BackgroundOsteochondral defects significantly affect patients¿ quality of life and represent challenging tissue lesions, because of the poor regenerative capacity of cartilage. Tissue engineering has long sought to promote cartilage repair, by employing artificial scaffolds to enhance cell capacity to deposit new cartilage. An ideal biomaterial should closely mimic the natural environment of the tissue, to promote scaffold colonization, cell differentiation and the maintenance of a differentiated cellular phenotype. The present study evaluated chitosan scaffolds enriched with D-(+) raffinose in osteochondral defects in rabbits. Cartilage defects were created in distal femurs, both on the condyle and on the trochlea, and were left untreated or received a chitosan scaffold. The animals were sacrificed after 2 or 4 weeks, and samples were analysed microscopically.ResultsThe retrieved implants were surrounded by a fibrous capsule and contained a noticeable inflammatory infiltrate. No hyaline cartilage was formed in the defects. Although defect closure reached approximately 100% in the control group after 4 weeks, defects did not completely heal when filled with chitosan. In these samples, the lesion contained granulation tissue at 2 weeks, which was then replaced by fibrous connective tissue by week 4. Noteworthy, chitosan never appeared to be integrated in the surrounding cartilage.ConclusionsIn conclusion, the present study highlights the limits of D-(+) raffinose-enriched chitosan for cartilage regeneration and offers useful information for further development of this material for tissue repair.

Chitosan-based scaffold modified with D-(+) raffinose for cartilage repair: an in vivo study / Ravanetti, Francesca; Galli, Carlo; Manfredi, Edoardo; Cantoni, Anna Maria; Scarpa, Edoardo; Macaluso, Guido Maria; Cacchioli, Antonio. - In: JOURNAL OF NEGATIVE RESULTS IN BIOMEDICINE. - ISSN 1477-5751. - 14:1(2015), p. 2. [10.1186/s12952-014-0021-5]

Chitosan-based scaffold modified with D-(+) raffinose for cartilage repair: an in vivo study

RAVANETTI, Francesca;GALLI, Carlo;MANFREDI, Edoardo;CANTONI, Anna Maria;MACALUSO, Guido Maria;CACCHIOLI, Antonio
2015

Abstract

BackgroundOsteochondral defects significantly affect patients¿ quality of life and represent challenging tissue lesions, because of the poor regenerative capacity of cartilage. Tissue engineering has long sought to promote cartilage repair, by employing artificial scaffolds to enhance cell capacity to deposit new cartilage. An ideal biomaterial should closely mimic the natural environment of the tissue, to promote scaffold colonization, cell differentiation and the maintenance of a differentiated cellular phenotype. The present study evaluated chitosan scaffolds enriched with D-(+) raffinose in osteochondral defects in rabbits. Cartilage defects were created in distal femurs, both on the condyle and on the trochlea, and were left untreated or received a chitosan scaffold. The animals were sacrificed after 2 or 4 weeks, and samples were analysed microscopically.ResultsThe retrieved implants were surrounded by a fibrous capsule and contained a noticeable inflammatory infiltrate. No hyaline cartilage was formed in the defects. Although defect closure reached approximately 100% in the control group after 4 weeks, defects did not completely heal when filled with chitosan. In these samples, the lesion contained granulation tissue at 2 weeks, which was then replaced by fibrous connective tissue by week 4. Noteworthy, chitosan never appeared to be integrated in the surrounding cartilage.ConclusionsIn conclusion, the present study highlights the limits of D-(+) raffinose-enriched chitosan for cartilage regeneration and offers useful information for further development of this material for tissue repair.
Chitosan-based scaffold modified with D-(+) raffinose for cartilage repair: an in vivo study / Ravanetti, Francesca; Galli, Carlo; Manfredi, Edoardo; Cantoni, Anna Maria; Scarpa, Edoardo; Macaluso, Guido Maria; Cacchioli, Antonio. - In: JOURNAL OF NEGATIVE RESULTS IN BIOMEDICINE. - ISSN 1477-5751. - 14:1(2015), p. 2. [10.1186/s12952-014-0021-5]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2786051
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