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Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents

BACKGROUND: Human cytomegalovirus (HCMV) is a worldwide infection, causing different troublesome in immunosupressed patients and very related to Human Immunodeficiency Virus 1 (HIV-1) infection, mainly in developing countries, with a co-infection rate of 80% in Africa. The high cost of present treat...

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Autores principales: Relaño-Rodríguez, I., Espinar-Buitrago, M. S., Martín-Cañadilla, V., Gómez-Ramirez, R., Jiménez, J. L., Muñoz-Fernández, M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927225/
https://www.ncbi.nlm.nih.gov/pubmed/33658029
http://dx.doi.org/10.1186/s12951-021-00809-4
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author Relaño-Rodríguez, I.
Espinar-Buitrago, M. S.
Martín-Cañadilla, V.
Gómez-Ramirez, R.
Jiménez, J. L.
Muñoz-Fernández, M. A.
author_facet Relaño-Rodríguez, I.
Espinar-Buitrago, M. S.
Martín-Cañadilla, V.
Gómez-Ramirez, R.
Jiménez, J. L.
Muñoz-Fernández, M. A.
author_sort Relaño-Rodríguez, I.
collection PubMed
description BACKGROUND: Human cytomegalovirus (HCMV) is a worldwide infection, causing different troublesome in immunosupressed patients and very related to Human Immunodeficiency Virus 1 (HIV-1) infection, mainly in developing countries, with a co-infection rate of 80% in Africa. The high cost of present treatments and the lack of routinely tests in these countries urge the necessity to develop new molecules or strategies against HCMV. The new treatments should be low-cost and capable of avoiding the emerging problem of resistant virus. Nanoparticles play an important role in several viral infections. Our main focus is to study the potential activity of polyanionic carbosilane dendrimers (PDC), which are hyperbranched molecules with several sulfonate or sulfate groups in their periphery, against different viruses. RESULTS: We studied the activity of G1-S4, G2-S16 and G2-S24P PDCs in MRC-5 cell line against HCMV infection by several plaque reduction assays. Our results show that dendrimers present good biocompatibility at the concentrations tested (1–50 µM) for 6 days in cell culture. Interestingly, both G2-S16 and G2-S24P showed a remarked inhibition at 10 µM against HCMV infection. Results on attachment and virucidal assays indicated that the inhibition was not directed to the virus or the virus-cell attachment. However, results of time of addition, showed a longer lasting activity of these dendrimers in comparison to ganciclovir, and the combination of G2-S16 or G2-S24P with ganciclovir increases the HCMV inhibition around 90 %. CONCLUSIONS: Nanotechnology, in particular polyanionic carbosilane dendrimers, have proved their potential application against HCMV, being capable of inhibiting the infection by themselves or enhancing the activity of ganciclovir, the actual treatment. These compounds represent a low-cost approach to fight HCMV infections. [Image: see text]
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spelling pubmed-79272252021-03-03 Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents Relaño-Rodríguez, I. Espinar-Buitrago, M. S. Martín-Cañadilla, V. Gómez-Ramirez, R. Jiménez, J. L. Muñoz-Fernández, M. A. J Nanobiotechnology Research BACKGROUND: Human cytomegalovirus (HCMV) is a worldwide infection, causing different troublesome in immunosupressed patients and very related to Human Immunodeficiency Virus 1 (HIV-1) infection, mainly in developing countries, with a co-infection rate of 80% in Africa. The high cost of present treatments and the lack of routinely tests in these countries urge the necessity to develop new molecules or strategies against HCMV. The new treatments should be low-cost and capable of avoiding the emerging problem of resistant virus. Nanoparticles play an important role in several viral infections. Our main focus is to study the potential activity of polyanionic carbosilane dendrimers (PDC), which are hyperbranched molecules with several sulfonate or sulfate groups in their periphery, against different viruses. RESULTS: We studied the activity of G1-S4, G2-S16 and G2-S24P PDCs in MRC-5 cell line against HCMV infection by several plaque reduction assays. Our results show that dendrimers present good biocompatibility at the concentrations tested (1–50 µM) for 6 days in cell culture. Interestingly, both G2-S16 and G2-S24P showed a remarked inhibition at 10 µM against HCMV infection. Results on attachment and virucidal assays indicated that the inhibition was not directed to the virus or the virus-cell attachment. However, results of time of addition, showed a longer lasting activity of these dendrimers in comparison to ganciclovir, and the combination of G2-S16 or G2-S24P with ganciclovir increases the HCMV inhibition around 90 %. CONCLUSIONS: Nanotechnology, in particular polyanionic carbosilane dendrimers, have proved their potential application against HCMV, being capable of inhibiting the infection by themselves or enhancing the activity of ganciclovir, the actual treatment. These compounds represent a low-cost approach to fight HCMV infections. [Image: see text] BioMed Central 2021-03-03 /pmc/articles/PMC7927225/ /pubmed/33658029 http://dx.doi.org/10.1186/s12951-021-00809-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Relaño-Rodríguez, I.
Espinar-Buitrago, M. S.
Martín-Cañadilla, V.
Gómez-Ramirez, R.
Jiménez, J. L.
Muñoz-Fernández, M. A.
Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents
title Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents
title_full Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents
title_fullStr Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents
title_full_unstemmed Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents
title_short Nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents
title_sort nanotechnology against human cytomegalovirus in vitro: polyanionic carbosilane dendrimers as antiviral agents
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927225/
https://www.ncbi.nlm.nih.gov/pubmed/33658029
http://dx.doi.org/10.1186/s12951-021-00809-4
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