<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(1)</volume><submitter>Sun H</submitter><pubmed_abstract>Our previous research identified that an oral mPEG-b-PCL polymeric micelle (PM) maintained satisfactory integrity but exhibited limited transcytosis efficiency. To enhance transcytosis and enable ROS-responsive release, we developed a series of hybrid PMs by blending a synthesized L-carnitine-grafted, thioketal-linked LC-PEG&lt;sub>5k&lt;/sub>-TK-PCL&lt;sub>7k&lt;/sub> polymer with mPEG&lt;sub>5k&lt;/sub>-PCL&lt;sub>7k&lt;/sub>. These hybrid PMs, similar in particle size (120 nm) and drug loading (10%) to the PM composed of pure mPEG&lt;sub>5k&lt;/sub>-PCL&lt;sub>7k&lt;/sub> (5-7E), retained good stability in SGF and SIF. However, the hybrid PM with a 40% LC-PEG&lt;sub>5k&lt;/sub>-TK-PCL&lt;sub>7k&lt;/sub> proportion showed reduced integrity and penetration in mucus layer. In Caco-2/E12 (7:3) cells, the hybrid PM with a 20% LC-PEG&lt;sub>5</pubmed_abstract><journal>Journal of nanobiotechnology</journal><pagination>182</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12918599</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>OCTN2-targeted and ROS-responsive hybrid polymeric micelles for oral delivery of docetaxel.</pubmed_title><pmcid>PMC12918599</pmcid><pubmed_authors>Bi X</pubmed_authors><pubmed_authors>Sui B</pubmed_authors><pubmed_authors>Jin X</pubmed_authors><pubmed_authors>Liu B</pubmed_authors><pubmed_authors>Gou J</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Song J</pubmed_authors></additional><is_claimable>false</is_claimable><name>OCTN2-targeted and ROS-responsive hybrid polymeric micelles for oral delivery of docetaxel.</name><description>Our previous research identified that an oral mPEG-b-PCL polymeric micelle (PM) maintained satisfactory integrity but exhibited limited transcytosis efficiency. To enhance transcytosis and enable ROS-responsive release, we developed a series of hybrid PMs by blending a synthesized L-carnitine-grafted, thioketal-linked LC-PEG&lt;sub>5k&lt;/sub>-TK-PCL&lt;sub>7k&lt;/sub> polymer with mPEG&lt;sub>5k&lt;/sub>-PCL&lt;sub>7k&lt;/sub>. These hybrid PMs, similar in particle size (120 nm) and drug loading (10%) to the PM composed of pure mPEG&lt;sub>5k&lt;/sub>-PCL&lt;sub>7k&lt;/sub> (5-7E), retained good stability in SGF and SIF. However, the hybrid PM with a 40% LC-PEG&lt;sub>5k&lt;/sub>-TK-PCL&lt;sub>7k&lt;/sub> proportion showed reduced integrity and penetration in mucus layer. In Caco-2/E12 (7:3) cells, the hybrid PM with a 20% LC-PEG&lt;sub>5</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-16T10:06:03.547Z</modification><creation>2026-07-09T10:48:53.49Z</creation></dates><accession>S-EPMC12918599</accession><cross_references><pubmed>41593744</pubmed><doi>10.1186/s12951-026-04067-0</doi></cross_references></HashMap>