Design of a Zn-based nanozyme injectable multifunctional hydrogel with ROS scavenging activity for myocardial infarction therapy

IF 9.6 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Yiming Zhong , Yi Yang , Yuze Xu , Bei Qian , Shixing Huang , Qiang Long , Zhaoxi Qi , Xiaojun He , Yecen Zhang , Lihui Li , Wangxi Hai , Xinming Wang , Qiang Zhao , Xiaofeng Ye
{"title":"Design of a Zn-based nanozyme injectable multifunctional hydrogel with ROS scavenging activity for myocardial infarction therapy","authors":"Yiming Zhong ,&nbsp;Yi Yang ,&nbsp;Yuze Xu ,&nbsp;Bei Qian ,&nbsp;Shixing Huang ,&nbsp;Qiang Long ,&nbsp;Zhaoxi Qi ,&nbsp;Xiaojun He ,&nbsp;Yecen Zhang ,&nbsp;Lihui Li ,&nbsp;Wangxi Hai ,&nbsp;Xinming Wang ,&nbsp;Qiang Zhao ,&nbsp;Xiaofeng Ye","doi":"10.1016/j.actbio.2024.01.015","DOIUrl":null,"url":null,"abstract":"<div><p><span>The existing strategies for myocardial infarction therapy mainly focus on reinstating myocardial blood supply<span>, often disregarding the intrinsic and intricate microenvironment created by elevated levels of reactive oxygen species (ROS) that accompanies myocardial infarction. This microenvironment entails cardiomyocytes apoptosis, substantial vascular cell death, excessive inflammatory infiltration and fibrosis. In such situation, the present study introduces a zinc-based nanozyme injectable multifunctional hydrogel, crafted from ZIF-8, to counteract ROS effects after myocardial infarction. The hydrogel exhibits both </span></span>superoxide dismutase<span> (SOD)-like and catalase<span><span><span> (CAT)-like enzymatic activities, proficiently eliminating surplus ROS in the infarcted region and interrupting ROS-driven inflammatory cascades. Furthermore, the hydrogel's exceptional immunomodulatory ability spurs a notable transformation of macrophages into the M2 phenotype, effectively neutralizing inflammatory factors and indirectly fostering vascularization in the infarcted region. For high ROS and demanding for zinc of the infarcted microenvironment, the gradual release of </span>zinc ions as the hydrogel degrades further enhances the bioactive and catalytic performance of the nanozymes, synergistically promoting cardiac function post myocardial infarction. In conclusion, this system of deploying catalytic </span>nanomaterials<span> within bioactive matrices for ROS-related ailment therapy not only establishes a robust foundation for biomedical material development, but also promises a holistic approach towards addressing myocardial infarction complexities.</span></span></span></p></div><div><h3>Statement of significance</h3><p><span>Myocardial infarction remains the leading cause of death worldwide. However, the existing strategies for myocardial infarction therapy mainly focus on reinstating myocardial blood supply. These therapies often ignore the intrinsic and intricate microenvironment created by elevated levels of reactive oxygen species (ROS). Hence, we designed an injectable Zn-Based nanozyme hydrogel with ROS scavenging activity for myocardial infarction therapy. ALG-(ZIF-8) can significantly reduce ROS in the infarcted area and alleviate the ensuing pathological process. ALG-(ZIF-8) gradually releases </span>zinc ions<span> to participate in the repair process and improves cardiac function. Overall, this multifunctional hydrogel equipped with ZIF-8 makes full use of the characteristics of clearing ROS and slowly releasing zinc ions, and we are the first to test the therapeutic efficacy of Zinc-MOFs crosslinked-alginate hydrogel for myocardial infarction.</span></p></div>","PeriodicalId":237,"journal":{"name":"Acta Biomaterialia","volume":"177 ","pages":"Pages 62-76"},"PeriodicalIF":9.6000,"publicationDate":"2024-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Biomaterialia","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1742706124000151","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0

