Fabrication and maturation of integrated biphasic anatomic mesenchymal stromal cell-laden composite scaffolds for osteochondral repair and joint resurfacing.
Fabrication and maturation of integrated biphasic anatomic mesenchymal stromal cell-laden composite scaffolds for osteochondral repair and joint resurfacing.
复制标题
DOI:
10.1002/jor.24969
复制
发表时间:
2021-11
期刊:
影响因子:
--
通讯作者:
Mauck RL
中科院分区:
文献类型:
--
作者:
Fryhofer GW;Zlotnick HM;Stoeckl BD;Farrell MJ;Steinberg DR;Mauck RL
Articular cartilage injury can lead to joint-wide erosion and the early onset of osteoarthritis. To address this, we recently developed a rapid fabrication method to produce patient-specific engineered cartilage tissues to replace an entire articular surface. Here, we extended that work by coupling a mesenchymal stromal cell-laden hydrogel (methacrylated hyaluronic acid, MeHA) with the porous polycaprolactone (PCL) bone integrating phase and assessed the composition and mechanical performance of these constructs over time. To improve initial construct stability, PCL/hydrogel interface parameters were first optimized by varying PCL pre-treatment (with sodium hydroxide before ethanol) prior to hydrogel infusion. Next, cylindrical osteochondral constructs were formed and cultured in media containing TGFβ3 for up to 8 weeks, with constructs evaluated for viability, histological features, and biochemical content. Mechanical properties were also assessed in axial compression and via an interface shear strength assay. Results showed that the fabrication process was compatible with cell viability, and that construct biochemical content and mechanical properties increased with time. Interestingly, compressive properties peaked at five weeks, while interfacial shear properties continued to improve beyond this time point. Lastly, these fabrication methods combined with a custom mold developed from limb-specific CT imaging data to create an anatomic implantable cell-seeded biologic joint surface, which showed similar maturation as the osteochondral cylinders. Future work will apply these advances in large animal models of critically-sized osteochondral repair and whole joint resurfacing.
登录
查看更多内容
影响因子:
7
作者:
Bian L;Angione SL;Ng KW;Lima EG;Williams DY;Mao DQ;Ateshian GA;Hung CT
通讯作者:
Hung CT
影响因子:
46.9
作者:
Kang, Hyun-Wook;Lee, Sang Jin;Atala, Anthony
通讯作者:
Atala, Anthony
影响因子:
4.1
作者:
Ballyns, Jeffery J.;Gleghorn, Jason P.;Bonassar, Lawrence J.
通讯作者:
Bonassar, Lawrence J.
DOI:
10.1007/s10856-019-6218-x
发表时间:
2019-02-01
影响因子:
3.7
作者:
Abdulghani, Saba;Morouco, Pedro G.
通讯作者:
Morouco, Pedro G.
影响因子:
9.7
作者:
Kim, Minwook;Farrell, Megan J.;Mauck, Robert L.
通讯作者:
Mauck, Robert L.