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矿化肌腱变形机制的同步加速器衍射研究

Synchrotron diffraction study of deformation mechanisms in mineralized tendon.

作者信息

Gupta H S, Messmer P, Roschger P, Bernstorff S, Klaushofer K, Fratzl P

机构信息

Max Planck Institute of Colloids and Interfaces, Department of Biomaterials, 14424 Potsdam, Germany.

出版信息

Phys Rev Lett. 2004 Oct 8;93(15):158101. doi: 10.1103/PhysRevLett.93.158101. Epub 2004 Oct 4.

Abstract

The high stiffness and toughness of biomineralized tissues are related to the material deformation mechanisms at different levels of organization, from trabeculae and osteons at the micrometer level to the mineralized collagen fibrils at the nanometer length scale. Quantitatively little is known about the sub-micrometer deformation mechanisms under applied load. Using a parallel-fibred mineralized tissue from the turkey leg tendon as a model for the mineralized collagen fibrils, we used in situ tensile testing with synchrotron x-ray diffraction to measure the average fibril deformation with applied external strain. Diffraction peak splitting occurred at large strains, implying an inhomogeneous elongation of collagen fibrils. Scanning electron microscopy measurements lead us to conclude that the inhomogeneous mineralization in mineralized tendon is at the origin of the high fracture strain.

摘要

生物矿化组织的高刚度和韧性与不同组织层次的材料变形机制有关,从微米级的骨小梁和骨单位到纳米长度尺度的矿化胶原纤维。关于施加负荷下亚微米级的变形机制,目前定量了解甚少。我们以火鸡腿部肌腱的平行纤维矿化组织作为矿化胶原纤维的模型,采用同步加速器X射线衍射原位拉伸试验,测量外加应变作用下胶原纤维的平均变形。在大应变时出现衍射峰分裂,这意味着胶原纤维伸长不均匀。扫描电子显微镜测量结果使我们得出结论,矿化肌腱中矿化不均匀是高断裂应变的根源。

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