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PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS
Published on: December 27, 2013
Outer eggshell membrane as delivery vehicle for polysaccharide/protein microcapsules incorporated with vitamin E
Zhi Chai1, Yuanyuan Li, Fei Liu
1CAU and ACC Joint-Laboratory of Space Food, Key Laboratory of Functional Dairy Science of Beijing and Ministry of Education, College of Food Science and Nutritional Engineering, China Agricultural University, Haidian, Beijing, China.
Journal of Agricultural and Food Chemistry
|December 19, 2012
Summary
A novel delivery system using outer eggshell membrane (OESM) and microcapsules enhances controlled release and enzymatic resistance. This natural composite material offers improved properties for various applications.
Area of Science:
- Biomaterials Science
- Drug Delivery Systems
- Materials Engineering
Background:
- Natural materials like outer eggshell membrane (OESM) offer unique structural properties.
- Emulsified microcapsules are widely used for controlled release applications.
- Combining natural structures with microcapsules can lead to advanced delivery systems.
Purpose of the Study:
- To investigate the features of a novel delivery system combining OESM with emulsified microcapsules.
- To evaluate the loading efficiency, controlled release, and forming mechanisms of the OESM/microcapsule system.
- To assess the impact of cross-linking agents and wall materials on system performance.
Main Methods:
- Preparation of polysaccharide/protein microcapsules incorporating vitamin E.
- Attachment of microcapsules to OESM and reinforcement with glutaraldehyde.
- Evaluation of controlled release kinetics and enzymatic degradation resistance.
- Analysis of structural properties and interaction mechanisms.
Main Results:
- Polysaccharide/protein microcapsules effectively attached to OESM, with attachment strength increased over 2-fold by glutaraldehyde.
- The OESM/microcapsule system demonstrated significantly improved controlled release compared to microcapsules alone due to steric blocking.
- OESM systems with pectin/protein microcapsules exhibited enhanced resistance to enzymatic degradation via compact aggregate formation.
Conclusions:
- The OESM/microcapsule composite system is a promising platform for enhanced controlled release applications.
- Glutaraldehyde cross-linking effectively improves the stability and integration of microcapsules within the OESM matrix.
- The choice of wall material (e.g., pectin/protein) influences the system's resistance to enzymatic degradation, highlighting tunable properties.
