Analysis of the hierarchical structure of biological tissues by scanning X-ray scattering using a micro-beam

Citation
O. Paris et al., Analysis of the hierarchical structure of biological tissues by scanning X-ray scattering using a micro-beam, CELL MOL B, 46(5), 2000, pp. 993-1004
Citations number
45
Categorie Soggetti
Cell & Developmental Biology
Journal title
CELLULAR AND MOLECULAR BIOLOGY
ISSN journal
01455680 → ACNP
Volume
46
Issue
5
Year of publication
2000
Pages
993 - 1004
Database
ISI
SICI code
0145-5680(200007)46:5<993:AOTHSO>2.0.ZU;2-L
Abstract
The outstanding mechanical properties of biological tissues such as wood or bone are mainly due to their hierarchical structure and to their optimizat ion at all levels of hierarchy. It is therefore essential to characterize t he structure at all levels to understand the complex behavior of such tissu es. Structures down to the micrometer level are accessible to light or scan ning electron microscopic observation. In the case of bone this includes, f or example, morphometry of the trabecular architecture or the bone mineral density distribution in cortical and trabecular bone. To characterize the s ub-micrometer structure of, e.g., the collagen-mineral composite in the cas e of bone or the cellulose microfibrils in the case of wood, other methods, such as transmission electron microscopy or X-ray scattering are necessary . The recent availability of extremely brilliant synchrotron X-ray sources has led to the development of the new techniques of scanning small-angle X- ray scattering and scanning X-ray microdiffraction, which are capable of pr oviding structural information on the micrometer and the nanometer level, s imultaneously. As a basic principle of the method the specimen is scanned a cross an X-ray beam which has a diameter of few micrometers. Measuring the X-ray absorption at each position provides an image of the specimen (:micro radiography) with resolution similar to light microscopy, in the micrometer range. Moreover, the X-ray scattering pattern is analyzed at each specimen position to provide parameters characterizing the structure in the nanomet er range. The present paper reviews the principles of the techniques and de monstrates their application to biological materials, such as wood or bone.