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Reference point indentation is not indicative of whole mouse bone measures of stress intensity fracture toughness

机译:参考点压痕不能指示整个小鼠骨骼的应力强度断裂韧度

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摘要

Bone fragility is a concern for aged and diseased bone. Measuring bone toughness and understanding fracture properties of the bone are critical for predicting fracture risk associated with age and disease and for preclinical testing of therapies. A reference point indentation technique (BioDent) has recently been developed to determine bone's resistance to fracture in a minimally invasive way by measuring the indentation distance increase (IDI) between the first and last indentations over cyclic indentations in the same position. In this study, we investigate the relationship between fracture toughness KC and reference point indentation parameters (i.e. IDI, total indentation distance (TID) and creep indentation distance (CID)) in bones from 38 mice from six types (C57Bl/6, Balb, oim/oim, oim/+, Phospho1−/− and Phospho1 wild type counterpart). These mice bone are models of healthy and diseased bone spanning a range of fracture toughness from very brittle (oim/oim) to ductile (Phospho1−/−). Left femora were dissected, notched and tested in 3-point bending until complete failure. Contralateral femora were dissected and indented in 10 sites of their anterior and posterior shaft surface over 10 indentation cycles. IDI, TID and CID were measured. Results from this study suggest that reference point indentation parameters are not indicative of stress intensity fracture toughness in mouse bone. In particular, the IDI values at the anterior mid-diaphysis across mouse types overlapped, making it difficult to discern differences between mouse types, despite having extreme differences in stress intensity based toughness measures. When more locations of indentation were considered, the normalised IDIs could distinguish between mouse types. Future studies should investigate the relationship of the reference point indentation parameters for mouse bone in other material properties of the bone tissue in order to determine their use for measuring bone quality.
机译:骨骼脆性是老化和患病骨骼的关注点。测量骨骼韧性和了解骨骼的骨折特性对于预测与年龄和疾病相关的骨折风险以及进行治疗前的临床测试至关重要。最近开发了一种参考点压痕技术(BioDent),通过测量同一位置的循环压痕中第一个和最后一个压痕之间的压痕距离增加(IDI),以最小的侵入性方式确定骨骼的抗骨折能力。在这项研究中,我们研究了六种类型(C57Bl / 6,Balb,Balb和Bb)的38只小鼠的骨骼中的断裂韧性KC与参考点压痕参数(即IDI,总压痕距离(TID)和蠕变压痕距离(CID))之间的关系。 oim / oim,oim / +,Phospho1 -/-和Phospho1野生型对应物)。这些小鼠骨骼是健康骨骼和患病骨骼的模型,涵盖了从非常脆性(oim / oim)到韧性(Phospho1 -// )的一系列断裂韧性。解剖左股骨,切开切口并进行三点弯曲测试,直到完全失败。在10个压痕周期中,解剖对侧股骨并在其前轴和后轴表面的10个位置进行压痕。测量了IDI,TID和CID。这项研究的结果表明,参考点压痕参数不能指示小鼠骨骼的应力强度,断裂韧性。尤其是,尽管基于应力强度的韧性测量方法存在极大差异,但不同鼠标类型的前中骨干处的IDI值重叠,因此很难辨别鼠标类型之间的差异。当考虑压痕的更多位置时,标准化的IDI可以区分鼠标类型。未来的研究应调查小鼠骨骼的参考点压痕参数与骨骼组织其他材料属性之间的关系,以确定它们在测量骨骼质量中的用途。

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