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The novel semi-biodegradable interpenetrating polymer networks based on urethane-dimethacrylate and epoxy-polyester components as alternative biomaterials

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Purpose: This paper presents the pilot study aimed at the development of new full interpenetrating polymer networks based on urethane-dimethacrylate and biodegradable epoxy-polyester as the proposition of new biomaterials with gradually emerging porosity. Methods: The urethane-dimethacrylate monomer was obtained from 4,4’-methylenebis(phenyl isocyanate) and tetraethylene glycol monomethacrylate. The redox-initiating system was employed for its radical polymerization. The epoxy-polyester was produced by oxidation of the polyester, synthesized from succinic anhydride and allyl glicydyl ether. It was cured in a step-growth process with biogenic, aliphatic amine – spermidine. The mixtures of both monomers with adequate curing agents were room temperature polymerized. The hardened materials were characterized for damping behavior and dynamic modulus, hardness, water sorption, the course of hydrolytic degradation as well as the morphology – before and during the degradation process. Results: The cured materials revealed the nonporous, dense morphology. In the hydrolytic environment, the epoxy-polyester network degraded and the porous urethane-dimethacrylate scaffold remained. The epoxy-polyester appeared to prevent the urethane-dimethacrylate from attaining a high degree of conversion, even if the polymerization rate and the molecular mobility of the latter one are higher than those of the epoxy-polyester. The most homogeneous material with the best physico-mechanical properties was obtained when the urethane-dimethacrylate content was smaller than the epoxy-polyester content, respectively 25 and 50 wt%. Conclusions: The system presented in this work could be useful in tissue engineering, where at the beginning of the tissue regeneration process it would meet the implant mechanical properties and then would deliver its porosity, facilitating the tissue regeneration process.
Rocznik
Strony
13--22
Opis fizyczny
Bibliogr. 24 poz., rys., tab., wykr.
Twórcy
  • Department of Physical Chemistry and Technology of Polymers, Silesian University of Technology, Gliwice, Poland
autor
  • Department of Physical Chemistry and Technology of Polymers, Silesian University of Technology, Gliwice, Poland
autor
  • Institute for Engineering of Polymer Materials and Dyes, Paint and Plastics Department, Gliwice, Poland
autor
  • Institute of Engineering Materials and Biomaterials, Silesian University of Technology, Gliwice, Poland
Bibliografia
  • [1] BARSZCZEWSKA-RYBAREK I., Characterization of urethanedimethacrylate derivatives as alternative monomers for the restorative composite matrix, Dent Mater, 2014, 30(12), 1336– 1344, DOI: 10.1016/j.dental.2014.09.008.
  • [2] BARSZCZEWSKA-RYBAREK I., Quantitative determination of degree of conversion in photocured poly(urethane-dimethacrylate)s by FTIR spectroscopy, J. Appl. Polym. Sci., 2012, Vol. 123(3), 1604–1611.
  • [3] BARSZCZEWSKA-RYBAREK I., GIBAS M., KURCOK M., Evaluation of the network parameter in aliphatic poly(urethane dimethacrylate)s by dynamic thermal analysis, Polymer, 2000, Vol. 41, 3129–3135.
  • [4] BARSZCZEWSKA-RYBAREK I., KORYTKOWSKA A., GIBAS M., Investigations on the structure of poly(dimethacrylate)s, Des Monomers Polym., 2001, Vol. 4(4), 301–314.
  • [5] DEB S., AIYATHURAI L., ROETHER J.A., LUKLINSKA Z.B., Development of high-viscosity, two-paste bioactive bone cements, Biomaterials, 2005, Vol. 26, 3713–3718.
  • [6] DICK J., GALE M., In Handbook of Polymer Testing: Physical Methods, R. Brown (ed.), New York Marcel, Dekker, 1999
  • [7] DOMB A.J., MANOR N., ELMALAK O., Biodegradable bone cement compositions based on acrylate and epoxide terminated poly(propylene fumarate) oligomers and calcium salt compositions, Biomaterials, 1996, Vol. 17, 411–417.
  • [8] FERRACANE J., Correlation between hardness and degree of conversion during the setting reaction of unfilled dental restorative resins, Dent. Mater., 1985, Vol. 1(1), 11–14.
