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Updated: Jun 5, 2025

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning

Published on: April 16, 2018

Multiple-Temperature-Responsive Double- and Triple-Network Hydrogels.

Supissra Boon-In¹, Daniel Crespy¹

¹Department of Material Science and Engineering, School of Molecular Science and Engineering, Vidyasirimedhi Institute of Science and Technology (VISTEC), Rayong, 21210, Thailand.

Macromolecular Rapid Communications

|December 14, 2024

Summary

This summary is machine-generated.

Researchers developed novel temperature-responsive hydrogels with multiple networks. These smart materials exhibit tunable volume transitions, showing promise for advanced applications in soft robotics and programmable reactors.

Keywords:

multiple‐network hydrogels multiple‐volume transitions temperature‐responsive polymers

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Synthesis of PolyN-isopropylacrylamide Janus Microhydrogels for Anisotropic Thermo-responsiveness and Organophilic/Hydrophilic Loading Capability

Published on: February 27, 2016

Area of Science:

Materials Science
Polymer Chemistry
Smart Materials

Background:

Temperature-responsive hydrogels are smart materials with reversible activation capabilities.
Existing hydrogels often lack precise control over volume transitions.
Developing advanced hydrogels is crucial for next-generation material applications.

Purpose of the Study:

To fabricate novel double- and triple-network hydrogels.
To investigate the temperature-responsive volume transition behavior of these multi-network hydrogels.
To explore the influence of superhydrophilic polymer networks on hydrogel swelling and shrinkage.

Main Methods:

Synthesis of double- and triple-network hydrogels.
Characterization of hydrogel volume transitions in response to temperature changes.
Incorporation of superhydrophilic polymer networks to modulate swelling/shrinkage properties.

Main Results:

Successfully fabricated double- and triple-network hydrogels.
Demonstrated dual- and triple-volume transitions upon temperature variation.
Observed significant differences in swelling/shrinkage due to superhydrophilic network incorporation.

Conclusions:

The developed multi-network hydrogels exhibit controlled, temperature-dependent volume transitions.
Superhydrophilic polymer networks enhance the responsiveness and tunability of these hydrogels.
Potential applications include soft robotics and programmable reactors.