Elevated iron levels have been identified in a variety of neurologic disorders, including Parkinson’s, Huntington’s, Alzheimer’s, Friedreich’s ataxia and multiple sclerosis. It has been hypothesized that excess iron may play a role in the progressive deterioration observed in patients suffering from those diseases. Current MRI techniques (e.g. magnetic susceptibility imaging, and T2 and T1 weighted MR images) used to detect excess iron deposits rely on differences of bulk water proton relaxivity. Unfortunately, these techniques suffer from the presence of artifacts, thereby complicating clinical interpretation. More direct imaging methods are needed that would specifically image iron and only iron in tissue. A UB chemist has developed a series of ligands that represent an entirely new class of contrast agents that respond only upon sequestering endogenous iron in cells, making it possible to image Fe(II) and only Fe(II) within a sea of metal ions and other cellular components. These PARACEST-based contrast agents appear to be useful tools for monitoring excess iron levels in tissue and may facilitate the tracking and treatment (e.g. chelating agents, CNS drugs, etc.) of diseases involving aberrant iron levels. Additionally, their development as clinical tools would provide a much-needed alternative to lanthanide contrast agents (e.g. gadolinium), which can be problematic for patients with compromised renal function.
由于技术保密工作限制,技术信息无法完全展现,请通过邮箱或短信联系我们,获取更多技术资料。
progressive deterioration observed
magnetic susceptibility imaging
direct imaging methods
compromised renal function
current mri techniques