The osteoinductive potential of printable, cell-laden hydrogel-ceramic composites

被引:19
作者
Fedorovich, Natalja E. [1 ]
Leeuwenburgh, Sander C. [2 ]
van der Helm, Yvonne J. M. [1 ]
Alblas, Jacqueline [1 ]
Dhert, Wouter J. A. [1 ,3 ]
机构
[1] Univ Med Ctr Utrecht, Dept Orthopaed, NL-3508 GA Utrecht, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Biomat, NL-6500 HB Nijmegen, Netherlands
[3] Univ Utrecht, Fac Vet Med, NL-3508 TD Utrecht, Netherlands
关键词
bone regeneration; organ printing; osteoinductive hydrogel matrices; apatitic nanoparticles; biphasic phosphate microparticles; CARBONATE-SUBSTITUTED HYDROXYAPATITE; ECTOPIC BONE-FORMATION; MARROW STROMAL CELLS; PARTICLE-SIZE; OSTEOGENIC CELLS; CAPPING AGENT; STEM-CELLS; PHOSPHATE; SCAFFOLDS; NANOCOMPOSITES;
D O I
10.1002/jbm.a.34171
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Hydrogels used as injectables or in organ printing often lack the appropriate stimuli to direct osteogenic differentiation of embedded multipotent stromal cells (MSCs), resulting in limited bone formation in these matrices. Addition of calcium phosphate (CaP) particles to the printing mixture is hypothesized to overcome this drawback. In this study we have investigated the effect of CaP particles on the osteoinductive potential of cell-laden hydrogel-CaP composite matrices. To this end, apatitic nanoparticles have been included in Matrigel constructs where after the viability of embedded progenitor cells was assessed in vitro. In addition, the osteoinductive potential of cell-laden Matrigel containing apatitic nanoparticles was investigated in vivo and compared with composites containing osteoinductive biphasic calcium phosphate (BCP) microparticles after subcutaneous implantation in immunodeficient mice. Histological and immunohistochemical analysis of the tissue response as well as in vivo bone formation revealed that apatitic nanoparticles were osteoinductive and induced osteoclast activation, but without bone formation. The BCP particles were more effective in inducing elaborate bone formation at the ectopic location. (c) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 100A: 24122420, 2012
引用
收藏
页码:2412 / 2420
页数:9
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