Drug Elution Rate Calculator
Model drug release from polymer matrices or drug-eluting implants using zero-order, first-order, Higuchi, and Korsmeyer-Peppas kinetic models.
Parameters
Model Rate Constants
Q = K0·t
Q = Q0(1−e−K1t)
Q = KH·√t
Q/Q0 = KKP·tn
Cumulative Release vs. Time
Results at t = 24 h
| Model | Released (µg) | Released (%) | Rate (µg/h) |
|---|---|---|---|
| Click Calculate to see results | |||
Summary
Model drug release from polymer matrices or drug-eluting implants using zero-order, first-order, Higuchi, and Korsmeyer-Peppas kinetic models.
How it works
- Enter the initial drug load (Q0, µg) and the plot duration in hours.
- Set the rate constant for each kinetic model you want to compare (zero-order, first-order, Higuchi, Korsmeyer-Peppas).
- Choose a query time point to read cumulative release at that exact moment.
- Click Calculate — the tool computes cumulative release (% and µg) and the instantaneous release rate for each model.
- Compare release profiles on the time-course chart and check the T50 and T80 milestones.
Use cases
- Compare predicted release profiles from drug-eluting stent coatings.
- Estimate drug remaining in a biodegradable PLGA implant at a given time.
- Fit experimental release data to an appropriate kinetic model.
- Determine the time to 50% or 80% cumulative release for formulation screening.
- Evaluate Fickian vs. anomalous transport using the Korsmeyer-Peppas n exponent.
Frequently Asked Questions
Last updated: 2026-06-09 ·
Reviewed by Nham Vu