Related Experiment Video
Updated: Jul 13, 2026

12:00
Synthesis of Gold Nanoparticle Integrated Photo-responsive Liposomes and Measurement of Their Microbubble Cavitation upon Pulse Laser Excitation
Published on: February 24, 2016
Gold nanoparticles enable selective light-induced contents release from liposomes.
Lauri Paasonen1, Timo Laaksonen, Christoffer Johans
1Department of Pharmaceutics, University of Kuopio, Kuopio, Finland. Lauri.Paasonen@helsinki.fi <Lauri.Paasonen@helsinki.fi>
Summary
Light-activated gold nanoparticles enable selective content release from liposomes. This novel drug delivery mechanism offers enhanced biological compatibility and localized release for various applications.
Area of Science:
- Biotechnology
- Materials Science
- Drug Delivery
Background:
- Liposomes are widely used for drug delivery but achieving controlled release remains a challenge.
- Selective activation of drug release mechanisms is crucial for minimizing side effects and improving therapeutic efficacy.
Purpose of the Study:
- To demonstrate a novel method for light-triggered content release from liposomes.
- To investigate the use of gold nanoparticles for localized heating and subsequent liposome destabilization.
Main Methods:
- Incorporation of hydrophobic or hydrophilic gold nanoparticles into liposomes.
- Monitoring the release of a fluorescent marker upon UV light exposure.
- Investigating the temperature-dependent release mechanism.
Main Results:
- Liposomes with incorporated gold nanoparticles showed intactness at 37°C.
- UV light irradiation triggered localized heating of gold nanoparticles, inducing content release.
- Release mechanism involves heat transfer from nanoparticles to lipids, causing phase transition.
Conclusions:
- Gold nanoparticles serve as efficient energy collectors, enabling selective, light-induced content release from liposomes.
- This approach offers a potentially more biologically compatible drug delivery system.
- The technology can be extended to other applications requiring localized content release.

