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Micropatterning and characterization of electrospun poly(ε‐caprolactone)/gelatin nanofiber tissue scaffolds by femtosecond laser ablation for tissue engineering applications
Authors:Yong Chae Lim  Jed Johnson  Zhengzheng Fei  Yun Wu  Dave F Farson  John J Lannutti  Hae Woon Choi  L James Lee
Institution:1. Laboratory for Multiscale Processing and Characterization, The Ohio State University, 1248 Arthur E. Adams Dr., Columbus, Ohio 43210;2. telephone: +614‐688‐4046;3. fax: +614‐292‐6842;4. Center for Affordable Nanoengineering of Polymeric Biomedical Devices, The Ohio State University, Columbus, Ohio;5. Department of Material Science and Engineering, The Ohio State University, Columbus, Ohio;6. Department of Chemical and Bimolecular Engineering, The Ohio State University, Columbus, Ohio;7. Department of Mechanical and Automotive Engineering, KeiMyoung University, Dalseo‐Gu, Daegu, Korea
Abstract:Experimental investigations aimed at assessing the effectiveness of femtosecond (FS) laser ablation for creating microscale features on electrospun poly(ε‐caprolactone) (PCL)/gelatin nanofiber tissue scaffold capable of controlling cell distribution are described. Statistical comparisons of the fiber diameter and surface porosity on laser‐machined and as‐spun surface were made and results showed that laser ablation did not change the fiber surface morphology. The minimum feature size that could be created on electrospun nanofiber surfaces by direct‐write ablation was measured over a range of laser pulse energies. The minimum feature size that could be created was limited only by the pore size of the scaffold surface. The chemical states of PCL/gelatin nanofiber surfaces were measured before and after FS laser machining by attenuated total reflectance Fourier transform infrared (ATR‐FTIR) spectroscopy and X‐ray photoelectron spectroscopy (XPS) and showed that laser machining produced no changes in the chemistry of the surface. In vitro, mouse embryonic stem cells (mES cells) were cultured on as‐spun surfaces and in laser‐machined microwells. Cell densities were found to be statistically indistinguishable after 1 and 2 days of growth. Additionally, confocal microscope imaging confirmed that spreading of mES cells cultured within laser‐machined microwells was constrained by the cavity walls, the expected and desired function of these cavities. The geometric constraint caused statistically significant smaller density of cells in microwells after 3 days of growth. It was concluded that FS laser ablation is an effective process for microscale structuring of these electrospun nanofiber tissue scaffold surfaces. Biotechnol. Bioeng. 2011; 108:116–126. © 2010 Wiley Periodicals, Inc.
Keywords:laser ablation  polycaprolactone  gelatin  tissue scaffold  micropatterning  stem cell
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