<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li X</submitter><funding>National Natural Science Foundation of China</funding><pagination>29256-29265</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9404477</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(33)</volume><pubmed_abstract>Current cancer treatment is not only limited to monotherapy but is also influenced by limited drug delivery options. Combined chemokinetic-photokinetic therapy has great promise in enhancing anticancer effects. Meanwhile, zein has superior self-assembly properties and can be loaded with photosensitizers. Herein, the targeted multifunctional nanoparticles based on zein/hyaluronate acid (HA)/tannin (TA)/Cu&lt;sup>2+&lt;/sup> loaded with IR780 (ZHTC@IR780) are constructed for synergetic cancer therapy by chemo-dynamic therapy (CDT) and photodynamic therapy (PDT). There is experimental proof that ZHTC@IR780 nanoparticles (NPs) can relieve the tumor hypoxic microenvironment by catalytic decomposition of endogenous H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> to O&lt;sub>2&lt;/sub> and further react with O&lt;sub>2&lt;/sub> to produce toxic &lt;sup>1&lt;/sup>O&lt;sub>2&lt;/sub> with 808 nm laser irradiation. The glutathione oxidase-like effects of ZHTC@IR780 NPs can generate Fenton-like Cu&lt;sup>+&lt;/sup> ions and deplete GSH for efficient hydroxyl radical (&lt;sup>•&lt;/sup>OH) production. In addition, CDT combined with PDT enhances the antitumor effect. Photodynamic therapy can cause immunogenic cell death, increase calreticulin eversion, release histone with high mobility, and promote apoptosis of tumor cells.</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Zein-Based Nanomedicines for Synergistic Chemodynamic/Photodynamic Therapy.</pubmed_title><pmcid>PMC9404477</pmcid><funding_grant_id>32072169</funding_grant_id><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Shi Q</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Zhen N</pubmed_authors><pubmed_authors>Zhou D</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Xue J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Zein-Based Nanomedicines for Synergistic Chemodynamic/Photodynamic Therapy.</name><description>Current cancer treatment is not only limited to monotherapy but is also influenced by limited drug delivery options. Combined chemokinetic-photokinetic therapy has great promise in enhancing anticancer effects. Meanwhile, zein has superior self-assembly properties and can be loaded with photosensitizers. Herein, the targeted multifunctional nanoparticles based on zein/hyaluronate acid (HA)/tannin (TA)/Cu&lt;sup>2+&lt;/sup> loaded with IR780 (ZHTC@IR780) are constructed for synergetic cancer therapy by chemo-dynamic therapy (CDT) and photodynamic therapy (PDT). There is experimental proof that ZHTC@IR780 nanoparticles (NPs) can relieve the tumor hypoxic microenvironment by catalytic decomposition of endogenous H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> to O&lt;sub>2&lt;/sub> and further react with O&lt;sub>2&lt;/sub> to produce toxic &lt;sup>1&lt;/sup>O&lt;sub>2&lt;/sub> with 808 nm laser irradiation. The glutathione oxidase-like effects of ZHTC@IR780 NPs can generate Fenton-like Cu&lt;sup>+&lt;/sup> ions and deplete GSH for efficient hydroxyl radical (&lt;sup>•&lt;/sup>OH) production. In addition, CDT combined with PDT enhances the antitumor effect. Photodynamic therapy can cause immunogenic cell death, increase calreticulin eversion, release histone with high mobility, and promote apoptosis of tumor cells.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2024-11-06T04:00:22.302Z</modification><creation>2024-11-06T04:00:22.302Z</creation></dates><accession>S-EPMC9404477</accession><cross_references><pubmed>36033651</pubmed><doi>10.1021/acsomega.2c03404</doi></cross_references></HashMap>