Treatment of full-thickness cartilage defects relies on osteochondral bilayer grafts, which mimic the microenvironment and structure of the two affected tissues: articular cartilage and subchondral bone. However, the integrity and stability of the grafts are hampered by the presence of a weak interphase, generated by the layering processes of scaffold manufacturing. We describe here the design and development of a bilayer monolithic osteochondral graft, avoiding delamination of the two distinct layers but preserving the cues for selective generation of cartilage and bone. A highly porous polycaprolactone-based graft was obtained by combining solvent casting/particulate leaching techniques. Pore structure and interconnections were designed to favour in vivo vascularization only at the bony layer. Hydroxyapatite granules were added as bioactive signals at the site of bone regeneration. Unconfined compressive tests displayed optimal elastic properties and low residual deformation of the graft after unloading (< 3%). The structural integrity of the graft was successfully validated by tension fracture tests, revealing high resistance to delamination, since fractures were never displayed at the interface of the layers (n=8). Ectopic implantation of grafts in nude mice, after seeding with bovine trabecular bone-derived mesenchymal stem cells and bovine articular chondrocytes, resulted in thick areas of mature bone surrounding ceramic granules within the bony layer, and a cartilaginous alcianophilic matrix in the chondral layer. Vascularization was mostly observed in the bony layer, with a statistically significant higher blood vessel density and mean area. Thus, the easily generated osteochondral scaffolds, since they are mechanically and biologically functional, are suitable for tissue-engineering applications for cartilage repair. Copyright (c) 2012 John Wiley & Sons, Ltd.
机构:
North Dakota State Univ, Dept Civil & Environm Engn, Fargo, ND 58105 USA
North Dakota State Univ, Ctr Engn Canc Test Beds, Fargo, ND 58105 USANorth Dakota State Univ, Dept Civil & Environm Engn, Fargo, ND 58105 USA
Katti, Dinesh R.
Katti, Kalpana S.
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North Dakota State Univ, Dept Civil & Environm Engn, Fargo, ND 58105 USA
North Dakota State Univ, Ctr Engn Canc Test Beds, Fargo, ND 58105 USANorth Dakota State Univ, Dept Civil & Environm Engn, Fargo, ND 58105 USA
机构:
Univ Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Univ Tokyo, Dept Sensory & Motor Syst Med, Grad Sch Med, Tokyo, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Ko, Edward Chengchuan
Fujihara, Yuko
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Univ Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Fujihara, Yuko
Ogasawara, Toru
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Univ Tokyo, Dept Sensory & Motor Syst Med, Grad Sch Med, Tokyo, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Ogasawara, Toru
Asawa, Yukiyo
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Univ Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Asawa, Yukiyo
Nishizawa, Satoru
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Univ Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Nishizawa, Satoru
Nagata, Satoru
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Nagata Microtia & Reconstruct Plast Surg Clin, Saitama, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Nagata, Satoru
Takato, Tsuyoshi
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Univ Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Univ Tokyo, Dept Sensory & Motor Syst Med, Grad Sch Med, Tokyo, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan
Takato, Tsuyoshi
Hoshi, Kazuto
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Univ Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, JapanUniv Tokyo, Dept Cartilage & Bone Regenerat Fujisoft, Grad Sch Med, Tokyo, Japan