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An inter-laboratory trial of the unified BARGE bioaccessibility method for arsenic, cadmium and lead in soil
Authors:Wragg Joanna  Cave Mark  Basta Nick  Brandon Esther  Casteel Stan  Denys Sebastien  Gron Christian  Oomen Agnes  Reimer Kenneth  Tack Karine  Van de Wiele Tom
Affiliation:
  • a British Geological Survey, Nottingham, United Kingdom
  • b School of Environment and Natural Resources, The Ohio State University, Columbus, OH, 43210-1085, USA
  • c National Institute for Public Health and the Environment, Bilthoven, The Netherlands
  • d College of Veterinary Medicine, University of Missouri, 65205, USA
  • e INERIS, Parc Technologique Alata, Verneuil-en-Halatte, France
  • f DHI Water Environment Health, Horsholm, Denmark
  • g Environmental Sciences Group, Royal Military College of Canada, Kingston, Ontario, Canada
  • h Laboratory of Microbial Ecology and Technology, University of Ghent, Ghent, Belgium
  • Abstract:The Bioaccessibility Research Group of Europe (BARGE) has carried out an inter-laboratory trial of a proposed harmonised in vitro physiologically based ingestion bioaccessibility procedure for soils, called the Unified BARGE Method (UBM). The UBM includes an initial saliva phase and simulated stomach and intestine compartments. The trial involved the participation of seven laboratories (five European and two North American) providing bioaccessibility data for As (11 samples), Cd (9 samples) and Pb (13 samples) using soils with in vivo relative bioavailability data measured using a swine model. The results of the study were compared with benchmark criteria for assessing the suitability of the UBM to provide data for human health risk assessments. Mine waste and slag soils containing high concentrations of As caused problems of poor repeatability and reproducibility which were alleviated when the samples were run at lower soil to solution ratios. The study showed that the UBM met the benchmark criteria for both the stomach and stomach & intestine phase for As. For Cd, three out of four criteria were met for the stomach phase but only one for the stomach & intestine phase. For Pb two, out of four criteria were met for the stomach phase and none for the stomach & intestine phase. However, the study recommends tighter control of pH in the stomach phase extraction to improve between-laboratory variability, more reproducible in vivo validation data and that a follow up inter-laboratory trial should be carried out.
    Keywords:Bioaccessibility   Bioavailability   Inter-laboratory trial   Soil   In vivo   In vitro
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