<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Toita R</submitter><funding>Niterra Co., Ltd.</funding><funding>Japan Society for the Promotion of Science</funding><pagination>e2302611</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11468989</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(5)</volume><pubmed_abstract>Implantable biomaterials trigger foreign body reactions (FBRs), which reduces the functional life of medical devices and prevents effective tissue regeneration. Although existing therapeutic approaches can circumvent collagen-rich fibrotic encapsulation secondary to FBRs, they disrupt native tissue repair. Herein, a new surface engineering strategy in which an apoptotic-mimetic, immunomodulatory, phosphatidylserine liposome (PSL) is released from an implant coating to induce the formation of a macrophage phenotype that mitigates FBRs and improves tissue healing is described. PSL-multilayers constructed on implant surfaces via the layer-by-layer method release PSLs over a 1-month period. In rat muscles, poly(etheretherketone) (PEEK), a nondegradable polymer implant model, induces FBRs with </pubmed_abstract><journal>Advanced healthcare materials</journal><pubmed_title>Releasable, Immune-Instructive, Bioinspired Multilayer Coating Resists Implant-Induced Fibrosis while Accelerating Tissue Repair.</pubmed_title><pmcid>PMC11468989</pmcid><funding_grant_id>JP18K12091</funding_grant_id><funding_grant_id>JP21H03833</funding_grant_id><funding_grant_id>JP23K18442</funding_grant_id><pubmed_authors>Tsuchiya A</pubmed_authors><pubmed_authors>Kasahara S</pubmed_authors><pubmed_authors>Kang JH</pubmed_authors><pubmed_authors>Toita R</pubmed_authors><pubmed_authors>Kitamura M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Releasable, Immune-Instructive, Bioinspired Multilayer Coating Resists Implant-Induced Fibrosis while Accelerating Tissue Repair.</name><description>Implantable biomaterials trigger foreign body reactions (FBRs), which reduces the functional life of medical devices and prevents effective tissue regeneration. Although existing therapeutic approaches can circumvent collagen-rich fibrotic encapsulation secondary to FBRs, they disrupt native tissue repair. Herein, a new surface engineering strategy in which an apoptotic-mimetic, immunomodulatory, phosphatidylserine liposome (PSL) is released from an implant coating to induce the formation of a macrophage phenotype that mitigates FBRs and improves tissue healing is described. PSL-multilayers constructed on implant surfaces via the layer-by-layer method release PSLs over a 1-month period. In rat muscles, poly(etheretherketone) (PEEK), a nondegradable polymer implant model, induces FBRs with </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-04T08:18:05.69Z</modification><creation>2025-04-04T08:18:05.69Z</creation></dates><accession>S-EPMC11468989</accession><cross_references><pubmed>38095751</pubmed><doi>10.1002/adhm.202302611</doi></cross_references></HashMap>