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Microcapsules with improved mechanical stability for hepatocyte culture
Chao Yin1, Ser Mien Chia, Chai Hoon Quek
1Johns Hopkins Singapore, Tissue & Therapeutic Engineering Lab, 117597 Singapore.
Biomaterials
|February 21, 2003
Summary
Increasing terpolymer molecular weight in microcapsules enhances mechanical stability for bioartificial liver devices. Hepatocyte function remains unaffected, crucial for improving liver assist device performance.
Area of Science:
- Biomaterials Engineering
- Hepatocyte Culture
- Bioartificial Organs
Background:
- Bioartificial liver assist devices (BLADs) utilize bioreactors with microencapsulated hepatocytes.
- Current microcapsule designs require improved mechanical stability for high perfusion rates.
- Optimizing microcapsule properties is key to successful BLAD applications.
Purpose of the Study:
- To investigate the impact of terpolymer molecular weight on microcapsule mechanical properties.
- To assess the effect of terpolymer molecular weight on encapsulated hepatocyte functions.
- To determine the suitability of modified microcapsules for BLADs.
Main Methods:
- Synthesis of six terpolymers with varying molecular weights (M(w)) via radical polymerization.
- Fabrication of microcapsules using terpolymers and methylated collagen.
- Evaluation of microcapsule mechanical properties, membrane thickness, and serum albumin permeability.
- Assessment of encapsulated hepatocyte functions: urea synthesis, albumin synthesis, and cytochrome P450 activity.
Main Results:
- Higher terpolymer M(w) significantly improved microcapsule mechanical properties.
- Terpolymer M(w) had minimal impact on capsule membrane thickness and albumin permeability.
- Encapsulated hepatocyte functions (urea, albumin synthesis, P450 activity) were not significantly affected by M(w).
Conclusions:
- Terpolymer molecular weight is a critical factor for enhancing microcapsule mechanical stability in BLADs.
- The developed microcapsules maintain optimal hepatocyte function, supporting their use in liver assist devices.
- This study provides a pathway for engineering more robust microcapsules for bioartificial liver applications.