<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Alimoradi H</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Anticancer drug delivery systems are often limited by hurdles, such as off-target distribution, slow cellular internalization, limited lysosomal escape, and drug resistance. To overcome these limitations, we have developed a stable nitric oxide (NO)-releasing nanoparticle (polystyrene-maleic acid [SMA]-&lt;i>tert&lt;/i>-dodecane S-nitrosothiol [tDodSNO]) with the aim of enhancing the anticancer properties of doxorubicin (Dox) and a Dox-loaded nanoparticle (SMA-Dox) carrier.&lt;h4>Materials and methods&lt;/h4>Effects of SMA-tDodSNO and/or in combination with Dox or SMA-Dox on cell viability, apoptosis, mitochondrial membrane potential, lysosomal membrane permeability, tumor tissue, and tumor growth were studied using in vitro and in vivo model of triple-negative breast cancer (TNBC). In</pubmed_abstract><journal>International journal of nanomedicine</journal><pagination>7771-7787</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6251458</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Nitric oxide-releasing nanoparticles improve doxorubicin anticancer activity.</pubmed_title><pmcid>PMC6251458</pmcid><pubmed_authors>Barzegar-Fallah A</pubmed_authors><pubmed_authors>Alshaibani L</pubmed_authors><pubmed_authors>Alimoradi H</pubmed_authors><pubmed_authors>Greish K</pubmed_authors><pubmed_authors>Pittala V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nitric oxide-releasing nanoparticles improve doxorubicin anticancer activity.</name><description>&lt;h4>Purpose&lt;/h4>Anticancer drug delivery systems are often limited by hurdles, such as off-target distribution, slow cellular internalization, limited lysosomal escape, and drug resistance. To overcome these limitations, we have developed a stable nitric oxide (NO)-releasing nanoparticle (polystyrene-maleic acid [SMA]-&lt;i>tert&lt;/i>-dodecane S-nitrosothiol [tDodSNO]) with the aim of enhancing the anticancer properties of doxorubicin (Dox) and a Dox-loaded nanoparticle (SMA-Dox) carrier.&lt;h4>Materials and methods&lt;/h4>Effects of SMA-tDodSNO and/or in combination with Dox or SMA-Dox on cell viability, apoptosis, mitochondrial membrane potential, lysosomal membrane permeability, tumor tissue, and tumor growth were studied using in vitro and in vivo model of triple-negative breast cancer (TNBC). In</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-05T12:59:55.512Z</modification><creation>2019-03-27T00:11:27Z</creation></dates><accession>S-EPMC6251458</accession><cross_references><pubmed>30538458</pubmed><doi>10.2147/IJN.S187089</doi></cross_references></HashMap>