Albumin-binding MR blood pool agents as MRI contrast agents in an intracranial mouse glioma model

被引:26
|
作者
Adzamli, K
Yablonskiy, DA
Chicoine, MR
Won, EK
Galen, KP
Zahner, MC
Woolsey, TA
Ackerman, JJH
机构
[1] Washington Univ, Sch Med, Mallinckrodt Inst Radiol, St Louis, MO 63110 USA
[2] Mallinckrodt Inc, Imaging Div, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Neurosurg, St Louis, MO USA
[4] Barnes Jewish Hosp, St Louis, MO 63110 USA
[5] Univ Washington, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
[6] Univ Washington, Sch Med, Siteman Canc Ctr, St Louis, MO 63110 USA
[7] Univ Washington, Dept Chem Arts & Sci, St Louis, MO USA
关键词
MR contrast media; blood pool agent; brain tumor; mouse glioma model; MRI;
D O I
10.1002/mrm.10382
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
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 mumole/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 mumole/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. (C) 2003 Wiley-Liss, Inc.
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页码:586 / 590
页数:5
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