Multilayer Nanocarrier for the Codelivery of Interferons: A Promising Strategy for Biocompatible and Long-Acting Antiviral Treatment

<b>Background:</b> Interferons (IFNs) are cytokines involved in the immune response with a synergistic regulatory effect on the immune response. They are therapeutics for various viral and proliferative conditions, with proven safety and efficacy. Their clinical application is challenging due to the molecules' size, degradation, and pharmacokinetics. We are working on new drug delivery systems that provide adequate therapeutic concentrations for these cytokines and prolong their half-life in the circulation, such as nanoformulations. <b>Methods:</b> Through nanoencapsulation using electrospray technology and biocompatible and biodegradable polymers, we are developing a controlled release system based on nanoparticles for viral infections of the respiratory tract. <b>Results:</b> We developed a controlled release system for viral respiratory tract infections. A prototype nanoparticle with a core was created, which hydrolyzed the polyvinylpyrrolidone (PVP) shell , releasing the active ingredients interferon-alpha (IFN-α) and interferon-gamma (IFN-γ). The chitosan (QS) core degraded slowly, with a controlled release of IFN-α. The primary and rapid effect of the interferon combination ensured an antiviral and immunoregulatory response from day one, induced by IFN-α and enhanced by IFN-γ. The multilayer design demonstrated an optimal toxicity profile. <b>Conclusions:</b> This formulation is an inhaled dry powder intended for the non-invasive intranasal route. The product does not require a cold chain and has the potential for self-administration in the face of emerging viral infections. This novel drug has applications in multiple infectious, oncological, and autoimmune conditions, and further development is proposed for its therapeutic potential. This prototype would ensure greater bioavailability, controlled release, fewer adverse effects, and robust biological action through the simultaneous action of both molecules.

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Publication Details

Journal
Pharmaceutics
Published
2024-10-22
DOI
https://doi.org/10.3390/pharmaceutics16111349
Citations
4
Primary Topic
Viral Infectious Diseases and Gene Expression in Insects
Type
article
Field-Weighted Citation Impact
0.94

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article

Multilayer Nanocarrier for the Codelivery of Interferons: A Promising Strategy for Biocompatible and Long-Acting Antiviral Treatment

Claudia Altamirano, Marbel Torres Arias, Raquel Montesino, Thelvia I. Ramos et al.
4 citations
Pharmaceutics
Viral Infectious Diseases and Gene Expression in Insects
0.94
article

Multilayer Nanocarrier for the Codelivery of Interferons: A Promising Strategy for Biocompatible and Long-Acting Antiviral Treatment

Claudia Altamirano, Marbel Torres Arias, Raquel Montesino, Thelvia I. Ramos, Leandro Santiago Padilla, Sarah Martin-Solano, Carlos A. Villacis-Aguirre, Jorge R. Toledo, Alexis Debut, Ignacio Cabezas, Oliberto Sánchez, Viana Manrique Suárez, Hortensia Rodrı́guez, Nelson Santiago Vispo, Florence Hugues, Natalie C. Parra, Emilio Lamazares, Felipe Sandoval Sandoval, Carolina Gómez-Gaete
article en
4 citations

Abstract

<b>Background:</b> Interferons (IFNs) are cytokines involved in the immune response with a synergistic regulatory effect on the immune response. They are therapeutics for various viral and proliferative conditions, with proven safety and efficacy. Their clinical application is challenging due to the molecules' size, degradation, and pharmacokinetics. We are working on new drug delivery systems that provide adequate therapeutic concentrations for these cytokines and prolong their half-life in the circulation, such as nanoformulations. <b>Methods:</b> Through nanoencapsulation using electrospray technology and biocompatible and biodegradable polymers, we are developing a controlled release system based on nanoparticles for viral infections of the respiratory tract. <b>Results:</b> We developed a controlled release system for viral respiratory tract infections. A prototype nanoparticle with a core was created, which hydrolyzed the polyvinylpyrrolidone (PVP) shell , releasing the active ingredients interferon-alpha (IFN-α) and interferon-gamma (IFN-γ). The chitosan (QS) core degraded slowly, with a controlled release of IFN-α. The primary and rapid effect of the interferon combination ensured an antiviral and immunoregulatory response from day one, induced by IFN-α and enhanced by IFN-γ. The multilayer design demonstrated an optimal toxicity profile. <b>Conclusions:</b> This formulation is an inhaled dry powder intended for the non-invasive intranasal route. The product does not require a cold chain and has the potential for self-administration in the face of emerging viral infections. This novel drug has applications in multiple infectious, oncological, and autoimmune conditions, and further development is proposed for its therapeutic potential. This prototype would ensure greater bioavailability, controlled release, fewer adverse effects, and robust biological action through the simultaneous action of both molecules.

PharmaceuticsVol. 16(11)
Universidad de las Fuerzas Armadas ESPE (EC), Pontificia Universidad Católica de Valparaíso (CL), University of Concepción (CL), Max Delbrück Center (DE), Universidad Yachay Tech (EC)
University of Miami, Universidad de Concepción, Universidad de las Fuerzas Armadas ESPE, Leonard M. Miller School of Medicine, Leonard M. Miller School of Medicine, University of Miami
Good health and well-being
Openalex Percentile: Top 25%
Viral Infectious Diseases and Gene Expression in Insects
0.94
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