Oligomers of styrene are not endocrine disruptors

Author:

Gelbke Heinz-Peter1,Banton Marcy2,Block Christian3,Dawkins Gordon4,Leibold Edgar5,Pemberton Mark6,Sakoda Atsunobu7,Yasukawa Atsushi8

Affiliation:

1. CinTox, Nice, France;

2. Lyondell Chemical Company, Houston, TX, USA;

3. PlasticsEurope AISBL, Brussels, Belgium;

4. INEOS Styrolution Group GmbH, Frankfurt am Main, Germany;

5. Product Safety, BASF SE, Ludwigshafen, Germany;

6. Systox Limited, Wilmslow, UK;

7. Japan Styrene Industry Association (JSIA), Tokyo, Japan;

8. PS Japan Corporation, Tokyo, Japan

Publisher

Informa UK Limited

Subject

Toxicology

Reference75 articles.

1. Aiba T, Nagao Y, Hatakeyama O, Yoneda Y, Mizuno Y, Harada R, Yamada T, Chiba M. 1998. Metabolic fate of styrene oligomers: blood levels in rats after a single oral or intravenous administration. 4th Annual Joint Meeting of the Japanese Society of Environmental Toxicology and the Society of Bioassay Studies. Abstract. p. 29 (in Japanese).

2. Biological Evaluation of Styrene Oligomers for Endocrine-disrupting Effects. (II).

3. Uterotrophic Assay of two Concentrations of Migrates from each of 23 Polystyrenes Administered Orally (by Gavage) to Immature Female Wistar Rats

4. BfR. 2016. Gemessene Gehalte an Styrol-Oligomeren in Lebensmittelsim-ulanzien: Ge-sundheitliche Risiken sind unwahrscheinlich. Aktualisierte Stellungnahme 023/2016 des BfR vom 21. April 2016.

5. BKH. 2000. European Commission DG ENV. Towards the establishment of a priority list of substances for further evaluation of their role in endocrine disruption – preparation of a candidate list of substances as a basis for priority setting. Delft, The Netherlands: BKH Consulting Engineers.

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