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Engineering 3D Cellularized Collagen Gels for Vascular Tissue Regeneration
Published on: June 16, 2015
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Electroactive graphene oxide-incorporated collagen assisting vascularization for cardiac tissue engineering
Mohammad Hadi Norahan1, Masoud Amroon1, Ramin Ghahremanzadeh2
1Department of Biomedical Engineering, Yazd Branch, Islamic Azad University, Yazd, Iran.
Journal of Biomedical Materials Research. Part A
|October 30, 2018
Summary
This study developed an electroactive collagen and graphene oxide (Col-GO) cardiac patch. The Col-GO patch shows promise for cardiac tissue engineering by enhancing electrical conductivity and supporting cardiomyocyte function post-infarction.
Area of Science:
- Biomaterials Science
- Tissue Engineering
- Cardiovascular Research
Background:
- Cardiac patches protect heart function post-myocardial infarction.
- Electroactive materials can improve electrical signal propagation in cardiac cells.
- Collagen-graphene oxide (Col-GO) composites offer potential for cardiac tissue engineering.
Purpose of the Study:
- To fabricate and characterize an electroactive Col-GO composite as a cardiac patch.
- To evaluate the biocompatibility, mechanical properties, and electrical conductivity of the Col-GO patch.
- To assess the potential of the Col-GO patch in promoting cardiomyocyte adhesion and cardiac gene expression.
Main Methods:
- Col-GO scaffolds were fabricated using freeze-drying and covalently coated with graphene oxide (GO).
- Scaffolds were reduced to restore GO conductivity; properties like pore size, tensile strength, and electrical conductivity were measured.
- Cytotoxicity assays using human umbilical vein endothelial cells (HUVECs) and assessment of cardiomyocyte adhesion and gene expression were performed.
Main Results:
- Col-GO scaffolds exhibited suitable pore sizes (120-138 ± 8 μm) and enhanced tensile strength with increasing GO concentration.
- The scaffolds demonstrated semi-conductive electrical properties (~10-4 S/m) and were non-toxic to HUVECs.
- Reduced Col-GO scaffolds promoted neonatal cardiomyocyte adhesion and upregulated cardiac-specific genes (Cx43, Actin4, Trpt-2), indicating angiogenic potential.
Conclusions:
- The developed Col-GO cardiac patch is biocompatible, mechanically robust, and electrically conductive.
- Reduced Col-GO materials show promise for cardiovascular applications by supporting cardiomyocyte function and promoting angiogenesis.
- This electroactive cardiac patch represents a viable strategy for cardiac tissue engineering and post-infarction repair.
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