2009
DOI: 10.1016/j.jchromb.2009.09.028
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Separation of microcystins and nodularins by ultra performance liquid chromatography

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Cited by 23 publications
(12 citation statements)
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“…Rapid analyses of microcystins and nodularins in cyanobacterial samples have already been described for LC-MS [17] and for HPLC-DAD [40,41]. The longer 30 min gradient used in this study did not provide further benefits as measured by selectivity and resolution as compared to the 5 min gradient.…”
Section: Chromatographic Performancementioning
confidence: 79%
“…Rapid analyses of microcystins and nodularins in cyanobacterial samples have already been described for LC-MS [17] and for HPLC-DAD [40,41]. The longer 30 min gradient used in this study did not provide further benefits as measured by selectivity and resolution as compared to the 5 min gradient.…”
Section: Chromatographic Performancementioning
confidence: 79%
“…In particular, the microcystins associated with some strains of Microcystis, have caused concern due to their hepatotoxicity in both humans and wildlife [4]. Microcystins are cyclic heptapeptide toxins, whose chemical structures vary primarily in the demethylation of amino acids and substitution of l-amino acids [5]. The chemical structures of microcystin-LR (MC-LR) and its demethyl derivative, [Dha 7 ] MC-LR, are shown in Fig.…”
Section: Introductionmentioning
confidence: 99%
“…Microcystins are cyanobacterial secondary metabolites delivered in water, which have been characterized as strong hepatotoxins [2][3][4][5][6][7]. The contamination of drinking water by microcystins has been suggested as a risk factor for cancer [1,4,6,7].…”
Section: Introductionmentioning
confidence: 99%
“…Microcystins have been determined in water by employing different separation strategies associated with several detection techniques, such as ultra-performance liquid chromatography [2], capillary electrophoresis [5], spectrophotometry [3,8,12], surface plasmon resonance immunobiosensor [15], quantum dots exploiting the photoluminescence quenching effect [16], extraction using cloud point and ionic liquid [17], and on-line microsolid-phase extraction-capillary liquid chromatography [18]. Nevertheless, the preferred method has predominantly been liquid chromatography coupled to mass spectrometry [2,[10][11][12]14,17,18].…”
Section: Introductionmentioning
confidence: 99%
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