<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang H</submitter><funding>Fundamental Research Funds for the Central Universities</funding><funding>National Natural Science Foundation of China</funding><funding>Third People's Hospital of Chengdu Scientific Research Project</funding><funding>Chengdu Science and Technology Bureau project</funding><pagination>e09998</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12697898</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(46)</volume><pubmed_abstract>A multifunctional high internal phase Pickering emulsion (HIPPE-QU) is developed to address immune dysregulation in periodontitis by reprogramming macrophage metabolism and promoting tissue regeneration. Fabricated via one-step homogenization, HIPPE-QU features a 75% internal phase and is co-stabilized by gelatin nanoparticles (GNPs) and copper-doped hydroxyapatite (HA-Cu), forming a gel-like, injectable emulgel suitable for clinical application. Hydrophobic quercetin (QU) is encapsulated in the internal phase and chelates with Cu&lt;sup>2&lt;/sup>⁺ and Ca&lt;sup>2&lt;/sup>⁺ at the interface, enabling sustained and pH-responsive release under the acidic periodontal environment. The spatially organized loading strategy across dispersed, interfacial, and internal phases yields synergistic antibacterial </pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Interfacial Coordination-Engineered Emulgel Modulates the Osteo-Immune Microenvironment in Periodontitis Treatment Via HIF1 Signaling Pathway-Induced Metabolic Reprogramming.</pubmed_title><pmcid>PMC12697898</pmcid><funding_grant_id>CSY-YN-01-2023-014</funding_grant_id><funding_grant_id>2024-YF05-00183-SN</funding_grant_id><funding_grant_id>2023PI13</funding_grant_id><funding_grant_id>2024-YF05-00178-SN</funding_grant_id><funding_grant_id>82101012</funding_grant_id><funding_grant_id>22172120</funding_grant_id><funding_grant_id>2682025ZTPY044</funding_grant_id><pubmed_authors>Peng X</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Tan H</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Yuan Q</pubmed_authors><pubmed_authors>Lin W</pubmed_authors><pubmed_authors>Weng J</pubmed_authors><pubmed_authors>Guo T</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Chen R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interfacial Coordination-Engineered Emulgel Modulates the Osteo-Immune Microenvironment in Periodontitis Treatment Via HIF1 Signaling Pathway-Induced Metabolic Reprogramming.</name><description>A multifunctional high internal phase Pickering emulsion (HIPPE-QU) is developed to address immune dysregulation in periodontitis by reprogramming macrophage metabolism and promoting tissue regeneration. Fabricated via one-step homogenization, HIPPE-QU features a 75% internal phase and is co-stabilized by gelatin nanoparticles (GNPs) and copper-doped hydroxyapatite (HA-Cu), forming a gel-like, injectable emulgel suitable for clinical application. Hydrophobic quercetin (QU) is encapsulated in the internal phase and chelates with Cu&lt;sup>2&lt;/sup>⁺ and Ca&lt;sup>2&lt;/sup>⁺ at the interface, enabling sustained and pH-responsive release under the acidic periodontal environment. The spatially organized loading strategy across dispersed, interfacial, and internal phases yields synergistic antibacterial </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-07-15T11:20:47.68Z</modification><creation>2026-07-04T03:11:27.764Z</creation></dates><accession>S-EPMC12697898</accession><cross_references><pubmed>41020683</pubmed><doi>10.1002/advs.202509998</doi></cross_references></HashMap>