  • [9] GONZÁLEZ M., CABANELAS J.C., BASELGA J., [in:] Infrared Spectroscopy – Materials Science, Engineering and Technology, T. Theophanides (ed.), Rijeka In Tech, 2012.
  • [10] HAMID Z.A., BLENCOWE A., OZCELIK B., PALMER J.A., STEVENS G.W., ABBERTON K.M., MORRISON W.A., PENINGTON A.J., QIAO G.G., Epoxy-amine synthesised hydrogel scaffolds for soft-tissue engineering, Biomaterials, 2010, Vol. 31(25), 6454–6467.
  • [11] HO J.E., BARBER T.A., VIRDI A.S., SUMNER D.R., HEALY K.E., The effect of enzymatically degradable IPN coatings on peri implant bone formation and implant fixation, J. Biomed. Mater. Res. A, 2007,Vol. 81, 720–727.
  • [12] KAUPPINEN L., Regulation of the human spermidine synthase mRNA translation by its 5'-untranslated region, FEBS Letters, 1995, Vol. 365(1), 61–65.
  • [13] ŁUKASZCZYK J., JASZCZ K., Studies of copolymerization of succinic anhydride and allyl glycidyl ether, React. Funct. Polym., 2000, Vol. 43, 25–32.
  • [14] ŁUKASZCZYK J., JASZCZ K., Synthesis and characteristics of biodegradable epoxy-polyester resins cured with glutaric anhydride, Macromol. Chem. Phys., 2002, Vol. 203, 301–308.
  • [15] ŁUKASZCZYK J., ŚMIGA-MATUSZOWICZ M., JASZCZ K., SRICHANA T., Preliminary studies on the hydrolytic degradation and biocompatibility of poly(3-allyloxy-1,2-propylene succinate), J. Biomater. Sci. Polymer Ed., 2010, Vol. 21, 691–700.
  • [16] MARTIN J.R., GUPTA M.K., PAGE J.M., YU F., DAVIDSON J.M., GUELCHER S.A., DUVALL C.L., A porous tissue engineering scaffold selectively degraded by cell-generated reactive oxygen species, Biomaterials, 2014, Vol. 35(12), 3766–3776.
  • [17] MATRICARDI P., DI MEO C., COVIELLO T., HENNINK W.E., ALHAIQUE F., Interpenetrating polymer networks polysaccharide hydrogels for drug delivery and tissue engineering, Adv. Drug. Deliv. Rev., 2013, Vol. 65, 1172–1187.
  • [18] NOWERS J.R., COSTANZO J.A., NARASIMHAN B., Structure– property relationships in acrylate/epoxy interpenetrating polymer networks: effects of the reaction sequence and composition, J. Appl. Polym. Sci., 2007, Vol. 104(2), 891–901.
  • [19] OLAH L., BORBAS L., Properties of calcium carbonatecontaining composite scaffolds, Acta Bioeng. Biomech., 2008, Vol. 10(1), 61–67.
  • [20] RUMIAN Ł., WOJAK I., SCHARNWEBER D., PAMULA E., Resorbable scaffolds modified with collagen type I or hydroxyapatite: in vitro studies on human mesenchymal stem cells, Acta Bioeng. Biomech., 2013, Vol. 15(1), 61–67.
  • [21] SANGERMANO M., COOK W.D., PAPAGNA S., GRASSINI S., Hybrid UV-cured organic–inorganic IPNs, Eur. Polym. J., 2012, Vol. 48, 1796–1804.
  • [22] SEAL B.L., OTERO T.C., PANITCH A., Polymeric biomaterials for tissue and organ regeneration, Mater Sci. Eng. R, 2001, Vol. 34, 147–230.
  • [23] SOKOŁOWSKI J., SZYNKOWSKA M.I., KLECZEWSKA J., KOWALSKI Z., SOBCZAK-KUPIEC A., PAWLACZYK A., SOKOŁOWSKI K., ŁUKOMSKA-SZYMAŃSKA M., Evaluation of resin composites modified with nanogold and nanosilver, Acta Bioeng. Biomech., 2014, Vol. 16(1), 51–61.
  • [24] VALLITTU P.K., Interpenetrating polymer networks (IPNs) in dental polymers and composites, J. Adhes. Sci. Technol., 2009, Vol. 23(7–8), 961–992.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-cf2ffcf8-49ca-42d8-8fcd-3318b1d35a95
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