Risk Assessment of Dietary Exposure to Organophosphorus Flame Retardants in Children by Using HBM-Data.

HBM4EU children dietary exposure organophosphorus flame retardants

Journal

Toxics
ISSN: 2305-6304
Titre abrégé: Toxics
Pays: Switzerland
ID NLM: 101639637

Informations de publication

Date de publication:
03 May 2022
Historique:
received: 31 03 2022
revised: 26 04 2022
accepted: 27 04 2022
entrez: 27 5 2022
pubmed: 28 5 2022
medline: 28 5 2022
Statut: epublish

Résumé

Due to their extensive usage, organophosphorus flame retardants (OPFRs) have been detected in humans and in the environment. Human are exposed to OPFRs via inhalation of indoor air, dust uptake or dietary uptake through contaminated food and drinking water. Only recently, few studies addressing dietary exposure to OPFRs were published. In this study, we used human biomonitoring (HBM) data of OPFRs to estimate how much the dietary intake may contribute to the total exposure. We estimated by reverse dosimetry, the daily intake of tris (2-chloroethyl) phosphate (TCEP), tris (1-chloro-2-propyl) phosphate (TCIPP), tris (1,3-dichloro-2-propyl) phosphate (TDCIPP) for children using HBM data from studies with sampling sites in Belgium, Denmark, France, Germany, Slovenia and Slovakia. For estimating the dietary exposure, a deterministic approach was chosen. The occurrence data of selected food categories were used from a published Belgium food basket study. Since the occurrence data were left-censored, the Lower bound (LB)-Upper bound (UB) approach was used. The estimated daily intake (EDI) calculated on the basis of urine metabolite concentrations ranged from 0.03 to 0.18 µg/kg bw/d for TDCIPP, from 0.05 to 0.17 µg/kg bw/d for TCIPP and from 0.02 to 0.2 µg/kg bw/d for TCEP. Based on national food consumption data and occurrence data, the estimated dietary intake for TDCIPP ranged from 0.005 to 0.09 µg/kg bw/d, for TCIPP ranged from 0.037 to 0.2 µg/kg bw/d and for TCEP ranged from 0.007 to 0.018 µg/kg bw/d (summarized for all countries). The estimated dietary intake of TDCIPP contributes 11-173% to the EDI, depending on country and LB-UB scenario. The estimated dietary uptake of TCIPP was in all calculations, except in Belgium and France, above 100%. In the case of TCEP, it is assumed that the dietary intake ranges from 6 to 57%. The EDI and the estimated dietary intake contribute less than 3% to the reference dose (RfD). Therefore, the estimated exposure to OPFRs indicates a minimal health risk based on the current knowledge of available exposure, kinetic and toxicity data. We were able to show that the dietary exposure can have an impact on the general exposure based on our underlying exposure scenarios.

Identifiants

pubmed: 35622647
pii: toxics10050234
doi: 10.3390/toxics10050234
pmc: PMC9144966
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : European Unions Horizon 2020 research and innovation program
ID : 733032, HBM4EU

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Auteurs

Veronika Plichta (V)

Austrian Agency for Health and Food Safety(AGES), Division of Integrative Risk Assessment, Data & Statistics, Department of Risk Assessment, 1220 Vienna, Austria.

Johann Steinwider (J)

Austrian Agency for Health and Food Safety(AGES), Division of Integrative Risk Assessment, Data & Statistics, Department of Risk Assessment, 1220 Vienna, Austria.

Nina Vogel (N)

German Environment Agency (UBA), 06844 Dessau-Roßlau, Germany.

Till Weber (T)

German Environment Agency (UBA), 06844 Dessau-Roßlau, Germany.

Marike Kolossa-Gehring (M)

German Environment Agency (UBA), 06844 Dessau-Roßlau, Germany.

Lubica Palkovičová Murínová (LP)

Faculty of Public Health, Slovak Medical University, 833 03 Bratislava, Slovakia.

Soňa Wimmerová (S)

Faculty of Public Health, Slovak Medical University, 833 03 Bratislava, Slovakia.

Janja Snoj Tratnik (JS)

Department of Environmental Sciences, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.

Milena Horvat (M)

Department of Environmental Sciences, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.

Gudrun Koppen (G)

VITO Health, Flemish Institute for Technological Research (VITO), 2400 Mol, Belgium.

Eva Govarts (E)

VITO Health, Flemish Institute for Technological Research (VITO), 2400 Mol, Belgium.

Liese Gilles (L)

VITO Health, Flemish Institute for Technological Research (VITO), 2400 Mol, Belgium.

Laura Rodriguez Martin (L)

VITO Health, Flemish Institute for Technological Research (VITO), 2400 Mol, Belgium.

Greet Schoeters (G)

VITO Health, Flemish Institute for Technological Research (VITO), 2400 Mol, Belgium.
Department of Biomedical Sciences, University of Antwerp, 2610 Wilrijk, Belgium.

Adrian Covaci (A)

Toxicological Center, University of Antwerp, 2610 Wilrijk, Belgium.

Clémence Fillol (C)

Santé Publique France, French Public Health Agency (ANSP), 94415 Saint-Maurice, France.

Loïc Rambaud (L)

Santé Publique France, French Public Health Agency (ANSP), 94415 Saint-Maurice, France.

Tina Kold Jensen (TK)

Department of Environmental Medicine, Institute of Public Health, University of Southern Denmark, 5000 Odense, Denmark.

Elke Rauscher-Gabernig (E)

Austrian Agency for Health and Food Safety(AGES), Division of Integrative Risk Assessment, Data & Statistics, Department of Risk Assessment, 1220 Vienna, Austria.

Classifications MeSH