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Phase Behavior of Charged Vesicles Under Symmetric and Asymmetric Solution Conditions Monitored with Fluorescence Microscopy
Published on: October 24, 2017
Gelation of charged catanionic vesicles prepared by a semispontaneous process
Zheng-Lin Huang1, Jhen-Yi Hong, Chien-Hsiang Chang
1Department of Chemical Engineering, National Cheng Kung University, Tainan 701, Taiwan.
Stable charged catanionic vesicles were created and gelled with polymers. Their interactions, studied via phase maps and rheology, suggest potential for drug delivery applications.
Area of Science:
- Supramolecular Chemistry
- Materials Science
- Colloid Science
Background:
- Catanionic vesicles are self-assembled structures formed from oppositely charged surfactants.
- Controlling vesicle charge and properties is crucial for their application in delivery systems.
Purpose of the Study:
- To prepare stable charged catanionic vesicles with tunable zeta-potentials.
- To investigate the gelation of these vesicles using various water-soluble polymers.
- To understand the interactions governing vesicle-polymer systems for potential drug delivery.
Main Methods:
- Semispontaneous formation of catanionic vesicles using an ion-pair amphiphile and component ionic surfactants with a cosolvent.
- Gelation studies using tube inversion and rheological analysis with four different polymers.
- Construction of phase maps to delineate regions of phase separation, viscous solution, and gel.
Main Results:
- Stable catanionic vesicles with zeta-potentials ranging from +59 mV to -96 mV were successfully prepared.
- Phase maps were constructed, illustrating gelation behavior based on vesicle composition and polymer content.
- Rheological data indicated electrostatic and hydrophobic interactions between vesicles and polymers.
Conclusions:
- The study successfully prepared tunable charged catanionic vesicles.
- The gelation behavior is dependent on vesicle charge and polymer characteristics.
- The findings provide insights into vesicle-polymer interactions, supporting their use in mucosal and transdermal drug delivery.
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