Development and in vitro assessment of a bi-layered chitosan-nano-hydroxyapatite osteochondral scaffold

被引:37
|
作者
Pitrolino, Katherine A. [1 ]
Felfel, Reda M. [2 ,3 ]
Pellizzeri, Laura Macri [1 ]
McLaren, Jane [4 ]
Popov, Alexander A. [1 ,2 ]
Sottile, Virginie [1 ,5 ]
Scotchford, Colin A. [2 ]
Scammell, Brigitte E. [4 ]
Roberts, George A. F. [2 ]
Grant, David M. [2 ]
机构
[1] Univ Nottingham, Sch Med, Acad Unit Translat Med Sci, Nottingham, England
[2] Univ Nottingham, Fac Engn, Adv Mat Res Grp, Nottingham, England
[3] Mansoura Univ, Fac Sci, Phys Dept, Mansoura 35516, Egypt
[4] Univ Nottingham, Sch Med, Acad Unit Inflammat Injury & Recovery Sci, Nottingham, England
[5] Univ Pavia, Dept Mol Med, Pavia, Italy
基金
英国工程与自然科学研究理事会;
关键词
Chitosan; Osteochondral scaffold; Nano-hydroxyapatite; Graded porosity; Mesenchymal stem cells; Tissue engineering; AUTOLOGOUS CHONDROCYTE IMPLANTATION; MESENCHYMAL STEM-CELLS; OSTEOGENIC DIFFERENTIATION; BONE-MARROW; REPAIR; DEGRADATION; PHOSPHATE; HYDROGEL; GENIPIN; MICROFRACTURE;
D O I
10.1016/j.carbpol.2022.119126
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An innovative approach was developed to engineer a multi-layered chitosan scaffold for osteochondral defect repair. A combination of freeze drying and porogen-leaching out methods produced a porous, bioresorbable scaffold with a distinct gradient of pore size (mean = 160-275 mu m). Incorporation of 70 wt% nanohydroxyapatite (nHA) provided additional strength to the bone-like layer. The scaffold showed instantaneous mechanical recovery under compressive loading and did not delaminate under tensile loading. The scaffold supported the attachment and proliferation of human mesenchymal stem cells (MSCs), with typical adherent cell morphology found on the bone layer compared to a rounded cell morphology on the chondrogenic layer. Osteogenic and chondrogenic differentiation of MSCs preferentially occurred in selected layers of the scaffold in vitro, driven by the distinct pore gradient and material composition. This scaffold is a suitable candidate for minimally invasive arthroscopic delivery in the clinic with potential to regenerate damaged cartilage and bone.
引用
收藏
页数:13
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