Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, 1304 West Green Street, Urbana, IL 61801, USA.
Biomaterials. 2010 May;31(13):3552-63. doi: 10.1016/j.biomaterials.2010.01.052. Epub 2010 Feb 11.
The role of macropore size (>100 microm) and geometry in synthetic scaffolds for bone regeneration has been studied extensively, but successful translation to the clinic has been slow. Significantly less attention has been given to porosity at the microscale (0.5-10 microm). While some have shown that microporosity in calcium phosphate (CaP)-based scaffolds can improve rate and extent of bone formation in macropores, none has explored microporosity as an additional and important space for bone ingrowth. Here we show osteointegration of biphasic calcium phosphate (BCP) scaffolds at both the macro and micro length scales. Bone, osteoid, and osteogenic cells fill micropores in scaffold rods and osteocytes are embedded in mineralized matrix in micropores, without the addition of growth factors. This work further highlights the importance of considering design parameters at the microscale and demonstrates the possibility for a bone-scaffold composite with no "dead space." Embedded osteocytes distributed throughout microporous rods may form a mechanosensory network, which would not be possible in scaffolds without microporosity. Multiscale osteointegration has the potential to greatly improve overall performance of these scaffolds through an improvement of mechanical properties, load transfer, and stability in the long and short term, and represents a new paradigm for scaffold design.
大孔尺寸(>100 微米)和形状在用于骨再生的合成支架中的作用已经得到了广泛的研究,但成功转化为临床应用的速度却很慢。人们对微孔尺寸(0.5-10 微米)的关注要少得多。虽然有人表明,基于磷酸钙(CaP)的支架中的微孔可以提高大孔中骨形成的速度和程度,但没有人探索微孔作为骨长入的额外重要空间。在这里,我们展示了双相磷酸钙(BCP)支架在宏观和微观长度尺度上的骨整合。骨、类骨质和成骨细胞填充在支架棒中的微孔中,骨细胞嵌入在微孔中的矿化基质中,而无需添加生长因子。这项工作进一步强调了在微观尺度上考虑设计参数的重要性,并展示了具有无“死区”的骨-支架复合材料的可能性。分布在微孔棒中的嵌入的成骨细胞可能形成一个机械敏感网络,如果支架中没有微孔,这是不可能的。多尺度骨整合有可能通过改善长期和短期的机械性能、负载传递和稳定性,极大地提高这些支架的整体性能,这代表了支架设计的一个新范例。