<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Khang MK</submitter><funding>National Heart, Lung and Blood Institute</funding><funding>NHLBI NIH HHS</funding><pagination>1102-1112</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7365982</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(4)</volume><pubmed_abstract>This work details a newly developed "sandwich" nanoplatform via neutravidin-biotin system for the detection and treatment of inflammation. First, biotinylated- and folate-conjugated optical imaging micelles targeted activated macrophages via folate/folate receptor interactions. Second, multivalent neutravidin proteins in an optimal concentration accumulated on the biotinylated macrophages. Finally, biotinylated anti-inflammatory drug-loaded micelles delivered drugs effectively at the inflammatory sites via a highly specific neutravidin-biotin affinity. Both &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> studies have shown that the "sandwich" pretargeting platform was able to diagnose inflammation by targeting activated macrophages as well as improve the therapeutic efficacy by amplifying the drug deli</pubmed_abstract><journal>Bioactive materials</journal><pubmed_title>A pretargeting nanoplatform for imaging and enhancing anti-inflammatory drug delivery.</pubmed_title><pmcid>PMC7365982</pmcid><funding_grant_id>T32 HL134613</funding_grant_id><funding_grant_id>NIH T32 HL134613</funding_grant_id><pubmed_authors>Khang MK</pubmed_authors><pubmed_authors>Tang L</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Co CM</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>A pretargeting nanoplatform for imaging and enhancing anti-inflammatory drug delivery.</name><description>This work details a newly developed "sandwich" nanoplatform via neutravidin-biotin system for the detection and treatment of inflammation. First, biotinylated- and folate-conjugated optical imaging micelles targeted activated macrophages via folate/folate receptor interactions. Second, multivalent neutravidin proteins in an optimal concentration accumulated on the biotinylated macrophages. Finally, biotinylated anti-inflammatory drug-loaded micelles delivered drugs effectively at the inflammatory sites via a highly specific neutravidin-biotin affinity. Both &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> studies have shown that the "sandwich" pretargeting platform was able to diagnose inflammation by targeting activated macrophages as well as improve the therapeutic efficacy by amplifying the drug deli</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2025-04-04T13:38:26.814Z</modification><creation>2025-04-04T13:38:26.814Z</creation></dates><accession>S-EPMC7365982</accession><cross_references><pubmed>32695939</pubmed><doi>10.1016/j.bioactmat.2020.06.019</doi></cross_references></HashMap>