Skip to main content
Log in

Bone-bonding behavior of three heat-treated silica gels implanted in mature rabbit bone

  • Orthopedic Surgical Forum
  • Published:
Calcified Tissue International Aims and scope Submit manuscript

Abstract

Silica gel has been reported to induce apatite nucleation on its surface in vitro and it can act as a stimulant that induces formation of chemical apatite (Ca-P) layers on the surfaces of bioactive glass-ceramics. In this study, apatite formation in response to and the bone-bonding behavior of solica gels implanted in the tibiae of mature rabbits were studied. Implants were made from three silica gels treated at 400, 800, and 1000°C, and the effects of such heat treatment on the above parameters were investigated. The silica gel was made by hydrolysis and polycondensation of tetraethoxysilane in aqueous solution containing polyethylene glycol. Rectangular implants (15 mm × 10 mm × 2 mm) of each heat-treated silica gel were implanted into both tibial bones of mature male rabbits, which were killed 4 or 8 weeks after implantation, and the tibiae containing the implants were dissected out. The bone-implant interfaces were investigated using Giemsa surface staining, contact microradiography, scanning electron microscopy-electron probe microanalysis, and X-ray diffraction. Histologically, no bonding of bone to any of the silica gels was observed at any time postimplantation. Soft tissue was observed at the bone-silica gel interface, but there were no giant foreign body or inflammatory cells. A Ca-P-rich layer was observed only on small areas of the surfaces of the silica gels treated at 400 and 800°C 4 and 8 weeks after implantation. X-Ray diffraction analysis confirmed the presence of hydroxyapatite in these Ca-P-rich layers. At no time after implantation was a Ca-P-rich layer observed on the surface of silica gel treated at 1000°C. It is thought that a special type of silanol group, which forms on silica gel treated below 800°C, is responsible for the apatite nucleation. A Ca-P layer does not always form reliably on the surfaces of silica gels.

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.

Similar content being viewed by others

References

  1. Kokubo T, Shigematsu M, Nagashima Y, Tashiro M, Nakamura T, Yamamuro T, Higashi S (1982) Apatite-and wollastonite-containing glass-ceramic for prosthetic application. Bull Inst Chem Res Kyoto Univ 60:260–268

    Google Scholar 

  2. Nakamura T, Yamamuro T, Higashi S, Kokubo T, Itoo S (1985) A new glass-ceramic for bone replacement: evaluation of its bonding ability to bone tissue. J Biomed Mater Res 19:685–698

    Google Scholar 

  3. Kitsugi T, Yamamuro T, Nakamura T, Higashi S, Kakutani Y, Hyakuna K, Ito S, Kokubo T, Takagi M, Shibuya T (1986) Bone bonding behavior of three kinds of apatite-containing glass-ceramics. J Biomed Mater Res 20:1295–1307

    Google Scholar 

  4. Kitsugi T, Yamamuro T, Nakamura T, Kokubo T, Shibuya T, Takagi M (1987) SEM-EPMA observation of three types of apatite-containing glass-ceramics implanted in bone: the variance of a Ca-P rich layer. J Biomed Mater Res 21:1255–1271

    Google Scholar 

  5. Kitsugi T, Yamamuro T, Nakamura T, Oka M, Kokubo T (1993) Influence of disodium (1-hydroxythylidene) diphosphonate on bonding between glass-ceramics containing apatite and wollastonite and mature male rabbit bone. Calcif Tissue Int 52:378–385

    Google Scholar 

  6. Kokubo T (1990) Surface chemistry of bioactive glass-ceramics. J Non-crystalline Solids 120:138–151

    Google Scholar 

  7. Kokubo T, Kushitani H, Sakka S, Kitsugi T, Yamamuro T (1990) Solutions able to reproduce in vivo surface-structure changes in bioactive glass-ceramic A-W3. J Biomed Mater Res 24:721–734

