Heparin-azithromycin microparticulate nasal gels block SARS-CoV-2 and bacterial respiratory infections
The SARS-CoV-2 pandemic highlighted the need for effective prophylactic and local treatment strategies against respiratory viruses. The nasal cavity is a critical site for pathogen entry and colonization, and is therefore a critical target for targeted interventions. SARS-CoV-2, as a plethora of other virus, primarily spreads via respiratory droplets infecting nasal epithelial cells. Concurrently, bacteria such as Streptococcus pneumoniae and Pseudomonas aeruginosa , frequently colonize the nasal cavity, causing co-infections and serving as reservoirs for further respiratory tract involvement. This study presents a nasal gel that combines heparin and azithromycin (AZM) microparticles to combat both viral and bacterial infections in the nasal cavity. The formulation exhibits a favorable safety profile with minimal haemolytic toxicity (HC 50 > 82 × 10⁷ μg/mL), potent activity against P. aeruginosa and S. pneumoniae at low concentrations (MIC of 15.6 µg/mL and 7.8 µg/mL, respectively), and effective antiviral properties (IC 50 of 0.062 µg/mL for Pseudovirus inhibition). These multifaceted properties position the formulation as a promising candidate for a convenient, dual-action therapy in respiratory infection management, offering potentially both treatment and prophylaxis.
Authors
- Brayan J. Anaya (ORCID: https://orcid.org/0000-0002-0846-9044)
- Karim Osouli-Bostanabad
- Diego F. Tirado (ORCID: https://orcid.org/0000-0002-6178-5660)
- Dolores R. Serrano (ORCID: https://orcid.org/0000-0002-0475-8420)
- Elena González‐Burgos
- Aikaterini Lalatsa (ORCID: https://orcid.org/0000-0003-4791-7468)
Institutions
- Universidad Complutense de Madrid (ES)
- University of Strathclyde (GB)
- Universidad Nacional de Colombia (CO)
- University of Portsmouth (GB)
Publication Details
- Journal
- Carbohydrate Polymer Technologies and Applications
- Published
- 2025-10-28
- DOI
- https://doi.org/10.1016/j.carpta.2025.101031
- Primary Topic
- Advanced Drug Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 0.00