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Researchers Collect First Direct Evidence Showing How Microbubbles Cause Blood Clot's Demise

Ultrasound-stimulated microbubbles have been showing promise in recent years as a non-invasive way to break up dangerous blood clots. But though many researchers have studied the effectiveness of this technique, not much was understood about why it works. Now a team of researchers in Toronto has collected the first direct evidence showing how these wiggling microbubbles cause a blood clot's demise. The team's findings are featured in the AIP Publishing journal Applied Physics Letters.

This is a time lapse image of a bubble (purple) burrowing into the network of a clot. The bubble is initially at rest in the fluid next to the clot. Exposure to ultrasound causes the bubble to shoot from left to right, penetrating the clot and causing damage to it in the process. (Credit:Christopher Acconcia)

Previous work on this technique, which is called sonothrombolysis, has focused on indirect indications of its effectiveness, including how much a blood clot shrinks or how well blood flow is restored following the procedure. The Toronto team, which included researchers from the University of Toronto and the Sunnybrook Research Institute, tried to catch the clot-killing process in action. Using high-speed photography and a 3-D microscopy technique, researchers discovered that stimulating the microbubbles with ultrasonic pulses pushes the bubbles toward the clots. The bubbles deform the clots' boundaries then begin to burrow into them, creating fluid-filled tunnels that break the clots up from the inside out.

These improvements in the understanding of how sonothrombolysis works will help researchers develop more sophisticated methods of breaking up blood clots, said lead author Christopher Acconcia.

Efforts so far "may only be scratching the surface with respect to effectiveness," said Acconcia. "Our findings provide a tool that can be used to develop more sophisticated sonothrombolysis techniques, which may lead to new tools to safely and efficiently dissolve clots in a clinical setting."

Source: http://www.aip.org

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