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Preparation and Characterization of Individual and Multi-drug Loaded Physically Entrapped Polymeric Micelles
Published on: August 28, 2015
Paclitaxel-loaded composite fibers: microstructure and emulsion stability
Amir Kraitzer1, Meital Zilberman
1Department of Biomedical Engineering, Faculty of Engineering, Tel-Aviv University, Tel-Aviv 69978, Israel.
New paclitaxel-loaded core/shell fibers offer advanced drug delivery. Formulation, not processing, controls porous structure and drug release for biomedical applications like stents.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Drug Delivery Systems
Background:
- Biomedical applications require advanced drug delivery systems.
- Core/shell fiber structures offer potential for localized drug release.
- Preventing restenosis and treating cancer are key therapeutic areas.
Purpose of the Study:
- To develop and characterize novel core/shell fiber structures loaded with paclitaxel.
- To investigate the influence of emulsion formulation and processing on fiber structure and drug release.
- To establish structure-property relationships for optimizing fiber performance.
Main Methods:
- Fabrication of core/shell fibers by coating nylon with paclitaxel-loaded poly(DL-lactic-co-glycolic acid).
- Shell preparation via freeze-drying of water-in-oil emulsions.
- Analysis of porous shell structure, emulsion stability, and drug release profiles.
Main Results:
- Achieved highly porous shell structures with excellent core adhesion.
- Emulsion drug content and copolymer composition significantly impacted pore size and distribution due to instability.
- Homogenization parameters had minimal effect on microstructure, indicating thermodynamic control.
Conclusions:
- Core/shell fibers loaded with paclitaxel are viable for biomedical applications.
- Emulsion thermodynamics, rather than kinetics, govern shell structure and drug release.
- Optimized formulations can yield tailored drug delivery profiles for applications like endovascular stents.
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