Please use this identifier to cite or link to this item:
http://hdl.handle.net/11189/6112| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Shephard, Gordon Seymour | en_US |
| dc.contributor.author | Thiel, PG | en_US |
| dc.contributor.author | Sydenham, Eric W. | en_US |
| dc.date.accessioned | 2017-11-09T12:22:34Z | - |
| dc.date.available | 2017-11-09T12:22:34Z | - |
| dc.date.issued | 1995 | - |
| dc.identifier.issn | 0021-9673 | - |
| dc.identifier.uri | http://hdl.handle.net/11189/6112 | - |
| dc.description.abstract | The fungus Fusarium moniliforme produces a group of mycotoxins, the fumonisins, of which the most abundant are fumonisins B 1 (FB1) and B 2 (FB2). Previously developed analytical methods for the determination of FB 1 in physiological samples have been modified for the determination of FB 2 by the use of less polar extraction solvents. Plasma and urine extracts were purified on strong anion-exchange solid-phase extraction cartridges and fecal extracts on reversed-phase (C18) cartridges. FB 2 in purified extracts was determined by reversed-phase HPLC with fluorescence detection using preformed o-phthaldialdehyde derivatives. These methods were reproducible (R.S.D. of less than 6%) with recoveries greater than 85%. In a short preliminary study, they have been applied to the determination of the fate of FB 2 dosed to rats by gavage. Of the dose given to the animals, over 90% was recovered unmetabolised in the feces within 48 h. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Journal of Chromatography A | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/3.0/za/ | - |
| dc.subject | Liquid chromatographic | en_US |
| dc.subject | Mycotoxin fumonisin B 2 | en_US |
| dc.subject | Fusarium moniliforme | en_US |
| dc.subject | Plasma | en_US |
| dc.title | Liquid chromatographic determination of the mycotoxin fumonisin B 2 in physiological samples | en_US |
| dc.type.patent | Article | en_US |
| Appears in Collections: | HWSci - Journal Articles (DHET subsidised) | |
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