Abstract

The existing strategies for myocardial infarction therapy mainly focus on reinstating myocardial blood supply, often disregarding the intrinsic and intricate microenvironment created by elevated levels of reactive oxygen species (ROS) that accompanies myocardial infarction. This microenvironment entails cardiomyocytes apoptosis, substantial vascular cell death, excessive inflammatory infiltration and fibrosis. In such situation, the present study introduces a zinc-based nanozyme injectable multifunctional hydrogel, crafted from ZIF-8, to counteract ROS effects after myocardial infarction. The hydrogel exhibits both superoxide dismutase (SOD)-like and catalase (CAT)-like enzymatic activities, proficiently eliminating surplus ROS in the infarcted region and interrupting ROS-driven inflammatory cascades. Furthermore, the hydrogel's exceptional immunomodulatory ability spurs a notable transformation of macrophages into the M2 phenotype, effectively neutralizing inflammatory factors and indirectly fostering vascularization in the infarcted region. For high ROS and demanding for zinc of the infarcted microenvironment, the gradual release of zinc ions as the hydrogel degrades further enhances the bioactive and catalytic performance of the nanozymes, synergistically promoting cardiac function post myocardial infarction. In conclusion, this system of deploying catalytic nanomaterials within bioactive matrices for ROS-related ailment therapy not only establishes a robust foundation for biomedical material development, but also promises a holistic approach towards addressing myocardial infarction complexities.

Statement of significance

Myocardial infarction remains the leading cause of death worldwide. However, the existing strategies for myocardial infarction therapy mainly focus on reinstating myocardial blood supply. These therapies often ignore the intrinsic and intricate microenvironment created by elevated levels of reactive oxygen species (ROS). Hence, we designed an injectable Zn-Based nanozyme hydrogel with ROS scavenging activity for myocardial infarction therapy. ALG-(ZIF-8) can significantly reduce ROS in the infarcted area and alleviate the ensuing pathological process. ALG-(ZIF-8) gradually releases zinc ions to participate in the repair process and improves cardiac function. Overall, this multifunctional hydrogel equipped with ZIF-8 makes full use of the characteristics of clearing ROS and slowly releasing zinc ions, and we are the first to test the therapeutic efficacy of Zinc-MOFs crosslinked-alginate hydrogel for myocardial infarction.

Abstract Image

Abstract Image

设计具有清除 ROS 活性的锌基纳米酶注射型多功能水凝胶,用于心肌梗死治疗
现有的心肌梗塞治疗策略主要侧重于恢复心肌供血,但往往忽视了心肌梗塞时活性氧(ROS)水平升高所造成的错综复杂的内在微环境。这种微环境包括心肌细胞凋亡、大量血管细胞死亡、过度炎症浸润和纤维化。在这种情况下,本研究引入了一种由 ZIF-8 制成的锌基纳米注射多功能水凝胶,以对抗心肌梗死后的 ROS 影响。这种水凝胶同时具有类似超氧化物歧化酶(SOD)和类似过氧化氢酶(CAT)的酶活性,能有效消除梗死区域过剩的 ROS,阻断 ROS 驱动的炎症级联反应。此外,水凝胶还具有出色的免疫调节能力,能促使巨噬细胞明显转变为 M2 表型,有效中和炎症因子,间接促进梗死区域的血管生成。对于高 ROS 和需要锌的梗塞微环境,锌离子随着水凝胶降解而逐渐释放,进一步增强了纳米酶的生物活性和催化性能,协同促进心肌梗塞后的心脏功能。总之,这种在生物活性基质中部署催化纳米材料以治疗 ROS 相关疾病的系统不仅为生物医学材料的开发奠定了坚实的基础,而且有望为解决心肌梗塞的复杂问题提供一种全面的方法。意义说明:心肌梗塞仍然是全球死亡的主要原因。然而,现有的心肌梗塞治疗策略主要侧重于恢复心肌供血。这些疗法往往忽视了活性氧(ROS)水平升高所造成的内在复杂微环境。因此,我们设计了一种具有清除 ROS 活性的可注射锌基纳米酶水凝胶,用于心肌梗死治疗。ALG-(ZIF-8)能显著减少心肌梗死区域的ROS,缓解随之而来的病理过程。ALG-(ZIF-8) 能逐渐释放锌离子参与修复过程,改善心脏功能。总之,这种配备了 ZIF-8 的多功能水凝胶充分利用了其清除 ROS 和缓慢释放锌离子的特性,我们首次测试了锌-MOFs 交联-精氨酸水凝胶对心肌梗死的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信