Previous Page  7 / 11 Next Page
Information
Show Menu
Previous Page 7 / 11 Next Page
Page Background

Volume 3, Issue 1 (Suppl)

Toxicol Open Access

ISSN: 2476-2067 TYOA, an open access journal

Toxicology Congress 2017

April 13-15, 2017

Page 40

Notes:

conference

series

.com

April 13-15, 2017 Dubai, UAE

8

th

World Congress on

Toxicology and Pharmacology

Endocrine disruption and antimicrobials

E

ndocrine disruptors are hormonally active substances of natural or synthetic origin affecting the endocrine (hormonal)

systems of humans. Such compounds can be found in chemical groups like steroids, cyclic hydrocarbons, phenols,

flavonoids, phtalates, parabens or toxic metals. They are used as antimicrobials, biocides, plasticizers, surfactants, UV filters

or fire retardants. They may be released from consumer products, e.g. cosmetics, toys, food packaging materials, household

products, medical devices and other products of industry or agriculture. In the EU, they are banned for consumer products.

Recently regulated CMR substances from the group of Antimicrobials/Preservatives (biocides) comprise: Chloracetamide

(Reprotox. Cat. 2), Phenol (Mutagenic Cat. 2), Nonylphenol (Reprotox. Cat. 2), Parabens (pentyl-, phenyl-, benzyl- for

absent data on reprotox.), Ketoconazole (Reprotox. Cat. 1B), Boron compounds

(Reprotox. Cat. 1B), Formaldehyde (Carcinogenic Cat. 1B), Polyaminopropyl

Biguanide-PHMB (Mutagenic Cat. 2). Significant reprotoxic effect has been

proved in the past namely for distinct bisphenols (Reprotox. Cat. 2) or phthalates

(Reprotox. Cat 1B or Cat. 2) which were subsequently banned. However, the

production of analogous compounds is increasing underlining the necessity to test

their safety including reprotoxicity. The European Commission's general policy is

the use of alternative toxicological methods

in vitro

instead of conventional tests on

vertebrates. Available methods

in vitro

to detect endocrine disruption are: OECD

TG 455/457–Estrogen Receptor Transactivation Test Method, OECD TG 456–

Effects on Steroidogenesis, OECD TG 236–ZFET, zebrafish embryo epigenetic

assay, MCF-7 cell proliferation assay, Xenoscreen YES/YAS yeast assay. Results of

a pilot study to prove applicability of methods

in vitro

to detect reprotoxicity are

presented.

Biography

Jirova Dagmar, MD, PhD, graduated and received her PhD at the Charles University in Prague. Her professional specialization is in Dermatotoxicology and

Immunotoxicology, focused on safety assessment of cosmetics and other consumer products. She is holding a position of the Head of Centre of Toxicology and

Health Safety at the National Institute of Public Health, Prague, Czech Republic. She is the author of more than 200 publications in scientific journals, proceedings

and monographs, posters or articles and publications for the public. She was the Principal Investigator in number of research projects in the field of alternative

toxicological methods for evaluation of health risks of chemicals and consumer products.

jirova@szu.cz

Jirova Dagmar

National Institute of Public Health, Czech Republic

Jirova Dagmar, Toxicol Open Access 2017, 3:1 (Suppl)

http://dx.doi.org/10.4172/2476-2067.C1.001

Figure 1:

OECD TG 455/457-VM7Luc4E2

cell line, kindly provided by Prof. M.

Denison, UCDAVIS, for research purposes.