



@article {2536,
	title = {Cellulose phosphates as biomaterials. I. Synthesis and characterization of highly phosphorylated cellulose gels},
	journal = {Journal of Applied Polymer ScienceJ. Appl. Polym. Sci.},
	volume = {82},
	year = {2001},
	note = {Cited By (since 1996): 27Export Date: 21 November 2012Source: ScopusCODEN: JAPNAdoi: 10.1002/app.2193Language of Original Document: EnglishCorrespondence Address: Granja, P.L.; Laborat{\'o}rio de Biomateriais, Instituto de Engenharia Biomedica, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal; email: pgranja@ibmc.up.ptReferences: Dumitriu, S., (1996) Polysaccharides in Medical Applications, , Marcel Dekker: New York;Franz, G., (1986) Adv Polym Sci, 76, p. 1; 
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},
	month = {2001///},
	pages = {3341 - 3353},
	abstract = {The present study concerns the investigation of a material expected to be biocompatible and able to promote bone regeneration. For this purpose, cellulose was chemically modified by phosphorylation. Once implanted, phosphorylated cellulose could promote the formation of calcium phosphates, thus having closer resemblance to bone functionality. In a previous investigation, the obtention and the preliminary characterization of cellulose phosphate gels were reported. In the present study, the synthesis by the H                        3PO
                        4/P
                        2O
                        5/Et
                        3PO 
                        4/hexanol method was optimized in terms of reaction parameters. The structure of materials was investigated by FTIR, Raman, and solid-state 
                        31P- and 
                        13C-NMR spectroscopic studies, and X-ray diffraction. Water swelling and stability to sterilization by gamma-radiation were also assessed. It was demonstrated that the present method allows highly phosphorylated cellulose derivatives to be obtained. Cellulose triphosphates gels are described here for the first time. Products obtained were poorly crystallized monoesters, apparently not significantly affected by gamma sterilization and showed a high water swelling capability. Chemical bonding was confirmed by FTIR, Raman, and both 
                        31P- and 
                        13C-NMR spectroscopies. It was also shown that the H
                        3PO
                        4/P
                        2O
                        5/Et
                        3PO 
                        4/hexanol method provides a versatile and interesting alternative route to some of the more widely used techniques for the phosphorylation of cellulose. {\textcopyright} 2001 John Wiley \&amp; Sons, Inc. J. Appl. Polym. Sci.
},
	keywords = {13C-NMR, 2O, 3PO, 4/hexanol method, 4/P, 5/Et, Biomaterials, Cellulose derivatives, Cellulose gels, Cellulose triphosphates, Chemical bonds, Fourier transform infrared spectroscopy, Gels, H, medical textile, Nuclear magnetic resonance spectroscopy, Phosphorylation, Raman scattering, Sterilizers, Synthesis (chemical), X ray diffraction analysis},
	isbn = {00218995 (ISSN)},
	url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-0035923986\&partnerID=40\&md5=7a58f84a4d86e26d35d7d90d44aecb63},
	author = {Granja, P.L. and Pouysgu, L. and Ptraud, M. and De Jso, B. and Baquey, C. and Barbosa, M.A.}
}
