<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(9)</volume><submitter>Zou L</submitter><pubmed_abstract>&lt;b>Rationale:&lt;/b> Combinations of two or more therapeutic agents targeting different signaling pathways involved in tumor progression can have synergistic anticancer effects. However, combination chemotherapies are greatly limited by the different pharmacokinetics, tumor targeting, and cellular uptake capacities of the combined drugs. We have previously demonstrated the potential synergistic efficacy of paclitaxel (PTX) and the natural anti-angiogenic agent tetramethylpyrazine (TMP) for suppressing ovarian carcinoma growth. An efficient, facile, and smart nanosystem to deliver PTX and TMP simultaneously &lt;i>in vivo&lt;/i> is greatly desired. &lt;b>Methods:&lt;/b> We constructed a redox-sensitive nanosystem based on the amphiphilic PTX-ss-TMP conjugate, in which PTX and TMP are linked by a disulfide </pubmed_abstract><journal>Theranostics</journal><pagination>4171-4186</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7977472</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Redox-sensitive carrier-free nanoparticles self-assembled by disulfide-linked paclitaxel-tetramethylpyrazine conjugate for combination cancer chemotherapy.</pubmed_title><pmcid>PMC7977472</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Fu C</pubmed_authors><pubmed_authors>Zou L</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Gu Z</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Redox-sensitive carrier-free nanoparticles self-assembled by disulfide-linked paclitaxel-tetramethylpyrazine conjugate for combination cancer chemotherapy.</name><description>&lt;b>Rationale:&lt;/b> Combinations of two or more therapeutic agents targeting different signaling pathways involved in tumor progression can have synergistic anticancer effects. However, combination chemotherapies are greatly limited by the different pharmacokinetics, tumor targeting, and cellular uptake capacities of the combined drugs. We have previously demonstrated the potential synergistic efficacy of paclitaxel (PTX) and the natural anti-angiogenic agent tetramethylpyrazine (TMP) for suppressing ovarian carcinoma growth. An efficient, facile, and smart nanosystem to deliver PTX and TMP simultaneously &lt;i>in vivo&lt;/i> is greatly desired. &lt;b>Methods:&lt;/b> We constructed a redox-sensitive nanosystem based on the amphiphilic PTX-ss-TMP conjugate, in which PTX and TMP are linked by a disulfide </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-04-25T18:40:30.998Z</modification><creation>2025-04-06T07:40:03.98Z</creation></dates><accession>S-EPMC7977472</accession><cross_references><pubmed>33754055</pubmed><doi>10.7150/thno.42260</doi></cross_references></HashMap>