(Press-News.org) BOSTON, Aug. 17, 2015 -- A blood clot is a dangerous health situation with the potential to trigger heart attacks, strokes and other medical emergencies. To treat a blood clot, doctors need to find its exact location. But current clinical techniques can only look at one part of the body at a time, slowing treatment and increasing the risk for complications. Now, researchers are reporting a method, tested in rats, that may someday allow health care providers to quickly scan the entire body for a blood clot.
The team will describe their approach in one of more than 9,000 presentations at the 250th National Meeting & Exposition of the American Chemical Society (ACS), the world's largest scientific society, taking place here through Thursday.
If a person suffers a stroke that stems from a blood clot, their risk for a second stroke skyrockets, says Peter Caravan, Ph.D. The initial blood clot can break apart and cause more strokes if it is not quickly found and treated. Depending on where the blood clot is located, the treatment varies -- some of them respond well to drugs, while others are better addressed with surgery.
To locate a blood clot, a physician may need to use three different methods: ultrasound to check the carotid arteries or legs, magnetic resonance imaging (MRI) to scan the heart and computed tomography to view the lungs. "It's a shot in the dark," Caravan says. "Patients could end up being scanned multiple times by multiple techniques in order to locate a clot. We sought a method that could detect blood clots anywhere in the body with a single whole-body scan."
In previous work, Caravan's team at the Martinos Center for Biomedical Imaging at Massachusetts General Hospital identified a peptide that binds specifically to fibrin -- an insoluble protein fiber found in blood clots. In the current study, they developed a blood clot probe by attaching a radionuclide to the peptide. Radionuclides can be detected anywhere in the body by an imaging method called positron emission tomography (PET). The researchers used different radionuclides and peptides, as well as different chemical groups for linking the radionuclide to the peptide, to identify which combination would provide the brightest PET signal in blood clots. They ultimately constructed and tested 15 candidate blood clot probes.
The researchers first analyzed how well each probe bound to fibrin in a test tube, and then they studied how well the probe detected blood clots in rats. "The probes all had a similar affinity to fibrin in vitro, but, in rats, their performances were quite different," says Caravan. He attributed these differences to metabolism. Some probes were broken down quickly in the body and could no longer bind to blood clots, but others were resistant to metabolism. "The best probe was the one that was the most stable," he says. The team is moving forward into the next phase of research with this best-performing probe, called FBP8, which stands for "fibrin binding probe #8." It contained copper-64 as the radionuclide.
"Of course, the big question is, 'How well will these perform in patients?'" he says. Caravan explains that the group is hoping to start testing the probe in human patients in the fall, but it could take an additional five years of research before the probe is approved for routine use in a clinical setting.
A press conference on this topic will be held Tuesday, Aug. 18, at 2:30 p.m. Eastern time in the Boston Convention & Exhibition Center. Reporters may check-in at Room 153B in person, or watch live on YouTube http://bit.ly/ACSLiveBoston. To ask questions online, sign in with a Google account.
INFORMATION:
Caravan acknowledges funding from the National Heart, Lung, and Blood Institute; HL109448.
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Title
Development of a fibrin-targeted radiopharmaceutical: effect of chelate type, linker, and radiometal on in vivo efficacy
Abstract
Thrombosis is often the underlying cause of major cardiovascular diseases including heart attack, stroke, and venous thromboembolism, which are leading causes of morbidity and mortality. Thrombus imaging would benefit from a whole-body approach instead of multiple examinations (current approach), especially for those cardiovascular events (e.g., thromboembolism) where the identification of both culprit embolus and source thrombus is required. We have been developing a fibrin-specific probe for thrombus detection by derivatizing a short, cyclic peptide that has high affinity and specificity for fibrin. We took an agnostic approach and compared different radionuclides (Cu-64, Ga-68, F-18, In-111, Tc-99m), different chelators, and different linkers. We characterized the affinity of the cold compound to fibrin and measured thrombus uptake, pharmacokinetics, biodistribution, and metabolism in a common rat model of arterial thrombosis. While all probes had similar affinity for fibrin, the in vivo studies showed a wide range of efficacy and these differences could be traced to differences in metabolic stability, either peptide metabolism or dechelation of the radiometal. There was no correlation of in vivo efficacy with in vitro measures of thermodynamic stability or kinetic inertness. Here we describe these structure-activity studies which led us to identify one specific probe for clinical translation.
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