<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Richardson SC</submitter><funding>Wellcome Trust</funding><funding>NIGMS NIH HHS</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>1-11</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6661902</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>127(1)</volume><pubmed_abstract>Macromolecular therapeutics and nano-sized drug delivery systems often require localisation to specific intracellular compartments. In particular, efficient endosomal escape, retrograde trafficking, or late endocytic/lysosomal activation are often prerequisites for pharmacological activity. The aim of this study was to define a fluorescence microscopy technique able to confirm the localisation of water-soluble polymeric carriers to late endocytic intracellular compartments. Three polymeric carriers of different molecular weight and character were studied: dextrin (Mw~50,000 g/mol), a N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer (Mw approximately 35,000 g/mol) and polyethylene glycol (PEG) (Mw 5000 g/mol). They were labelled with Oregon Green (OG) (0.3-3 wt.%; &lt;3% free OG in respect o</pubmed_abstract><journal>Journal of controlled release : official journal of the Controlled Release Society</journal><pubmed_title>The use of fluorescence microscopy to define polymer localisation to the late endocytic compartments in cells that are targets for drug delivery.</pubmed_title><pmcid>PMC6661902</pmcid><funding_grant_id>R01 GM058202-11</funding_grant_id><funding_grant_id>R01 GM058202</funding_grant_id><funding_grant_id>EP/C013220/1</funding_grant_id><pubmed_authors>Davies MW</pubmed_authors><pubmed_authors>Piper RC</pubmed_authors><pubmed_authors>Deacon SP</pubmed_authors><pubmed_authors>Wallom KL</pubmed_authors><pubmed_authors>Powell AJ</pubmed_authors><pubmed_authors>Duncan R</pubmed_authors><pubmed_authors>Ferguson EL</pubmed_authors><pubmed_authors>Richardson SC</pubmed_authors></additional><is_claimable>false</is_claimable><name>The use of fluorescence microscopy to define polymer localisation to the late endocytic compartments in cells that are targets for drug delivery.</name><description>Macromolecular therapeutics and nano-sized drug delivery systems often require localisation to specific intracellular compartments. In particular, efficient endosomal escape, retrograde trafficking, or late endocytic/lysosomal activation are often prerequisites for pharmacological activity. The aim of this study was to define a fluorescence microscopy technique able to confirm the localisation of water-soluble polymeric carriers to late endocytic intracellular compartments. Three polymeric carriers of different molecular weight and character were studied: dextrin (Mw~50,000 g/mol), a N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer (Mw approximately 35,000 g/mol) and polyethylene glycol (PEG) (Mw 5000 g/mol). They were labelled with Oregon Green (OG) (0.3-3 wt.%; &lt;3% free OG in respect o</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Apr</publication><modification>2025-04-22T15:09:33.472Z</modification><creation>2019-08-02T07:02:38Z</creation></dates><accession>S-EPMC6661902</accession><cross_references><pubmed>18281120</pubmed><doi>10.1016/j.jconrel.2007.12.015</doi></cross_references></HashMap>