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Microgel-Based Stretchable Reservoir Devices for Elongation Enhanced Small Molecule Release Rate
Yingnan Zhang1, Yongfeng Gao1, Wildemar S P Carvalho1
1Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada.
ACS Applied Materials & Interfaces
|April 8, 2020
Summary
Stretchable microgel devices control drug release. Thin gold coatings and stretching accelerate the release of crystal violet (CV) by altering microgel porosity and creating cracks, enabling tunable drug delivery systems.
Area of Science:
- Materials Science
- Biomedical Engineering
- Drug Delivery Systems
Background:
- Developing controlled drug release systems is crucial for effective therapeutics.
- Microgel-based devices offer tunable properties for drug encapsulation and release.
- Controlling release kinetics through external stimuli like mechanical stress is an active research area.
Purpose of the Study:
- To fabricate stretchable microgel reservoir devices for controlled release of crystal violet (CV).
- To investigate the influence of gold (Au) layer thickness and device elongation on CV release rates.
- To explore the potential for autonomous drug release systems triggered by natural movements.
Main Methods:
- Fabrication of stretchable poly(N-isopropylacrylamide)-co-acrylic acid (pNIPAm-co-10% AAc) microgel reservoir devices.
- Loading of crystal violet (CV) into microgels via electrostatic interactions at pH 6.5.
- Triggering CV release by changing solution pH to 3.0 and analyzing release kinetics under varying Au layer thickness and device elongation.
Main Results:
- CV release was triggered by a pH shift, breaking electrostatic interactions.
- Decreasing Au layer thickness and increasing device elongation accelerated CV release.
- Au layer thickness dominated release at low elongation, while elongation-induced cracks dominated at high elongation, enabling an 'off' to 'on' release transition.
Conclusions:
- Stretchable microgel devices with tunable Au coatings and mechanical properties can precisely control drug release kinetics.
- The interplay between Au layer porosity and elongation-induced cracking offers a mechanism for modulating release rates.
- These findings support the development of autonomous drug delivery systems activated by mechanical stimuli.

