Instantaneous In Vivo Imaging of Acute Myocardial Infarct by NIR‐II Luminescent Nanodots
Fast and precise localization of ischemic tissues in the myocardium after an acute infarct is required by clinicians as the first step toward accurate and efficient treatment. Nowadays, diagnosis of a heart attack at early times is based on biochemical blood analysis (detection of cardiac enzymes) o...
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Veröffentlicht in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2020-07, Vol.16 (29), p.e1907171-n/a, Article 1907171 |
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Sprache: | eng |
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Zusammenfassung: | Fast and precise localization of ischemic tissues in the myocardium after an acute infarct is required by clinicians as the first step toward accurate and efficient treatment. Nowadays, diagnosis of a heart attack at early times is based on biochemical blood analysis (detection of cardiac enzymes) or by ultrasound‐assisted imaging. Alternative approaches are investigated to overcome the limitations of these classical techniques (time‐consuming procedures or low spatial resolution). As occurs in many other fields of biomedicine, cardiological preclinical imaging can also benefit from the fast development of nanotechnology. Indeed, bio‐functionalized near‐infrared‐emitting nanoparticles are herein used for in vivo imaging of the heart after an acute myocardial infarct. Taking advantage of the superior acquisition speed of near‐infrared fluorescence imaging, and of the efficient selective targeting of the near‐infrared‐emitting nanoparticles, in vivo images of the infarcted heart are obtained only a few minutes after the acute infarction event. This work opens an avenue toward cost‐effective, fast, and accurate in vivo imaging of the ischemic myocardium after an acute infarct.
Angiotensine II‐functionalized Ag2S nanodots enable rapid in vivo NIR‐II imaging of damage to the myocardium after a heart attack in mice. Less than 10 min after their intravenous injection, specific images are obtained and can be distinguished from control cases (non‐targeted nanoparticles and healthy mice). |
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ISSN: | 1613-6810 1613-6829 |
DOI: | 10.1002/smll.201907171 |