Bioavailability Formula:
From: | To: |
Bioavailability is the systemically available fraction of a drug that reaches the systemic circulation and is available at the site of action. It is a crucial pharmacokinetic parameter that determines the efficacy of drug administration.
The calculator uses the Bioavailability formula:
Where:
Explanation: The formula calculates the fraction of administered drug that reaches systemic circulation, accounting for administration rate, dosing interval, and drug purity.
Details: Accurate bioavailability calculation is essential for determining appropriate drug dosing, comparing different drug formulations, and ensuring therapeutic efficacy while minimizing side effects.
Tips: Enter drug rate of administration in kg/s, dosing interval in seconds, administered dose in kg, and drug purity as a percentage. All values must be positive numbers.
Q1: What is considered good bioavailability?
A: Bioavailability values range from 0 to 1 (or 0-100%). Generally, values above 0.8 (80%) are considered excellent, while values below 0.3 (30%) may indicate poor absorption.
Q2: How does drug purity affect bioavailability?
A: Lower drug purity reduces the effective amount of active pharmaceutical ingredient, thereby decreasing the bioavailability calculation.
Q3: Why is dosing interval important?
A: The dosing interval affects how frequently the drug is administered, which influences the steady-state concentration and overall bioavailability.
Q4: Can bioavailability exceed 100%?
A: No, bioavailability is a fraction and cannot exceed 1 (100%). Values above 1 indicate calculation errors or measurement inaccuracies.
Q5: How does administration route affect bioavailability?
A: Intravenous administration typically has 100% bioavailability, while oral administration usually has lower bioavailability due to first-pass metabolism and absorption limitations.