## Abstract ## Purpose To quantify the effect of iodine on the gadolinium (Gd) contrast‐enhanced signal in MR arthrography. ## Materials and Methods Saline solutions of Gd contrast agent (0–1 mmol/liter) were mixed with iodinated contrast agent (0–185 mmol/liter). The T1 and T2 relaxation consta
Effect of the intracellular localization of a Gd-based imaging probe on the relaxation enhancement of water protons
✍ Scribed by Enzo Terreno; Simonetta Geninatti Crich; Simona Belfiore; Luigi Biancone; Claudia Cabella; Giovanna Esposito; Andrea D. Manazza; Silvio Aime
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 267 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Gd‐HPDO3A has been internalized into rat hepatocarcinoma cells in the cytoplasm (by electroporation) or in intracellular vesicles (by pinocytosis), respectively. In the former case, the observed relaxation rates are likely dependent upon the amount of internalized paramagnetic complex, whereas in the latter case the relaxation enhancement is “quenched” to a plateau value (about 3 s^−1^) when the entrapped amount of Gd‐chelate is higher than 1 × 10^10^ Gd/cell. The observed behavior has been accounted in terms of a theoretical treatment based on equations formally derived by Labadie et al. (J Magn Reson B 1994;105:99–102). On this basis, entrapment into intracellular vesicles has been treated as a three‐site water exchange (extracellular/cytoplasm/vesicle compartments), whereas the cell pellets containing the paramagnetic agent spread out in the cytoplasm can be analyzed by a two‐site exchange system. Magn Reson Med, 2006. © 2006 Wiley‐Liss, Inc.
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