Description
Computed Tomography (CT) allows for the cutting edge use of non-invasive anatomical imaging of the human body and is commonly used to diagnose cardiovascular disease. However, there are two main limitations of CT: limited soft tissue contrast and the lack of molecular readout. In recent years, the development of gold nanoparticles (GNRs) as CT contrast agents have gained major attention, with a specific focus on overcoming these CT limitations. The unique properties of GNRs, such as high X-ray attenuation, easy synthesis, and most importantly the ability to incorporate targeted photothermal therapy to imaging, make it an attractive agent for molecular imaging.
Activated platelets are known to play a major role in the pathogenesis of atherosclerosis and ischaemia/ reperfusion injury post myocardial infarction. In the Atherothrombosis lab, we have developed a single-chain antibody which only targets and binds to activated platelets present in areas of disease, but does not bind to resting circulating platelets. We aim to design activated platelet-targeted GNRs for molecular imaging of atherosclerosis and myocardial infarction. Further on, we aim to develop a theranostic agent, by incorporating photothermal therapy or a therapeutic drug to the activated platelet-targeted GNRs for localised therapy, whilst ensuring limited systemic side effects.
Technologies to learn/apply: Nanotechnology, molecular imaging, preclinical imaging, CT, MR, biotechnology, recombinant protein design and production.
Essential criteria:
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords
Atherosclerosis, Atherothrombosis, Cardiovascular, CT imaging
Available options
PhD/Doctorate
Masters by research
Masters by coursework
Honours
Time commitment
Full-time
Top-up scholarship funding available
Yes
Year 1:
$6000
Physical location
Baker Heart & Diabetes Instititute, Prahran (Next to Alfred Hospital)
Research webpage
Co-supervisors
Prof
Geoff Pietersz
(External)