<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(4)</volume><submitter>Palazzolo JS</submitter><pubmed_abstract>Thrombolysis with tissue-type plasminogen activator (tPA) remains the main treatment for acute ischemic stroke. Nevertheless, tPA intervention is limited by a short therapeutic window, low recanalization rates, and a risk of intracranial hemorrhage (ICH), highlighting the clinical demand for improved thrombolytic drugs. We examined a novel thrombolytic agent termed "SCE5-scuPA," comprising a single-chain urokinase plasminogen activator (scuPA) fused with a single-chain antibody (SCE5) that targets the activated glycoprotein IIb/IIIa platelet receptor, for its effects in experimental stroke. SCE5-scuPA was first tested in a whole blood clot degradation assay to show the benefit of platelet-targeted thrombolysis. The tail bleeding time, blood clearance, and biodistribution were then determin</pubmed_abstract><journal>Blood advances</journal><pagination>561-574</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9984306</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Platelet-targeted thrombolysis for treatment of acute ischemic stroke.</pubmed_title><pmcid>PMC9984306</pmcid><pubmed_authors>Alt K</pubmed_authors><pubmed_authors>Jagdale S</pubmed_authors><pubmed_authors>Broughton BRS</pubmed_authors><pubmed_authors>Wright DK</pubmed_authors><pubmed_authors>Hagemeyer CE</pubmed_authors><pubmed_authors>Palazzolo JS</pubmed_authors><pubmed_authors>Niego B</pubmed_authors><pubmed_authors>Medcalf RL</pubmed_authors><pubmed_authors>Ale A</pubmed_authors><pubmed_authors>Ho H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Platelet-targeted thrombolysis for treatment of acute ischemic stroke.</name><description>Thrombolysis with tissue-type plasminogen activator (tPA) remains the main treatment for acute ischemic stroke. Nevertheless, tPA intervention is limited by a short therapeutic window, low recanalization rates, and a risk of intracranial hemorrhage (ICH), highlighting the clinical demand for improved thrombolytic drugs. We examined a novel thrombolytic agent termed "SCE5-scuPA," comprising a single-chain urokinase plasminogen activator (scuPA) fused with a single-chain antibody (SCE5) that targets the activated glycoprotein IIb/IIIa platelet receptor, for its effects in experimental stroke. SCE5-scuPA was first tested in a whole blood clot degradation assay to show the benefit of platelet-targeted thrombolysis. The tail bleeding time, blood clearance, and biodistribution were then determin</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-05-29T16:30:27.09Z</modification><creation>2025-04-06T12:22:43.212Z</creation></dates><accession>S-EPMC9984306</accession><cross_references><pubmed>35482909</pubmed><doi>10.1182/bloodadvances.2021006691</doi></cross_references></HashMap>