Bioavailability Formula:
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The Bioavailability Of drug dose describes the fraction or percentage of an administered drug that reaches the systemic circulation in an unchanged and active form. It is a crucial pharmacokinetic parameter that determines the effectiveness of drug therapy.
The calculator uses the Bioavailability formula:
Where:
Explanation: This formula calculates the percentage of drug that reaches systemic circulation based on clearance rate, target concentration, and maintenance dose.
Details: Accurate bioavailability calculation is essential for determining appropriate drug dosing, optimizing therapeutic outcomes, and minimizing side effects in pharmaceutical development and clinical practice.
Tips: Enter drug clearance in m³/s, target plasma concentration in kg/m³, and maintenance dose in kg/s. All values must be valid positive numbers.
Q1: What factors affect drug bioavailability?
A: Bioavailability can be affected by route of administration, drug formulation, first-pass metabolism, chemical instability, and patient-specific factors.
Q2: What is considered good bioavailability?
A: Typically, bioavailability above 80% is considered excellent, while values below 20% may require special formulation strategies or alternative administration routes.
Q3: How does route of administration affect bioavailability?
A: Intravenous administration provides 100% bioavailability, while oral administration typically has lower bioavailability due to first-pass metabolism and absorption limitations.
Q4: Why is bioavailability important in drug development?
A: Bioavailability data helps determine appropriate dosing regimens, predict therapeutic efficacy, and guide formulation development for new drugs.
Q5: Can bioavailability change between individuals?
A: Yes, bioavailability can vary significantly between individuals due to factors like age, genetics, liver function, and concurrent medications.