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IARC MONOGRAPHS ON THE EVALUATION OF CARCINOGENIC ...

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174<br />

<strong>IARC</strong> <strong>M<strong>ON</strong>OGRAPHS</strong> VOLUME 82<br />

Table 1. Melting-points and ultraviolet absorption of aflatoxins<br />

Aflatoxin Melting-point (°C)<br />

Ultraviolet absorption (ethanol)<br />

λ max (nm) ε (L mol –1 cm –1 )<br />

B 1 268–269 (decomposition) 223 25 600<br />

(crystals from chloroform) 265 13 400<br />

362 21 800<br />

B 2 286–289 (decomposition) 265 11 700<br />

(crystals from chloroform-pentane) 363 23 400<br />

G 1 244–246 (decomposition) 243 11 500<br />

(crystals from chloroform-methane) 257 9 900<br />

264 10 000<br />

362 16 100<br />

G 2 237–240 (decomposition) 265 9 700<br />

(crystals from ethyl acetate) 363 21 000<br />

M 1 299 (decomposition) 226 23 100<br />

(crystals from methanol) 265 11 600<br />

357 19 000<br />

From O’Neil et al. (2001)<br />

columns, which are simple and rapid to use, and with reduction in the use of toxic<br />

solvents for extraction and clean-up.<br />

Quality assurance for the analysis of aflatoxins B 1, B 2, G 1, G 2 and M 1 in foods is<br />

available for laboratories through the American Association of Cereal Chemists’ Check<br />

Sample Program and the Analytical Proficiency Testing Programme administered in the<br />

USA and the United Kingdom, respectively.<br />

As contamination may not occur in a homogeneous way throughout a sample of<br />

maize or peanuts 1 , good sampling and sample preparation procedures must be used to<br />

obtain accurate quantitative results. Summaries of the procedures, variability and application<br />

of sampling plans for mycotoxins are included in Section 1.5 and in the European<br />

Commission directive 98/53/CE (European Commission, 1998a).<br />

A number of approaches have been used to analyse aflatoxins and their metabolites<br />

in human tissues and body fluids. These include immunoaffinity purification, immunoassay<br />

(Wild et al., 1987), high-performance liquid chromatography (HPLC) with fluorescence<br />

or ultraviolet detection and synchronous fluorescence spectroscopy (Groopman<br />

& Sabbioni, 1991). Molecular biomarkers, such as urinary markers, metabolites in milk<br />

and parent compounds in blood, are used for determining exposure to aflatoxins<br />

(Groopman, 1993).<br />

1 Maize (corn) and peanuts (groundnuts) will be used throughout this volume for corn and groundnuts.

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