<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Yang C</submitter><pubmed_abstract>The toxic effects of chemotherapy drugs on normal tissues are still a major limiting factor in cancer treatment. In this paper, we report a metal-organic framework (Zn-Co ZIF) with chitosan-coated outer layer as a carrier for the drug adriamycin hydrochloride (DOX), a treatment for liver cancer, as a novel anti-cancer nanodrug-enhanced carrier. Gold nanoparticles, a good photothermal conversion agent, were combined with the target SH-RGD during surface functionalisation to prepare Zn-Co ZIF@DOX-CS-Au-RGD (ZD-CAR), a nanoplatform with good photothermal conversion properties and targeting for combined liver cancer therapy. ZD-CAR was developed after RGD accurately targeted the tumour and entered the tumour microenvironment (TME), it cleaves and releases the liver cancer therapeutic agent (DOX) in a weak acidic environment to effectively kill tumour cells. The metal skeleton cleavage releases Co&lt;sup>2+&lt;/sup>, which catalyzes the production of oxygen from H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> to alleviate the tumour hypoxic environment. The dissolved oxygen could reach 14 mg/L after adding 80 mg/mL of ZD-CAR. Meanwhile, gold nanoparticles could convert light energy into heat energy under 808 NIR irradiation to induce local superheating and kill tumour cells. In summary, this study developed a nanoplatform that combines chemo-photothermal-targeted therapy. It has shown good therapeutic effeciency in cellular experiments and performance tests and has promising applications in anti-cancer therapy.</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1110909</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10154549</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Zn-Co metal organic frameworks coated with chitosand and Au nanoparticles for chemo-photothermal-targeted combination therapy of liver cancer.</pubmed_title><pmcid>PMC10154549</pmcid><pubmed_authors>Tiwari SK</pubmed_authors><pubmed_authors>Wang N</pubmed_authors><pubmed_authors>Guo L</pubmed_authors><pubmed_authors>Zheng H</pubmed_authors><pubmed_authors>Jiang L</pubmed_authors><pubmed_authors>Huang J</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>An G</pubmed_authors><pubmed_authors>Bai Z</pubmed_authors><pubmed_authors>Yang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Zn-Co metal organic frameworks coated with chitosand and Au nanoparticles for chemo-photothermal-targeted combination therapy of liver cancer.</name><description>The toxic effects of chemotherapy drugs on normal tissues are still a major limiting factor in cancer treatment. In this paper, we report a metal-organic framework (Zn-Co ZIF) with chitosan-coated outer layer as a carrier for the drug adriamycin hydrochloride (DOX), a treatment for liver cancer, as a novel anti-cancer nanodrug-enhanced carrier. Gold nanoparticles, a good photothermal conversion agent, were combined with the target SH-RGD during surface functionalisation to prepare Zn-Co ZIF@DOX-CS-Au-RGD (ZD-CAR), a nanoplatform with good photothermal conversion properties and targeting for combined liver cancer therapy. ZD-CAR was developed after RGD accurately targeted the tumour and entered the tumour microenvironment (TME), it cleaves and releases the liver cancer therapeutic agent (DOX) in a weak acidic environment to effectively kill tumour cells. The metal skeleton cleavage releases Co&lt;sup>2+&lt;/sup>, which catalyzes the production of oxygen from H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> to alleviate the tumour hypoxic environment. The dissolved oxygen could reach 14 mg/L after adding 80 mg/mL of ZD-CAR. Meanwhile, gold nanoparticles could convert light energy into heat energy under 808 NIR irradiation to induce local superheating and kill tumour cells. In summary, this study developed a nanoplatform that combines chemo-photothermal-targeted therapy. It has shown good therapeutic effeciency in cellular experiments and performance tests and has promising applications in anti-cancer therapy.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-22T00:26:36.299Z</modification><creation>2025-04-05T19:38:14.008Z</creation></dates><accession>S-EPMC10154549</accession><cross_references><pubmed>37152005</pubmed><doi>10.3389/fonc.2023.1110909</doi></cross_references></HashMap>