4.1 Article

Targeting Nanostrategies for Imaging of Atherosclerosis

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CONTRAST MEDIA & MOLECULAR IMAGING
卷 2021, 期 -, 页码 -

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WILEY-HINDAWI
DOI: 10.1155/2021/6664471

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  1. project Nanoparticles Based on a Theranostic Approach for the Delivery of a MicroRNA Set to Be Used for Breast and Thyroid Cancers Resistant to Drugs - MIUR Progetti di Ricerca di Rilevante Interesse Nazionale (PRIN) Bando 2017 [2017MHJJ55]

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Despite advancements in cardiovascular research, atherosclerosis remains the leading cause of death globally. Current imaging methods for diagnosing ASCVD lack the ability to accurately identify high-risk plaque rupture. Utilizing hydrogel nanoparticles encapsulating Gd-DTPA with active targeting of plaque macrophages can potentially enable earlier and more accurate diagnosis in the complex environment of human atherosclerotic plaque.
Despite the progress in cardiovascular research, atherosclerosis still represents the main cause of death worldwide. Clinically, the diagnosis of Atherosclerotic Cardiovascular Disease (ASCVD) relies on imaging methodologies including X-ray angiography and computed tomography (CT), which however still fails in the identification of patients at high risk of plaque rupture, the main cause of severe clinical events as stroke and heart attack. Magnetic resonance imaging, which is characterized by very high spatial resolution, could provide a better characterization of atherosclerotic plaque (AP) anatomy and composition, aiding in the identification of vulnerable plaques. In this context, hydrogel matrices, which have been demonstrated able to boost relaxometric properties of Gd-based contrast agents (CAs) by the effect of Hydrodenticity, represent a valuable tool towards the precision imaging of ASCVD improving the performance of this class of CAs while reducing systemic toxicity. In particular, hydrogel nanoparticles encapsulating Gd-DTPA can further contribute to providing CA-specific accumulation in the AP by nanoparticle surface decoration triggering an active targeting of the AP with the overall effect of allowing an earlier and more accurate diagnosis. In this work, we tested crosslinked Hyaluronic Acid Nanoparticles (cHANPs) in the complex environment of human atherosclerotic plaque. In addition, the surface of cHANPs was decorated with the antibody anti-CD36 (Ab36-cHANPs) for the active targeting of AP-associated macrophages. Results demonstrate that the Hydrodenticity of cHANPs and Ab36-cHANPs is preserved in this complex system and, preliminarily, that interaction of these probes with the AP is present.

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