RELAXOGRAPHIC IMAGING

被引:102
作者
LABADIE, C [1 ]
LEE, JH [1 ]
VETEK, G [1 ]
SPRINGER, CS [1 ]
机构
[1] SUNY STONY BROOK, DEPT RADIOL, STONY BROOK, NY 11794 USA
来源
JOURNAL OF MAGNETIC RESONANCE SERIES B | 1994年 / 105卷 / 02期
关键词
D O I
10.1006/jmrb.1994.1109
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
A fundamental extension of NMR imaging is described. The distribution of relaxation times, the relaxogram, is considered as the third (or fourth) dimension of a set of 2D (or 3D) image data. There is a relaxographic dimension for each type of relaxation: longitudinal, transverse, rotating frame, etc. It is the formal inverse Laplace transform of the relaxation decay data set. Thus, combined relaxography and imaging (CRI) approaches are de fined. CRI data can he displayed in two fundamental ways: localized relaxograms (relaxograms from any part of an image) or relaxographic images (images produced from discrete portions of a relaxogram). Relaxographic images are elemental components of the true spin-density image. The CRI concept is demonstrated with longitudinal relaxation data from samples of yeast cells suspended in media containing the contrast agent (CR) GdDTPA(2-). This allows the discrimination of subvoxel intra- and extracellular (H2O)-H-1 signals in the relaxograms from very small image voxels (about 400 nl). It is possible to isolate the intracellular (H2O)-H-1 resonance from as few as a million cells. Relaxographic images are shown of the extracellular space (i.e., the distribution space of the CR) and the cytoplasmic space of a cell suspension with a cytocrit gradient. These have important potential applications in the in vivo situation. Also, the extent of equilibrium transcytolemmal water exchange can be detected and quantified. (C) 1994 Academic Press, Inc.
引用
收藏
页码:99 / 112
页数:14
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