心肌损伤的靶向成像。

David E Sosnovik, Matthias Nahrendorf, Ralph Weissleder
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引用次数: 20

摘要

分子显像剂可以靶向心肌细胞表面的特定受体或蛋白质,也可以靶向释放到间质空间的酶,如组织蛋白酶、基质金属蛋白酶和髓过氧化物酶。然而,心肌分子成像要求显像剂体积小、灵敏度高(纳摩尔级或更高),并能进入间隙。一些符合这些标准的新型药物已被用于心肌靶向分子成像应用。磁共振、荧光和单光子发射CT已被用于成像这些试剂产生的分子信号。在心肌中使用靶向显像剂有可能为心肌损伤的病理生理学提供有价值的见解,并促进新的治疗策略的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted imaging of myocardial damage.

Molecular imaging agents can be targeted to a specific receptor or protein on the cardiomyocyte surface, or to enzymes released into the interstitial space, such as cathepsins, matrix metalloproteinases and myeloperoxidase. Molecular imaging of the myocardium, however, requires the imaging agent to be small, sensitive (nanomolar levels or better), and able to gain access to the interstitial space. Several novel agents that fulfill these criteria have been used for targeted molecular imaging applications in the myocardium. Magnetic resonance, fluorescence, and single-photon emission CT have been used to image the molecular signals generated by these agents. The use of targeted imaging agents in the myocardium has the potential to provide valuable insights into the pathophysiology of myocardial injury and to facilitate the development of novel therapeutic strategies.

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