Abstract
Abstract A rapid method is described for extraction and cleanup of raw and processed milk for determination of anatoxins M1 and M2 by using a C18 Sep-Pak/silica gel cleanup column combination. Anatoxins are separated by normal phase liquid chromatography and their concentrations are determined by fluorescence detection in a silica gel-packed flow cell. Recoveries ranged from 99 to 103% with coefficients of variation less than 2% for Mi levels of 0.117-1.17 ng/mL added to raw milk. Similar recoveries were obtained for M2. The coefficient of variation for analysis of 5 subsamples of naturally contaminated milk was Jess than 1%. Agreement with the official method is satisfactory. Each sample requires less than 25 mL solvent and 10 min actual handling time. Sample chromatograms show no interferences in the M1-M2 elution region and no late-eluting peaks, which permits spacing injections at 13-20 min intervals. Anatoxin levels as low as 0.03 ppb may be determined by this procedure. Extracts have also been analyzed by thin layer chromatography.
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Publication Info
- Year
- 1984
- Type
- article
- Volume
- 67
- Issue
- 6
- Pages
- 1111-1114
- Citations
- 12
- Access
- Closed
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Identifiers
- DOI
- 10.1093/jaoac/67.6.1111