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利用实时表面跟踪微拉曼光谱技术对骨表面成分进行成像。

Mapping Bone Surface Composition Using Real-Time Surface Tracked Micro-Raman Spectroscopy.

机构信息

Department of Biomaterials, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden,

Department of Biomaterials, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

Cells Tissues Organs. 2020;209(4-6):266-275. doi: 10.1159/000511079. Epub 2021 Feb 4.

Abstract

The surface of bone tells a story - one that is worth a thousand words - of how it is built and how it is repaired. Chemical (i.e., composition) and physical (i.e., morphology) characteristics of the bone surface are analogous to a historical record of osteogenesis and provide key insights into bone quality. Analysis of bone chemistry is of particular relevance to the advancement of human health, cell biology, anthropology/archaeology, and biomedical engineering. Although scanning electron microscopy remains a popular and versatile technique to image bone across multiple length scales, limited chemical information can be obtained. Micro-Raman spectroscopy is a valuable tool for nondestructive chemical/compositional analysis of bone. However, signal integrity losses occur frequently during wide-field mapping of non-planar surfaces. Samples for conventional Raman imaging are, therefore, rendered planar through polishing or sectioning to ensure uniform signal quality. Here, we demonstrate ν1 PO43- and ν1 CO32- peak intensity losses where the sample surface and the plane of focus are offset by over 1-2 μm when underfocused and 2-3 μm when overfocused at 0.5-1 s integration time (15 mW, 633 nm laser). A technique is described for mapping the composition of the inherently irregular/non-planar surface of bone. The challenge posed by the native topology characteristic of this unique biological system is circumvented via real-time focus-tracking based on laser focus optimization by continuous closed-loop feedback. At the surface of deproteinized and decellularized/defatted sheep tibial cortical bone, regions of interest up to 1 mm2 were scanned at micrometer and submicrometer resolution. Despite surface height deviations exceeding 100 μm, it is possible to seamlessly probe local gradients in organic and inorganic constituents of the extracellular matrix as markers of bone metabolism and bone turnover, blood vessels and osteocyte lacunae, and the rope-like mineralized bundles that comprise the mineral phase at the bone surface.

摘要

骨的表面讲述了一个故事——一个千言万语都无法描述的故事——讲述了它的构建方式和修复方式。骨表面的化学(即组成)和物理(即形态)特征类似于成骨的历史记录,为骨质量提供了关键的见解。骨化学分析对于人类健康、细胞生物学、人类学/考古学和生物医学工程的发展尤其重要。尽管扫描电子显微镜仍然是一种流行且多功能的技术,可以在多个长度尺度上对骨进行成像,但只能获得有限的化学信息。微拉曼光谱是一种用于骨的非破坏性化学/成分分析的有价值的工具。然而,在对非平面表面进行宽场映射时,信号完整性经常会丢失。因此,为了确保均匀的信号质量,用于传统拉曼成像的样品通过抛光或切片使其成为平面。在这里,我们证明了当离焦 1-2 μm 时,样品表面和焦点平面会发生偏移,当离焦 2-3 μm 时,在 0.5-1 s 积分时间(15 mW,633 nm 激光)下,ν1 PO43-和ν1 CO32-峰强度会发生损失。描述了一种用于绘制骨固有不规则/非平面表面成分的技术。通过基于激光焦点优化的实时焦点跟踪,通过连续闭环反馈进行连续闭环反馈,克服了这种独特生物系统的固有拓扑特征所带来的挑战。在脱蛋白和去细胞/脱脂绵羊胫骨皮质骨的表面上,以亚微米分辨率扫描了高达 1 mm2 的感兴趣区域。尽管表面高度偏差超过 100 μm,但可以探测到细胞外基质中有机和无机成分的局部梯度,这些梯度是骨代谢和骨转换、血管和骨细胞腔以及构成骨表面矿物质相的绳状矿化束的标志物。

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