<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(11)</volume><submitter>Chen W</submitter><pubmed_abstract>Acute respiratory distress syndrome (ARDS) is the leading cause of respiratory failure with high morbidity and mortality. Pulmonary surfactant (PS)-based complementary therapies have exhibited potential for ARDS healing and applied as an adjunctive therapy strategy. Coacervate (Coac) has the characteristics of softness, deformability and excellent molecular enrichment properties, and has attracted extensive attention in the biomedical field. Here PS and coacervate were combined for the potential ARDS treatment. The Coac, fabricated from polyallylamine hydrochloride (PAH) and adenosine triphosphate (ATP) by simple mixing, exhibited soft droplet property and high enrichment for dexamethasone sodium phosphate (DSP). To avoid the fusion effect of membraneless coacervate and endow it with biolo</pubmed_abstract><journal>Acta pharmaceutica Sinica. B</journal><pagination>5945-5965</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12648001</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pulmonary surfactant-biomimetic membranized coacervate injection for acute respiratory distress syndrome therapy.</pubmed_title><pmcid>PMC12648001</pmcid><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Kong L</pubmed_authors><pubmed_authors>Fu C</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Xie Q</pubmed_authors><pubmed_authors>Kang J</pubmed_authors><pubmed_authors>Yang C</pubmed_authors><pubmed_authors>Zhou Z</pubmed_authors><pubmed_authors>Batur S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pulmonary surfactant-biomimetic membranized coacervate injection for acute respiratory distress syndrome therapy.</name><description>Acute respiratory distress syndrome (ARDS) is the leading cause of respiratory failure with high morbidity and mortality. Pulmonary surfactant (PS)-based complementary therapies have exhibited potential for ARDS healing and applied as an adjunctive therapy strategy. Coacervate (Coac) has the characteristics of softness, deformability and excellent molecular enrichment properties, and has attracted extensive attention in the biomedical field. Here PS and coacervate were combined for the potential ARDS treatment. The Coac, fabricated from polyallylamine hydrochloride (PAH) and adenosine triphosphate (ATP) by simple mixing, exhibited soft droplet property and high enrichment for dexamethasone sodium phosphate (DSP). To avoid the fusion effect of membraneless coacervate and endow it with biolo</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T17:56:37.214Z</modification><creation>2026-05-19T03:12:08.74Z</creation></dates><accession>S-EPMC12648001</accession><cross_references><pubmed>41311384</pubmed><doi>10.1016/j.apsb.2025.08.025</doi></cross_references></HashMap>