全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Silica Aerogel Improves the Biocompatibility in a Poly- -Caprolactone Composite Used as a Tissue Engineering Scaffold

DOI: 10.1155/2013/402859

Full-Text   Cite this paper   Add to My Lib

Abstract:

Poly- -caprolactone (PCL) is a biodegradable polyester that has received great attentions in clinical and biomedical applications as sutures, drug delivery tool, and implantable scaffold material. Silica aerogel is a material composed of SiO2 that has excellent physical properties for use in drug release formulations and biomaterials for tissue engineering. The current study addresses a composite of silica aerogel with PCL as a potential bone scaffold material for bone tissue engineering. The biocompatibility evaluation of this composite indicates that the presence of silica aerogel effectively prevented any cytotoxic effects of the PCL membrane during extended tissue culture periods and improved the survival, attachment, and growth of 3T3 cells and primary mouse osteoblastic cells. The beneficial effect of silica aerogel may be due to neutralization of the acidic condition that develops during PCL degradation. Specifically, it appears that silica aerogel to PCL wt/wt ratio at 0.5?:?1 maintains a constant pH environment for up to 4 weeks and provides a better environment for cell growth. 1. Introduction Poly- -caprolactone (PCL) is one of the polyester polymers that possess several advantages including benign biocompatibility, low cost, biodegradability, and easy fabrication. Previous studies have suggested that PCL was a good candidate biomaterial for cartilage tissue engineering in terms of cell attachment, proliferation, and matrix production [1–4]. Positive effects of PCL composites on osteoblasts when using as bone graft substitute have also been demonstrated [3, 5–7]. In addition, PCL has been investigated for reconstruction of many other tissues such as skin, nerve, and retina [8]. The major drawback to the use of PCL as tissue scaffold is the production of an acidic environment during the PCL degradation process, which may influence the local microenvironment and cell viability. Aerogels are materials with extremely high porosity and a high surface area [9]. They are usually produced by supercritical extraction of a stable gel using sol-gel technology [10, 11]. Aerogels have useful properties such as high heat insulation [12, 13], low refractive index [14, 15], and dielectric constant close to gas properties [16, 17]. For the past decade, aerogels have gained increased attention in the biomedical field as a potential tool for targeted drug delivery systems [18–20]. Silica aerogel is a material composed of SiO2 with physical properties that include (1) amorphous properties with extremely low bulk density (0.003–0.35?g/cm3), (2) optical

