Chromatography of mycotoxins on precoated reverse-phase thin-layer plates

1989 ◽  
Vol 18 (3) ◽  
pp. 327-330 ◽  
Author(s):  
D. Abramson ◽  
T. Thorsteinson ◽  
D. Forest
Keyword(s):  
1980 ◽  
Vol 16 (2) ◽  
pp. 219-221 ◽  
Author(s):  
William Bress ◽  
Kenneth Ziminski ◽  
Walter Long ◽  
Thomas Manning ◽  
Leslie Lukash

2003 ◽  
Vol 1 (3) ◽  
pp. 260-276 ◽  
Author(s):  
Marioara Bem ◽  
Miron Caproiu ◽  
Dan Stoicescu ◽  
Titus Constantinescu ◽  
Alexandru Balaban

Abstract4-Chloro-7-nitrobenzofurazan reacts by nucleophilic substitution with phenoxide anions derived from estriol (2c), ethynylestradiol (2d), phenol (3e), guaiacol (3f), 2,6-dimethoxyphenol (3g), eugenol (3h), isoeugenol (3i), the cytostatic Etoposide (4), and Reichardt’s betaine (5) in the presence of crown ethers affording the corresponding 4-aryloxy-7-nitrobenzofurazan derivatives 6c, 6d, 7e-7i, 8, and 9. The structure of these compounds was confirmed by NMR spectra. Hydrophobicity/hydrophilicity parameters were investigated by reverse phase thin-layer chromatography.


2002 ◽  
Vol 3 (7) ◽  
pp. 755-763 ◽  
Author(s):  
Maria Das Graças Cardoso ◽  
David Nelson ◽  
Antônia Tavares do Amaral ◽  
Custódio Dos Santos ◽  
Alcilene De Abreu Pereira ◽  
...  

1988 ◽  
Vol 71 (5) ◽  
pp. 949-953 ◽  
Author(s):  
Andrzej A Frohlich ◽  
Ronald R Marquardt ◽  
Aniko Bernatsky

Abstract An improved procedure for sample preparation and quantitation of ochratoxin A in moldy grain was developed. Grain samples were acidified and extracted, and extracts were subjected to reverse phase thin-layer chromatography (RPTLC). The separated spots, which were identified under UV light, were scraped and collected into recovery devices. Ochratoxin A was eluted from the adsorbent and analyzed by either liquid chromatography with fluorescence detection or direct spectrofluorometric measurement. The method yielded values that were proportional to the concentrations of toxin in the sample, had relatively high levels of recovery (94%), and required considerably less volume of solvents and preparation time than a standard packed column method.


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