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Pb and Cu speciation and bioavailability in port wine
1LAQUIPAI, Chemistry Department, Faculdade de Ciências da Universidade do Porto, R. Campo Alegre 687, P-4169-007 Oporto, Portugal.
Journal of Agricultural and Food Chemistry
|November 23, 2000
Summary
This study analyzed lead (Pb) and copper (Cu) speciation in Port wines to assess human bioavailability. Results indicate varying metal complexation and low Pb dialyzability, suggesting limited absorption.
Area of Science:
- Food Chemistry
- Environmental Chemistry
- Toxicology
Background:
- Port wine contains lead (Pb) and copper (Cu), essential to assess human bioavailability.
- Metal speciation influences metal absorption and potential toxicity.
- Understanding metal-ligand interactions in wine is crucial for dietary exposure assessment.
Purpose of the Study:
- To investigate the speciation of Pb and Cu in various Port wine types.
- To estimate the bioavailability of Pb and Cu through in vitro simulated gastrointestinal digestion.
- To determine metal distribution and complexation across different wine matrices and digestion stages.
Main Methods:
- In vitro simulated gastrointestinal digestion of Port wines.
- Potentiometry and cathodic voltammetry to determine metal complex stability constants (K(av), K'(av)) and ligand concentrations (CC, CC(inert)).
- Reverse-phase high-performance liquid chromatography (RP-HPLC) for metal distribution analysis based on molecular weight and polarity.
- Quantification of total, soluble, and dialyzable metal fractions.
Main Results:
- White and very aged red Port wines exhibited lower Pb complexing affinity compared to other wines.
- Cu ligands in white wines were weaker but more concentrated than in other types.
- Pb complexing ligand concentrations (CC(inert)) increased post-digestion, while stability (K'(av)) decreased.
- Low dialyzable fractions for Pb (10-22%) and approximately 50% for Cu were observed during intestinal digestion.
Conclusions:
- Port wine type significantly influences Pb and Cu speciation and complexation.
- The bioavailable fraction of Pb is limited due to low intestinal dialyzability.
- Cu bioavailability is higher than Pb, with approximately half being potentially absorbable.