Abstract
Many investigations have been attempted to promote calcification of synthetic polymers for applications as orthopaedic and dental implants. In this study, novel titanium dioxide (TiO2) reinforced porous poly(2-hydroxyethyl methacrylate) (pHEMA) hydrogels were synthesized. Calcification capacity of the composite polymers was examined using light microscopy, scanning electron microscopy and Fourier transform infrared spectroscopy after incubation of the materials in a simulated body fluid up to 53 days. Mechanical strength, porosity and in vitro cytotoxicity were also investigated. Calcification capacity of porous pHEMA was significantly enhanced by the addition of TiO2 particulates. Infiltration of calcium phosphate, up to 1000 μm, was observed. The diffusion capacity of calcium ions was affected by the porosity and the interconnectivity of pores in the hydrogel polymers which were influenced by the presence of TiO2 and the monomer concentration. Cell viability tests indicated that porous hydrogels containing 7.5% TiO2 were not toxic to 3T3 fibroblast cells. These results demonstrate that incorporating TiO2 nanoparticulates can promote enhanced formation of calcium phosphate whilst maintaining the porosity and interconnectivity of the hydrogel polymers and would be very useful for the development of orthopaedic tissue engineering scaffolds.
Similar content being viewed by others
References
Refojo MF. Polymers in ophthalmology: an overview. In: Williams DF, editor. Biocompatibility in clinical practice, vol. II. Boca Raton, FL: CRC Press; 1982. p. 3.
Mack EJ, Okano T, Kim SW. Biomedical applications of poly(2-hydroxyethyl methacrylate) and its copolymers. In: Peppas NA, editor. Hydrogels in medicine and pharmacy, vol. II. Boca Raton, FL: CRC Press; 1987. p. 65.
Hick CR, Crawford G, Chirla TV, Wiffen S, Vijayasekeran S, Lou X, et al. Development and clinical assessment of an artificial cornea. Prog Retin Eye Res. 2000;19:149–70. doi:10.1016/S1350-9462(99)00013-0.
Hicks CR, Morrison D, Lou X, Crawford GJ, Gadjatsy A, Constable IJ. Orbit implants: potential new directions. Expert Rev Med Devices. 2006;3:805–15. doi:10.1586/17434440.3.6.805.
Calnan JS, Pflug JJ, Chhabra AS, Raghupati N. Clinical and experimental studies of polyhydroxyethyl methacrylate gel (“Hydron”) for reconstructive surgery. Br J Plast Surg. 1971;24:113–24. doi:10.1016/S0007-1226(71)80029-2.
Tripathi RC, Tripathi BJ, Silverman RA, Rao GN. Contact lens deposits and spoilage: identification and management. Int Ophthalmol Clin. 1991;31:91–120. doi:10.1097/00004397-199103120-00012.
Bowers RWJ, Tighe BJ. Studies in the ocular compatibility of hydrogels: a review of the clinical manifestations of spoilation. Biomaterials. 1987;8:83–8. doi:10.1016/0142-9612(87)90094-9.
Lou X, Vijayasekaran S, Sugiharti R, Robertson T. Morphological and topographic effect on calcification tendency of pHEMA hydrogels. Biomaterials. 2005;26:5808–17. doi:10.1016/j.biomaterials.2005.02.034.
Chirila TV, Zainuddin. Calcification of synthetic polymers functionalized with negatively ionizable groups: a critical review. React Funct Polym. 2007;67:165–72. doi:10.1016/j.reactfunctpolym.2006.10.008.
Chirila TV, Zainuddin, Hill DJT, Whittaker AK, Kemp A. Effect of phosphate functional groups on the calcification capacity of acrylic hydrogels. Acta Biomater. 2007;3:95–102. doi:10.1016/j.actbio.2006.07.011.
Yokogawa Y, Reyes JP, Mucalo MR, Toriyama M, Kawamoto Y, Suzuki T, et al. Growth of calcium phosphate on phosphorylated chitin fibres. J Mater Sci: Mater Med. 1997;8:407–12. doi:10.1023/A:1018549404092.
Crawford GJ, Hicks CR, Lou X, Vijayasekaran S, Tan D, Chirila TV, et al. Ophthalmology. 2002;109:883. doi:10.1016/S0161-6420(02)00958-2.
Chirila TV, Hicks CR, Dalton PD, Vijayasekaran S, Lou X, Hong Y, et al. Artificial cornea. Prog Polym Sci. 1998;23:447–73. doi:10.1016/S0079-6700(97)00036-1.
Chirila TV, Constable IJ, Crawford GJ, Vijayasekaran S, Thompson DE, Chen YC, et al. Poly(2-hydroxyethyl methacrylate) sponges as implant materials: in vivo and in vitro evaluation of cellular invasion. Biomaterials. 1993;14:26–38. doi:10.1016/0142-9612(93)90072-A.
Webster TJ, Savaiano JK. Altered responses of chondrocytes to nanophase PLGA/nanophase titania composites. Biomaterials. 2004;25:1205–13. doi:10.1016/j.biomaterials.2003.08.012.
Liu HN, Slamovich EB, Webster TJ. Increased osteoblast functions among nanophase titania/poly(lactide-co-glycolide) composites of the highest nanometer surface roughness. J Biomed Mater Res A. 2006;78A:798–807. doi:10.1002/jbm.a.30734.
Tanahashi M, Yao T, Kokubo T, Minoda M, Miyamoto T, Nakamura T, et al. Apatite coating on organic polymers by a biomimetic process. J Am Ceram Soc. 1994;77:2805–8. doi:10.1111/j.1151-2916.1994.tb04508.x.
Lou X, Munro S, Wang S. Drug release characteristics of phase separation pHEMA sponge materials. Biomaterials. 2004;25:5071–80. doi:10.1016/j.biomaterials.2004.01.058.
Lou X, Wang S, Tan SY. Mathematics-aided quantitative analysis of diffusion characteristics of pHEMA sponge hydrogels. Asia-Pac J Chem Eng. 2007;2:609–17. doi:10.1002/apj.62.
Kokubo T, Takadama H. How useful is SBF in predicting in vivo bone bioactivity? Biomaterials. 2007;27:2907–15. doi:10.1016/j.biomaterials.2006.01.017.
Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983;65:55–63. doi:10.1016/0022-1759(83)90303-4.
Hicks CR, Crawford GJ, Lou X, Tan DT, Snibson GR, Sutton G, et al. Corneal replacement using a synthetic hydrogel cornea, AlphaCorT: device, preliminary outcomes and complications. Eye. 2003;17:385–92. doi:10.1038/sj.eye.6700333.
Acknowledgement
This work was supported by the Australian Research Council Discovery Project Grant (DP0557148). We thank Dr Choo-May Lai of Lions Eye Institute Perth for technical assistance in cell culture experiments.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Li, C., Zheng, YF. & Lou, X. Calcification capacity of porous pHEMA–TiO2 composite hydrogels. J Mater Sci: Mater Med 20, 2215–2222 (2009). https://doi.org/10.1007/s10856-009-3793-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10856-009-3793-2