A Cardiac-Targeted Nanozyme Interrupts the Inflammation-Free Radical Cycle in Myocardial Infarction

© 2023 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 36(2024), 2 vom: 08. Jan., Seite e2308477
1. Verfasser: Liu, Xueliang (VerfasserIn)
Weitere Verfasser: Chen, Binghua, Chen, Jingqi, Wang, Xuan, Dai, Xinfeng, Li, Yuqing, Zhou, Huayuan, Wu, Lian-Ming, Liu, Zhuang, Yang, Yu
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2024
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article block of inflammation-free radical cycle cardiac targeting myocardial infarction nanozyme tannic acid Anti-Inflammatory Agents Free Radicals Polyphenols
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520 |a Severe systemic inflammation following myocardial infarction (MI) is a major cause of patient mortality. MI-induced inflammation can trigger the production of free radicals, which in turn ultimately leads to increased inflammation in cardiac lesions (i.e., inflammation-free radicals cycle), resulting in heart failure and patient death. However, currently available anti-inflammatory drugs have limited efficacy due to their weak anti-inflammatory effect and poor accumulation at the cardiac site. Herein, a novel Fe-CurTA nanozyme is developed for targeted therapy of MI, which is generated by coordinating Fe3+ and anti-inflammatory drug curcumin (Cur) with further modification of tannic acid (TA). Such Fe-Cur@TA nanozyme exhibits excellent free radicals scavenging and anti-inflammatory properties by reducing immune cell infiltration, promoting macrophage polarization toward the M2-like phenotype, suppressing inflammatory cytokine secretion, and blocking the inflammatory free radicals cycle. Furthermore, due to the high affinity of TA for cardiac tissue, Fe-Cur@TA shows an almost tenfold greater in cardiac retention and uptake than Fe-Cur. In mouse and preclinical beagle dog MI models, Fe-Cur@TA nanozyme preserves cardiac function and reduces scar size, suggesting promising potential for clinical translation in cardiovascular disease 
650 4 |a Journal Article 
650 4 |a block of inflammation-free radical cycle 
650 4 |a cardiac targeting 
650 4 |a myocardial infarction 
650 4 |a nanozyme 
650 7 |a tannic acid  |2 NLM 
650 7 |a Anti-Inflammatory Agents  |2 NLM 
650 7 |a Free Radicals  |2 NLM 
650 7 |a Polyphenols  |2 NLM 
700 1 |a Chen, Binghua  |e verfasserin  |4 aut 
700 1 |a Chen, Jingqi  |e verfasserin  |4 aut 
700 1 |a Wang, Xuan  |e verfasserin  |4 aut 
700 1 |a Dai, Xinfeng  |e verfasserin  |4 aut 
700 1 |a Li, Yuqing  |e verfasserin  |4 aut 
700 1 |a Zhou, Huayuan  |e verfasserin  |4 aut 
700 1 |a Wu, Lian-Ming  |e verfasserin  |4 aut 
700 1 |a Liu, Zhuang  |e verfasserin  |4 aut 
700 1 |a Yang, Yu  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Advanced materials (Deerfield Beach, Fla.)  |d 1998  |g 36(2024), 2 vom: 08. Jan., Seite e2308477  |w (DE-627)NLM098206397  |x 1521-4095  |7 nnas 
773 1 8 |g volume:36  |g year:2024  |g number:2  |g day:08  |g month:01  |g pages:e2308477 
856 4 0 |u http://dx.doi.org/10.1002/adma.202308477  |3 Volltext 
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