Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/84446
Title: Grafting of glycidyl methacrylate upon coralline hydroxyapatite in conjugation with demineralized bone matrix using redox initiating system
Authors: Murugan, R. 
Panduranga Rao, K.
Keywords: Coralline hydroxyapatite
DBM
FT-IR
GMA
Grafting
Issue Date: Feb-2003
Citation: Murugan, R.,Panduranga Rao, K. (2003-02). Grafting of glycidyl methacrylate upon coralline hydroxyapatite in conjugation with demineralized bone matrix using redox initiating system. Macromolecular Research 11 (1) : 14-18. ScholarBank@NUS Repository.
Abstract: Grafting of glycidyl methacrylate (GMA) upon coralline hydroxyapatite in conjugation with demineralized bone matrix (CHA-DBM) using equal molar ratio of potassium persulfate/sodium metabisulfite redox initiating system was investigated in aqueous medium. The optimum reaction condition was standardized by varying the concentrations of backbone, monomer, initiator, temperature and time. The results obtained imply that the percent grafting was found to increase initially and then decrease in most of the cases. The optimum temperature and time were found to be 50°C and 180 min, respectively, to obtain higher grafting yield. Fourier transform infrared (FT-IR) spectroscopy and X-ray powder diffraction (XRD) method were employed for the proof of grafting. The FT-IR spectrum of grafted CHA-DBM showed epoxy groups at 905 and 853 cm-1 and ester carbonyl group at 1731 cm-1 of poly(glycidyl methacrylate) (PGMA) in addition to the characteristic absorptions of CHA-DBM, which provides evidence of the grafting. The XRD results clearly indicated that the crystallographic structure of the grafted CHA-DBM has not changed due to the grafting reaction. Further, no phase transformation was detected by the XRD analysis, which suggests that the PGMA is grafted only on the surface of CHA-DBM backbone. The grafted CHA-DBM will have better functionality because of their surface modification and hence they may be more useful in coupling of therapeutic agents through epoxy groups apart from being used as osteogenic material.
Source Title: Macromolecular Research
URI: http://scholarbank.nus.edu.sg/handle/10635/84446
ISSN: 15985032
Appears in Collections:Staff Publications

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