References

[1]  R. Izquierdo, N. Garcia-Giralt, M. T. Rodriguez et al., “Biodegradable PCL scaffolds with an interconnected spherical pore network for tissue engineering,” Journal of Biomedical Materials Research A, vol. 85, no. 1, pp. 25–35, 2008.
[2]  J. M. Kemppainen and S. J. Hollister, “Differential effects of designed scaffold permeability on chondrogenesis by chondrocytes and bone marrow stromal cells,” Biomaterials, vol. 31, no. 2, pp. 279–287, 2010.
[3]  H. W. Kim, J. C. Knowles, and H. E. Kim, “Hydroxyapatite/poly(ε-caprolactone) composite coatings on hydroxyapatite porous bone scaffold for drug delivery,” Biomaterials, vol. 25, no. 7-8, pp. 1279–1287, 2004.
[4]  W. J. Li, R. Tuli, C. Okafor et al., “A three-dimensional nanofibrous scaffold for cartilage tissue engineering using human mesenchymal stem cells,” Biomaterials, vol. 26, no. 6, pp. 599–609, 2005.
[5]  L. Calandrelli, B. Immirzi, M. Malinconico et al., “Natural and synthetic hydroxyapatite filled PCL: mechanical properties and biocompatibility analysis,” Journal of Bioactive and Compatible Polymers, vol. 19, no. 4, pp. 301–313, 2004.
[6]  S. C. Rizzi, D. J. Heath, A. G. A. Coombes, N. Bock, M. Textor, and S. Downes, “Biodegradable polymer/hydroxyapatite composites: surface analysis and initial attachment of human osteoblasts,” Journal of Biomedical Materials Research, vol. 55, no. 4, pp. 475–486, 2001.
[7]  H. Yu, P. J. VandeVord, L. Mao, H. W. Matthew, P. H. Wooley, and S. Y. Yang, “Improved tissue-engineered bone regeneration by endothelial cell mediated vascularization,” Biomaterials, vol. 30, no. 4, pp. 508–517, 2009.
[8]  L. Ghasemi-Mobarakeh, M. P. Prabhakaran, M. Morshed, M. H. Nasr-Esfahani, and S. Ramakrishna, “Bio-functionalized PCL nanofibrous scaffolds for nerve tissue engineering,” Materials Science and Engineering C, vol. 30, no. 8, pp. 1129–1136, 2010.
[9]  H. Ren and L. Zhang, “In situ growth approach for preparation of Au nanoparticle-doped silica aerogel,” Colloids and Surfaces A, vol. 372, no. 1–3, pp. 98–101, 2010.
[10]  M. Alnaief and I. Smirnova, “In situ production of spherical aerogel microparticles,” Journal of Supercritical Fluids, vol. 55, no. 3, pp. 1118–1123, 2011.
[11]  J. Ge, Y. Z. Zhang, M. Li, and L. Song, “Research of bioactive PLGA tissue engineering materials processed by sol-gel method,” Polymeric Materials Science and Engineering, vol. 27, no. 10, pp. 169–172, 2011.
[12]  W. C. Ackerman, M. Vlachos, S. Rouanet, and J. Fruendt, “Use of surface treated aerogels derived from various silica precursors in translucent insulation panels,” Journal of Non-Crystalline Solids, vol. 285, no. 1–3, pp. 264–271, 2001.
[13]  A. Abu Obaid, S. Andersen, J. W. Gillespie Jr., R. Vaidyanathan, and A. Studley, “Investigation of thermal and acoustic performance of aerogel-based glass fiber composites,” in Proceedings of the International SAMPE Symposium and Exhibition, pp. 2279–2290, May 2005.
[14]  N. D. Hegde and A. V. Rao, “Effect of processing temperature on gelation and physical properties of low density TEOS based silica aerogels,” Journal of Sol-Gel Science and Technology, vol. 38, no. 1, pp. 55–61, 2006.
[15]  E. J. Lerner, “Less is more with aerogels,” Industrial Physicist, vol. 10, no. 5, pp. 26–30, 2004.
[16]  H. Fan, H. R. Bentley, K. R. Kathan, P. Clem, Y. Lu, and C. J. Brinker, “Self-assembled aerogel-like low dielectric constant films,” Journal of Non-Crystalline Solids, vol. 285, no. 1-3, pp. 79–83, 2001.
[17]  G. S. Kim and S. H. Hyun, “Synthesis and characterization of silica aerogel films for inter-metal dielectrics via ambient drying,” Thin Solid Films, vol. 460, no. 1-2, pp. 190–200, 2004.
[18]  M. Alnaief and I. Smirnova, “Effect of surface functionalization of silica aerogel on their adsorptive and release properties,” Journal of Non-Crystalline Solids, vol. 356, no. 33-34, pp. 1644–1649, 2010.
[19]  I. Smirnova, S. Suttiruengwong, and W. Arlt, “Feasibility study of hydrophilic and hydrophobic silica aerogels as drug delivery systems,” Journal of Non-Crystalline Solids, vol. 350, pp. 54–60, 2004.
[20]  I. Smirnova, J. Mamic, and W. Arlt, “Adsorption of drugs on silica aerogels,” Langmuir, vol. 19, no. 20, pp. 8521–8525, 2003.
[21]  S. Sakka, “Application of sol-gel technolgy,” in Handbook of Sol-Gel Science and Technology, pp. 1–138, Kluwer Academic, New York, NY, USA, 2005.
