Advances in Nanotechnology for the Treatment of Herpes Virus Infections

Herpes simplex virus (HSV) infections present a major global health burden due to their high morbidity. Conventional therapies offer limited efficacy due to poor bioavailability, the need for frequent administration and potential drug resistance. Recent advances in nanotechnology provide opportunities to overcome these limitations. This review summarizes the latest advances in nanocarrier-based formulations, highlighting their role in improving bioavailability, sustained release, mucosal penetration and antiviral activity. An integrative search was conducted from January 2010 to December 2025. Inclusion and exclusion criteria were used to select the articles. After analyzing the articles, 34 were included in this review with in vitro studies and 14 with in vivo assays. These articles were evaluated in relation to physicochemical characterization studies and in vitro and in vivo assays. Studies were found involving polymeric nanoparticles, metal nanoparticles, solid lipid nanoparticles, liposomes, niosomes, nanoemulsions and nanofibers. Regarding in vitro assays, it was observed that the nanosystems showed increased antiviral activity in cell cultures infected with the herpes simplex virus. In addition, developed nanosystems showed prolonged antiviral activity and lowered toxicity in animal models. Thus, these systems prove to be effective when compared to conventional therapy and can be considered an advance in HSV infection therapy.

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Publication Details

Journal
Viruses
Published
2026-03-13
DOI
https://doi.org/10.3390/v18030351
Primary Topic
Herpesvirus Infections and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Advances in Nanotechnology for the Treatment of Herpes Virus Infections

Gabriela Lopes Gama e Silva, Tatielle do Nascimento, Bruna Coelho de Almeida, Eduardo Ricci-Junior et al.
Viruses
Herpesvirus Infections and Treatments
article

Advances in Nanotechnology for the Treatment of Herpes Virus Infections

Gabriela Lopes Gama e Silva, Tatielle do Nascimento, Bruna Coelho de Almeida, Eduardo Ricci-Junior, Mariana Sato de Souza Bustamante Monteiro, Yohan Oliveira de Carvalho
article en

Abstract

Herpes simplex virus (HSV) infections present a major global health burden due to their high morbidity. Conventional therapies offer limited efficacy due to poor bioavailability, the need for frequent administration and potential drug resistance. Recent advances in nanotechnology provide opportunities to overcome these limitations. This review summarizes the latest advances in nanocarrier-based formulations, highlighting their role in improving bioavailability, sustained release, mucosal penetration and antiviral activity. An integrative search was conducted from January 2010 to December 2025. Inclusion and exclusion criteria were used to select the articles. After analyzing the articles, 34 were included in this review with in vitro studies and 14 with in vivo assays. These articles were evaluated in relation to physicochemical characterization studies and in vitro and in vivo assays. Studies were found involving polymeric nanoparticles, metal nanoparticles, solid lipid nanoparticles, liposomes, niosomes, nanoemulsions and nanofibers. Regarding in vitro assays, it was observed that the nanosystems showed increased antiviral activity in cell cultures infected with the herpes simplex virus. In addition, developed nanosystems showed prolonged antiviral activity and lowered toxicity in animal models. Thus, these systems prove to be effective when compared to conventional therapy and can be considered an advance in HSV infection therapy.

VirusesVol. 18(3)
Universidade do Estado do Rio de Janeiro (BR)
Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro
Openalex Percentile: Top 25%
Herpesvirus Infections and Treatments
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Advances in Nanotechnology for the Treatment of Herpes Virus Infections — Gabriela Lopes Gama e Silva, Tatielle do Nascimento, et al. · Viruses (2026) | TGRS Research Map | TGRS