<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(11)</volume><submitter>Baez-Diaz C</submitter><funding>Instituto de Salud Carlos III</funding><funding>Agencia Estatal de Investigación</funding><funding>Consejería de Economía, Ciencia y Agenda Digital, Junta de Extremadura</funding><pubmed_abstract>The administration of cardiosphere-derived cells (CDCs) after acute myocardial infarction (AMI) is very promising. CDC encapsulation in alginate-poly-l-lysine-alginate (APA) could increase cell survival and adherence. The intrapericardial (IP) approach potentially achieves high concentrations of the therapeutic agent in the infarcted area. We aimed to evaluate IP therapy using a saline vehicle as a control (CON), a dose of 30 × 10&lt;sup>6&lt;/sup> CDCs (CDCs) or APA microcapsules containing 30 × 10&lt;sup>6&lt;/sup> CDCs (APA-CDCs) at 72 h in a porcine AMI model. Magnetic resonance imaging (MRI) was used to determine the left ventricular ejection fraction (LVEF), infarct size (IS), and indexed end diastolic and systolic volumes (EDVi; ESVi) pre- and 10 weeks post-injection. Programmed electrical stimulation (PES) was performed to test arrhythmia inducibility before euthanasia. Histopathological analysis was carried out afterwards. The IP infusion was successful in all animals. At 10 weeks, MRI revealed significantly higher LVEF in the APA-CDC group compared with CON. No significant differences were observed among groups in IS, EDVi, ESVi, PES and histopathological analyses. In conclusion, the IP injection of CDCs (microencapsulated or not) was feasible and safe 72 h post-AMI in the porcine model. Moreover, CDCs APA encapsulation could have a beneficial effect on cardiac function, reflected by a higher LVEF at 10 weeks.</pubmed_abstract><journal>Pharmaceutics</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8626005</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Intrapericardial Delivery of APA-Microcapsules as Promising Stem Cell Therapy Carriers in an Experimental Acute Myocardial Infarction Model.</pubmed_title><pmcid>PMC8626005</pmcid><funding_grant_id>Sara Borrell CD19/00048</funding_grant_id><funding_grant_id>PI20/00247</funding_grant_id><funding_grant_id>GR18199</funding_grant_id><funding_grant_id>IB20184</funding_grant_id><funding_grant_id>CB16/11/00494</funding_grant_id><funding_grant_id>PID2019-107329RA-C22/AEI/10.13039/501100011033</funding_grant_id><funding_grant_id>IB20191</funding_grant_id><pubmed_authors>Martin H</pubmed_authors><pubmed_authors>Espona-Noguera A</pubmed_authors><pubmed_authors>Crisostomo V</pubmed_authors><pubmed_authors>Casado JG</pubmed_authors><pubmed_authors>Ciriza J</pubmed_authors><pubmed_authors>Pedraz JL</pubmed_authors><pubmed_authors>Baez-Diaz C</pubmed_authors><pubmed_authors>Blanco-Blazquez V</pubmed_authors><pubmed_authors>Lopez E</pubmed_authors><pubmed_authors>Sanchez-Margallo FM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intrapericardial Delivery of APA-Microcapsules as Promising Stem Cell Therapy Carriers in an Experimental Acute Myocardial Infarction Model.</name><description>The administration of cardiosphere-derived cells (CDCs) after acute myocardial infarction (AMI) is very promising. CDC encapsulation in alginate-poly-l-lysine-alginate (APA) could increase cell survival and adherence. The intrapericardial (IP) approach potentially achieves high concentrations of the therapeutic agent in the infarcted area. We aimed to evaluate IP therapy using a saline vehicle as a control (CON), a dose of 30 × 10&lt;sup>6&lt;/sup> CDCs (CDCs) or APA microcapsules containing 30 × 10&lt;sup>6&lt;/sup> CDCs (APA-CDCs) at 72 h in a porcine AMI model. Magnetic resonance imaging (MRI) was used to determine the left ventricular ejection fraction (LVEF), infarct size (IS), and indexed end diastolic and systolic volumes (EDVi; ESVi) pre- and 10 weeks post-injection. Programmed electrical stimulation (PES) was performed to test arrhythmia inducibility before euthanasia. Histopathological analysis was carried out afterwards. The IP infusion was successful in all animals. At 10 weeks, MRI revealed significantly higher LVEF in the APA-CDC group compared with CON. No significant differences were observed among groups in IS, EDVi, ESVi, PES and histopathological analyses. In conclusion, the IP injection of CDCs (microencapsulated or not) was feasible and safe 72 h post-AMI in the porcine model. Moreover, CDCs APA encapsulation could have a beneficial effect on cardiac function, reflected by a higher LVEF at 10 weeks.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2022-02-11T13:31:58.493Z</modification><creation>2022-02-11T13:31:58.493Z</creation></dates><accession>S-EPMC8626005</accession><cross_references><pubmed>34834235</pubmed><doi>10.3390/pharmaceutics13111824</doi></cross_references></HashMap>