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Updated: Jun 18, 2025

PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS
Published on: December 27, 2013
Scientific opinion on the tolerable upper intake level for vitamin E
The tolerable upper intake level (UL) for vitamin E (alpha-tocopherol) remains unchanged for most age groups. The critical effect for establishing the UL is impaired blood clotting and bleeding risk.
Area of Science:
- Nutrition Science
- Food Safety
- Toxicology
Background:
- The European Commission requested a review of the tolerable upper intake level (UL) for vitamin E.
- Alpha-tocopherol is the only essential form of vitamin E.
- Previous ULs were established by the Scientific Committee on Food.
Purpose of the Study:
- To revise the tolerable upper intake level (UL) for vitamin E (alpha-tocopherol).
- To assess adverse health effects of excess vitamin E intake, including impaired coagulation, bleeding, cardiovascular disease, and prostate cancer.
Main Methods:
- Systematic literature reviews were conducted.
- The critical effect for establishing the UL was identified as impaired blood clotting and associated bleeding risk.
- No new dose-response data were available to refine the UL.
Main Results:
- Existing ULs for vitamin E were retained for all population groups.
- Specific ULs were set for infants (50 mg/day for 4-6 months, 60 mg/day for 7-11 months).
- ULs apply to all alpha-tocopherol stereoisomers but exclude individuals on anticoagulants or with vitamin K malabsorption.
Conclusions:
- Existing tolerable upper intake levels for vitamin E are maintained.
- Vitamin E intake exceeding ULs is unlikely in European populations, except for high-dose supplement users.
- The established ULs are based on the risk of impaired blood coagulation and bleeding.
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