## Abstract We compared __in vivo__ and __in vitro__ Hahn echo T~2~ measurements in rat lungs in both imaging and nonimaging modes. All measurements could be characterized by multiexponential functions consisting of either two or three exponentials. Essentially the same values of the time constants
An in vivo NMR imaging determination of multiexponential Hahn T2 of normal lung
✍ Scribed by Sumie Shioya; Rebecca Christman; David C. Ailion
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 484 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We describe the first in vivo imaging determination of normal lung tissue's multiexponential transverse magnetization decay. Normal spontaneously breathing rats were used for the measurements. To obtain motion‐insensitive images, we used a modified line scan imaging technique which we call the interleaved line scan (ILS). The ILS overcomes the following difficulties associated with imaging lungs: low signal‐to‐noise ratio (S/N) due to lung's low proton density and short T~2~ decay, artifacts associated with cardiac and respiratory motion, and excessively long imaging times with conventional line scan techniques. Using the ILS, a 16‐line 32‐average image with an 8‐s repetition time requires 4.3 min. From a series of 16 Hahn spin‐echo images with echo times ranging from 16 to 90 ms, we obtained a two‐component T~2~ decay for normal peripheml lung tissue. The measured fast and slow T~2~ components were 9.5 ± 1.0 and 34 ± 5.0 ms for the right lung and 9.0 ± 1.5 and 32 ± 4.5 for the left lung. The relative magnetization for the slow T~2~ component was 7.0 ± 4.5% for the right lung and 10 ± 3.0% for the left lung. © 1990 Academic Press, Inc.
📜 SIMILAR VOLUMES
## Abstract The rotating frame method of localized spectroscopy can be augmented by the inclusion of a refocusing pulse to enable the measurement of T~2~ relaxation times. This technique is particularly appropriate for determining short relaxation parameters due to the absence of time consuming swi
To generate non-small cell lung cancer (NSCLC)-reactive lymphocytes, we transfected an HLA-A2-expressing human NSCLC line (1355) with the cDNA encoding the lymphocyte co-stimulatory molecule CD80. Following selection in G418, 1355.7 demonstrated stable cell-surface expression of CD80. Allogeneic mix