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在骨骼早期加热阶段的纳米级修饰在微观结构尺度上是不均匀的。

Nanoscale modifications in the early heating stages of bone are heterogeneous at the microstructural scale.

作者信息

Gourrier Aurélien, Chadefaux Céline, Lemaitre Estelle, Bellot-Gurlet Ludovic, Reynolds Michael, Burghammer Manfred, Plazanet Marie, Boivin Georges, Farlay Delphine, Bunk Oliver, Reiche Ina

机构信息

Université Grenoble Alpes, Laboratoire Interdisciplinaire de Physique (LIPHY), Grenoble, France.

CNRS, LIPHY, Grenoble, France.

出版信息

PLoS One. 2017 Apr 19;12(4):e0176179. doi: 10.1371/journal.pone.0176179. eCollection 2017.

Abstract

Nanoscale studies of bone provide key indicators to evidence subtle structural changes that may occur in the biomedical, forensic and archaeological contexts. One specific problem encountered in all those disciplines, for which the identification of nanostructural cues could prove useful, is to properly monitor the effect of heating on bone tissue. In particular, the mechanisms at work at the onset of heating are still relatively unclear. Using a multiscale approach combining Raman microspectroscopy, transmission electron microscopy (TEM), synchrotron quantitative scanning small-angle X-ray scattering imaging (qsSAXSI) and polarized light (PL) microscopy, we investigate the ultrastructure of cortical bovine bone heated at temperatures < 300°C, from the molecular to the macroscopic scale. We show that, despite limited changes in crystal structure, the mineral nanoparticles increase in thickness and become strongly disorganized upon heating. Furthermore, while the nanostructure in distinct anatomical quadrants appears to be statistically different, our results demonstrate this stems from the tissue histology, i.e. from the high degree of heterogeneity of the microstructure induced by the complex cellular processes involved in bone tissue formation. From this study, we conclude that the analysis of bone samples based on the structure and organization of the mineral nanocrystals requires performing measurements at the histological level, which is an advantageous feature of qsSAXSI. This is a critical aspect that extends to a much broader range of questions relating to nanoscale investigations of bone, which could also be extended to other classes of nanostructured heterogeneous materials.

摘要

对骨骼的纳米尺度研究提供了关键指标,以证明在生物医学、法医和考古背景下可能发生的细微结构变化。在所有这些学科中遇到的一个特定问题,即纳米结构线索的识别可能有用的问题,是如何正确监测加热对骨组织的影响。特别是,加热开始时起作用的机制仍然相对不清楚。我们采用拉曼显微光谱、透射电子显微镜(TEM)、同步加速器定量扫描小角X射线散射成像(qsSAXSI)和偏振光(PL)显微镜相结合的多尺度方法,研究了温度低于300°C时加热的皮质牛骨从分子尺度到宏观尺度的超微结构。我们表明,尽管晶体结构变化有限,但矿物纳米颗粒在加热时厚度增加并变得高度无序。此外,虽然不同解剖象限的纳米结构在统计学上似乎不同,但我们的结果表明,这源于组织结构,即源于骨组织形成过程中复杂细胞过程所诱导的微观结构的高度异质性。从这项研究中,我们得出结论,基于矿物纳米晶体的结构和组织对骨样品进行分析需要在组织学水平上进行测量,这是qsSAXSI的一个优势特征。这是一个关键方面,扩展到与骨骼纳米尺度研究相关的更广泛的问题范围,也可以扩展到其他类别的纳米结构异质材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37e6/5397064/d5deee47e839/pone.0176179.g001.jpg

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