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        <r:String xml:lang="en">Flash nanoprecipitation for co-delivery of magnetic nanoparticles and small molecules in polymeric nanocarriers</r:String>
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          <r:String xml:lang="sv">Uppsala universitet</r:String>
          <r:String xml:lang="en">Uppsala University</r:String>
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          <r:String xml:lang="sv">Uppsala universitet</r:String>
          <r:String xml:lang="en">Uppsala University</r:String>
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        <r:SimpleDate>2026-03-05</r:SimpleDate>
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      <r:Content xml:lang="en">Chronic inflammatory diseases may benefit from nanocarrier platforms that co-deliver hydrophobic anti-inflammatory drugs and imaging agents. Here, we report polymeric theranostic nanocarrier dispersions produced by flash nanoprecipitation (FNP) that encapsulate flame-made manganese-doped superparamagnetic iron oxide nanoparticles (SPIONs; Mn0.25Fe2.75O4) together with T‑5224, a model small-molecule inhibitor of the c‑Fos/c‑Jun activator protein‑1 (AP‑1) complex. We first mapped key formulation and process parameters governing dispersion properties, including PLA–PEG molecular weight, total solute concentration, solvent-to-antisolvent ratio, and SPION:polymer mass ratio. These studies identified conditions yielding smaller, narrowly distributed dispersions. Using the optimized formulation, T‑5224/SPION nanocarrier dispersions were purified by magnetic separation and exhibited hydrodynamic diameters</r:Content>
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        <r:Subject xml:lang="sv" controlledVocabularyID="21003" controlledVocabularyName="Standard för svensk indelning av forskningsämnen 2025">Nanoteknisk materialvetenskap</r:Subject>
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