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Updated: Dec 24, 2025

Preparation of Functional Silica Using a Bioinspired Method
Published on: August 1, 2018
A facile and efficient strategy to encapsulate the model basic protein lysozyme into porous CaCO3
Pengzhong Shi1, Shan Luo, Brigitte Voit
1School of Ophthalmology and Optometry, Eye Hospital, School of Biomedical Engineering, Wenzhou Medical University, Wenzhou, Zhejiang Province 325035, P. R. China.
This study presents a novel method for efficiently encapsulating basic proteins, like lysozyme, into porous calcium carbonate carriers using heparin doping. This approach achieves high loading efficiency and preserves protein activity, overcoming previous limitations in protein drug delivery.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Drug Delivery
Background:
- Basic proteins are crucial for biological functions and therapies but are limited by instability and short half-lives.
- Protein encapsulation in carriers enhances stability and controls release, but achieving high loading under mild conditions remains challenging.
- Layer-by-layer (LBL) assembly with sacrificial templates is used for protein encapsulation, though porous CaCO3 struggles with basic proteins.
Purpose of the Study:
- To develop a highly efficient and simple method for encapsulating basic proteins, specifically lysozyme, into porous calcium carbonate (CaCO3) carriers.
- To overcome the poor loading ability of porous CaCO3 for basic proteins by incorporating a doping agent.
- To ensure the retention of the encapsulated protein's biological activity and control its release during subsequent processing.
Main Methods:
- Development of a method involving doping porous CaCO3 with heparin to enhance lysozyme encapsulation.
- Utilizing the layer-by-layer (LBL) technique with sacrificial CaCO3 templates for protein carrier fabrication.
- Investigating the encapsulation efficiency and protein activity retention post-encapsulation and during LBL wrapping.
Main Results:
- Achieved a 99.5% encapsulation efficiency and a capacity of 91.6 mg g-1 for lysozyme under mild conditions.
- Demonstrated near 100% retention of lysozyme activity after encapsulation.
- Showed that lysozyme loss during LBL wrapping is controllable by selecting appropriate polyelectrolyte pairs.
Conclusions:
- Heparin doping significantly enhances the efficiency and capacity of basic protein (lysozyme) encapsulation in porous CaCO3.
- The developed method preserves the biological activity of encapsulated proteins, crucial for therapeutic applications.
- This approach offers a versatile platform for encapsulating various functional proteins for applications in catalysis, disease treatment, and tissue engineering.
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