Hostname: page-component-77c89778f8-fv566 Total loading time: 0 Render date: 2024-07-20T19:28:54.474Z Has data issue: false hasContentIssue false

Development of Cartilage and Bone During Formation of Phalanges by Tissue Engineering

Published online by Cambridge University Press:  02 July 2020

W. Landis
Affiliation:
Department of Biochemistry and Molecular Pathology, Northeastern Ohio Universities College of Medicine, Rootstown, OH44272
N. Isogai
Affiliation:
Department of Surgery, Children’s Hospital, Boston, MA02115
J. Vacanti
Affiliation:
Department of Surgery, Massachusetts General Hospital, Boston, MA02114
Get access

Extract

Treatment of human congenital malformations and for loss of tissue or organ function is a serious clinical concern, frequently supported by harvesting autogenous tissue for reconstructive surgery. This paper summarizes an alternate approach through novel tissue engineering methods and describes cell-polymer composites that could be fundamental in developing advances for digit and joint replacement. The work utilizes cells from different sources transplanted on biodegradable polymer matrices to form structures with defined shape, morphological features and composition resembling those of human phalanges and intact joints.

Polyglycolic acids (PGA) fibers (Albany International, Mansfield, MA) 15 μm in diameter were used as a mesh support for cell attachment and matrix formation. For cartilage and tendon cells, PGA alone served as a flat surface without specific shape. For bone cells, PGA was copolymerized with poly-L-lactic acid (PLLA) (Polysciences, Warrington, PA) and shaped after a human phalanx molded from cadaveric distal and middle phalangeal bones. Polymers were sterilized with ethylene oxide before use.

Type
Biomaterials
Copyright
Copyright © Microscopy Society of America

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.Cima, L. G.et al., J. Biomech. Eng., 113 (1991) 143CrossRefGoogle Scholar
2.Kim, T. H.et al., Mat. Res. Soc. Symp. Proc, 394 (1995) 91CrossRefGoogle Scholar
3.Vacanti, C. A.et al., Plast. Reconstr. Surg., 88 (1991) 753CrossRefGoogle Scholar
4.Cao, Y.et al., Transplant. Proc., 26 (1994) 3390Google Scholar