4.4 Article

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

期刊

CELLS TISSUES ORGANS
卷 209, 期 4-6, 页码 266-275

出版社

KARGER
DOI: 10.1159/000511079

关键词

Bone; Bone surface; Biomineralization; Raman spectroscopy

资金

  1. Svenska Sallskapet for Medicinsk Forskning (SSMF) postdoctoral scholarship
  2. Adlerbertska Foundation
  3. IngaBritt and Arne Lundberg Foundation
  4. Hjalmar Svensson Foundation
  5. Dr. Felix Neubergh Foundation
  6. Promobilia
  7. Materials Science Area of Advance at Chalmers
  8. Department of Biomaterials, University of Gothenburg

向作者/读者索取更多资源

The surface of bone serves as a historical record of osteogenesis, providing key insights into bone quality. Chemical analysis of bone is crucial for various fields such as human health, cell biology, anthropology/archaeology, and biomedical engineering.
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 nu(1) PO43- and nu(1) CO32- peak intensity losses where the sample surface and the plane of focus are offset by over 1-2 mu m when underfocused and 2-3 mu m 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 mm(2) were scanned at micrometer and submicrometer resolution. Despite surface height deviations exceeding 100 mu m, 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.

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