analyzed on a Develosil ODScolumn with MeCN-MeOH-H2O (8 : 1 : 1). The fluorescence intensities of both toxin derivatives measuredat an excitation of 365nmand an emission of 412nmshowed good linearity in the range 1~80ng.

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Cited by 225 publications
(51 citation statements)
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“…Such inconvenience has led to the development of chemical detection and quantification methods based on the chromatographic properties of biotoxins [18,19]. The chemical methods most frequently used for the detection of OA are based on Liquid Chromatography (LC) or High Performance Liquid Chromatography (HPLC) separation strategies, coupled with several detection methods including Mass Spectrometry (LC-MS), tandem mass spectrometry (LC-MS/MS), FLuorimetric Detection (HPLC-FLD) and UltraViolet Detection (HPLC-UVD) [12,20,21]. In addition, alternative chromatography-based chemical methods are also available for the detection of OA (though much less used) including Gas Chromatography (GS) [22] and Micellar Electro Kinetic Chromatography (MEKC) [23].…”
Section: Methods Used For the Detection Of Okadaic Acidmentioning
confidence: 99%
“…Such inconvenience has led to the development of chemical detection and quantification methods based on the chromatographic properties of biotoxins [18,19]. The chemical methods most frequently used for the detection of OA are based on Liquid Chromatography (LC) or High Performance Liquid Chromatography (HPLC) separation strategies, coupled with several detection methods including Mass Spectrometry (LC-MS), tandem mass spectrometry (LC-MS/MS), FLuorimetric Detection (HPLC-FLD) and UltraViolet Detection (HPLC-UVD) [12,20,21]. In addition, alternative chromatography-based chemical methods are also available for the detection of OA (though much less used) including Gas Chromatography (GS) [22] and Micellar Electro Kinetic Chromatography (MEKC) [23].…”
Section: Methods Used For the Detection Of Okadaic Acidmentioning
confidence: 99%
“…This explains why PTXs and YTXs, together with OAs, were all included in the old “DSP toxin complex”. To overcome the lack of established cultures of Dinophysis , Lee et al developed a highly sensitive HPLC method (at that time) with fluorimetric detection (HPLC-FLD) that allowed chemical analyses of samples composed of several hundreds of individually picked cells of Dinophysis [69]. These early analyses showed that OA and/or DTX1 were the main toxins in Dinophysis spp, that only D. fortii (Japanese strains) was found to contain PTXs, and that large differences in toxin content per cell could be found, even within the same species and locality [70].…”
Section: Historic Overviewmentioning
confidence: 99%
“…injection and survival monitored over a 24-h period. In efforts to improve the specificity of the assay, several modifications to the technique (generally involving an additional partitioning step) have been developed [11,69,312,313]. …”
Section: Assessment Of Sample Collection Procedures and Available mentioning
confidence: 99%
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“…As most lipophilic marine toxins lack chromophores, a derivatisation step was required. For toxins of the OA group 9-anthryldiazomethane (ADAM) [134] and for PTXs and YTXs 4-[2-(6,7–dimethoxy-4-methyl-3-oxo-3,4-dihydroquinoxalinyl)ethyl]-1,2,4-triazoline-3,5-dione (DMEQ-TAD) have been used as derivatisation reagents [135,136]. A major drawback of LC-FLD is its limited selectivity for the OA group toxins as well as for the PTXs and YTXs.…”
Section: Methods Of Analysismentioning
confidence: 99%