Advancing influenza virus treatment: in vitro and ex vivo studies of PI3K inhibitor-loaded lipid nanoparticles
Influenza A viruses (IAVs) remain a significant global health concern, causing seasonal outbreaks and pandemics with substantial morbidity and mortality, particularly among vulnerable groups. Annual vaccination serves as the primary preventative measure, but its limited effectiveness against emerging subtypes and insufficient coverage underscore the urgent need for novel antiviral strategies. Resistance to Food and Drug Administration (FDA)- and European Medicines Agency (EMA)-approved direct antivirals further emphasizes this necessity. Host-directed therapeutic strategies, such as those targeting phosphatidylinositol 3-kinases (PI3Ks), which are utilized by IAVs during replication, offer promising alternatives to reduce infection severity. In parallel, advances in nanotechnology have facilitated the use of lipid nanoparticles (LNPs) as efficient drug delivery systems, enhancing bioavailability, optimizing therapeutic stability, and enabling precise site-specific delivery to infected cells. This study investigates the combined use of pictilisib, a PI3K inhibitor, and LNPs, as a novel approach to combat IAV infections. Polyethylene glycol (PEG)- and poly(2-oxazoline) (POx)-Lipids were incorporated into the drug delivery carriers, with POx-Lipids emerging as promising alternatives due to allergenic concerns associated with PEG. Pictilisib was successfully encapsulated in LNPs and demonstrated comparable antiviral and anti-inflammatory properties to the free drug <i>in vitro</i>. Notably, <i>ex vivo</i> experiments revealed that POx-Lipid LNPs encapsulating pictilisib had a more potent effect on infection compared to free pictilisib, suggesting improved pharmacokinetics, drug stability, and targeted delivery. This integrated approach combining targeted PI3K inhibition and advanced nanocarrier technology represents a significant advance in addressing the challenges associated with IAV treatment, paving the way for further exploration of these strategies to combat infectious diseases.
Authors
- Carsten Hoffmann (ORCID: https://orcid.org/0000-0003-0884-9300)
- Bettina Löffler (ORCID: https://orcid.org/0009-0009-6792-9328)
- Laura Klement (ORCID: https://orcid.org/0009-0008-3956-6059)
- Christina Ehrhardt (ORCID: https://orcid.org/0000-0002-8879-6087)
- Christian Kosan (ORCID: https://orcid.org/0000-0002-8387-3653)
- Jana Ismail (ORCID: https://orcid.org/0000-0002-8475-5683)
- Michaela Schmidtke (ORCID: https://orcid.org/0000-0001-9163-5682)
- Caroline T. Holick (ORCID: https://orcid.org/0009-0000-1724-2725)
- Stephanie M. Schubert (ORCID: https://orcid.org/0000-0001-9527-7763)
- Josefine Schroeder (ORCID: https://orcid.org/0009-0003-3732-2476)
- Johannes Jungwirth (ORCID: https://orcid.org/0009-0003-5917-9527)
- Christine Weber (ORCID: https://orcid.org/0000-0003-0712-5255)
- Stephanie Hoeppener (ORCID: https://orcid.org/0000-0002-5770-5197)
Institutions
- Helmholtz Institute Jena (DE)
- Helmholtz-Zentrum Berlin für Materialien und Energie (DE)
- Jena University Hospital (DE)
- Friedrich Schiller University Jena (DE)
Publication Details
- Journal
- Materials Today Bio
- Published
- 2025-11-26
- DOI
- https://doi.org/10.1016/j.mtbio.2025.102587
- Primary Topic
- Influenza Virus Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00