Wieneke Bil, Julia Hartmann, Martine Bakker, Bas Bokkers
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引用次数: 0
Abstract
Per- and polyfluoroalkyl substances (PFAS) often co-occur as contaminants in drinking water and food. Various mixture risk assessment (MRA) approaches have been published to address the associated human health risks.
The Dutch National Institute for Public Health and the Environment (RIVM) organized an online workshop to discuss PFAS MRA approaches. Over 50 experts participated, representing research institutes, universities and government organizations internationally. A discussion document with scientific literature and considerations on PFAS MRA approaches was shared with participants ahead of the workshop.
The workshop yielded overall agreement among participants in support of evidence pointing towards no interaction and dose-additivity of PFAS mixtures. Participants broadly supported the need for a flexible, component-based MRA approach to accommodate the variability in PFAS mixtures and the integration of new PFAS. Overall, the workshop underscored the need to ensure that risk assessments are both scientifically robust and practically feasible, and showed that the global mixture risk assessment community is largely in agreement regarding evaluation of PFAS.
The input received as well as the outcomes of this workshop were used by RIVM in a recommendation to the World Health Organisation (WHO) on suitable approaches for assessment of PFAS in food and drinking water.
期刊介绍:
Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health.
Types of peer-reviewed articles published:
-Original research articles of relevance for regulatory aspects covering aspects including, but not limited to:
1.Factors influencing human sensitivity
2.Exposure science related to risk assessment
3.Alternative toxicological test methods
4.Frameworks for evaluation and integration of data in regulatory evaluations
5.Harmonization across regulatory agencies
6.Read-across methods and evaluations
-Contemporary Reviews on policy related Research issues
-Letters to the Editor
-Guest Editorials (by Invitation)