Hostname: page-component-7bb8b95d7b-5mhkq Total loading time: 0 Render date: 2024-09-12T15:36:43.290Z Has data issue: false hasContentIssue false
  • English
  • Français

Osteocompatibility of Photopolymerizable Anhydride Networks

Published online by Cambridge University Press:  15 February 2011

V.R. Shastri ,
R.P. Marini ,
R.F. Padera ,
S. Kirchain ,
P. Tarcha  and
R. Langer
V.R. Shastri
Affiliation:
Department of Chemical Engineering and Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA [email protected]
R.P. Marini
Affiliation:
Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, MA 02139
R.F. Padera
Affiliation:
Department of Chemical Engineering and Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA 02139
S. Kirchain
Affiliation:
Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, MA 02139
P. Tarcha
Affiliation:
Abbott Laboratories, Hospital Products Division, Department of Advanced Drug Delivery, Abbott Park, IL 60064-3500
R. Langer
Affiliation:
Department of Chemical Engineering and Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA 02139
Get access

Abstract

A new family of polyanhydrides has been developed which can be cured photochemically to produce degradable networks. These degradable polyanhydride networks can be useful in orthopedics as bone cements and for drug delivery. This system, which is a semi-interpenetrating network (semi-IPN), has been evaluated for tissue compatibility in subcutaneous sites in rats and shown to undergo degradation by surface erosion. It was observed that the inflammatory response to the semi-IPN implants was minimal at both short (3, 6 weeks) and long (28 weeks) time points and the fibrotic response was largely absent throughout the duration of this study. Furthermore, excellent tissue infiltration and integration with good neovascularization was observed around the semi-IPN implants. The osteocompatibility and osteoconductive properties of this system have been evaluated in a longitudinal defect model in the articular surface of the distal femur in adult rabbits. This study compared the semi-IPN implants to control groups consisting of unfilled defects and PLA implants. Histological evaluation (H&E and Trichrome Masson staining) of the implant site revealed that the semi-IPN implant is osteocompatible and well tolerated by the surrounding cancellous bone and marrow constituents. The tissue reaction to the implant is characterized by an ingrowth of vascularized connective tissue and a mild fibrous capsule. Furthermore, partial to complete closure of the articular surface with fibrocartilage and fibrous tissue was observed in all experimental animals containing the semi-IPN polymer implants.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 530: Symposium CC – Biomaterials Regulating Cell Function & Tissue Development , 1998 , 93
Copyright
Copyright © Materials Research Society 1998

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1 Mojola, A., Vainionpää, S., Vihtonen, K., Mero, M., Vasenius, J., Törmälä, P., and Rokkanen, P., Clin. Ortho. Rel. Res. 268, 260 (1991).Google Scholar
2 Bone Graft and Bone Substitutes, Eds. Habal, M. B. and Reddi, A. H., Saunders, W. B. Co., Chp. 26, pg. 276 (1992).Google Scholar
3 Suganuma, J., Alexander, H., Traub, J., and Ricci, J. C., Tissue Inducing Biomaterials in MRS. Proceedings (1992).Google Scholar
4 Bone Graft and Bone Substitutes, Eds. Habal, M. B. and Reddi, A. H., Saunders, W. B. Co., pg. 399 (1992).Google Scholar
5 Savarino, L., Stea, S., Ciapetti, G., Paganetto, G., Donati, M. E., Alvergna, P. and Pizzoferrato, A., J. Biomed. Mat. Res. 29, 701 (1995) and Glowacki, J., Jasty, M., and Goldring, S., J. Bone Miner. Res. 1, 327 (1986)Google Scholar
6 Anseth, K. S., Shastri, V. R., Laurencin, C. T., and Langer, R., ACS: PMSE 74, 385 (1996).Google Scholar
7 Hill, J. W. andW. Carothers, H., J. Am. Chem. Soc. 54, 1569 (1932).Google Scholar
8 Rosen, H. G., Chang, J., Wnek, G. E., Linhardt, R., and Langer, R., Biomaterials 4, 131 (1983). and A. Domb and R. Langer, J. Polym. Sci. 23, 3375 (1987).Google Scholar
9 Shastri, V., Marini, R. P., Lindberg, J., Tarcha, P., and Langer, R., Manuscript in preparation.Google Scholar