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Diffusion in and around alginate and chitosan films with embedded sub-millimeter voids
Subhajit Patra1, Dharmendra Kumar Bal1, Somenath Ganguly1
1Department of Chemical Engineering, Indian Institute of Technology, Kharagpur 721302, India.
Summary
Alginate and chitosan hydrogel films with embedded voids enhance drug diffusion. These porous biopolymer scaffolds show improved controlled release for potential tissue engineering and drug delivery applications.
Area of Science:
- Biomaterials Science
- Materials Engineering
- Drug Delivery
Background:
- Hydrogel scaffolds from biopolymers are promising for controlled drug release and tissue engineering.
- Alginate and chitosan are widely studied biopolymers for scaffold fabrication.
Purpose of the Study:
- To investigate the solute release behavior of alginate and chitosan films containing sub-millimeter voids.
- To quantify the effect of these voids on diffusion and mass transfer coefficients.
Main Methods:
- Fabrication of hydrogel films with embedded voids using nitrogen gas bubbles prior to crosslinking.
- Characterization of void dimensions using digital microscopy and scanning electron microscopy.
- Measurement of porosity and gravimetric analysis.
- Solute (Vitamin B-12) release studies in PBS buffer at ambient and 37°C with lysozyme.
- Estimation of diffusion and mass transfer coefficients using a mathematical model.
Main Results:
- Embedded voids significantly enhanced the diffusion coefficient within the hydrogel films.
- The presence of voids altered the mass transfer characteristics at the gel-interface.
- Comparison with void-free films highlighted the void-induced enhancement in solute release.
Conclusions:
- Porous hydrogel scaffolds with embedded voids offer improved controlled release properties.
- This approach can be utilized to optimize drug delivery systems and tissue engineering scaffolds.
- The study provides insights into the relationship between scaffold architecture and solute transport kinetics.

