Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/141169
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Type: Journal article
Title: Detection of atherosclerotic plaques with HDL-like porphyrin nanoparticles using an intravascular dual-modality optical coherence tomography and fluorescence system
Author: Chen, R.
Sandeman, L.
Nankivell, V.
Tan, J.T.M.
Rashidi, M.
Psaltis, P.J.
Zheng, G.
Bursill, C.
McLaughlin, R.A.
Li, J.
Citation: Scientific Reports, 2024; 14(1):12359-1-12359-10
Publisher: Nature Portfolio
Issue Date: 2024
ISSN: 2045-2322
2045-2322
Statement of
Responsibility: 
Rouyan Chen, Lauren Sandeman, Victoria Nankivell, JoanneT. M.Tan, Mohammad Rashidi, Peter J. Psaltis, Gang Zheng, Christina Bursill, Robert A. McLaughlin, Jiawen Li
Abstract: Atherosclerosis is the build-up of fatty plaques within blood vessel walls, which can occlude the vessels and cause strokes or heart attacks. It gives rise to both structural and biomolecular changes in the vessel walls. Current single-modality imaging techniques each measure one of these two aspects but fail to provide insight into the combined changes. To address this, our team has developed a dual-modality imaging system which combines optical coherence tomography (OCT) and fluorescence imaging that is optimized for a porphyrin lipid nanoparticle that emits fluorescence and targets atherosclerotic plaques. Atherosclerosis-prone apolipoprotein (Apo)e-/- mice were fed a high cholesterol diet to promote plaque development in descending thoracic aortas. Following infusion of porphyrin lipid nanoparticles in atherosclerotic mice, the fiber-optic probe was inserted into the aorta for imaging, and we were able to robustly detect a porphyrin lipid-specific fluorescence signal that was not present in saline-infused control mice. We observed that the nanoparticle fluorescence colocalized in areas of CD68+ macrophages. These results demonstrate that our system can detect the fluorescence from nanoparticles, providing complementary biological information to the structural information obtained from simultaneously acquired OCT.
Keywords: Biophotonics; Cardiovascular diseases; Nanoparticles
Rights: © The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
DOI: 10.1038/s41598-024-63132-6
Grant ID: http://purl.org/au-research/grants/nhmrc/2022337
http://purl.org/au-research/grants/nhmrc/1178912
http://purl.org/au-research/grants/nhmrc/1184571
http://purl.org/au-research/grants/nhmrc/2001646
http://purl.org/au-research/grants/nhmrc/2002254
http://purl.org/au-research/grants/nhmrc/2008462
Published version: http://dx.doi.org/10.1038/s41598-024-63132-6
Appears in Collections:Research Outputs

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