<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Guo X</submitter><funding>Translational Medicine Cross Research Fund of Shanghai Jiao Tong University</funding><funding>Clinical Research Plan of Shanghai Hospital Development Center</funding><funding>Shanghai Collaborative Innovation Center for Translational Medicine Fund</funding><funding>National Natural Science Foundation of China</funding><pagination>531</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9749152</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>Acute myocardial infarction (AMI) is usually caused by coronary thrombosis. However, the short half-life, lack of targetability and inevitable ischemia/reperfusion injury secondary to revascularization, which characterizes tissue plasminogen activator (tPA) limit its thrombolytic efficacy for AMI. To address the targeted and site-specific delivery of tPA, the current study reports the construction of a thrombus-targeting and responsive biomimetic nanoparticle (PTPN) for spatiotemporal treatment of AMI. PTPN was constituted by the thrombus microenvironment- responsive phenylboronic acid (PBA) nanocarrier, antioxidant molecular protocatechualdehyde (PC) and tPA with thrombolytic effect, which were enclosed by the platelet membrane. The thrombus-targeting capability of the platelet membrane e</pubmed_abstract><journal>Journal of nanobiotechnology</journal><pubmed_title>Thrombus-specific/responsive biomimetic nanomedicine for spatiotemporal thrombolysis and alleviation of myocardial ischemia/reperfusion injury.</pubmed_title><pmcid>PMC9749152</pmcid><funding_grant_id>NO.TM202013</funding_grant_id><funding_grant_id>No.SHDC2020CR3084B</funding_grant_id><funding_grant_id>No.YG2021ZD27, YG2022QN101 and YG2022ZD025</funding_grant_id><funding_grant_id>Nos.81901419, 82072199 and 82172168</funding_grant_id><pubmed_authors>Zang J</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Hong T</pubmed_authors><pubmed_authors>Shao R</pubmed_authors><pubmed_authors>Hou X</pubmed_authors><pubmed_authors>He B</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><pubmed_authors>Su F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Thrombus-specific/responsive biomimetic nanomedicine for spatiotemporal thrombolysis and alleviation of myocardial ischemia/reperfusion injury.</name><description>Acute myocardial infarction (AMI) is usually caused by coronary thrombosis. However, the short half-life, lack of targetability and inevitable ischemia/reperfusion injury secondary to revascularization, which characterizes tissue plasminogen activator (tPA) limit its thrombolytic efficacy for AMI. To address the targeted and site-specific delivery of tPA, the current study reports the construction of a thrombus-targeting and responsive biomimetic nanoparticle (PTPN) for spatiotemporal treatment of AMI. PTPN was constituted by the thrombus microenvironment- responsive phenylboronic acid (PBA) nanocarrier, antioxidant molecular protocatechualdehyde (PC) and tPA with thrombolytic effect, which were enclosed by the platelet membrane. The thrombus-targeting capability of the platelet membrane e</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-05T15:42:27.004Z</modification><creation>2025-04-05T15:42:27.004Z</creation></dates><accession>S-EPMC9749152</accession><cross_references><pubmed>36514154</pubmed><doi>10.1186/s12951-022-01686-1</doi></cross_references></HashMap>