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Bone Defect Model Dependent Optimal Pore Sizes of 3D‐Plotted Beta‐Tricalcium Phosphate Scaffolds for Bone Regeneration
Author(s) -
Diao Jingjing,
Ding Huanwen,
Huang Minqiang,
Fu Xiaoling,
Zou Fen,
Li Tianjie,
Zhao Naru,
Mao Chuanbin,
Wang Yingjun
Publication year - 2019
Publication title -
small methods
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.66
H-Index - 46
ISSN - 2366-9608
DOI - 10.1002/smtd.201900237
Subject(s) - intramembranous ossification , endochondral ossification , materials science , biomedical engineering , ossification , cartilage , regeneration (biology) , tibia , chemistry , anatomy , biophysics , microbiology and biotechnology , biology , medicine
Abstract Bones such as long bone and flat bone vary physiologically and anatomically. How pore sizes affect bone regeneration in different bone defects and its mechanisms are not well studied. Herein, typical long bone (tibia) defect model and flat bone (calvarial) defect model are applied to investigate their bone regeneration capacity and the underlying mechanism mediated by the pore sizes. Pore sizes (100, 250, and 400 µm) of the beta‐tricalcium phosphate (β‐TCP) scaffolds are strictly controlled utilizing a 3D plotting method. Bone regeneration capability in vivo by these pore sizes is related to the defect models (tibial defects and calvarial defects). Among the three pore sizes being studied, 100 µm pore size is most efficient in inducing bone formation in repairing flat bone defects, which is owing to the enhanced osteoblast differentiation in the intramembranous ossification. Differently, the scaffolds with a pore size of 400 µm display the best ability of bone formation for repairing long bone defects, which is speculated to be related to the accelerated formation of cartilage templates and ossification centers in endochondral ossification. This study suggests that bone defect type should be concerned in the design of the porous structure of an artificial material.