Antiviral and anti-inflammatory efficacy of nanoencapsulated brazilian green propolis against SARS-CoV-2

Abstract The global COVID-19 pandemic, caused by SARS-CoV-2, continues to pose a significant threat to public health and the economy. SARS-CoV-2 is highly contagious, transmitted primarily through direct contact or inhalation of droplets, and can cause severe respiratory illnesses and other health c...

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Main Authors: Iasmin Rosanne Silva Ferreira, Isabela Araújo Justino, Ronaldo Bragança Martins, Maria Vitória Oliveira Souza, Thais Melquiades de Lima, Ana Maria de Freitas Pinheiro, Eurico Arruda, Jairo Kenupp Bastos, Priscyla Daniely Marcato
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-05683-w
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Summary:Abstract The global COVID-19 pandemic, caused by SARS-CoV-2, continues to pose a significant threat to public health and the economy. SARS-CoV-2 is highly contagious, transmitted primarily through direct contact or inhalation of droplets, and can cause severe respiratory illnesses and other health complications, including post-acute COVID-19 syndrome. This study explored the antiviral potential of Brazilian green propolis, a natural product rich in flavonoids and phenolic compounds encapsulated in a microemulsion, to enhance its stability and antiviral effects. Brazilian green propolis extract was encapsulated in a microemulsion (ME-GP) and characterized using various physicochemical techniques. Furthermore, the antiviral and anti-inflammatory activities of ME-GP was evaluated in vitro and ex-vivo against SARS-CoV-2. For this, cells or tonsils were treated with ME-GP followed by infection with SARS-CoV-2. The microemulsion showed a size of approximately 217 nm, negative zeta potential, high encapsulation efficiency for artepillin C and baccharin (< 99%), and a spherical morphology. The ME-GP formulation was evaluated for antiviral activity against multiple SARS-CoV-2 variants (Wuhan, Gamma, Delta, and Omicron) in Caco-2 cells. The results demonstrated a significant reduction in viral load, particularly for the Wuhan and Delta variants, with up to a 99% reduction in viral load under prophylactic treatment conditions. Time-of-addition assays revealed that ME-GP acts at an early stage in the viral life cycle, likely by interfering with viral entry or immediate post-entry events. Additionally, ME-GP was evaluated in human tonsils, demonstrating an 80% reduction in viral load, suggesting its potential to reduce the transmission and progression of infection. Furthermore, ME-GP exhibited anti-inflammatory activity in human tonsils, significantly decreasing IL-1β, IL-6, TNF-α, and TNF-β levels. Thus, this study highlights the promising prophylactic and therapeutic potential of nanoencapsulated green propolis for combating SARS-CoV-2 and its variants, providing a natural adjunct in COVID-19 therapy.
ISSN:2045-2322