<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carvalho AM</submitter><funding>Horizon 2020 Framework Programme</funding><funding>Children&amp;apos;s Cancer and Leukaemia Group</funding><pagination>6503-6514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11480974</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(10)</volume><pubmed_abstract>Paediatric acute myeloid leukemia (AML) is a heterogeneous hematological malignancy still heavily reliant on traditional chemotherapeutic approaches. Combination treatments have shown to be a superior approach, but their success is often hindered by side effects and different drugs' pharmacokinetics. Here, we investigated ABT-737 and Purvalanol A as a potential drug pairing for pediatric AML and described the development of CD33-targeted polymeric nanoparticles (NPs) to enable their simultaneous targeted codelivery. Separate drug encapsulation within poly(lactic-&lt;i>co&lt;/i>-glycolic acid) (PLGA) NPs was optimized prior to coencapsulation of both drugs at a synergistic ratio in PEGylated PLGA NPs. The therapeutic effects of formulations were evaluated in a panel of pediatric AML cells, and du</pubmed_abstract><journal>Biomacromolecules</journal><pubmed_title>Development of CD33-Targeted Dual Drug-Loaded Nanoparticles for the Treatment of Pediatric Acute Myeloid Leukemia.</pubmed_title><pmcid>PMC11480974</pmcid><funding_grant_id>CCLGA 2019 01</funding_grant_id><funding_grant_id>859458</funding_grant_id><pubmed_authors>Greene MK</pubmed_authors><pubmed_authors>Scott CJ</pubmed_authors><pubmed_authors>Smyth P</pubmed_authors><pubmed_authors>Mutch A</pubmed_authors><pubmed_authors>Cairns LV</pubmed_authors><pubmed_authors>Mills KI</pubmed_authors><pubmed_authors>McLaughlin KM</pubmed_authors><pubmed_authors>McCloskey KD</pubmed_authors><pubmed_authors>Carvalho AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of CD33-Targeted Dual Drug-Loaded Nanoparticles for the Treatment of Pediatric Acute Myeloid Leukemia.</name><description>Paediatric acute myeloid leukemia (AML) is a heterogeneous hematological malignancy still heavily reliant on traditional chemotherapeutic approaches. Combination treatments have shown to be a superior approach, but their success is often hindered by side effects and different drugs' pharmacokinetics. Here, we investigated ABT-737 and Purvalanol A as a potential drug pairing for pediatric AML and described the development of CD33-targeted polymeric nanoparticles (NPs) to enable their simultaneous targeted codelivery. Separate drug encapsulation within poly(lactic-&lt;i>co&lt;/i>-glycolic acid) (PLGA) NPs was optimized prior to coencapsulation of both drugs at a synergistic ratio in PEGylated PLGA NPs. The therapeutic effects of formulations were evaluated in a panel of pediatric AML cells, and du</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-04T07:40:42.467Z</modification><creation>2025-04-04T07:40:42.467Z</creation></dates><accession>S-EPMC11480974</accession><cross_references><pubmed>39235263</pubmed><doi>10.1021/acs.biomac.4c00672</doi></cross_references></HashMap>