Chitosan-based hydrogels for developing a small-diameter vascular graft: in vitro and in vivo evaluation
JAMES, J.
Biologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
Centre Hospitalier Universitaire de Bordeaux [CHU Bordeaux]
Biologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
Centre Hospitalier Universitaire de Bordeaux [CHU Bordeaux]
BORDENAVE, L.
Service de médecine nucléaire [Bordeaux]
Bioingénierie tissulaire [BIOTIS]
CIC Bordeaux
< Réduire
Service de médecine nucléaire [Bordeaux]
Bioingénierie tissulaire [BIOTIS]
CIC Bordeaux
Langue
en
Article de revue
Ce document a été publié dans
Biomedical Materials. 2017-12-01, vol. 12, n° 6, p. 065003
IOP Publishing
Résumé en anglais
Aims: Vascular grafts made of synthetic polymers perform poorly in small-diameter applications (cardiac and peripheral bypass). Chitosan is a biocompatible natural polymer that can provide a novel biological scaffold for ...Lire la suite >
Aims: Vascular grafts made of synthetic polymers perform poorly in small-diameter applications (cardiac and peripheral bypass). Chitosan is a biocompatible natural polymer that can provide a novel biological scaffold for tissue engineering development. The goal of this study was to demonstrate the biocompatibility of a novel chitosan preparation in vitro and in vivo, and to assess its potential as a scaffold for vascular applications.Methods and results: A series of experiments of increasing complexity, ranging from in vitro biocompatibility and hemocompatibility tests to in vivo studies in small and large animals (rats and sheep), was performed to provide a comprehensive analysis of chitosan hydrogels' biological properties. In vitro studies established that: (i) chitosan supported human endothelial progenitor cells adhesion, proliferation and resistance to physiological shear stress; (ii) chitosan did not activate platelets, the complement system, or the intrinsic coagulation pathway. In vivo results showed: (iii) no resorption of chitosan and no chronic inflammation at 60 days in a rat heterotopic implantation model (magnetic resonance imaging and histology); (iv) no flow obstruction (Doppler ultrasound) and no thrombus formation (histology and scanning electron microscopy) at 2 h after a carotid arteriotomy repair with chitosan patches in sheep. Finally, two chitosan tubes were implanted as carotid interposition grafts for 3 days in sheep showing that chitosan was strong enough to be sutured, to withstand arterial pressure, and no flow obstruction was observed through this short period.Conclusion: Chitosan-based hydrogels displayed promising in vitro biocompatibility and hemocompatibility properties as well as in vivo short-term performance.< Réduire
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