<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carini V</submitter><funding>Liverpool John Moores University</funding><pagination>13</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12845076</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(1)</volume><pubmed_abstract>&lt;b>Background/Objectives:&lt;/b> The growing threat posed by antimicrobial resistance to worldwide public health highlights the urgent need not only for new anti-infective candidates, but also for innovative formulation strategies capable of mediating effective delivery of anti-infective compounds. The current study, therefore, aimed to demonstrate the feasibility of formulating lipid-polymer hybrid nanoparticles (LPHNPs) with dual loading of both core and shell compartments for combination anti-infective delivery. &lt;b>Methods:&lt;/b> LPHNPs containing the antibiotic cefotaxime within a chitosan polymer core and the novel antimicrobial peptide RN7IN6 within a bacteria-mimicking lipid shell were produced by microfluidic mixing, and optimized with respect to parameters including total flow rate, fl</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Dual Core-Shell Loaded Lipid-Polymer Hybrid Nanoparticles as Combination Anti-Infective Delivery Platforms.</pubmed_title><pmcid>PMC12845076</pmcid><funding_grant_id>SCS ECR PhD Studentship</funding_grant_id><pubmed_authors>Scagnetti G</pubmed_authors><pubmed_authors>Saleem I</pubmed_authors><pubmed_authors>Foulkes J</pubmed_authors><pubmed_authors>Evans K</pubmed_authors><pubmed_authors>Carini V</pubmed_authors><pubmed_authors>Gordon S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dual Core-Shell Loaded Lipid-Polymer Hybrid Nanoparticles as Combination Anti-Infective Delivery Platforms.</name><description>&lt;b>Background/Objectives:&lt;/b> The growing threat posed by antimicrobial resistance to worldwide public health highlights the urgent need not only for new anti-infective candidates, but also for innovative formulation strategies capable of mediating effective delivery of anti-infective compounds. The current study, therefore, aimed to demonstrate the feasibility of formulating lipid-polymer hybrid nanoparticles (LPHNPs) with dual loading of both core and shell compartments for combination anti-infective delivery. &lt;b>Methods:&lt;/b> LPHNPs containing the antibiotic cefotaxime within a chitosan polymer core and the novel antimicrobial peptide RN7IN6 within a bacteria-mimicking lipid shell were produced by microfluidic mixing, and optimized with respect to parameters including total flow rate, fl</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-15T03:12:15.905Z</modification><creation>2026-06-15T03:08:38.196Z</creation></dates><accession>S-EPMC12845076</accession><cross_references><pubmed>41599120</pubmed><doi>10.3390/pharmaceutics18010013</doi></cross_references></HashMap>