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A specific groove design for individualized healing in a canine partial sternal defect model by a polycaprolactone/hydroxyapatite scaffold coated with bone marrow stromal cells
Author(s) -
Xuan Yiwen,
Tang Hua,
Wu Bin,
Ding Xinyu,
Lu Zhongyuan,
Li Wei,
Xu Zhifei
Publication year - 2014
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.35012
Subject(s) - polycaprolactone , scaffold , materials science , biomedical engineering , stromal cell , bone marrow , bone healing , medicine , anatomy , pathology , composite material , polymer
The reconstruction of sternal defects remains clinically challenging for thoracic surgeons. Here we aimed to explore the individualized reconstruction of partial sternal defects with new biodegradable material in a large animal model. We used the fused deposition modeling (FDM) technique to manufacture polycaprolactone/hydroxyapatite (PCL/HA) tissue scaffolds with individualized grooves to repair the sternal defect. The defects were surgically created in a sternocostal joint of eighteen Beagle dogs. The animals were separated into three groups ( n = 6): Blank group, PCL/HA group, and PCL/HA/BMSCs group. Radiographic examination, histological, and histomorphometric analyses were performed to evaluate the result. In the blank group, the defect site couldn't maintain its original integrity due to no bone union. In the PCL/HA group and PCL/HA/BMSCs group, it was observed that the scaffolds retained their shapes without significant degradation at 12 weeks. Both groups could observe new bone‐union by radiographic and histological examination. And PCL/HA/BMSCs would be more mineralized tissue area at implant sites ( p < 0.05). These results reveal that using the FDM technique to manufacture the PCL/HA scaffolds with specific grooves could repair the sternal defect satisfactorily. Furthermore the scaffolds with BMSCs‐seeded could enhance the amount of bone ingrowth and seemed to be more promising. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 102A: 3401–3408, 2014.