## Abstract Accurate knowledge of relaxation times is imperative for adjustment of MRI parameters to obtain optimal signalβtoβnoise ratio (SNR) and contrast. As small animal MRI studies are extended to increasingly higher magnetic fields, these parameters must be assessed anew. The goal of this stu
Gadodiamide T1 relaxivity in brain tissue in vivo is lower than in saline
β Scribed by Stephen Pickup; Andrew K. W. Wood; Harold L. Kundel
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 330 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
In vivo measurements of gadodiamide (GdβDTPAβBMA) T~1~ relaxivity were performed at 4.7 T in injured and normal rat brains. Cerebral lesions were induced in nine rats by a localized freezing method. T~1~ maps of the lesions were generated before and after injection of GdβDTPAβBMA (0.1β0.6 mmol/kg). Samples of normal and necrotic brain were collected postmortem; the wet and dry weights were determined, and Gd content was measured by inductively coupled plasma mass spectroscopy. The in vivo relaxivity was determined by a linear fit of a plot of the change in relaxation rate following injection of the contrast agent as a function of Gd content. This analysis yielded a relaxivity in the injured brain of 2.8 sec^β1^ mmol^β1^ kg tissue water at 36Β°C. The water weight fraction was 0.90 Β± SD 0.02 wt/wt in injured brain and 0.79 Β± 0.02 in normal brain. Relaxivity measurements were also performed on solutions of GdβDTPAβBMA (0.0β0.6 mmol) and albumin (0β30% wt/wt) in normal saline at room and physiologic temperatures. The relaxivity in the albumin/saline increased with increasing solids content with values of 4.0β4.9 sec^β1^ mmol^β1^kg at 21Β°C and 3.4β4.5 sec^β1^ mmol^β1^ kg at 37Β°C. The relaxivity of the tissues differed significantly from that of the saline solutions of comparable solids content, suggesting that the solids content of a tissue is not the only factor that determines in vivo relaxivity. Magn Reson Med 53:35β40, 2005. Β© 2004 WileyβLiss, Inc.
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