Non-Invasive Photoacoustic Imaging of In Vivo Mice with Erythrocyte Derived Optical Nanoparticles to Detect CAD/MI

Autor: Georges El Fakhri, Joseph C. Wu, Zhen Cheng, Yonggang Liu, Taylor Hanley, Sanjiv S. Gambhir, Hao Chen, Raiyan T. Zaman, Bahman Anvari, Steven R. Long
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
Pathology
medicine.medical_specialty
Erythrocytes
Myocardial Infarction
lcsh:Medicine
Bioengineering
Coronary Artery Disease
030204 cardiovascular system & hematology
Cardiovascular
Article
Photoacoustic Techniques
Coronary artery disease
Mice
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Fibrosis
In vivo
medicine
Animals
Nanotechnology
lcsh:Science
Heart Disease - Coronary Heart Disease
Multidisciplinary
Animal
business.industry
Optical Imaging
lcsh:R
Atherosclerosis
medicine.disease
Coronary Vessels
Stenosis
Heart Disease
Good Health and Well Being
030104 developmental biology
medicine.anatomical_structure
Cardiovascular diseases
chemistry
Disease Models
Nanoparticles
Biomedical Imaging
lcsh:Q
Ligation
business
Indocyanine green
Interventional cardiology
Preclinical imaging
Artery
Zdroj: Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-9 (2020)
Scientific reports, vol 10, iss 1
ISSN: 2045-2322
Popis: Coronary artery disease (CAD) causes mortality and morbidity worldwide. We used near-infrared erythrocyte-derived transducers (NETs), a contrast agent, in combination with a photoacoustic imaging system to identify the locations of atherosclerotic lesions and occlusion due to myocardial-infarction (MI). NETs (≈90 nm diameter) were fabricated from hemoglobin-depleted mice erythrocyte-ghosts and doped with Indocyanine Green (ICG). Ten weeks old male C57BL/6 mice (n = 9) underwent left anterior descending (LAD) coronary artery ligation to mimic vulnerable atherosclerotic plaques and their rupture leading to MI. 150 µL of NETs (20 µM ICG,) was IV injected via tail vein 1-hour prior to photoacoustic (PA) and fluorescence in vivo imaging by exciting NETs at 800 nm and 650 nm, respectively. These results were verified with histochemical analysis. We observed ≈256-fold higher PA signal from the accumulated NETs in the coronary artery above the ligation. Fluorescence signals were detected in LAD coronary, thymus, and liver. Similar signals were observed when the chest was cut open. Atherosclerotic lesions exhibited inflammatory cells. Liver demonstrated normal portal tract, with no parenchymal necrosis, inflammation, fibrosis, or other pathologic changes, suggesting biocompatibility of NETs. Non-invasively detecting atherosclerotic plaques and stenosis using NETs may lay a groundwork for future clinical detection and improving CAD risk assessment.
Databáze: OpenAIRE