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 Met with Singaporeans!  Presented final proposal of collaboration to AOS staff  Finished Experimental Design › Turned in final and revised editions.

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Presentation on theme: " Met with Singaporeans!  Presented final proposal of collaboration to AOS staff  Finished Experimental Design › Turned in final and revised editions."— Presentation transcript:

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2  Met with Singaporeans!  Presented final proposal of collaboration to AOS staff  Finished Experimental Design › Turned in final and revised editions  Finished ISEF forms  Started updates to Background Research paper

3  Biocompatible polymer  Biodegradable at a slow enough rate to allow increased cell growth and stability  Proven to have potential for scaffolds in relation to tissue regeneration › Has created scaffolds w/ ideal conditions  High porosities  Large amounts of surface areas

4  Chitosan › Advantages  natural polymer, biocompatible and biodegradable  Cellular binding capabilities  Accelerates wound healing  Anti-bacterial properties

5  Chitosan: › Disadvantages  high viscosity limits spinnability  Fibers can swell in aqueous solution- need to be cross linked to maintain structural qualities

6  Alginate › Advantages  Good for health reasons (low toxicity, immunogenic)  Low cost › Disadvantages  Poor spinnability (possibly be fixed with addition of a synthetic polymer)

7  Universal solvent- can be used for PCL, CHT, & Alg  Acetic Acid › Previous research for PCL & CHT › Alginate?  Another possibility: formic acid/acetone › If acetic acid doesn’t work

8  Create control meshes of pure PCL › Mix solution  PCL & acetic acid › Electrospin  Starting parameters: 15 wt.% concentration, 20 cm from tip of syringe to collector plate, & 20 kV

9  Vary voltage to create 9 meshes › 3 Voltages- 3 trials for each  20 kV  15 kV  25 kV  Examine pieces of meshes under scanning electron microscope (SEM)  Culture fibroblast cells onto other pieces of meshes

10  Observing cells › Examine under TC inverted light microscope  Analyze cell growth › Conduct cell counts in cells per unit area (mm 2 ) › Means and standard deviations › ANOVA (Analysis of Variants) tests

11  Create solutions of PCL and chitosan  Electrospin  Vary concentration of chitosan to PCL › 5% CHT › 15% CHT › 25% CHT  Total of 9 meshes (3 trials of each concentration)

12  Analyze with Scanning Electron Microscope (SEM)  Culture fibroblast cells and seed into meshes created  Determine cell density  Analyze with means, standard deviations, and ANOVA tests

13  Data obtained: › Fiber diameter and pore diameter of mesh › Cell density amounts  Analysis includes: › Means* › Standard Deviations* › ANOVA tests  3 comparisons *5-7 measurements/areas for these methods

14  Pure PCL mesh vs. chitosan/PCL mesh  AOS & HCI › With pure PCL mesh: › AFM (atomic force microscope) vs. SEM › Fibroblast cells vs. Drosophila cells › pure PCL mesh vs. alginate/PCL mesh › Chitosan/PCL mesh vs. alginate/PCL mesh

15  Basic Timeline › Includes any work either side does during each month  Background Research Paper  Experimental Design drafts  Any PowerPoint presentations  References › Links to all relevant journal articles either have found

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17  Finish last revision to ISEF forms  Finish the update on background research  Research more into alginate for potential universal solvent  Acquisition forms

18 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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