{"title":"A hydrated HA/F127 biointerface for polyphenol release modulation and active–passive antibacterial protection on EGCG-loaded UHMWPE joint materials","authors":"Yu Han, Jiang-Yu Li, Shu-Min Pan, Peiqi Yu, Mengfan Jing, Yaming Wang, Yue Ren, Ke Tian, Chuntai Liu, Changyu Shen","doi":"10.1007/s42114-026-02059-0","DOIUrl":null,"url":null,"abstract":"<div><p>Periprosthetic joint infection remains a major challenge for artificial joint materials, highlighting the need for antibacterial and anti-adhesive ultrahigh molecular weight polyethylene (UHMWPE) surfaces. Here, a hydrated hyaluronic acid (HA)/Pluronic F127 biointerface was constructed on epigallocatechin gallate (EGCG)-loaded UHMWPE to couple polyphenol release modulation with active–passive antibacterial protection. The HA/F127 layer contributed to enhancing the outward migration of EGCG from the UHMWPE matrix. Compared with uncoated EGCG/UHMWPE, this hydrated interface increased the 24 h cumulative EGCG release by 52%, with micro-FTIR depth profiling revealing surface-biased residual EGCG redistribution rather than broad matrix depletion. This release-modulating interface enhanced antibacterial activity, achieving inhibition ratios of 95% against <i>Staphylococcus aureus</i> and 91% against <i>Escherichia coli</i>. By reducing protein adsorption and bacterial retention, the hydrated HA/F127 surface further provided passive anti-adhesive protection complementary to EGCG-mediated bacterial inhibition. The modified surface maintained good cytocompatibility and exhibited a short-term boundary-lubrication effect. Overall, this work presents an active-release/passive-antifouling biointerface strategy to address infection-related challenges of UHMWPE-based biomaterials.</p><h3>Graphical abstract</h3><p>A hydrated HA/F127 biointerface was constructed on EGCG-loaded UHMWPE through stepwise interfacial immobilization. The polymeric interface modulates EGCG release while reducing bacterial/protein adhesion, thereby coupling EGCG-mediated active antibacterial activity with passive anti-adhesion and boundary lubrication for infection-resistant UHMWPE joint materials.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":7220,"journal":{"name":"Advanced Composites and Hybrid Materials","volume":"9 5","pages":""},"PeriodicalIF":15.5000,"publicationDate":"2026-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s42114-026-02059-0.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Composites and Hybrid Materials","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s42114-026-02059-0","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/29 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MATERIALS SCIENCE, COMPOSITES","Score":null,"Total":0}
引用次数: 0
Abstract
Periprosthetic joint infection remains a major challenge for artificial joint materials, highlighting the need for antibacterial and anti-adhesive ultrahigh molecular weight polyethylene (UHMWPE) surfaces. Here, a hydrated hyaluronic acid (HA)/Pluronic F127 biointerface was constructed on epigallocatechin gallate (EGCG)-loaded UHMWPE to couple polyphenol release modulation with active–passive antibacterial protection. The HA/F127 layer contributed to enhancing the outward migration of EGCG from the UHMWPE matrix. Compared with uncoated EGCG/UHMWPE, this hydrated interface increased the 24 h cumulative EGCG release by 52%, with micro-FTIR depth profiling revealing surface-biased residual EGCG redistribution rather than broad matrix depletion. This release-modulating interface enhanced antibacterial activity, achieving inhibition ratios of 95% against Staphylococcus aureus and 91% against Escherichia coli. By reducing protein adsorption and bacterial retention, the hydrated HA/F127 surface further provided passive anti-adhesive protection complementary to EGCG-mediated bacterial inhibition. The modified surface maintained good cytocompatibility and exhibited a short-term boundary-lubrication effect. Overall, this work presents an active-release/passive-antifouling biointerface strategy to address infection-related challenges of UHMWPE-based biomaterials.
Graphical abstract
A hydrated HA/F127 biointerface was constructed on EGCG-loaded UHMWPE through stepwise interfacial immobilization. The polymeric interface modulates EGCG release while reducing bacterial/protein adhesion, thereby coupling EGCG-mediated active antibacterial activity with passive anti-adhesion and boundary lubrication for infection-resistant UHMWPE joint materials.
期刊介绍:
Advanced Composites and Hybrid Materials is a leading international journal that promotes interdisciplinary collaboration among materials scientists, engineers, chemists, biologists, and physicists working on composites, including nanocomposites. Our aim is to facilitate rapid scientific communication in this field.
The journal publishes high-quality research on various aspects of composite materials, including materials design, surface and interface science/engineering, manufacturing, structure control, property design, device fabrication, and other applications. We also welcome simulation and modeling studies that are relevant to composites. Additionally, papers focusing on the relationship between fillers and the matrix are of particular interest.
Our scope includes polymer, metal, and ceramic matrices, with a special emphasis on reviews and meta-analyses related to materials selection. We cover a wide range of topics, including transport properties, strategies for controlling interfaces and composition distribution, bottom-up assembly of nanocomposites, highly porous and high-density composites, electronic structure design, materials synergisms, and thermoelectric materials.
Advanced Composites and Hybrid Materials follows a rigorous single-blind peer-review process to ensure the quality and integrity of the published work.