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Scaffolds for bone tissue engineering fabricated from two different materials by the rapid prototyping technique: PCL versus PLGA

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Abstract

Three dimensional tissue engineered scaffolds for the treatment of critical defect have been usually fabricated by salt leaching or gas forming technique. However, it is not easy for cells to penetrate the scaffolds due to the poor interconnectivity of pores. To overcome these current limitations we utilized a rapid prototyping (RP) technique for fabricating tissue engineered scaffolds to treat critical defects. The RP technique resulted in the uniform distribution and systematic connection of pores, which enabled cells to penetrate the scaffold. Two kinds of materials were used. They were poly(ε-caprolactone) (PCL) and poly(d, l-lactic-glycolic acid) (PLGA), where PCL is known to have longer degradation time than PLGA. In vitro tests supported the biocompatibility of the scaffolds. A 12-week animal study involving various examinations of rabbit tibias such as micro-CT and staining showed that both PCL and PLGA resulted in successful bone regeneration. As expected, PLGA degraded faster than PCL, and consequently the tissues generated in the PLGA group were less dense than those in the PCL group. We concluded that slower degradation is preferable in bone tissue engineering, especially when treating critical defects, as mechanical support is needed until full regeneration has occurred.

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References

  1. Persidis A. Tissue engineering. Nat Biotechnol. 1999;17:508–10.

    Article  CAS  Google Scholar 

  2. Sachlos E, Czernuszka JT. Making tissue engineering scaffolds work review on the application of solid freeform fabrication technology to the production of tissue engineering scaffolds. Eur Cells Mater. 2009;5:29–40.

    Google Scholar 

  3. Chen G, Ushida T, Tateishi T. Scaffold design for tissue engineering. Macromol Biosci. 2002;2:67–77.

    Article  CAS  Google Scholar 

  4. Pathiraja AG, Raju A. Biodegradable synthetic polymers for tissue engineering. Eur Cells Mater. 2003;5:1–16.

    Google Scholar 

  5. Sabir MI, Xu X, Li L. A review on biodegradable polymeric materials for bone tissue engineering applications. J Mater Sci. 2009;44:5713–24.

    Article  CAS  Google Scholar 

  6. Nair LS, Laurencin CT. Biodegradable polymers as biomaterials. Prog Polym Sci. 2007;32:762–98.

    Article  CAS  Google Scholar 

  7. Hutmacher DW. Scaffolds in tissue engineering bone and cartilage. Biomaterials. 2000;21:2529–43.

    Article  CAS  Google Scholar 

  8. Barbanti SH, Carvalho Zavaglia CA, de Rezende Duek EA. Effect of salt leaching on PCL and PLGA(50/50) resorbable scaffolds. Mater Res. 2008;11:75–80.

    Article  CAS  Google Scholar 

  9. Mooney DJ, Baldwin DF, Suh NP, Vacanti JP, Langer R. Novel approach to fabricate porous sponges of poly(d,l lactic-co-glycolic acid) without the use of organic solvents. Biomaterials. 1996;17:1417–22.

    Article  CAS  Google Scholar 

  10. Harris LD, Kim BS, Mooney DJ. Open pore biodegradable matrices formed with gas foaming. J Biomed Mater Res. 1998;42:396–402.

    Article  CAS  Google Scholar 

  11. Yun H, Kim S, Hyun Y, Heo S, Shin J. Three-dimensional mesoporous-giantporous inorganic/organic composite scaffolds for tissue engineering. Chem Mater. 2007;19:6363–6.

    Article  CAS  Google Scholar 

  12. Heo S, Kim S, Wei J, Kim DH, Hyun Y, Yun H, Kim HK, Yoon TR, Kim S, Park S, Shin JW, Shin J. In vitro and animal study of novel nano-hydroxyapatite/poly(ε-caprolactone) composite scaffolds fabricated by layer manufacturing process. Tissue Eng Part A. 2009;15:977–89.

    Article  CAS  Google Scholar 

  13. De Santis R, Gloria A, Russo T, D’Amora U, Zeppetelli S, Dionigi C, Sytcheva A, Herrmannsdörfer T, Dediu V, Ambrosio L. A basic approach toward the development of nanocomposite magnetic scaffolds for advanced bone tissue engineering. J Appl Polym Sci. 2010;122:3599–605.

