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7.1 St Amand
1. Interpreting Population Level Biomonitoring
Data in a Risk-Based Context:
A Canadian Perspective
Annie St-Amand1, Kate Werry1, Andy Nong1,
Sean M. Hays2, Lesa L. Aylward2
1Healthy Environments and Consumer Safety Branch, Health Canada;
2Summit Toxicology LLP
September 10, 2013
4. Biomonitoring Equivalents (BE)
“Safe” human dose
RfD, TDI: mg/kg-d
Uncertainty
Factors
Human (equivalent)
Point of Departure
Human
urine/blood level
BE: µg/L
Uncertainty
Factors
Human
Pharmacokinetics
BE - Concentration of biomarker that is
consistent with existing exposure guidance
or reference values such as RfDs, TDIs,
etc (Hays et al., 2007).
POD: mg/kg-d
Human
urine/blood level
BEPOD: µg/L
12. Discussion
• HQs < 1 for majority of biomarkers
– suggest exposure levels are below existing
guidance values
• HQs > 1 at upper bound of the CHMS
population distributions for inorganic arsenic
and cadmium.
• BEs do not represent diagnostic criteria
• BEs are interim values (screening)
13. Conclusion
• Cadmium and inorganic arsenic: more detailed
examinations required
• Useful for prioritization efforts
www.health.gc.ca/biomonitoring
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