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Synthesis and Characterization of Polyphosphazenes Modified with Hydroxyethyl Methacrylate and Lactic Acid

DOI: 10.1155/2013/645869

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Abstract:

Poly(dichlorophosphazene) was prepared by melt ring-opening polymerization of the hexachlorocyclotriphosphazene. Poly[bis(2-hydroxyethyl-methacrylate)-phosphazene] and poly[(2-hydroxyethyl-methacrylate)-graft-poly(lactic-acid)-phosphazene] were obtained by nucleophilic condensation reactions at different concentrations of the substituents. The properties of the synthesized copolymers were assessed by FTIR, 1H-NMR and 31P-NMR, thermal analysis (DSC-TGA), and electron microscopy (SEM). The copolymers have a block structure and show two 's below room temperature. They are stable up to a temperature of 100°C. The type of the substituents attached to the PZ backbone determines the morphology of the polymers. 1. Introduction Polyesters, polyorthoesters, polyanhydrides, poly(R-amino acids), and polyphosphazenes are degradable polymers that have been investigated for a variety of biomedical applications such as sutures, drug delivery systems, and scaffolds for tissue engineering [1]. Useful properties can be obtained by blending two different polymers. However, compatible polymer blends require strong molecular interactions between polymer chains [2]. Poly(organophosphazenes) offer an appealing platform for the design and synthesis of novel biodegradable polymers as well as critical advantages for the design of biologically functional macromolecules with a broad structural diversity [3], high functional density, and tailored biodegradability [4]. These polymers are of scientific and technological concern since the first work of synthesis reported by Allcock et al. [5, 6]. Polyphosphazenes (PZs) posses special characteristics, including flame-retardant properties, high resistance to oil and solvents, and feasibility for tailored properties according to the choice of organic, inorganic, or organometallic side groups [7]. As biomaterials they have inherent advantages, due to their biocompatibility and fast degradation rate. In addition, degradation residues, phosphate, ammonia, and side groups are either nontoxic when they are present in small quantities or are easily metabolized by the human body [8, 9]. Polyphosphazenes are hybrid polymers with a flexible inorganic backbone of alternating phosphorus and nitrogen atoms and organic side groups. Their composition vary from 3 to 10,000 (–N=P–) repetitive units having two substituents (–R) attached to the phosphorus atom [7]. Polyphosphazenes are synthesized by reactions with alkoxides, aryloxides, or amines from a highly reactive macromolecular intermediate, poly(dichlorophosphazene), which is prepared by thermal

References

[1]  J. Jagur-Grodzinski, “Biomedical application of functional polymers,” Reactive and Functional Polymers, vol. 39, no. 2, pp. 99–138, 1999.
[2]  N. R. Krogman, A. L. Weikel, N. Q. Nguyen, et al., “Hydrogen bonding in blends of polyesters with dipeptide-containing polyphosphazenes,” Journal of Applied Polymer Science, vol. 115, no. 1, pp. 431–437, 2010.
[3]  H. R. Allcock, “Recent developments in polyphosphazene materials science,” Current Opinion in Solid State and Materials Science, vol. 10, no. 5-6, pp. 231–240, 2006.
[4]  A. Singh, N. R. Krogman, S. Sethuraman et al., “Effect of side group chemistry on the properties of biodegradable l-alanine cosubstituted polyphosphazenes,” Biomacromolecules, vol. 7, no. 3, pp. 914–918, 2006.
[5]  H. R. Allcock and S. R. Pucher, “Polyphosphazenes with glucosyl and methylamino, trifluoroethoxy, phenoxy, or (methoxyethoxy)ethoxy side groups,” Macromolecules, vol. 24, no. 1, pp. 23–34, 1991.
[6]  H. R. Allcock and K. B. Visscher, “Preparation and characterization of poly(organophosphazene) blends,” Chemistry of Materials, vol. 4, no. 6, pp. 1182–1187, 1992.
[7]  M. Gleria and R. De Jaeger, “Aspects of Phosphazene Research,” Journal of Inorganic and Organometallic Polymers, vol. 11, no. 1, pp. 1–45, 2001.
[8]  A. K. Andrianov, Y. Y. Svirkin, and M. P. LeGolvan, “Synthesis and biologically relevant properties of polyphosphazene polyacids,” Biomacromolecules, vol. 5, no. 5, pp. 1999–2006, 2004.
[9]  D. Puppi, F. Chiellini, A. M. Piras, and E. Chiellini, “Polymeric materials for bone and cartilage repair,” Progress in Polymer Science, vol. 35, no. 4, pp. 403–440, 2010.
[10]  Y. Cui, X. Zhao, X. Tang, and Y. Luo, “Novel micro-crosslinked poly(organophosphazenes) with improved mechanical properties and controllable degradation rate as potential biodegradable matrix,” Biomaterials, vol. 25, no. 3, pp. 451–457, 2004.
[11]  P. Sharrock and G. Grégoire, “HEMA reactivity with demineralized dentin,” Journal of Dentistry, vol. 38, no. 4, pp. 331–335, 2010.
[12]  B. Gupta, N. Revagade, and J. Hilborn, “Poly(lactic acid) fiber: an overview,” Progress in Polymer Science, vol. 32, no. 4, pp. 455–482, 2007.
[13]  E. Martínez-Ceballos, Síntesis y caracterización de biopolímeros modificados para usos biomédicos [M.S. thesis], Universidad Autónoma del Estado de México, 2011.
[14]  R. Vera-Grazianoa, J. Palacios-Aiquisiraa, A. Martínez-Richab, F. Barcelóc, T. Halachevd, and V. M. Casta?od, “On the structure and physicochemical properties of acrylic compounds,” International Journal of Polymeric Materials and Polymeric Biomaterials, vol. 52, no. 2, pp. 85–95, 2003.
[15]  G. Kister, G. Cassanas, and M. Vert, “Effects of morphology, conformation and configuration on the IR and Raman spectra of various poly(lactic acid)s,” Polymer, vol. 39, no. 2, pp. 267–273, 1998.
[16]  Y. Zhou, D. Yang, X. Gao, et al., “Semi-interpenetrating polymer network hydrogels based on water-soluble N-carboxylethyl chitosan and photopolymerized poly (2-hydroxyethyl methacrylate),” Carbohydrate Polymers, vol. 75, no. 2, pp. 293–298, 2009.
[17]  L.T. Lima, R. Auras, and M. Rubino, “Processing technologies for poly(lactic acid),” Progress in Polymer Science, vol. 33, no. 8, pp. 820–852, 2008.
[18]  H. R. Allcock, K. B. Visscher, and Y.-B. Kim, “New polyphosphazenes with unsaturated side groups: Use as reaction intermediates, cross-linkable polymers, and components of interpenetrating polymer networks,” Macromolecules, vol. 29, no. 8, pp. 2721–2728, 1996.
[19]  N. R. Krogman, A. L. Weikel, N. Q. Nguyen, L. S. Nair, C. T. Laurencin, and H. R. Allcock, “Synthesis and characterization of new biomedical polymers: serine-and threonine-containing polyphosphazenes and poly(L-lactic acid) grafted copolymers,” Macromolecules, vol. 41, no. 21, pp. 7824–7828, 2008.

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