[22]  Z. Jia, J. Zhang, C. Jia, J. Nie, and K. Chu, “Preparation and characterization of mechanical properties of carbon nanotube/45S5Bioglass composites for biologic applications,” Materials Science and Engineering A, vol. 528, no. 3, pp. 1553–1557, 2011.
[23]  H. R. Stanley, M. B. Hall, A. E. Clark, C. J. King III, L. L. Hench, and J. J. Berte, “Using 45S5 bioglass cones as endosseous ridge maintenance implants to prevent alveolar ridge resorption: a 5-year evaluation,” International Journal of Oral and Maxillofacial Implants, vol. 12, no. 1, pp. 95–105, 1997.
[24]  I. D. Xynos, M. V. J. Hukkanen, J. J. Batten, L. D. Buttery, L. L. Hench, and J. M. Polak, “Bioglass 45S5 stimulates osteoblast turnover and enhances bone formation in vitro: implications and applications for bone tissue engineering,” Calcified Tissue International, vol. 67, no. 4, pp. 321–329, 2000.
[25]  L. L. Hench, R. J. Splinter, W. C. Allen, and T. K. Greenlee, “Bonding mechanisms at the interface of ceramic prosthetic materials,” Journal of Biomedical Materials Research, vol. 5, no. 6, pp. 117–141, 1972.
[26]  A. L. Andrade, D. M. Souza, W. A. Vasconcellos, R. V. Ferreira, and R. Z. Domingues, “Tetracycline and/or hydrocortisone incorporation and release by bioactive glasses compounds,” Journal of Non-Crystalline Solids, vol. 355, no. 13, pp. 811–816, 2009.
[27]  M. Corno and A. Pedone, “Vibrational features of phospho-silicate glasses: periodic B3LYP simulations,” Chemical Physics Letters, vol. 476, no. 4–6, pp. 218–222, 2009.
[28]  G. Jiang, M. E. Evans, I. A. Jones, C. D. Rudd, C. A. Scotchford, and G. S. Walker, “Preparation of poly(ε-caprolactone)/continuous bioglass fibre composite using monomer transfer moulding for bone implant,” Biomaterials, vol. 26, no. 15, pp. 2281–2288, 2005.
[29]  P. P. Lopes, B. J. M. L. Ferreira, N. A. F. Almeida, M. C. Fredel, M. H. V. Fernandes, and R. N. Correia, “Preparation and study of in vitro bioactivity of PMMA-co-EHA composites filled with a Ca3(PO4)2-SiO2-MgO glass,” Materials Science and Engineering C, vol. 28, no. 4, pp. 572–577, 2008.
[30]  S. N. Salama, H. Darwish, and H. A. Abo-Mosallam, “HA forming ability of some glass-ceramics of the CaMgSi2O6-Ca5(PO4)3F-CaAl2SiO6 system,” Ceramics International, vol. 32, no. 4, pp. 357–364, 2006.
[31]  Y. Zhou, H. Li, K. Lin, W. Zhai, W. Gu, and J. Chang, “Effect of heat treatment on the properties of SiO2-CaO-MgO-P2O5 bioactive glasses.,” Journal of Materials Science Materials in Medicine, vol. 23, no. 9, pp. 2101–2108, 2012.
[32]  F. Sabri, J. D. Boughter Jr., D. Gerth et al., “Histological evaluation of the biocompatibility of polyurea crosslinked silica aerogel implants in a rat model: a pilot study,” PLoS ONE, vol. 7, no. 12, Article ID e50686, 2012.
[33]  Y. Jiang, T. Jia, W. Gong, P. H. Wooley, and S. Y. Yang, “Titanium particle-challenged osteoblasts promote osteoclastogenesis and osteolysis in a murine model of periprosthestic osteolysis,” Acta Biomaterialia, vol. 9, no. 7, pp. 7564–7572, 2013.
[34]  H. Yu, P. H. Wooley, and S. Yang, “Biocompatibility of poly-caprolactone-hydroxyapatite composite on mouse bone marrow-derived osteoblasts and endothelial cells,” Journal of Orthopaedic Surgery and Research, vol. 4, no. 1, article 5, 2009.
[35]  Y. Jiang, T. Jia, W. Gong, P. H. Wooley, and S.-Y. Yang, “Effects of Ti, PMMA, UHMWPE, and Co–Cr wear particles on differentiation and functions of bone marrow stromal cells,” Journal of Biomedical Materials Research A, 2013.
[36]  H. L. Wamocha, H. E. Misak, Z. Song et al., “Cytotoxicity of release products from magnetic nanocomposites in targeted drug delivery,” Journal of Biomaterials Applications, vol. 27, no. 6, pp. 661–667, 2013.
[37]  K. T. Shalumon, K. H. Anulekha, K. P. Chennazhi, H. Tamura, S. V. Nair, and R. Jayakumar, “Fabrication of chitosan/poly(caprolactone) nanofibrous scaffold for bone and skin tissue engineering,” International Journal of Biological Macromolecules, vol. 48, no. 4, pp. 571–576, 2011.
[38]  N. S. Binulal, M. Deepthy, N. Selvamurugan et al., “Role of nanofibrous poly(caprolactone) scaffolds in human mesenchymal stem cell attachment and spreading for in vitro bone tissue engineering-response to osteogenic regulators,” Tissue Engineering A, vol. 16, no. 2, pp. 393–404, 2010.
[39]  A. Polini, D. Pisignano, M. Parodi, R. Quarto, and S. Scaglione, “Osteoinduction of human mesenchymal stem cells by bioactive composite scaffolds without supplemental osteogenic growth factors,” PLoS ONE, vol. 6, no. 10, Article ID e26211, 2011.

Full-Text

Contact Us

[email protected]

QQ:3279437679

WhatsApp +8615387084133