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Updated: Apr 21, 2026

Alternating Magnetic Field-Responsive Hybrid Gelatin Microgels for Controlled Drug Release
Published on: February 13, 2016
Refillable and magnetically actuated drug delivery system using pear-shaped viscoelastic membrane
Hongyun So1, Young Ho Seo2, Albert P Pisano
1Department of Mechanical Engineering, University of California , Berkeley, California 94720, USA.
A novel magnetic drug delivery device offers on-demand, controlled medication release for localized diseases. This refillable, valveless system precisely dispenses therapeutic doses using external magnetic fields.
Area of Science:
- Biomedical Engineering
- Materials Science
- Drug Delivery Systems
Background:
- Localized diseases require precise drug delivery for efficacy and reduced side effects.
- Existing drug delivery systems often lack on-demand control or require complex mechanisms.
- Valveless and refillable systems are desirable for improved patient compliance and usability.
Purpose of the Study:
- To develop and characterize a novel refillable and valveless drug delivery device.
- To demonstrate on-demand drug release actuated by an external magnetic field.
- To investigate the controlled discharge of therapeutic agents for localized disease treatment.
Main Methods:
- Design of a dome-shaped drug reservoir with a pear-shaped viscoelastic magnetic membrane.
- Actuation of the membrane using an external magnetic field (up to 500 mT).
- Quantification of drug release based on magnetic field strength and number of actuations.
Main Results:
- The device achieved controlled drug release via magnetic actuation of the membrane.
- Maximum drug release of 18 ± 1.5 μg per actuation was observed at 500 mT.
- Variable drug doses were successfully controlled by adjusting magnetic field parameters and actuations.
Conclusions:
- The developed magnetic drug delivery device enables precise, on-demand medication release.
- The valveless, refillable design presents a promising platform for localized disease therapy.
- Further optimization could enhance therapeutic outcomes and patient-specific dosing.
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