DocumentCode :
438584
Title :
High resolution Ca/P maps of bone architecture
Author :
Tzaphlidou, Margaret ; Speller, Robert ; Royle, Gary ; Griffiths, Jenny
Author_Institution :
Lab. of Med. Phys., Ioannina Univ., Greece
Volume :
5
fYear :
2004
fDate :
16-22 Oct. 2004
Firstpage :
3267
Abstract :
The Ca/P ratio was measured in cortical bone samples from the femoral neck, front and rear tibia of female rats (1.5 yr of age), using synchrotron radiation microtomography. Use of a monoenergetic X-ray beam, as provided by the synchrotron facility, generates accurate 3D maps of the linear attenuation coefficient within the sample and hence gives the ability to map different chemical components. MicroCT data sets were collected at 20 and 28 keV for each bone sample and two calibration phantoms. From the 3D data sets, multiple 2D slices were reconstructed with a slice thickness of ∼14 μm. Regions of interest were defined around suitable sites and were converted to Ca/P ratios using the data collected from the test phantoms. Mean values (M+SD) for cortical femoral, front and rear tibias are: 2.12+0.08, 1.75+0.06 and 1.94+0.07 respectively. Differences between the same bone sites from different animals are not significant (0.3-3). Differences between estimates made at 20 and 28 keV are not significant (p>0.5).
Keywords :
bone; calibration; computerised tomography; phantoms; 3D maps; Ca; P; bone architecture; calibration phantoms; chemical components; cortical bone samples; female rats; femoral neck; front tibia; high resolution Ca/P maps; linear attenuation coefficient; microCT data sets; monoenergetic X-ray beam; rear tibia; synchrotron radiation microtomography; Animals; Attenuation; Bones; Calibration; Chemicals; Imaging phantoms; Neck; Rats; Synchrotron radiation; Testing;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Nuclear Science Symposium Conference Record, 2004 IEEE
ISSN :
1082-3654
Print_ISBN :
0-7803-8700-7
Electronic_ISBN :
1082-3654
Type :
conf
DOI :
10.1109/NSSMIC.2004.1466384
Filename :
1466384
Link To Document :
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