<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Lin J</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The development of nanodrug carriers utilizing tumor microenvironment has become a hotspot in reversing multidrug resistance (MDR).&lt;h4>Materials and methods&lt;/h4>This study synthesized a redox-sensitive copolymer, Pluronic F127-disulfide bond-d-α-tocopheryl polyethylene glycol 1000 succinate (FSST), through the connection of the reduction-sensitive disulfide bond between F127 and d-α-tocopheryl polyethylene glycol 1000 succinate. This polymer could induce the elevation of reactive oxygen species (ROS) levels, ultimately resulting in cytotoxicity. Moreover, the redox-responsive mixed micelles, F127-folate (FA)/FSST/P123 (FFSSTP), based on FSST, Pluronic F127-FA, and Pluronic P123, were prepared to load paclitaxel (PTX).&lt;h4>Results&lt;/h4>The in vitro release study demonstra</pubmed_abstract><journal>International journal of nanomedicine</journal><pagination>805-830</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5808690</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Redox-responsive F127-folate/F127-disulfide bond-d-α-tocopheryl polyethylene glycol 1000 succinate/P123 mixed micelles loaded with paclitaxel for the reversal of multidrug resistance in tumors.</pubmed_title><pmcid>PMC5808690</pmcid><pubmed_authors>Fu S</pubmed_authors><pubmed_authors>Zhao C</pubmed_authors><pubmed_authors>Han L</pubmed_authors><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Yang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Redox-responsive F127-folate/F127-disulfide bond-d-α-tocopheryl polyethylene glycol 1000 succinate/P123 mixed micelles loaded with paclitaxel for the reversal of multidrug resistance in tumors.</name><description>&lt;h4>Introduction&lt;/h4>The development of nanodrug carriers utilizing tumor microenvironment has become a hotspot in reversing multidrug resistance (MDR).&lt;h4>Materials and methods&lt;/h4>This study synthesized a redox-sensitive copolymer, Pluronic F127-disulfide bond-d-α-tocopheryl polyethylene glycol 1000 succinate (FSST), through the connection of the reduction-sensitive disulfide bond between F127 and d-α-tocopheryl polyethylene glycol 1000 succinate. This polymer could induce the elevation of reactive oxygen species (ROS) levels, ultimately resulting in cytotoxicity. Moreover, the redox-responsive mixed micelles, F127-folate (FA)/FSST/P123 (FFSSTP), based on FSST, Pluronic F127-FA, and Pluronic P123, were prepared to load paclitaxel (PTX).&lt;h4>Results&lt;/h4>The in vitro release study demonstra</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-04T14:48:51.575Z</modification><creation>2019-03-26T23:02:57Z</creation></dates><accession>S-EPMC5808690</accession><cross_references><pubmed>29445276</pubmed><doi>10.2147/IJN.S152395</doi></cross_references></HashMap>