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Novel MRI Contrast Agent for Molecular Imaging of Fibrin

Authors :
Patrick J. Gaffney
Stefan Fischer
Gregorio A. Sicard
Patrick M. Winter
John S. Allen
Gregory M. Lanza
Mark McLean
Ralph Fuhrhop
Samuel A. Wickline
Michael J. Scott
Sebastian Flacke
Source :
Circulation. 104:1280-1285
Publication Year :
2001
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2001.

Abstract

Background Molecular imaging of thrombus within fissures of vulnerable atherosclerotic plaques requires sensitive detection of a robust thrombus-specific contrast agent. In this study, we report the development and characterization of a novel ligand-targeted paramagnetic molecular imaging agent with high avidity for fibrin and the potential to sensitively detect active vulnerable plaques. Methods and Results The nanoparticles were formulated with 2.5 to 50 mol% Gd-DTPA-BOA, which corresponds to >50 000 Gd 3+ atoms/particle. Paramagnetic nanoparticles were characterized in vitro and evaluated in vivo. In contradistinction to traditional blood-pool agents, T1 relaxation rate as a function of paramagnetic nanoparticle number was increased monotonically with Gd-DTPA concentration from 0.18 mL · s −1 · pmol −1 (10% Gd-DTPA nanoparticles) to 0.54 mL · s −1 · pmol −1 for the 40 mol% Gd-DTPA formulations. Fibrin clots targeted in vitro with paramagnetic nanoparticles presented a highly detectable, homogeneous T1-weighted contrast enhancement that improved with increasing gadolinium level (0, 2.5, and 20 mol% Gd). Higher-resolution scans and scanning electron microscopy revealed that the nanoparticles were present as a thin layer over the clot surface. In vivo contrast enhancement under open-circulation conditions was assessed in dogs. The contrast-to-noise ratio between the targeted clot (20 mol% Gd-DTPA nanoparticles) and blood was ≈118±21, and that between the targeted clot and the control clot was 131±37. Conclusions These results suggest that molecular imaging of fibrin-targeted paramagnetic nanoparticles can provide sensitive detection and localization of fibrin and may allow early, direct identification of vulnerable plaques, leading to early therapeutic decisions.

Details

ISSN :
15244539 and 00097322
Volume :
104
Database :
OpenAIRE
Journal :
Circulation
Accession number :
edsair.doi.dedup.....aa33ea490b2c8d2d5a8b5747aea914cd
Full Text :
https://doi.org/10.1161/hc3601.094303