| Literature DB >> 22581131 |
Guillaume Potdevin1, Andreas Malecki, Thomas Biernath, Martin Bech, Torben H Jensen, Robert Feidenhans'l, Irene Zanette, Timm Weitkamp, Johannes Kenntner, Jürgen Mohr, Paul Roschger, Michael Kerschnitzki, Wolfgang Wagermaier, Klaus Klaushofer, Peter Fratzl, Franz Pfeiffer.
Abstract
The understanding of large biophysical systems at the systems level often depends on a precise knowledge of their microstructure. This is difficult to obtain, especially in vivo, because most imaging methods are either limited in terms of achievable field of view, or make use of penetrating ionizing radiations such as x-rays, in which case the resolution is severely limited by the deposited dose. Here, we describe a new method, x-ray vector radiography (XVR), which yields various types of information about the local orientation, anisotropy and average size of the sample microstructures. We demonstrate the feasibility by showing first experimental XVRs of human vertebra bone samples, giving information on the trabecular structures even with a pixel resolution of half a millimetre, much larger than the structures themselves. This last point is critical for the development of low-dose measurement methods which will allow for in vivo studies and potentially in the future for new medical diagnostics methods of bone metabolic disorder diseases such as osteoporosis.Entities:
Mesh:
Year: 2012 PMID: 22581131 DOI: 10.1088/0031-9155/57/11/3451
Source DB: PubMed Journal: Phys Med Biol ISSN: 0031-9155 Impact factor: 3.609