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Updated: Apr 28, 2026

An Integrated System to Remotely Trigger Intracellular Signal Transduction by Upconversion Nanoparticle-mediated Kinase Photoactivation
Published on: August 30, 2017
Nanovalve activation by surface-attached photoacids
T M Guardado-Alvarez1, M M Russell, J I Zink
1Department of Chemistry and Biochemistry and California NanoSystems Institute, University of California, Los Angeles, California 90095-1569, USA. zink@chem.ucla.edu.
Light-activated photoacids on nanoparticles trigger molecular release from nanovalves. This pH-responsive system demonstrates externally controlled drug delivery using light activation.
Area of Science:
- Nanotechnology
- Materials Science
- Photochemistry
Background:
- Mesoporous silica nanoparticles (MSNs) are widely used for drug delivery.
- Controlling molecular release from MSNs remains a challenge.
- Developing externally triggered release systems is crucial for targeted therapies.
Purpose of the Study:
- To develop a light-responsive nanovalve system for controlled molecular release.
- To investigate the mechanism of light-induced proton transfer for nanovalve activation.
- To demonstrate pH-responsive molecular delivery using photoacid-functionalized MSNs.
Main Methods:
- Synthesized photoacid-functionalized mesoporous silica nanoparticles.
- Attached an aniline-based stalk and cyclodextrin to block nanoparticle pores.
- Used UV light excitation to trigger proton transfer and nanovalve opening.
- Analyzed the release of trapped molecules using spectroscopy.
Main Results:
- Photoacid excitation induced proton transfer, leading to aniline stalk protonation.
- Protonation caused the release of the cyclodextrin gatekeeper molecule.
- Successfully demonstrated light-triggered release of encapsulated molecules from MSNs.
- Confirmed the pH-responsive nature of the nanovalve system.
Conclusions:
- Light-triggered proton transfer effectively activates nanovalves on MSNs.
- Photoacid-functionalized MSNs provide a controllable platform for molecular delivery.
- This system offers a novel approach for externally regulated drug release.
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