Nanophase bone substitute in vivo response to subcutaneous implantation

被引:10
作者
Baskin, Jonathan Z. [1 ,2 ,3 ]
Vasanji, Amit [4 ]
McMasters, James [3 ]
Soenjaya, Yohannes [3 ]
Barbu, Anca M. [1 ]
Eppell, Steven J. [1 ,3 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Cleveland, OH 44106 USA
[2] Louis Stokes Cleveland VA Med Ctr, Dept Otolaryngol Head & Neck Surg, Cleveland, OH USA
[3] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[4] ImageIQ Inc, Cleveland, OH USA
关键词
bone substitute; mineralized collagen; histological response; morphology; porosity; HYDROXYAPATITE/COLLAGEN HAP/COL COMPOSITE; POROUS SCAFFOLDS; BIOACTIVE GLASS; TRAUMA SURGERY; COLLAGEN; BIOMATERIAL; PARTICLES; MATRIX; VITRO; RATS;
D O I
10.1002/jbm.a.34175
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
A collagen-apatite composite designed as a load-bearing bone substitute implant is used to characterize the relationship between implant morphology and in vivo behavior. This nanophase bone substitute (NBS) is studied morphologically using a nondestructive imaging technique and biologically using the rodent subcutaneous model. Porosity and pore interconnectivity are correlated with histological outcomes showing cellular invasion occurs with average pore sizes below 100 mu m. Crosslinking with D-ribose is shown to affect cellular infiltration in a dose-response manner. These data suggest that collagen-apatite bone substitutes can support cellular infiltration with pore size significantly smaller than 100 mu m, an encouraging result regarding development of the NBS into a platform of biomaterials with enhanced mechanical properties. The data also indicate that increasing crosslinking density decreases cellular infiltration of NBS. Thus, modulating mechanical properties of the material by altering crosslink density is likely to produce decreased biological response within the material. (c) 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 100A: 24622473, 2012.
引用
收藏
页码:2462 / 2473
页数:12
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