首页> 外文期刊>Journal of biomedical materials research, Part A >Evaluation of bone regeneration by DNA release from composites of oligo(poly(ethylene glycol) fumarate) and cationized gelatin microspheres in a critical-sized calvarial defect.
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Evaluation of bone regeneration by DNA release from composites of oligo(poly(ethylene glycol) fumarate) and cationized gelatin microspheres in a critical-sized calvarial defect.

机译:寡核苷酸(聚富马酸乙二醇酯)和阳离子化明胶微球复合物在临界大小的颅骨缺损中的复合物释放DNA来评估骨再生。

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摘要

This research examines the bone formation response to release of plasmid DNA encoding human Bone Morphogenetic Protein-2 from hydrogel composites consisting of cationized gelatin microspheres (CGMS) embedded within a crosslinked oligo(poly(ethylene glycol) fumarate) (OPF) hydrogel network in a critical-sized rat cranial defect model after 30 days. Four composite groups were investigated: (1) composites with 10 microg DNA loaded into the CGMS phase, (2) composites with 10 microg DNA loaded into the OPF phase, (3) composites with 100 microg DNA loaded into the OPF phase, and (4) composites without DNA (material control). Light microscopy revealed no enhancement in bone formation for groups releasing plasmid DNA, relative to the material control group. Limited formation of new bone was observed from the defect margins and within the defect for some samples. The hydrogels swelled appreciably and fragmentation of the implants was noted to varying degrees among samples within groups, with a presence of inflammatory cells related to the degree of fragmentation. The lack of enhancement in bone formation indicates that the release of plasmid DNA from the composites was not sufficient to elicit a bone regeneration response.
机译:这项研究检查了骨形成对从人类凝胶形成的水凝胶复合物中释放编码人骨形态发生蛋白2的质粒DNA的反应,该复合物由嵌入明胶的交联的寡聚(聚乙二醇富马酸酯)(OPF)水凝胶网络中的阳离子明胶微球(CGMS)组成。 30天后达到临界大小的大鼠颅骨缺损模型。研究了四个复合材料组:(1)CGMS相中载有10 microg DNA的复合物,(2)OPF相中载有10 microg DNA的复合物,(3)OPF相中载有100 microg DNA的复合物,和( 4)没有DNA的复合材料(材料控制)。相对于材料对照组,光学显微镜显示释放质粒DNA的组的骨形成没有增强。对于某些样品,从缺陷边缘和缺陷内部观察到新骨的形成有限。水凝胶明显膨胀,并且在组内的样品之间注意到植入物的碎裂程度不同,存在与碎裂程度有关的炎性细胞。骨形成缺乏增强表明从复合物中释放质粒DNA不足以引起骨再生反应。

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