In vitro degradation of a chitosan-based osteochondral construct points to a transient effect on cellular viability

被引:1
|
作者
Pitrolino, Katherine [1 ,2 ]
Felfel, Reda [3 ,4 ,5 ]
Roberts, George [3 ]
Scotchford, Colin [3 ]
Grant, David [3 ]
Sottile, Virginie [6 ,7 ]
机构
[1] Univ Nottingham, Sch Med, Nottingham, England
[2] Univ Derby, Coll Sci & Engn, Derby, England
[3] Univ Nottingham, Fac Engn, Adv Mat Res Grp, Nottingham, England
[4] Univ Strathclyde, Mech & Aerosp Engn, Glasgow, Scotland
[5] Mansoura Univ, Fac Sci, Phys Dept, Mansoura, Egypt
[6] Univ Pavia, Dept Mol Med, Pavia, Italy
[7] Fdn IRCCS Policlin San Matteo, UOC Bioscaffolds & Transplantat, Pavia, Italy
基金
英国工程与自然科学研究理事会;
关键词
chitosan; scaffold; degradation; glucosamine; osteochondral repair; MESENCHYMAL STEM-CELLS; AUTOLOGOUS CHONDROCYTE IMPLANTATION; ARTICULAR-CARTILAGE DEFECTS; N-ACETYLATED CHITOSANS; VIVO DEGRADATION; COMPOSITE SCAFFOLDS; REPAIR; GLUCOSAMINE; GENIPIN; DIFFERENTIATION;
D O I
10.1088/1748-605X/ad6547
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Bioresorbable chitosan scaffolds have shown potential for osteochondral repair applications. The in vivo degradation of chitosan, mediated by lysozyme and releasing glucosamine, enables progressive replacement by ingrowing tissue. Here the degradation process of a chitosan-nHA based bioresorbable scaffold was investigated for mass loss, mechanical properties and degradation products released from the scaffold when subjected to clinically relevant enzyme concentrations. The scaffold showed accelerated mass loss during the early stages of degradation but without substantial reduction in mechanical strength or structure deterioration. Although not cytotoxic, the medium in which the scaffold was degraded for over 2 weeks showed a transient decrease in mesenchymal stem cell viability, and the main degradation product (glucosamine) demonstrated a possible adverse effect on viability when added at its peak concentration. This study has implications for the design and biomedical application of chitosan scaffolds, underlining the importance of modelling degradation products to determine suitability for clinical translation.
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页数:15
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