
ISO 19040:2018
ISO 19040:2018 Water quality – Determination of the estrogenic potential of water and waste water – Part 3: In vitro human cell-based reporter gene assay
CDN $347.00
Description
This document specifies a method for the determination of the estrogenic potential of water and waste water by means of a reporter gene assay utilizing stably transfected human cells. This reporter gene assay is based on the activation of the human estrogen receptor alpha.
This method is applicable to:
– fresh water;
– waste water;
– aqueous extracts and leachates;
– eluates of sediments (fresh water);
– pore water;
– aqueous solutions of single substances or of chemical mixtures;
– drinking water;
– the limit of quantification (LOQ) of this method for the direct analysis of water samples is between 0,3 ng/l and 1 ng/l 17Œ≤-estradiol equivalents (EEQ) based on the results of the international interlaboratory trial (see Annex F). The upper working range was evaluated [based on the results of the international interlaboratory trial (see Table F.3)] up to a level of 75 ng EEQ/l. Samples showing estrogenic potencies above this threshold have to be diluted for a valid quantification. Extraction and pre concentration of water samples can prove necessary if their estrogenic potential is below the given LOQ.
Edition
1
Published Date
2018-08-07
Status
PUBLISHED
Pages
40
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Abstract
This document specifies a method for the determination of the estrogenic potential of water and waste water by means of a reporter gene assay utilizing stably transfected human cells. This reporter gene assay is based on the activation of the human estrogen receptor alpha.
This method is applicable to:
- fresh water;
- waste water;
- aqueous extracts and leachates;
- eluates of sediments (fresh water);
- pore water;
- aqueous solutions of single substances or of chemical mixtures;
- drinking water;
- the limit of quantification (LOQ) of this method for the direct analysis of water samples is between 0,3 ng/l and 1 ng/l 17β-estradiol equivalents (EEQ) based on the results of the international interlaboratory trial (see Annex F). The upper working range was evaluated [based on the results of the international interlaboratory trial (see Table F.3)] up to a level of 75 ng EEQ/l. Samples showing estrogenic potencies above this threshold have to be diluted for a valid quantification. Extraction and pre concentration of water samples can prove necessary if their estrogenic potential is below the given LOQ.
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