Title :
Novel design of a chitosan-collagen scaffold for hepatocyte implantation
Author :
Khamna, H.J. ; Klein, Michael D. ; Matthew, H.W.T.
Author_Institution :
Dept. of Biomed. Eng., Wayne State Univ., Detroit, MI, USA
Abstract :
Implantation of a bioartificial liver, composed of a hepatocyte seeded scaffold, has the potential to offer new treatment options for liver diseases. One of the problems associated with hepatocyte transplantation is the need to ensure adequate oxygenation in the short term and angiogenesis in the long term. The primary goal of this project is to develop a chitosan based scaffold capable of overcoming these problems. In this study we describe the design of a cylindrical shaped chitosan-collagen scaffold with radial pores originating at a central port. To generate this microstructure a chitosan-collagen solution was frozen under controlled rate and radial thermal gradient conditions and then lyophilized. Microstructure was examined using SEM. Rehydrated scaffolds were equilibrated with culture medium and seeded with either aggregated or single cell hepatocytes through a central injection port. MTT staining, fluorescence microscopy, and SEM were used to examine cell distribution, attachment, viability and morphology. SEM imaging showed that scaffolds had long tapering pores with diameters ranging from 50 μm at the port to 10 μm at the external surface. This microstructure allowed for efficient cell seeding via the central port. Single cells and aggregated hepatocytes were evenly distributed throughout the scaffold and attached to pore walls. Also discussed is the next phase of scaffold design, which addresses the need for immediate oxygenation by seeded cells
Keywords :
aggregation; artificial organs; biochemistry; biomedical materials; cellular biophysics; fluorescence; liver; optical microscopy; polymers; proteins; scanning electron microscopy; adequate oxygenation; aggregated hepatocytes; aggregation; angiogenesis; artificial liver implantation; biodegradable polymer; cell attachment; cell distribution; cell morphology; cell viability; chitosan-collagen scaffold; controlled rate conditions; fluorescence microscopy; hepatocyte implantation; hepatocyte seeded scaffold; hepatocyte transplantation; liver diseases; lyophilized; microstructure; radial pores; radial thermal gradient conditions; scaffold design; scanning electron microscopy; tissue engineering; Biodegradable materials; Bovine; Heat treatment; Liver diseases; Medical treatment; Microstructure; Polymers; Scanning electron microscopy; Size control; Testing;
Conference_Titel :
Engineering in Medicine and Biology Society, 2000. Proceedings of the 22nd Annual International Conference of the IEEE
Conference_Location :
Chicago, IL
Print_ISBN :
0-7803-6465-1
DOI :
10.1109/IEMBS.2000.897975