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Area Under Curve Given Average Plasma Concentration Calculator

Formula Used:

\[ \text{Area Under Curve} = \text{Average Plasma Concentration} \times \text{Dosing Interval} \] \[ \text{AUC} = C_{av} \times \tau \]

mol/m³
seconds

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1. What is Area Under Curve (AUC)?

Area under Curve (AUC) is the definite integral of a curve that describes the variation of a drug concentration in blood plasma as a function of time. It represents the total drug exposure over a specific time period.

2. How Does the Calculator Work?

The calculator uses the formula:

\[ \text{AUC} = C_{av} \times \tau \]

Where:

Explanation: The formula calculates the total drug exposure by multiplying the average plasma concentration by the dosing interval duration.

3. Importance of AUC Calculation

Details: AUC is a crucial pharmacokinetic parameter that helps determine drug bioavailability, compare different formulations, and establish dosing regimens for optimal therapeutic effects.

4. Using the Calculator

Tips: Enter average plasma concentration in mol/m³ and dosing interval in seconds. Both values must be positive numbers.

5. Frequently Asked Questions (FAQ)

Q1: What does AUC represent in pharmacokinetics?
A: AUC represents the total drug exposure over time, which is important for determining bioavailability and comparing different drug formulations.

Q2: How is average plasma concentration determined?
A: Average plasma concentration is typically calculated from multiple blood samples taken at different time points after drug administration.

Q3: What factors can affect AUC values?
A: Factors include drug absorption rate, distribution, metabolism, elimination, and individual patient characteristics like age, weight, and organ function.

Q4: Why is AUC important for drug dosing?
A: AUC helps establish appropriate dosing regimens to achieve therapeutic drug levels while minimizing toxicity and ensuring consistent drug exposure.

Q5: How does AUC relate to bioavailability?
A: AUC is directly proportional to bioavailability - the fraction of administered drug that reaches systemic circulation unchanged.

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