Mingqian He , Yuan Li , Dashuai Zhu , Junlang Li , Meggie Cangu , Panagiotis Tasoudis , Jiazhu Xu , Thomas G. Caranasos , Yi Hong , Ke Huang
{"title":"Stromal-platelet membrane-inspired nanoparticles (SPIN) for targeted heart repair","authors":"Mingqian He , Yuan Li , Dashuai Zhu , Junlang Li , Meggie Cangu , Panagiotis Tasoudis , Jiazhu Xu , Thomas G. Caranasos , Yi Hong , Ke Huang","doi":"10.1016/j.bioactmat.2025.06.055","DOIUrl":null,"url":null,"abstract":"<div><div>Myocardial infarction (MI), commonly known as a heart attack, remains a leading cause of death worldwide. Standard treatments, such as coronary stent placement or coronary artery bypass graft surgery, aim to restore blood flow to ischemic myocardial tissue. However, a significant complication of these procedures is ischemia/reperfusion (I/R) injury, which occurs when blood flow is restored, triggering oxidative stress, inflammation, and calcium overload that can further damage the heart. To limit the I/R injury following the coronary recanalization of an MI heart, we designed stromal-platelet membrane-inspired nanoparticles (SPINs) that consist of a poly (lactic-co-glycolic acid) (PLGA) core, decorated by a dual membrane coating: a platelet membrane for precise adhesion to the damaged endothelium area and a stromal cell membrane to enhance receptor-ligand interactions and immune-evasiveness. This unique dual-membrane configuration synergistically reduces fibrosis and inflammation while promoting angiomyogenesis. This combination integrates the vascular injury targeting and immune-evasive properties of the nanoparticle, making this dual-membrane design a promising add-on intervention to augment post- percutaneous coronary intervention recovery, enhancing outcomes and offering potential improved cardiac repair.</div></div>","PeriodicalId":8762,"journal":{"name":"Bioactive Materials","volume":"53 ","pages":"Pages 45-57"},"PeriodicalIF":18.0000,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioactive Materials","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452199X25002919","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
Myocardial infarction (MI), commonly known as a heart attack, remains a leading cause of death worldwide. Standard treatments, such as coronary stent placement or coronary artery bypass graft surgery, aim to restore blood flow to ischemic myocardial tissue. However, a significant complication of these procedures is ischemia/reperfusion (I/R) injury, which occurs when blood flow is restored, triggering oxidative stress, inflammation, and calcium overload that can further damage the heart. To limit the I/R injury following the coronary recanalization of an MI heart, we designed stromal-platelet membrane-inspired nanoparticles (SPINs) that consist of a poly (lactic-co-glycolic acid) (PLGA) core, decorated by a dual membrane coating: a platelet membrane for precise adhesion to the damaged endothelium area and a stromal cell membrane to enhance receptor-ligand interactions and immune-evasiveness. This unique dual-membrane configuration synergistically reduces fibrosis and inflammation while promoting angiomyogenesis. This combination integrates the vascular injury targeting and immune-evasive properties of the nanoparticle, making this dual-membrane design a promising add-on intervention to augment post- percutaneous coronary intervention recovery, enhancing outcomes and offering potential improved cardiac repair.
Bioactive MaterialsBiochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
28.00
自引率
6.30%
发文量
436
审稿时长
20 days
期刊介绍:
Bioactive Materials is a peer-reviewed research publication that focuses on advancements in bioactive materials. The journal accepts research papers, reviews, and rapid communications in the field of next-generation biomaterials that interact with cells, tissues, and organs in various living organisms.
The primary goal of Bioactive Materials is to promote the science and engineering of biomaterials that exhibit adaptiveness to the biological environment. These materials are specifically designed to stimulate or direct appropriate cell and tissue responses or regulate interactions with microorganisms.
The journal covers a wide range of bioactive materials, including those that are engineered or designed in terms of their physical form (e.g. particulate, fiber), topology (e.g. porosity, surface roughness), or dimensions (ranging from macro to nano-scales). Contributions are sought from the following categories of bioactive materials:
Bioactive metals and alloys
Bioactive inorganics: ceramics, glasses, and carbon-based materials
Bioactive polymers and gels
Bioactive materials derived from natural sources
Bioactive composites
These materials find applications in human and veterinary medicine, such as implants, tissue engineering scaffolds, cell/drug/gene carriers, as well as imaging and sensing devices.