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

  1. Enter the initial drug load (Q0, µg) and the plot duration in hours.
  2. Set the rate constant for each kinetic model you want to compare (zero-order, first-order, Higuchi, Korsmeyer-Peppas).
  3. Choose a query time point to read cumulative release at that exact moment.
  4. Click Calculate — the tool computes cumulative release (% and µg) and the instantaneous release rate for each model.
  5. 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