Abstract
The demineralized bone matrix (DBM) putty is a traditional bone graft utilized to facilitate the repair and reconstruction of bone. Recent studies indicated the DBM putties with the various carriers were different in bone repairing ability. In order to prepare a kind of DBM putty with a good biocompatibility and bioactivity, the DBM gel was processed from the DBM and the feasibility as a carrier for the DBM putty was evaluated. After the bovine DBM gel was prepared, the BMPs content as well as the ability to promote osteogenic differentiation of MC3T3-E1 cells in vitro were investigated. Then the DBM putty was prepared and filled into the rat calvarial defect model to evaluate the bone repairing ability by micro-CT and histology. The result showed there was 2.953 ± 0.054 ng BMP contained in per gram of the DBM gel. And the ALP production of MC3T3-E1 cells in the DBM gels group increased with prolonged culturing, the mineralized nodules formed in MC3T3-E1 cells on 14th day after co-culture. The putty prepared by DBM gel was easy to handle without loss of DBM particles at room temperature. In the rat calvarial bone defect experiment, histological observation showed more mature bone formed in the DBM putty group than that in the type I collagen group at 12 weeks, which indicated the bone putty prepared by DBM gel exhibited a better bone repair capability.
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Acknowledgements
This work was supported by the research funding from Natural Science Foundation of Shandong Province (Nos. BS2015SW021; ZR2014HM009; ZR2016HP13), the Project of Science and Technology of Binzhou Medical University (Nos. BY2014KYQD25; BY2014KJ08), the National Natural Science Foundation of China (No. 81301570), and The development of medical science and technology project of Shandong Province (No. 2013WS0306).
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Zhang, N., Ma, L., Liu, X. et al. In vitro and in vivo evaluation of xenogeneic bone putty with the carrier of hydrogel derived from demineralized bone matrix. Cell Tissue Bank 19, 591–601 (2018). https://doi.org/10.1007/s10561-018-9708-z
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DOI: https://doi.org/10.1007/s10561-018-9708-z