| Literature DB >> 12594765 |
Kofi Adzamli1, Dmitriy A Yablonskiy, Michael R Chicoine, Eun Kyung Won, Karen P Galen, Michael C Zahner, Thomas A Woolsey, Joseph J H Ackerman.
Abstract
Intravenous MRI contrast agents are commonly used to improve the detection of intracranial tumors and other central nervous system (CNS) lesions for diagnosis and treatment planning. Two small-molecule, albumin-binding blood pool contrast agents (MP-2269 and MS-325) of potential clinical significance were evaluated at 1.5 Tesla in a mouse glioma model and compared with an extracellular contrast agent (OptiMARK). Tumor image contrast was significantly enhanced and long-lived following administration of 30 micromole/kg of the blood pool agents: specifically, contrast enhancement peaked slowly at 25-30 min following administration, remained constant for >3 hr, and returned to baseline within 20 hr. Comparable but "transient" enhancement was achieved using 100 micromole/kg OptiMARK: specifically, contrast enhancement peaked rapidly at 2-5 min following administration and then declined over 40 min. The blood pool contrast agents demonstrated an approximately threefold increased dose-effectiveness and a lengthened window of tumor contrast enhancement in comparison to commonly available extracellular contrast agents. This demonstrates the potential of alternative contrast-enhanced (CE) MRI examination protocols for tumor detection. Copyright 2003 Wiley-Liss, Inc.Entities:
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Year: 2003 PMID: 12594765 DOI: 10.1002/mrm.10382
Source DB: PubMed Journal: Magn Reson Med ISSN: 0740-3194 Impact factor: 4.668