<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Chen X</submitter><pubmed_abstract>Non-small-cell lung cancer (NSCLC) accounts for over 85% of clinical lung cancer cases, which is the leading cause of cancer-related death. To develop new therapeutic strategy for NSCLC, a library of L-phenylalanine-based poly(ester amide) (Phe-PEA) polymers was synthesized and assembled with docetaxel (Dtxl) to form Dtxl-loaded Phe-PEA nanoparticles (NPs). The hydrophobic Phe-PEA polymers were able to form NPs by nanoprecipitation method and the characterization results showed that the screened Dtxl-8P4 NPs have small particle size (∼100 nm) and high Dtxl loading (∼20 wt%). In vitro experiments showed that Dtxl-8P4 NPs were rapidly trafficked into cancer cells, then effectively escaped from lysosomal degradation and achieved significant tumor cell inhibition. In vivo results demonstrated </pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>118</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5835838</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Significant Suppression of Non-small-cell Lung Cancer by Hydrophobic Poly(ester amide) Nanoparticles with High Docetaxel Loading.</pubmed_title><pmcid>PMC5835838</pmcid><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Zhao L</pubmed_authors><pubmed_authors>He Z</pubmed_authors><pubmed_authors>Ling X</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Kang Y</pubmed_authors><pubmed_authors>Xiong F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Significant Suppression of Non-small-cell Lung Cancer by Hydrophobic Poly(ester amide) Nanoparticles with High Docetaxel Loading.</name><description>Non-small-cell lung cancer (NSCLC) accounts for over 85% of clinical lung cancer cases, which is the leading cause of cancer-related death. To develop new therapeutic strategy for NSCLC, a library of L-phenylalanine-based poly(ester amide) (Phe-PEA) polymers was synthesized and assembled with docetaxel (Dtxl) to form Dtxl-loaded Phe-PEA nanoparticles (NPs). The hydrophobic Phe-PEA polymers were able to form NPs by nanoprecipitation method and the characterization results showed that the screened Dtxl-8P4 NPs have small particle size (∼100 nm) and high Dtxl loading (∼20 wt%). In vitro experiments showed that Dtxl-8P4 NPs were rapidly trafficked into cancer cells, then effectively escaped from lysosomal degradation and achieved significant tumor cell inhibition. In vivo results demonstrated </description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-19T02:28:35.861Z</modification><creation>2019-03-26T23:17:51Z</creation></dates><accession>S-EPMC5835838</accession><cross_references><pubmed>29541026</pubmed><doi>10.3389/fphar.2018.00118</doi></cross_references></HashMap>