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3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection
Herpes viruses are widespread in the human population and can cause many different diseases. Genital herpes is common and can increase the risk of HIV infection and neonatal herpes. Acyclovir is the most used drug for herpes treatment; however, it presents some disadvantages due to its poor oral bio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696101/ https://www.ncbi.nlm.nih.gov/pubmed/36423110 http://dx.doi.org/10.3390/v14112501 |
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author | de Carvalho Rodrigues, Victor Guterres, Iara Zanella Savi, Beatriz Pereira Silva, Izabella Thaís Fongaro, Gislaine Salmoria, Gean Vitor |
author_facet | de Carvalho Rodrigues, Victor Guterres, Iara Zanella Savi, Beatriz Pereira Silva, Izabella Thaís Fongaro, Gislaine Salmoria, Gean Vitor |
author_sort | de Carvalho Rodrigues, Victor |
collection | PubMed |
description | Herpes viruses are widespread in the human population and can cause many different diseases. Genital herpes is common and can increase the risk of HIV infection and neonatal herpes. Acyclovir is the most used drug for herpes treatment; however, it presents some disadvantages due to its poor oral bioavailability. In this study, some ethylene vinyl acetate devices with different acyclovir amounts (0, 10, and 20 wt.%) were manufactured by fused filament fabrication in two different geometries, an intrauterine device, and an intravaginal ring. Thermal analyses suggested that the crystallinity of EVA decreased up to 8% for the sample loaded with 20 wt.% of acyclovir. DSC, SEM, and FTIR analyses confirmed that the drug was successfully incorporated into the EVA matrix. Moreover, the drug release tests suggested a burst release during the first 24 h followed by a slower release rate sustained up to 80 days. Biological assays showed the biocompatibility of the EVA/ACV device, as well as a 99% reduction in vitro replication of HSV-1. Finally, the EVA presented a suitable performance for 3D printing manufacturing that can contribute to developing personalized solutions for long-term herpes treatment. |
format | Online Article Text |
id | pubmed-9696101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96961012022-11-26 3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection de Carvalho Rodrigues, Victor Guterres, Iara Zanella Savi, Beatriz Pereira Silva, Izabella Thaís Fongaro, Gislaine Salmoria, Gean Vitor Viruses Article Herpes viruses are widespread in the human population and can cause many different diseases. Genital herpes is common and can increase the risk of HIV infection and neonatal herpes. Acyclovir is the most used drug for herpes treatment; however, it presents some disadvantages due to its poor oral bioavailability. In this study, some ethylene vinyl acetate devices with different acyclovir amounts (0, 10, and 20 wt.%) were manufactured by fused filament fabrication in two different geometries, an intrauterine device, and an intravaginal ring. Thermal analyses suggested that the crystallinity of EVA decreased up to 8% for the sample loaded with 20 wt.% of acyclovir. DSC, SEM, and FTIR analyses confirmed that the drug was successfully incorporated into the EVA matrix. Moreover, the drug release tests suggested a burst release during the first 24 h followed by a slower release rate sustained up to 80 days. Biological assays showed the biocompatibility of the EVA/ACV device, as well as a 99% reduction in vitro replication of HSV-1. Finally, the EVA presented a suitable performance for 3D printing manufacturing that can contribute to developing personalized solutions for long-term herpes treatment. MDPI 2022-11-11 /pmc/articles/PMC9696101/ /pubmed/36423110 http://dx.doi.org/10.3390/v14112501 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article de Carvalho Rodrigues, Victor Guterres, Iara Zanella Savi, Beatriz Pereira Silva, Izabella Thaís Fongaro, Gislaine Salmoria, Gean Vitor 3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection |
title | 3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection |
title_full | 3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection |
title_fullStr | 3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection |
title_full_unstemmed | 3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection |
title_short | 3D-Printed EVA Devices for Antiviral Delivery and Herpes Virus Control in Genital Infection |
title_sort | 3d-printed eva devices for antiviral delivery and herpes virus control in genital infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696101/ https://www.ncbi.nlm.nih.gov/pubmed/36423110 http://dx.doi.org/10.3390/v14112501 |
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