<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ismail J</submitter><funding>Deutsche Forschungsgemeinschaft</funding><pagination>187</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10891717</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>Hybrid nanoparticles (HNPs) were designed by combining a PLGA core with a lipid shell that incorporated PEG-Lipid conjugates with various functionalities (-RGD, -cRGD, -NH&lt;sub>2&lt;/sub>, and -COOH) to create targeted drug delivery systems. Loaded with a neutral lipid orange dye, the HNPs were extensively characterized using various techniques and investigated for their uptake in human monocyte-derived macrophages (MDMs) using FC and CLSM. Moreover, the best-performing HNPs (i.e., HNP-COOH and HNP-RGD as well as HNP-RGD/COOH mixed) were loaded with the anti-inflammatory drug BRP-201 and prepared in two size ranges (d&lt;sub>H&lt;/sub> ~140 nm and d&lt;sub>H&lt;/sub> ~250 nm). The HNPs were examined further for their stability, degradation, MDM uptake, and drug delivery efficiency by studying the inhibiti</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>PEG-Lipid-PLGA Hybrid Particles for Targeted Delivery of Anti-Inflammatory Drugs.</pubmed_title><pmcid>PMC10891717</pmcid><funding_grant_id>471397362</funding_grant_id><funding_grant_id>316213987</funding_grant_id><funding_grant_id>INST 275/315-1 FUGG</funding_grant_id><pubmed_authors>Ismail J</pubmed_authors><pubmed_authors>Pretzel D</pubmed_authors><pubmed_authors>Rezaei K</pubmed_authors><pubmed_authors>Nischang I</pubmed_authors><pubmed_authors>Dahlke P</pubmed_authors><pubmed_authors>Czaplewska JA</pubmed_authors><pubmed_authors>Jordan PM</pubmed_authors><pubmed_authors>Schubert US</pubmed_authors><pubmed_authors>Beringer-Siemers B</pubmed_authors><pubmed_authors>Tsarenko E</pubmed_authors><pubmed_authors>Stumpf S</pubmed_authors><pubmed_authors>Vollrath A</pubmed_authors><pubmed_authors>Klepsch LC</pubmed_authors><pubmed_authors>Hoeppener S</pubmed_authors><pubmed_authors>Werz O</pubmed_authors></additional><is_claimable>false</is_claimable><name>PEG-Lipid-PLGA Hybrid Particles for Targeted Delivery of Anti-Inflammatory Drugs.</name><description>Hybrid nanoparticles (HNPs) were designed by combining a PLGA core with a lipid shell that incorporated PEG-Lipid conjugates with various functionalities (-RGD, -cRGD, -NH&lt;sub>2&lt;/sub>, and -COOH) to create targeted drug delivery systems. Loaded with a neutral lipid orange dye, the HNPs were extensively characterized using various techniques and investigated for their uptake in human monocyte-derived macrophages (MDMs) using FC and CLSM. Moreover, the best-performing HNPs (i.e., HNP-COOH and HNP-RGD as well as HNP-RGD/COOH mixed) were loaded with the anti-inflammatory drug BRP-201 and prepared in two size ranges (d&lt;sub>H&lt;/sub> ~140 nm and d&lt;sub>H&lt;/sub> ~250 nm). The HNPs were examined further for their stability, degradation, MDM uptake, and drug delivery efficiency by studying the inhibiti</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-04-19T14:47:46.113Z</modification><creation>2025-04-19T14:47:46.113Z</creation></dates><accession>S-EPMC10891717</accession><cross_references><pubmed>38399248</pubmed><doi>10.3390/pharmaceutics16020187</doi></cross_references></HashMap>