Skip to main content

Advertisement

Log in

Tissue engineering scaffolds of mesoporous magnesium silicate and poly(ε-caprolactone)–poly(ethylene glycol)–poly(ε-caprolactone) composite

  • Published:
Journal of Materials Science: Materials in Medicine Aims and scope Submit manuscript

Abstract

Mesoporous magnesium silicate (m-MS) and poly(ε-caprolactone)–poly(ethylene glycol)–poly(ε-caprolactone) (PCL–PEG–PCL) composite scaffolds were fabricated by solvent-casting and particulate leaching method. The results suggested that the incorporation of m-MS into PCL–PEG–PCL could significantly improve the water adsorption of the m-MS/PCL–PEG–PCL composite (m-MPC) scaffolds. The in vitro degradation behavior of m-MPC scaffolds were determined by testing weight loss of the scaffolds after soaking into phosphate buffered saline (PBS), and the result showed that the degradation of m-MPC scaffolds was obviously enhanced by addition of m-MS into PCL–PEG–PCL after soaking for 10 weeks. Proliferation of MG63 cells on m-MPC was significantly higher than MPC scaffolds at 4 and 7 days. ALP activity on the m-MPC was obviously higher than MPC scaffolds at 7 days, revealing that m-MPC could promote cell differentiation. Histological evaluation showed that the introduction of m-MS into PCL–PEG–PCL enhanced the efficiency of new bone formation when the m-MPC scaffolds implanted into bone defect of rabbits. The results suggested that the inorganic/organic composite of m-MS and PCL–PEG–PCL scaffolds exhibited good biocompatibility, degradability and osteogenesis.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10
Fig. 11

Similar content being viewed by others

References

  1. Camilleri J, Sorrentino F, Damidot D. Investigation of the hydration and bioactivity of radiopacified tricalcium silicate cement, Biodentine and MTA Angelus. Dent Mater. 2013;29:580–93.

    Article  Google Scholar 

  2. Wang M. Developing bioactive composite materials for tissue replacement. Biomaterials. 2003;24:2133–51.

    Article  Google Scholar 

  3. Vallet-Regi M, Colilla M, Gonzalez B. Medical applications of organic–inorganic hybrid materials within the field of silica-based bioceramics. Chem Soc Rev. 2011;40:596–607.

    Article  Google Scholar 

  4. Verron E, Gauthier O, Janvier P, Pilet P, Lesoeur J, Bujoli B, Bouler JM. In vivo bone augmentation in an osteoporotic environment using bisphosphonate-loaded calcium deficient apatite. Biomaterials. 2010;31:7776–84.

    Article  Google Scholar 

  5. Wang S. Ordered mesoporous materials for drug delivery. Microporous Mesoporous Mater. 2009;117:1–9.

    Article  Google Scholar 

  6. Li X, Wang X, Chen H, Jiang P, Dong X, Shi J. Hierarchically porous bioactive glass scaffolds synthesized with a PUF and P123 cotemplated approach. Chem Mater. 2007;19:4322–6.

    Article  Google Scholar 

  7. Lee HS, Hwang SJ, Kim HK, Lee YS, Park J, Yu JS, Cho YW. In situ NMR study on the interaction between LiBH4–Ca (BH4) 2 and mesoporous scaffolds. J Phys Chem Lett. 2012;3:2922–7.

    Article  Google Scholar 

  8. Jia JF, Zhou HJ, Wei J, Jiang X, Hua H, Chen FP, Wei SC, Shin JW, Liu CS. Development of magnesium calcium phosphate biocement for bone regeneration. J R Soc Interface. 2010;7:1171–80.

    Article  Google Scholar 

  9. Zhao Q, Zhang P, Antonietti M, Yuan J. Poly (ionic liquid) complex with spontaneous micro-/mesoporosity: template-free synthesis and application as catalyst support. J Am Chem Soc. 2012;134:11852–5.

    Article  Google Scholar 

  10. Murphy CM, Haugh MG, Obrien FJ. The effect of mean pore size on cell attachment, proliferation and migration in collagen–glycosaminoglycan scaffolds for bone tissue engineering. Biomaterials. 2010;31:461–6.

    Article  Google Scholar 

  11. Gong C, Shi S, Wu L, Gou M, Yin Q, Guo Q, Qian Z. Biodegradable in situ gel-forming controlled drug delivery system based on thermosensitive PCL–PEG–PCL hydrogel. Part 2: Sol–gel–sol transition and drug delivery behavior. Acta Biomater. 2009;5:3358–70.

    Article  Google Scholar 

  12. Kehoe S, Zhang XF, Boyd D. FDA approved guidance conduits and wraps for peripheral nerve injury: a review of materials and efficacy. Injury. 2012;43:553–72.

    Article  Google Scholar 

  13. Gou M, Gong C, Zhang J, Wang X, Wang X, Gu Y, Qian Z. Polymeric matrix for drug delivery: Honokiol-loaded PCL–PEG–PCL nanoparticles in PEG–PCL–PEG thermosensitive hydrogel. J Biomed Mater Res. 2010;93:219–26.

