Dual-ligand supramolecular nanofibers inspired by the renin-angiotensin system for the targeting and synergistic therapy of myocardial infarction

• Published in: Theranostics Vol. 11; no. 8; pp. 3725 - 3741
• Main Authors: Wen, Zhanpeng, Zhan, Jie, Li, Hekai, Xu, Guanghui, Ma, Shaodan, Zhang, Jianwu, Li, Zehua, Ou, Caiwen, Yang, Zhimou, Cai, Yanbin, Chen, Minsheng
• Format: Journal Article
• Language: English
• Published: Australia Ivyspring International Publisher Pty Ltd 01.01.2021; Ivyspring International Publisher
• Subjects: Cardiac function; Drugs; Efficiency; Endocrine system; Heart attacks; Heart failure; Hydrogels; Ligands; Medical prognosis; Nanoparticles; Peptides; Research Paper; Rheology; Spectrum analysis; targeted therapy; supramolecular self-assembly; renin-angiotensin system (RAS); myocardial infarction; synergistic effect
• ISSN: 1838-7640; 1838-7640
• DOI: 10.7150/thno.53644

The compensatory activation of the renin-angiotensin system (RAS) after myocardial infarction (MI) plays a crucial role in the pathogenesis of heart failure. Most existing studies on this subject focus on mono- or dual-therapy of blocking the RAS, which exhibit limited efficacy and often causes serious adverse reactions. Few studies have been conducted on targeted therapy based on the activated RAS post-MI. Thus, the development of multiple-functional nanomedicine with concurrent targeting ability and synergistic therapeutic effect against RAS may show great promise in improving cardiac function post-MI. We utilized a cooperative self-assembly strategy constructing supramolecular nanofibers- telmisartan-doped co-assembly nanofibers ( ) to counter-regulate RAS through targeted delivery and combined therapy. were prepared through serial steps of solvent exchange, heating incubation, gelation, centrifugation, and lyophilization, in which the telmisartan was doped in the self-assembly process of to obtain the co-assembly nanofibers wherein they act as both therapeutic agents and target-guide agents. exhibited the desired binding affinity to the two different receptors, AT1R and MasR. Through the dual ligand-receptor interactions to mediate the coincident downstream pathways, not only displayed favorably targeted properties to hypoxic cardiomyocytes, but also exerted synergistic therapeutic effects in apoptosis reduction, inflammatory response alleviation, and fibrosis inhibition and , significantly protecting cardiac function and mitigating post-MI adverse outcomes. A dual-ligand nanoplatform was successfully developed to achieve targeted and synergistic therapy against cardiac deterioration post-MI. We envision that the integration of multiple therapeutic agents through supramolecular self-assembly would offer new insight for the systematic and targeted treatment of cardiovascular diseases.