Use of Intravital Microscopy to Study the Microvascular Behavior of Microbubble-Based Ultrasound Contrast Agents

作者：Schneider Michel; Broillet Anne; Tardy Isabelle^*; Pochon Sibylle; Bussat Philippe; Bettinger Thierry; Helbert Alexandre; Costa Maria; Tranquart Francois

来源：Microcirculation, 2012, 19(3): 245-259.

DOI：10.1111/j.1549-8719.2011.00152.x

• cremaster muscle
• dorsal skin-fold chamber
• hamster cheek pouch
• intravital microscopy
• liver
• microbubble
• microcirculation
• mouse
• rat
• spinotrapezius muscle
• BR55
• SonoVue (R)
• BR14
• P-selectin

Purpose: The study describes the use of intravital microscopy (IVM) to assess the behavior of ultrasound contrast agents (UCAs), including targeted UCAs, in the microcirculation of rodents. Materials and Methods: IVM was performed on various exteriorized organs: hamster cheek pouch, rat mesentery, liver, spinotrapezius muscle, and mouse cremaster muscle. A dorsal skin-fold chamber with MatBIII tumor cells was also implanted in rats. Nontargeted UCAs (SonoVue (R) and BR14) and targeted UCAs (BR55 and P-selectin targeted microbubbles) were tested. IVM was used to measure microbubble size, determine their persistence, and observe their behavior in the blood circulation. Results: Intravenous and intra-arterial injections of high doses of UCAs did not modify the local microvascular hemodynamics. No microbubble coalescence and no increased size were observed. Adhesion of some microbubbles to leukocytes was observed in various microcirculation models. Microbubbles are captured by Kupffer cells in the liver. Targeted microbubbles were shown to adhere specifically to endothelial receptors without compromising local blood flow. Conclusion: These results support the safety of both targeted and nontargeted UCAs as no microvascular flow alteration or plugging of microvessels were observed. They confirm that binding observed with targeted microbubbles are due to the binding of these microbubbles to specific endothelial receptors.

• 出版日期2012-4