    Google Scholar 

  14. Hoppe A, Guldal NS, Boccaccini AR. A review of the biological response to ionic dissolution products from bioactive glasses and glass-ceramics. Biomaterials. 2011;32:2757–74.

    Article  Google Scholar 

  15. Wu C, Miron R, Sculean A, Kaskel S, Doert T, Schulze R, Zhang Y. Proliferation, differentiation and gene expression of osteoblasts in boron-containing associated with dexamethasone deliver from mesoporous bioactive glass scaffolds. Biomaterials. 2011;32:7068–78.

    Article  Google Scholar 

  16. Kokubo T, Matsushita T, Takadama H, Kizuki T. Development of bioactive materials based on surface chemistry. J Eur Ceram Soc. 2009;29:1267–74.

    Article  Google Scholar 

  17. Nayak S, Dey T, Naskar D, Kundu SC. The promotion of osseointegration of titanium surfaces by coating with silk protein sericin. Biomaterials. 2013;34:2855–64.

    Article  Google Scholar 

  18. Wharmby MT, Mowat JP, Thompson SP, Wright PA. Extending the pore size of crystalline metal phosphonates toward the mesoporous regime by isoreticular synthesis. J Am Chem Soc. 2011;133:1266–9.

    Article  Google Scholar 

  19. Wu Z, Zhao D. Ordered mesoporous materials as adsorbents. Chem Commun. 2011;47:3332–8.

    Article  Google Scholar 

  20. Arcos D, Vallet-Regi M. Sol–gel silica-based biomaterials and bone tissue regeneration. Acta Biomater. 2010;6:2874–88.

    Article  Google Scholar 

  21. Nandakumar A, Fernandes H, de Boer J, Moroni L, Habibovic P, van Blitterswijk CA. Fabrication of bioactive composite scaffolds by electrospinning for bone regeneration. Macromol Bio. 2010;10:1365–73.

    Article  Google Scholar 

  22. Gerhardt LC, Widdows KL, Erol MM, Burch CW, Sanz-Herrera JA, Ochoa I, Boccaccini AR. The pro-angiogenic properties of multi-functional bioactive glass composite scaffolds. Biomaterials. 2011;32:4096–108.

    Article  Google Scholar 

  23. Bechara S, Wadman L, Popat KC. Electroconductive polymeric nanowire templates facilitates in vitro C17. 2 neural stem cell line adhesion, proliferation and differentiation. Acta Biomater. 2011;7:2892–901.

    Article  Google Scholar 

  24. Callahan LA, Ganios AM, Childers EP, Weiner SD, Becker ML. Primary human chondrocyte extracellular matrix formation and phenotype maintenance using RGD-derivatized PEGDM hydrogels possessing a continuous Young’s modulus gradient. Acta Biomater. 2013;9:6095–104.

    Article  Google Scholar 

  25. Wang HX, Guan SK, Wang X, Ren CX, Wang LG. In vitro degradation and mechanical integrity of Mg–Zn–Ca alloy coated with Ca-deficient hydroxyapatite by the pulse electrodeposition process. Acta Biomater. 2009;6:1743–8.

    Article  Google Scholar 

  26. Zhang Z, Ni J, Chen L, Yu L, Xu J, Ding J. Biodegradable and thermoreversible PCLA–PEG–PCLA hydrogel as a barrier for prevention of post-operative adhesion. Biomaterials. 2011;32:4725–36.

    Article  Google Scholar 

  27. Steen EJ, Kang Y, Bokinsky G, Hu Z, Schirmer A, McClure A, Keasling JD. Microbial production of fatty-acid-derived fuels and chemicals from plant biomass. Nature. 2010;463:559–62.

    Article  Google Scholar 

  28. Delcroix GJR, Garbayo E, Sindji L, Thomas O, Vanpouille-Box C, Schiller PC, Montero-Menei CN. The therapeutic potential of human multipotent mesenchymal stromal cells combined with pharmacologically active microcarriers transplanted in hemi-parkinsonian rats. Biomaterials. 2011;2:1560–73.

    Article  Google Scholar 

  29. Tang J, Peng R, Ding J. The regulation of stem cell differentiation by cell–cell contact on micropatterned material surfaces. Biomaterials. 2010;31:2470–6.

    Article  Google Scholar 

Download references

Acknowledgments

This study was supported by grants from the National Natural Science Foundation of China (No. 81000799, 81271705, 31100680 and 51173041), Nano special program of Science and Technology Development of Shanghai (No. 12nm0500400), and the Key Medical Program of Science and Technology Development of Shanghai (No. 12441902800, 12441903600).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Ming Li or Yunfei Niu.

Additional information

Wei Dong is the co-first author.

Rights and permissions

Reprints and permissions

About this article

Cite this article

He, D., Dong, W., Tang, S. et al. Tissue engineering scaffolds of mesoporous magnesium silicate and poly(ε-caprolactone)–poly(ethylene glycol)–poly(ε-caprolactone) composite. J Mater Sci: Mater Med 25, 1415–1424 (2014). https://doi.org/10.1007/s10856-014-5183-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10856-014-5183-7

Keywords

Navigation