<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wan M</submitter><funding>Jiangsu Natural Science Foundation</funding><funding>Jiangsu Provincial Key Medical Talent Foundation, and Six Talent Peaks Project of Jiangsu Province</funding><funding>National Science Foundation of China</funding><funding>National Natural Science Foundation of China</funding><funding>Jiangsu Key Technology RD Program</funding><funding>Excellent Young Scholars NSFC</funding><funding>Social Development Project of Jiangsu Provincial Science and Technology Department</funding><funding>Technology Support Program of Science and Technology Department of Jiangsu Province</funding><funding>Huaian Biofunctional Materials and Analysis Technology Innovation Platform</funding><pagination>eaaz9014</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7385437</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(22)</volume><pubmed_abstract>The treatment difficulties of venous thrombosis include short half-life, low utilization, and poor penetration of drugs at thrombus site. Here, we develop one kind of mesoporous/macroporous silica/platinum nanomotors with platelet membrane (PM) modification (MMNM/PM) for sequentially targeting delivery of thrombolytic and anticoagulant drugs for thrombus treatment. Regulated by the special proteins on PM, the nanomotors target the thrombus site and then PM can be ruptured under near-infrared (NIR) irradiation to achieve desirable sequential drug release, including rapid release of thrombolytic urokinase (3 hours) and slow release of anticoagulant heparin (>20 days). Meantime, the motion ability of nanomotors under NIR irradiation can effectively promote them to penetrate deeply in thrombus site to enhance retention ratio. The in vitro and in vivo evaluation results confirm that the synergistic effect of targeting ability from PM and motion ability from nanomotors can notably enhance the thrombolysis effect in both static/dynamic thrombus and rat model.</pubmed_abstract><journal>Science advances</journal><pubmed_title>Platelet-derived porous nanomotor for thrombus therapy.</pubmed_title><pmcid>PMC7385437</pmcid><funding_grant_id>HAP201612</funding_grant_id><funding_grant_id>81622033</funding_grant_id><funding_grant_id>81572129</funding_grant_id><funding_grant_id>BE2015703</funding_grant_id><funding_grant_id>WSW-061</funding_grant_id><funding_grant_id>BE2016609</funding_grant_id><funding_grant_id>21603105, 21571104</funding_grant_id><funding_grant_id>BE2019744),</funding_grant_id><funding_grant_id>BE2016010, BE2015603</funding_grant_id><pubmed_authors>Fang D</pubmed_authors><pubmed_authors>Zhao B</pubmed_authors><pubmed_authors>Wan M</pubmed_authors><pubmed_authors>Jiang Q</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Mao C</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Wu R</pubmed_authors><pubmed_authors>Shi D</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Fang L</pubmed_authors><pubmed_authors>Miao Z</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Platelet-derived porous nanomotor for thrombus therapy.</name><description>The treatment difficulties of venous thrombosis include short half-life, low utilization, and poor penetration of drugs at thrombus site. Here, we develop one kind of mesoporous/macroporous silica/platinum nanomotors with platelet membrane (PM) modification (MMNM/PM) for sequentially targeting delivery of thrombolytic and anticoagulant drugs for thrombus treatment. Regulated by the special proteins on PM, the nanomotors target the thrombus site and then PM can be ruptured under near-infrared (NIR) irradiation to achieve desirable sequential drug release, including rapid release of thrombolytic urokinase (3 hours) and slow release of anticoagulant heparin (>20 days). Meantime, the motion ability of nanomotors under NIR irradiation can effectively promote them to penetrate deeply in thrombus site to enhance retention ratio. The in vitro and in vivo evaluation results confirm that the synergistic effect of targeting ability from PM and motion ability from nanomotors can notably enhance the thrombolysis effect in both static/dynamic thrombus and rat model.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2025-04-04T07:40:49.447Z</modification><creation>2025-04-04T07:40:49.447Z</creation></dates><accession>S-EPMC7385437</accession><cross_references><pubmed>32766445</pubmed><doi>10.1126/sciadv.aaz9014</doi></cross_references></HashMap>