farmacokinetiek absorption bioavailability pharmacokinetics
Conditions
Interventions
During the test day, participants will ingest a drink consisting of 65 mg AME
(16 mg anthocyanins), and 200 ml water.
Sponsors
Universiteit Maastricht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: • Men and women, aged between 18-35 years, or between 55-75 years old • BMI between 18-35 kg/m2 • Systolic blood pressure
Exclusion criteria
Exclusion criteria: • Smoking or smoking cessation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The bioavailability and pharmacokinetics of AME will be assessed via frequent blood sampling, urine collection, and faecal sampling, in which AME and metabolite profiles will be quantified. Blood samples will be collected at t=0h, t=0.5h, t=1h, t=1.5h t=2h, t=2.5h, t=3h, t=4h, t=6h, t=8h, t=10h, t=12h, t=24h, t=48h following AME intake. Urine samples will be collected at t=0h, and in 6 different time intervals, i.e. t=0-4h, t=4-8h, t=8-12h, t=12-16h, t=16-24h, and t=24h-48h. Available faecal samples will be collected and combined into one sample until t=48h on a voluntary basis. | — |
Secondary
| Measure | Time frame |
|---|---|
| n.a. | — |
Countries
Netherlands
Outcome results
None listed