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Dual Photo- and pH-Responsive Spirooxazine-Functionalized Dextran Nanoparticles
Shahnaz Rahimi1,2, Steffi Stumpf2,3, Oliver Grimm2
1Laboratory of Organic and Polymer Chemistry, College of Science, University of Tehran, 16th Azar St., Enghelab Sq., 141556455 Tehran, Iran.
This study presents a novel dual photo- and pH-responsive polymer nanoparticle system. These smart nanoparticles change structure under UV light and varying acidity, showing potential for drug delivery applications.
Area of Science:
- Polymer Chemistry
- Materials Science
- Nanotechnology
Background:
- Developing smart materials with tunable properties is crucial for advanced applications.
- Stimuli-responsive polymers offer dynamic control over material behavior.
- Dextran-based nanomaterials are biocompatible and versatile platforms.
Purpose of the Study:
- To synthesize and characterize dual photo- and pH-responsive spirooxazine-functionalized dextran nanoparticles.
- To investigate the nanoparticle's structural and aggregation behavior under UV light and acidic conditions.
- To evaluate the potential of these nanoparticles for controlled drug delivery using Nile Red as a model drug.
Main Methods:
- Functionalization of dextran with a spirooxazine derivative (SO-COOH).
- Formation of nanoparticles in aqueous media.
- Stimulation studies using UV light, visible light, and varying pH conditions (pH 5 and 3).
- Encapsulation and tracking of Nile Red fluorescent dye to monitor structural changes.
Main Results:
- Successfully synthesized spirooxazine-functionalized dextran (Dex-SO) nanoparticles.
- Demonstrated reversible nanoparticle aggregation upon UV light (forming Dex-MC) and visible light stimuli.
- Observed nanoparticle aggregation and swelling at pH 5 and 3, respectively, due to spirooxazine protonation.
- Nile Red encapsulation provided insights into light- and pH-induced structural transformations.
Conclusions:
- The developed Dex-SO nanoparticles exhibit dual responsiveness to light and pH.
- The reversible photoisomerization and pH-dependent protonation enable tunable nanoparticle assembly.
- These findings highlight the potential of these stimuli-responsive nanoparticles for controlled release and drug delivery systems.
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