    Article  Google Scholar 

  14. Kim GH, Son JG. 3D polycarprolactone (PCL) scaffold with hierarchical structure fabricated by a piezoelectric transducer (PZT)-assisted bioplotter. Appl Phys A. 2009;94:781–5.

    Article  CAS  Google Scholar 

  15. Seyednejad H, Gawlitta D, Kuiper RV, Bruin A, Nostrum CF, Vermonden T, Dhert W, Hennink WE. In vivo biocompatibility and biodegradation of 3D-printed porous scaffolds based on a hydroxyl-functionalized poly(ε-caprolactone). Biomaterials. 2012;33:4309–18.

    Article  CAS  Google Scholar 

  16. Jia YT, Zhu XY, Liu QQ. In vitro degradation of electrospun fiber membranes of PCL/PVP blends. AMR. 2011;332–334:1330–4.

    Article  Google Scholar 

  17. Sun H, Mei L, Song C, Cui X, Wang P. The in vivo degradation, absorption and excretion of PCL-based implant. Biomaterials. 2006;27:1735–40.

    Article  CAS  Google Scholar 

  18. Kim J, McBride S, Tellis B, Alvarez-Urena P, Song YH, Dean DD, Sylvia VL, Elgendy H, Ong J, Hollinger JO. Rapid-prototyped PLGA/β-TCP/hydroxyapatite nanocomposite scaffolds in a rabbit femoral defect model. Biofabrication. 2012;4:1–11.

    Article  Google Scholar 

  19. Baker SC, Rohman G, Southgate J, Cameron NR. The relationship between the mechanical properties and cell behaviour on PLGA and PCL scaffolds for bladder tissue engineering. Biomaterials. 2009;30:1321–8.

    Article  CAS  Google Scholar 

  20. Hulbert SF, Morrison SJ, Klawitter JJ. Tissue reaction to three ceramics of porous and non-porous structures. J Biomed Mater Res. 1972;6:347–74.

    Article  CAS  Google Scholar 

  21. Flatley TJ, Lynch KL, Benson M. Tissue response to implants of calcium phosphate ceramics in rabbit spine. Clin Orthop. 1983;179:246–52.

    Google Scholar 

  22. Slagada AJ, Coutinho OP, Reis RL. Bone tissue engineering: state of they are and future trends. Macromol Biosci. 2004;4:743–65.

    Article  Google Scholar 

  23. Yao J, Tao SL, Young MJ. Synthetic polymer scaffolds for stem cell transplantation in retinal tissue engineering. Polymers. 2011;3:899–914.

    Article  CAS  Google Scholar 

  24. Hoffmeister BK, Smith SR, Handley SM, Rho JY. Anisotropy of Young’s modulus of human tibial cortical bone. Med Biol Eng Comput. 2000;38:333–8.

    Article  CAS  Google Scholar 

  25. Rho JY, Ashman RB, Turner CH. Young’s modulus of trabecular and cortical bone material: ultrasonic and microtensile measurements. J Biomech. 1993;26:111–9.

    Article  CAS  Google Scholar 

  26. Karageorgiou V, Kaplan D. Porosity of 3D biomaterial scaffolds and osteogenesis. Biomaterials. 2005;26:5474–91.

    Article  CAS  Google Scholar 

  27. Schieker M, Seitz H, Drosse I, Seitz S, Mutschler W. Biomaterials as scaffold for bone tissue engineering. Eur J Trauma. 2006;2:114–24.

    Article  Google Scholar 

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Acknowledgments

This work was supported by the grants of Technology Innovation Program (10038667, Ministry of Knowledge Economy, ROK) and Priority Research Centers Program (2010-0020224, the Ministry of Education, Science and Technology).

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Correspondence to Taek Rim Yoon or Jung-Woog Shin.

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Park, S.H., Park, D.S., Shin, J.W. et al. Scaffolds for bone tissue engineering fabricated from two different materials by the rapid prototyping technique: PCL versus PLGA. J Mater Sci: Mater Med 23, 2671–2678 (2012). https://doi.org/10.1007/s10856-012-4738-8

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  • DOI: https://doi.org/10.1007/s10856-012-4738-8

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