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Fabrication of an electrospun nanofibrous scaffold for use in the field of tissue engineering
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To create a nanofibrous mesh consisting of polycaprolactone and another biological polymer which enables cell activity and seeks to eventually provide an application in the field of tissue engineering toward a biomimetic skin graft.
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Protection from infection Prevent fluid/heat loss Ability to support and maintain tissue growth Skin properties › Friction & elasticity For easy movement and manipulation
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ECM - main structural tissue of skin › Helps skin renew and generate › Provides signals to intercellular pathways Main components › Glycoproteins (such as collagen) › Proteoglycans › Hyaluronic Acid Engineered ECMs are known as scaffolds
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Ability to create scaffolds › mimic the ECM in size and porosity › Have high surface to volume ratio More space for cells to attach and grow Increases biocompatibility Easy to vary mechanical and biological properties through changing materials Flexible- allows cells to manipulate their environment
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Biocompatible polymer Biodegradable at a slow enough rate to allow increased cell growth and stability Easy to manipulate Relatively low melting point- easy to use Clinically safe (FDA approval) Proven to have potential for scaffolds in relation to tissue regeneration › Has created scaffolds w/ ideal conditions High porosities Large amounts of surface areas
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Much research has shown that adding another biochemical can: Increase stress resistance Provide better adhesion of cells to the final scaffold Increase the potential for cell proliferation Biochemical should › Be a component of skin naturally › Must be able to be combined in a solution to be electrospun
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Collagen › Advantages biodegradable and biocompatible plays important role in tissue formation › Disadvantages Very expensive complex handling properties Gelatin › Advantages naturally derived from collagen, similar properties Cost efficient and easy to manipulate › Disadvantages can provoke inflammatory response Poor electrospinnability unless combined with specific solvents
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Hyaluronic Acid › Advantages: Excellent biocompatibility and biodegradability Main component of ECM › Disadvantages High viscosity, surface tension, and water retention make it difficult to form uniform sized fibers Elastin › Advantages Provides elasticity to skin- essential for this skin quality › Disadvantages highly insoluble Potential health risk Fibrinogen › Advantages Essential for wound healing Promotes cell migration and cellular interaction › Disadvantages difficult to control matrix properties
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Alginate › Advantages Good for health reasons (low toxicity, immunogenic) Low cost › Disadvantages Poor spinnability (possibly be fixed with addition of a synthetic polymer) Chitosan › Advantages natural polymer, biocompatible and biodegradable Cellular binding capabilities Accelerates wound healing Anti-bacterial properties › Disadvantages high viscosity limits spinnability Fibers can swell in aqueous solution- need to be cross linked to maintain structural qualities
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Create solutions of PCL and other polymer varying the concentrations Spin these solutions creating nanofilament meshes Analyze meshes for fiber and pore qualities using scanning electron microscope Culture fibroblast cells and seed into meshes created
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Data obtained will include: › Fiber diameter and pore diameter of the mesh › Concentration of the chemical › Amount of cell activity throughout mesh Analysis will include: › For what concentration of chemical did the most cell activity occur
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Akhyari, P., Kamiya, H., Haverich, A., Karck, M., & Lichtenberg, A. (2008). Myocardial tissue engineering: The extracellular matrix. European Journal of Cardio-Thoracic Surgery, 34, 229-241. doi: 10.1016/j.ejcts.2008.03.062 Bhardwaj, N. & Kundu, S. C. (2010). Electrospinning: A fascinating fiber fabrication technique. Biotechnology Advances, 28, 325-347. doi: 10.1016/j.biotechadv.2010.01.004 Chong, E.J., Phan, T.T., Lim, I.J., Zhang, Y.Z., Bay, B.H., Ramakrishna, S., & Lim, C.T. (2007). Evaluation of electrospun PCL/gelatin nanofibrous scaffold for wound healing and layered dermal reconstitution. Acta Biomaterialia, 3, 321-330. doi: 10.1016/j.actbio.2007.01.002 Geng, X., Kwon, O-H., & Jang, J. (2005). Electrospinning of chitosan dissolved in concentrated acetic acid solution. Biomaterials, 26, 5427-5432. Han, J., Branford-White, C.J., & Zhu, L.M. (2010). Preparation of poly(є-caprolactone)/poly(trimethylene carbonate) blend nanofibers by electrospinning. Carbohydrate Polymers, 79, 214-218. doi: 10.1016/j.carbpol.2009.07.052 Homayoni, H., Ravandi, S.A.H., & Valizadeh, M. (2009). Electrospinning of chitosan nanofibers: Processing optimization. Carbohydrate Polymers, 77, 656-661. Lowery, J.L., Datta, N., & Rutledge, G.C. (2010). Effect of fiber diameter, pore size and seeding method on growth of human dermal fibroblasts in electrospun poly(є-caprolactone) fibrous mats. Biomaterials, 31, 491-504. doi: 10.1016/j.biomaterials.2009.09.072 Nisbet, D.R., Forsythe, J.S., Shen, W., Finkelstein, D.I., & Horne, M.K. (2009). A review of the cellular response on electrospun nanofibers for tissue engineering. Journal of Biomaterials Application, 24, 7-29. Pham, Q.P., Sharama, V., & Mikos, A.G. (2006). Electrospinning of polymeric nanofibers for tissue engineering applications: A review. Tissue Engineering, 12,1197-1211. Shevchenko, R.V., James, S.L., & James, S.E. (2010). A review of tissue-engineered skin bioconstructs available for skin reconstruction. Journal of the Royal Society Interface, 7, 229-258. doi: 10.1098/rsif.2009.0403 Sill, T.J., & von Recum, H.A. (2008). Electrospinning: Applications in drug delivery and tissue engineering. Biomaterials, 29, 1989-2006. doi: 10.1016/j.biomaterials.2008.01.011 Woodruff, M.A., & Hutmacher, D.W. (in press). The return of a forgotten polymer- Polycaprolactone in the 21 st century. Progress in Polymer Science. doi: 10.1016/j.progpolymsci.2010.04.002
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