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Advisory Committee on Health Effects of Endocrine Disruptors
The Supplement II to the Intermediary Report
1.2.5

 

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5 Ensuring reliability of analytical results
Variance of analytical results from different laboratories increases with decreasing analyte concentrations, as W. Horwitz1 pointed out. For the analysis of BPA, phthalic acid esters or nonylphenol in biological samples or animal feeds, which are at concentrations of ppb order, this is one of the most important issue for the reliability of analytical results.
Another problem is that these substances exist in the laboratory environment and readily contaminate the samples resulting in gross errors in analytical results. The analytical procedures should therefore be so designed as to preclude contamination.
The guidelines described in this document have been developed with these problems taken into account.

(1) Evaluation of reliability of analysis
As stated in the Interim Report, evaluation of analytical results of different laboratories on the same samples is an indispensable step for determining the reliability of an analytical procedure.
Unfortunately, however, it was impossible to find laboratories which would participate in systematic inter-laboratory cross checks of the present guidelines which deal with microanalysis of very small amounts of biological samples for components readily confounded with contaminations. Although cross checks for some samples was carried out among the laboratories which took part in the development of the present guidelines, a more general project involving more laboratories is still needed.

(2) Measures for maintenance and assurance of precision
In order to confirm that a laboratory provides sufficient sensitivity and precision in analysis of a specific sample, it is recommended to perform beforehand a cross check with one (preferably more than one) reference laboratory using the same sample.

1 J. Assoc. Off. Anal. Chem., 63, 1344(1980)
 

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