<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Blanco-Blazquez V</submitter><funding>ISCIII</funding><funding>Instituto de Salud Carlos III</funding><funding>European Union</funding><funding>Junta de Extremadura, Consejeria de Economía e Infraestructuras</funding><funding>Agencia Estatal de Investigación</funding><funding>Junta de Extremadura, Consejería de Economía, Ciencia y Agenda Digital</funding><pagination>86</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9960949</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(2)</volume><pubmed_abstract>Therapy microencapsulation allows minimally invasive, safe, and effective administration. Hepatocyte growth factor (HGF) has angiogenic, anti-inflammatory, anti-apoptotic, and anti-fibrotic properties. Our objective was to evaluate the cardiac safety and effectiveness of intracoronary (IC) administration of HGF-loaded extended release microspheres in an acute myocardial infarction (AMI) swine model. An IC infusion of 5 × 10&lt;sup>6&lt;/sup> HGF-loaded microspheres (MS+HGF, &lt;i>n&lt;/i> = 7), 5 × 10&lt;sup>6&lt;/sup> placebo microspheres (MS, &lt;i>n&lt;/i> = 7), or saline (SAL, &lt;i>n&lt;/i> = 7) was performed two days after AMI. TIMI flow and Troponin I (TnI) values were assessed pre- and post-treatment. Cardiac function was evaluated with magnetic resonance imaging (cMR) before injection and at 10 weeks. Plasma c</pubmed_abstract><journal>Journal of cardiovascular development and disease</journal><pubmed_title>Intracoronary Administration of Microencapsulated HGF in a Reperfused Myocardial Infarction Swine Model.</pubmed_title><pmcid>PMC9960949</pmcid><funding_grant_id>PID2019-107329RAC22/AEI/10.13039/501100011033</funding_grant_id><funding_grant_id>PI20/00247</funding_grant_id><funding_grant_id>GR21201</funding_grant_id><funding_grant_id>GR18199</funding_grant_id><funding_grant_id>IB20191</funding_grant_id><pubmed_authors>Martin H</pubmed_authors><pubmed_authors>Palacios I</pubmed_authors><pubmed_authors>Gonzalez-Bueno I</pubmed_authors><pubmed_authors>Blazquez R</pubmed_authors><pubmed_authors>Crisostomo V</pubmed_authors><pubmed_authors>Solares J</pubmed_authors><pubmed_authors>Casado JG</pubmed_authors><pubmed_authors>Steendam R</pubmed_authors><pubmed_authors>Blanco-Blazquez V</pubmed_authors><pubmed_authors>Baez-Diaz C</pubmed_authors><pubmed_authors>Uson A</pubmed_authors><pubmed_authors>Sanchez-Margallo FM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intracoronary Administration of Microencapsulated HGF in a Reperfused Myocardial Infarction Swine Model.</name><description>Therapy microencapsulation allows minimally invasive, safe, and effective administration. Hepatocyte growth factor (HGF) has angiogenic, anti-inflammatory, anti-apoptotic, and anti-fibrotic properties. Our objective was to evaluate the cardiac safety and effectiveness of intracoronary (IC) administration of HGF-loaded extended release microspheres in an acute myocardial infarction (AMI) swine model. An IC infusion of 5 × 10&lt;sup>6&lt;/sup> HGF-loaded microspheres (MS+HGF, &lt;i>n&lt;/i> = 7), 5 × 10&lt;sup>6&lt;/sup> placebo microspheres (MS, &lt;i>n&lt;/i> = 7), or saline (SAL, &lt;i>n&lt;/i> = 7) was performed two days after AMI. TIMI flow and Troponin I (TnI) values were assessed pre- and post-treatment. Cardiac function was evaluated with magnetic resonance imaging (cMR) before injection and at 10 weeks. Plasma c</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-04-07T13:24:00.87Z</modification><creation>2025-04-07T00:31:59.199Z</creation></dates><accession>S-EPMC9960949</accession><cross_references><pubmed>36826582</pubmed><doi>10.3390/jcdd10020086</doi></cross_references></HashMap>