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Updated: Jun 11, 2026

Models and Methods to Evaluate Transport of Drug Delivery Systems Across Cellular Barriers
Published on: October 17, 2013
Design of optimized diffusion-controlled transdermal drug delivery systems
E Bruce Nauman1, Kandarp Patel, Pankaj Karande
1Department of Chemical and Biological Engineering, Rensselaer Polytechnic Institute, Troy, NY, USA.
This study optimized multilayer transdermal patch design for maximum drug release. The ideal design uses specific drug concentrations and barrier layer thickness for effective therapeutic delivery.
Area of Science:
- Materials Science
- Pharmaceutical Sciences
- Chemical Engineering
Background:
- A systematic approach for designing multilayer transdermal patches is presented.
- Design is based on therapeutically relevant drug specifications.
Purpose of the Study:
- To optimize drug release from transdermal patches using random search optimization.
- To identify key design parameters for multilayer transdermal patches.
Main Methods:
- Utilized random search optimization techniques.
- Optimized maximum drug release subject to therapeutic specifications.
- Varied barrier layer thickness and drug concentrations in drug-containing layers as design parameters.
Main Results:
- An optimal patch design was identified.
- The optimal design featured two drug-containing layers of equal thickness with 20% and 80% relative drug concentrations.
- A barrier layer thickness of 14% (relative to total drug-containing layer thickness) was determined to be optimal.
Conclusions:
- The proposed transdermal patch design is broadly applicable.
- The design effectively satisfies therapeutic specifications.
- The design maximizes drug utilization.
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