Skip to main content
Log in

Tissue reactions to lead samples in a late infection rat model

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

Abstract

Tissue reactions to rat lead samples, modelling for clinically used leads, were investigated in a late infection model, in which injection of bacteria was performed after a 3-week encapsulation process. At the site of injection, detachment of the original fibrous capsule, wound fluid infiltration, fibrin formation and granulocyte and macrophage infiltrations, occurred. Spreading of infection did not occur via the generally assumed direct bacterial adhesion to materials, but through blood vessels at the outside of capsules and through wound fluid passage at the interface and in the lumen of the lead sample. At day 5, infection had spread all over, but, apart from two small abscesses, seemed to be suppressed at day 10. However, probably due to luminal bacterial growth, at weeks 3 and 6 the reaction intensified showing larger abscesses with accumulations of lymphocytes. The results of this study represent a good basis for further studies aimed at developing infection-resistent lead material. Research efforts are first directed on modification of material surfaces to provide controlled release of antimicrobial agents.

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. J. BLACK, “Biological performance of materials: Fundamentals of biocompatibility”, 2nd Edn (Marcel Dekker, New York, 1992).

    Google Scholar 

  2. J. DANKERT, A. H. HOGT and J. FEIJEN, CRC Crit. Rev. Biocompat. 2 (1986) 219.

    Google Scholar 

  3. S. H. DOUGHERTY and R. L. SIMMONS. Curr. Probl. Surg. 19 (1982) 217.

    Google Scholar 

  4. F. J. SCHOEN, American Society for Artificial Organs, J. 33 (1987) 8.

    Google Scholar 

  5. A. F.VON RECUM and E. BARTH. J. Invest. Surg. 2 (1989) 351.

    Google Scholar 

  6. P. B.VAN WACHEM, M. J. A.VAN LUYN, E. H. BLAAUW, D. RAATJES, P. T. CAHALAN and M. HENDRIKS. J. Mater. Sci. Mater. Med. 5 (1994) 628.

    Google Scholar 

  7. A. E. KHOURY, K. LAM, B. ELLIS and J. W. COSTERTON. American Society for Artificial Organs, J 38 (1991) M174.

  8. G. D. CHRISTENSEN, L. M. BADDOUR and W. A. SIMPSON. Zbl. Bakt. Suppl. 16 (1987) 103.

    Google Scholar 

  9. J. W. COSTERTON, Rev. Infect. Dis. 6 (suppl. 3) (1984) S608.

  10. W. P. REED and R. C. WILLIAMS. J. Chron. Dis. 31 (1978) 67.

    Google Scholar 

  11. K. MERRITT, J. W. SHAFER and S. A. BROWN. J. Biomed. Mater. Res. 13 (1979) 101.

    Google Scholar 

  12. J. M. ANDERSON. Cardiovasc. Pathol. 2 (1993) 335.

    Google Scholar 

  13. F. A. WALDVOGEL. in “Principles and practice of infectious diseases”, 3rd Edn (Churchill Livingston, New York, 1990) pp. 1489–1511.

    Google Scholar 

  14. A. K. ABBAS, A. H. LICHTMAN and J. S. POBER. “Cellular and molecular immunology” (W. B. Saunders, Philadelphia, PA, 1991).

    Google Scholar 

  15. J. BROSTOFF, G. K. SCADDING, D. K. MALE and I. M. ROITT. “Clinical immunology” (Gower Medical Publishing, London, 1991).

    Google Scholar 

  16. J. B.VAN DER MEER and M. C. J. M.DE JONG. Neth. J. Med. 40 (1992) 244.

    Google Scholar 

  17. B. JANSEN, J. SCHIERHOLZ, F. SCHUMACHER-PERDREAU, G. PETERS and G. PULVERER. Adv. Biomater. 9 (1990) 117.

    Google Scholar 

  18. G. COLOMB and A. SHPIGELMAN. J. Biomed. Mater. Res. 25 (1991) 937.

    Google Scholar 

  19. B. JANSEN, F. SCHUMACHER-PERDREAU, G. PETERS and G. PULVERER, J. Inv. Surg. 2 (1989) 361.

    Google Scholar 

  20. A. G. GRISTINA. Science 237 (1987) 1588.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Van Wachem, P.B., Van Luyn, M.J.A., De Wit, A.W. et al. Tissue reactions to lead samples in a late infection rat model. J Mater Sci: Mater Med 7, 415–423 (1996). https://doi.org/10.1007/BF00122011

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00122011

Keywords

Navigation