Completed Brain & Nervous System Heart, Stroke & Blood

Molecular magnetic resonance imaging with microparticles of iron oxide.

In plain English

AI plain-English summary

Tiny iron particles, each coated with a targeting molecule, are being tested as a new way to spot disease on MRI scans before any visible damage appears. Current MRI contrast agents highlight anatomy but cannot reveal what is happening at a molecular level. This team has developed microparticles of iron oxide (MPIO) that bind to specific biological targets, producing a strong, clear signal on the scan. The problem is that most molecular imaging agents never get tested in the real-world roles they were designed for. This project will change that. The researchers will test MPIO in three specific situations: measuring molecular expression non-invasively and confirming it with tissue samples; detecting early molecular signals that predict future atherosclerosis before any plaque forms; and monitoring whether a treatment is working when standard scans show no change. They will also refine the particles themselves, making them biodegradable and testing how tightly and quickly they bind to targets under flow conditions. If successful, this could give clinicians a tool to catch cardiovascular disease earlier, track treatment response more accurately, and move beyond the limits of anatomical imaging. The work is applied and device-focused, with clear translational potential.

View original technical description
We have designed, developed and applied a new class of molecular magnetic resonance imaging agent. Ligand-conjugated iron oxide microparticles (MPIO). For the majority of contrast agent approaches there has been no attempt to apply the agent in the very roles for which they were developed. However, for MPIO, where contrast effects are highly conspicuous and readily quantifiable, there is a compelling case to proceed to a more sophisticated assessment of utility. Therefore, in Aim 1 we will tes t MPIO in three critical areas: (A) Non-invasive quantification of molecular expression and distribution with corroboration through tissue analyses. (B) Identification of pre-lesion molecular signals that anticipate the later development of atherosclerosis. (C) Monitoring responses to treatment that are not apparent using conventional anatomical imaging techniques. Aim 2 will focus on refinements in targeting strategies and MPIO design to make more biologically effective contrast agents. We will test association / dissociation kinetics and affinities of MPIO conjugated to a range of ligands (including novel synthetic glycoproteins) under flow conditions in vitro and we will evaluate the properties of a new class of biodegradable MPIO in vitro and in vivo, including disposal and dispersal if the iron oxide core.

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Researchers

Robin Choudhury (EPMC Awardee)

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Original classification

Senior Research Fellowship Clinical

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