## Abstract This work presents a methodology for obtaining quantitative oxygen concentration images in the tumor‐bearing legs of living C3H mice. The method uses high‐resolution electron paramagnetic resonance imaging (EPRI). Enabling aspects of the methodology include the use of injectable, narrow
Comparison of 1H blood oxygen level–dependent (BOLD) and 19F MRI to investigate tumor oxygenation
✍ Scribed by Dawen Zhao; Lan Jiang; Eric W. Hahn; Ralph P. Mason
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 408 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Fluorine‐19 [^19^F] MRI oximetry and ^1^H blood oxygen level–dependent (BOLD) MRI were used to investigate tumor oxygenation in rat breast 13762NF carcinomas, and correlations between the techniques were examined. A range of tissue oxygen partial pressure (pO~2~) values was found in the nine tumors while the anesthetized rats breathed air, with individual tumor pO~2~ ranging from a mean of 1 to 36 torr and hypoxic fraction (HF10) (<10 torr) ranging from 0% to 75%, indicating a large intra‐ and intertumor heterogeneity. Breathing oxygen produced significant increase in tumor pO~2~ (mean ΔpO~2~ = 50 torr) and decrease in HF~10~ (P < 0.01). ^1^H BOLD MRI observed using a spin echo‐planar imaging (EPI) sequence revealed a heterogeneous response and significant increase in mean tumor signal intensity (SI) (ΔSI = 7%, P < 0.01). R measured by multigradient‐echo (MGRE) MRI decreased significantly in response to oxygen (mean Δ__R__ = −4 s^−1^; P < 0.05). A significant correlation was found between changes in mean tumor pO~2~ and mean EPI BOLD ΔSI accompanying oxygen breathing (r^2^ > 0.7, P < 0.001). Our results suggest that BOLD MRI provides information about tumor oxygenation and may be useful to predict pO~2~ changes accompanying interventions. Significantly, the magnitude of the BOLD response appears to be predictive for residual tumor HFs. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.
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