Background and Purpose-Molecular imaging of therapeutic interventions with targeted agents that simultaneously carry drugs or genes for local delivery is appealing. We investigated the ability of a novel microbubble carrier (immunobubble) for abciximab, a glycoprotein IIb/IIIa receptor inhibitor, for ultrasonographic molecular imaging of human clots. Methods-Human thrombi were incubated with immunobubbles conjugated with abciximab. Control clots were incubated in either saline or with immunobubbles conjugated with nonspecific antibody. We evaluated immunobubble suspensions with variable concentrations of encapsulated gas and measured mean acoustic intensity of the incubated clots. In vivo molecular imaging of human thrombi with abciximab immunobubbles was evaluated in a rat model of carotid artery occlusion. Results-Mean acoustic intensity was significantly higher for abciximab immunobubbles as compared with control immunobubbles under all conditions tested with maximum difference in intensity at a gas volume of 0.2 L (Pϭ0.0013 for mechanical index 0.05, Pϭ0.0001 for mechanical index 0.7). Binding of abciximab immunobubbles to clots in vitro led to enhanced echogenicity dependent on bubble concentration. In vivo ultrasonic detectability of carotid thrombi was significantly higher for clots targeted with abciximab immunobubbles (PϽ0.05). Quantification of in vivo contrast enhancement displayed a highly significant increment for abciximab immunobubble-targeted clots compared with nonspecific immunobubble-targeted clots (PϽ0.0001) and to native clots (PϽ0.0001). Conclusions-This study demonstrates the feasibility of using a therapeutic agent for selective targeting in vascular imaging. Abciximab immunobubbles improve visualization of human clots both in vitro and in an in vivo model of acute arterial thrombotic occlusion.

No abstract

No abstract

This article describes the preparation of macroporous cross-linked poly(dicyclopentadiene) by chemically induced phase separation. Dicyclopentadiene was polymerized and cross-linked by metathesis in the presence of 2-propanol, using a ruthenium-based catalyst, and then dried under vacuum. The resulting porous materials were characterized by SEM, density measurements, and mercury porosimetry. By varying the initial 2-propanol content, it was shown that closed or open cell porosity could be obtained, with narrow pore size distributions and micrometric average access diameters. A linear dependence of the pore volume fraction and the initial 2-propanol content was also observed, suggesting easy tailoring of the former.

This article describes the pore size modification and in situ surface functionalization of macroporous crosslinked poly(dicyclopentadiene), produced by chemically induced phase separation, with norbornene‐functionalized poly(ethylene glycol) telechelic oligomers. The microstructure of the open porosity materials produced with this technique consisted of agglomerated particles. The incorporation of these telechelic oligomers allowed a substantial decrease in the pore size and a related increase in the internal surface area. These functionalized oligomers acted as stabilizers around the primary particles produced by phase separation and blocked their growth so that the materials resulting from the agglomeration of these smaller particles showed finer microstructures. The resulting porous materials were characterized by scanning electron microscopy, density measurements, nitrogen adsorption, and mercury porosimetry. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 2036–2046, 2003