    Google Scholar 

  8. Kokubo T, Ito S, Huang ZT, Hayashi T, Sakka S, Kitsugi T, Yamamuro T (1990) Ca, P-rich layer formed on high-strength bioactive glass-ceramic A-W. J Biomed Mater Res 24:331–343

    Google Scholar 

  9. Pereira MM, Clark AE, Hench LL (1994) Calcium phosphate formation on sol-gel-derived bioactive glasses in vitro. J Biomed Mater Res 28:693–698

    Google Scholar 

  10. Li P, Ohtsuki C, Kokubo T, Nakanishi K, Soga N, Nakamura T, Yamamuro T (1993) Process of formation of bone-like apatite layer on silica gel. J Mater Sci: Mater Med 4:127–131

    Google Scholar 

  11. Li P, Ohtsuki C, Kokubo T, Nakanishi K, Soga N, Nakamura T, Yamamuro T (1992) Apatite formation induced by silica gel in a simulated body fluid. J Am Ceram Soc 75:2094–2097

    Google Scholar 

  12. Li P, Otsuki C, Kokubo T, Nakanishi K, Soga N, Nakamura T, Yamamuro T (1993) Effects of ions in aqueous media on hydroxyapatite induction by silica gel and its relevance to bioactivity of bioactive glasses and glass-ceramics. J Appl Biomaterials 4:221–229

    Google Scholar 

  13. Li P, Ohtsuki C, Kokubo T, Nakanishi K, Soga N, de Groot K (1994) The role of hydrated silica, titania, and alumina in inducing apatite on implants. J Biomed Mater Res 28:7–15

    Google Scholar 

  14. Gross UM, Strunz V (1977) Surface staining of sawed sections of undecalcified bone containing alloplastic implants. Stain Technol 52:217–219

    Google Scholar 

  15. Carlisl EM (1970) Silicon: a possible factor in bone calcification. Science 167:279–280

    Google Scholar 

  16. Landis WJ, Lee DD, Brenna JT, Chandra S, Morrison GH (1986) Detection and localization of silicon and associated elements in vertebrate bone tissue by imaging ion microscopy. Calcif Tissue Int 38:52–59

    Google Scholar 

  17. Nagase M, Abe Y, Chigira M, Udagawa E (1981) Toxicology and biocompatibility of bioglasses. J Biomed Mater Res 15:805–817

    Google Scholar 

  18. Kangasniemi IMO, Vahatalo K, Happonen R-P, Yli-Urpo A, de Groot K (1994) In vivo reactions of Ca, P particle containing surface reactive glasses. J Biomed Mater Res 28:993–1002

    Google Scholar 

  19. Kawanabe K, Yamamuro T, Nakamura T, Kotani S (1991) Effects of injecting massive amounts of bioactive ceramics in mice. J Biomed Mater Res 25:117–128

    Google Scholar 

  20. West JH, Hench LL (1991) Reaction kinetics of bioactive ceramics, part V: molecular orbital modeling of bioactive glass surface reactions. pp. 75–86 In: Yamamuro T, Kokubo T, Nakamura T (eds) Bioceramics, vol 5. Kobunshi Kankokai. Kyoto

    Google Scholar 

  21. Kitsugi T, Yamamuro T, Nakamura T, Kokubo T (1989) Bonding behavior of MgO-CaO-SiO2-P2O5-CaF2 glass (mother glass of A.W-glass ceramics). J Biomed Mater Res 23:631–648

    Google Scholar 

  22. Hench LL, Ethridge EC (1982) Biomaterials: an interfacial approach. In: Biophysics and bioengineerings series, vol 4. Academic Press, New York, pp 62–86, 126–148

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Deceased

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kitsugi, T., Nakamura, T., Oka, M. et al. Bone-bonding behavior of three heat-treated silica gels implanted in mature rabbit bone. Calcif Tissue Int 57, 155–160 (1995). https://doi.org/10.1007/BF00298437

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00298437

Key words

Navigation