Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98966
Title: Immobilization of gelatin onto poly(glycidyl methacrylate)-grafted polycaprolactone substrates for improved cell-material interactions
Authors: Yuan, Shaojun
Xiong, Gordon
Roguin, Ariel
Choong, Cleo Swee Neo
Keywords: DRNTU::Engineering::Materials::Biomaterials
Issue Date: 2012
Source: Yuan, S., Xiong, G., Roguin, A., & Choong, C. (2012). Immobilization of gelatin onto poly(glycidyl methacrylate)-grafted polycaprolactone substrates for improved cell–material interactions. Biointerphases, 7, 1-12.
Series/Report no.: Biointerphases
Abstract: To enhance the cytocompatibility of polycaprolactone (PCL), cell-adhesive gelatin is covalently immobilized onto the PCL film surface via two surfacemodified approaches: a conventional chemical immobilization process and a surface-initiated atom transfer radical polymerization (ATRP) process. Kinetics studies reveal that the polymer chain growth from the PCL film using the ATRP process is formed in a controlled manner, and that the amount of immobilized gelatin increases with an increasing concentration of epoxide groups on the grafted P(GMA) brushes. In vitro cell adhesion and proliferation studies demonstrate that cell affinity and growth are significantly improved by the immobilization of gelatin on PCL film surfaces, and that this improvement is positively correlated to the amount of covalently immobilized gelatin. With the versatility of the ATRP process and tunable grafting efficacy of gelatin, this study offers a suitable methodology for the functionalization of biodegradable polyesters scaffolds to improve cell–material interactions.
URI: https://hdl.handle.net/10356/98966
http://hdl.handle.net/10220/12729
DOI: http://dx.doi.org/10.1007/s13758-012-0030-1
Rights: © 2012 The Authors. This paper was published in Biointerphases and is made available as an electronic reprint (preprint) with permission of the authors. The paper can be found at the following official DOI: [http://dx.doi.org/10.1007/s13758-012-0030-1]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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