Methods for vascular imaging using nanoparticulate contrast agents
OwnerReinhard Koenig, Taffy J. Williamsinventors
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OwnerReinhard Koenig, Taffy J. Williamsinventors
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New and sensitive methods for imaging the perfusion of tissues and the extravasation of blood out vessels have been developed. The present invention is useful in the imaging of microperfusion in organ tissues (e.g., heart, liver, brain and kidneys) to aid in evaluating the perfusion status of organs on the level of the smallest blood vessels (i.e. capillaries). The present invention also provides methods and compositions for imaging and evaluating macrophages and plaque, e.g., vulnerable plaque. Such evaluations are important in a number of clinical diagnoses, including assessing organ damage associated with angina pectoris, heart attack, stroke, and the like, as well as assessing vessel leakages associated with aneurisms, diffuse bleedings after trauma, and the like.
An in vivo method for detecting or evaluating accumulated macrophages in a blood vessel of a subject comprising:
An in vivo method for detecting or evaluating plaque accumulation in a blood vessel of a subject comprising:
An in vivo method for predicting risk of vascular disease by detecting or evaluating accumulated macrophages within a blood vessel of a subject comprising:
An in vivo method for detecting or evaluating the perfusion status of a blood vessel or an organ in a subject comprising:
An in vivo method for detecting or evaluating the microperfusion status of a small blood vessel comprising:
An in vivo method for detecting or evaluating the perfusion status of a tumor in a subject comprising:
An in vivo method for assessing organ damage in a subject comprising
In one embodiment, said organ is selected from the group consisting of heart, brain, lung, kidney, liver, pancreas, or spleen.
An in vivo method for assessing leakage of blood from vessels in a subject comprising
A composition comprising a non-water soluble, nanoparticulate contrast agent having a mean particle size sufficient to allow the nanoparticulate contrast agent to be taken up by activated macrophages.
Dependencies are inferred from the claim text.