Absorbed Fractions for
-Particles in Tissues of Trabecular Bone: Considerations of Marrow Cellularity Within the ICRP Reference Male
Christopher J. Watchman, MS1,
Derek W. Jokisch, PhD2,
Phillip W. Patton, PhD3,
Didier A. Rajon, PhD4,
George Sgouros, PhD5 and
Wesley E. Bolch, PhD1,6
1 Department of Nuclear and Radiological Engineering, University of Florida, Gainesville, Florida
2 Department of Physics and Astronomy, Francis Marion University, Florence, South Carolina
3 Department of Health Physics, University of NevadaLas Vegas, Las Vegas, Nevada
4 Department of Neurosurgery, University of Florida, Gainesville, Florida
5 Department of Radiology, Johns Hopkins University, Baltimore, Maryland
6 Department of Biomedical Engineering, University of Florida, Gainesville, Florida

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FIGURE 1. Histology slides of normal human bone marrow at 2 different marrow cellularities. At lower cellularity, a greater proportion of bone trabecula surface is covered by adipocytes (i.e., the first fat layer).
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FIGURE 2. Geometric model used to partition sampled marrow cavity chords into subtrajectories of -particle through active (red) marrow and inactive (yellow) marrow, the latter represented by individual adipocytes (white spheres).
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FIGURE 3. Absorbed fractions for an active marrow target (100% cellularity) from active marrow source (TAM) (A), trabecular bone endosteum source (TBE) (B), trabecular bone surface source (TBS) (C), and trabecular bone volume source (TBV) (D).
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FIGURE 4. Absorbed fractions for endosteum target from -sources emitted within the TAM (A), TBE (B), TBS (C), and TBV (D).
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FIGURE 5. Dependence of active marrow absorbed fraction with changes in marrow cellularity within lumbar vertebrae: TAM source (A), TBE source (B), TBS source (C), and TBV source (D).
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Copyright © 2005 by the Society of Nuclear Medicine.