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Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial
Canine distemper is caused by canine distemper virus (CDV), a multisystemic infectious disease with a high morbidity and mortality rate in dogs. Nanotechnology represents a development opportunity for new molecules with antiviral effects that may become effective treatments in veterinary medicine. T...
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/PMC9694365/ https://www.ncbi.nlm.nih.gov/pubmed/36366427 http://dx.doi.org/10.3390/v14112329 |
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author | Gastelum-Leyva, Fabian Pena-Jasso, Antonio Alvarado-Vera, Martha Plascencia-López, Ismael Patrón-Romero, Leslie Loera-Castañeda, Verónica Gándara-Mireles, Jesús Alonso Lares-Asseff, Ismael Leal-Ávila, María Ángeles Alvelais-Palacios, J. A. Almeida-Pérez, Javier Bogdanchikova, Nina Pestryakov, Alexey Almanza-Reyes, Horacio |
author_facet | Gastelum-Leyva, Fabian Pena-Jasso, Antonio Alvarado-Vera, Martha Plascencia-López, Ismael Patrón-Romero, Leslie Loera-Castañeda, Verónica Gándara-Mireles, Jesús Alonso Lares-Asseff, Ismael Leal-Ávila, María Ángeles Alvelais-Palacios, J. A. Almeida-Pérez, Javier Bogdanchikova, Nina Pestryakov, Alexey Almanza-Reyes, Horacio |
author_sort | Gastelum-Leyva, Fabian |
collection | PubMed |
description | Canine distemper is caused by canine distemper virus (CDV), a multisystemic infectious disease with a high morbidity and mortality rate in dogs. Nanotechnology represents a development opportunity for new molecules with antiviral effects that may become effective treatments in veterinary medicine. This study evaluated the efficacy and safety of silver nanoparticles (AgNPs) in 207 CDV, naturally infected, mixed-breed dogs exhibiting clinical signs of the non-neurological and neurological phases of the disease. Group 1a included 52 dogs (experimental group) diagnosed with non-neurologic distemper treated with 3% oral and nasal AgNPs in addition to supportive therapy. Group 1b included 46 dogs (control group) diagnosed with non-neurological distemper treated with supportive therapy only. Group 2a included 58 dogs with clinical signs of neurological distemper treated with 3% oral and nasal AgNPs in addition to supportive therapy. Group 2b included 51 dogs (control group) diagnosed with clinical signs of neurological distemper treated with supportive therapy only. Efficacy was measured by the difference in survival rates: in Group 1a, the survival rate was 44/52 (84.6%), versus 7/46 in Group 1b (15.2%), while both showed clinical signs of non-neurological distemper. The survival rate of dogs with clinical signs of neurological distemper in Group 2a (38/58; 65.6%) was significantly higher than those in Control Group 2b (0/51; 0%). No adverse reactions were detected in experimental groups treated with AgNPs. AgNPs significantly improved survival in dogs with clinical signs of neurological and non-neurological distemper. The use of AgNPs in the treatment of neurological distemper led to a drastic increase in the proportion of dogs recovered without sequels compared to dogs treated without AgNPs. The evidence demonstrates that AgNP therapy can be considered as a targeted treatment in dogs severely affected by canine distemper virus. |
format | Online Article Text |
id | pubmed-9694365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96943652022-11-26 Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial Gastelum-Leyva, Fabian Pena-Jasso, Antonio Alvarado-Vera, Martha Plascencia-López, Ismael Patrón-Romero, Leslie Loera-Castañeda, Verónica Gándara-Mireles, Jesús Alonso Lares-Asseff, Ismael Leal-Ávila, María Ángeles Alvelais-Palacios, J. A. Almeida-Pérez, Javier Bogdanchikova, Nina Pestryakov, Alexey Almanza-Reyes, Horacio Viruses Article Canine distemper is caused by canine distemper virus (CDV), a multisystemic infectious disease with a high morbidity and mortality rate in dogs. Nanotechnology represents a development opportunity for new molecules with antiviral effects that may become effective treatments in veterinary medicine. This study evaluated the efficacy and safety of silver nanoparticles (AgNPs) in 207 CDV, naturally infected, mixed-breed dogs exhibiting clinical signs of the non-neurological and neurological phases of the disease. Group 1a included 52 dogs (experimental group) diagnosed with non-neurologic distemper treated with 3% oral and nasal AgNPs in addition to supportive therapy. Group 1b included 46 dogs (control group) diagnosed with non-neurological distemper treated with supportive therapy only. Group 2a included 58 dogs with clinical signs of neurological distemper treated with 3% oral and nasal AgNPs in addition to supportive therapy. Group 2b included 51 dogs (control group) diagnosed with clinical signs of neurological distemper treated with supportive therapy only. Efficacy was measured by the difference in survival rates: in Group 1a, the survival rate was 44/52 (84.6%), versus 7/46 in Group 1b (15.2%), while both showed clinical signs of non-neurological distemper. The survival rate of dogs with clinical signs of neurological distemper in Group 2a (38/58; 65.6%) was significantly higher than those in Control Group 2b (0/51; 0%). No adverse reactions were detected in experimental groups treated with AgNPs. AgNPs significantly improved survival in dogs with clinical signs of neurological and non-neurological distemper. The use of AgNPs in the treatment of neurological distemper led to a drastic increase in the proportion of dogs recovered without sequels compared to dogs treated without AgNPs. The evidence demonstrates that AgNP therapy can be considered as a targeted treatment in dogs severely affected by canine distemper virus. MDPI 2022-10-24 /pmc/articles/PMC9694365/ /pubmed/36366427 http://dx.doi.org/10.3390/v14112329 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 Gastelum-Leyva, Fabian Pena-Jasso, Antonio Alvarado-Vera, Martha Plascencia-López, Ismael Patrón-Romero, Leslie Loera-Castañeda, Verónica Gándara-Mireles, Jesús Alonso Lares-Asseff, Ismael Leal-Ávila, María Ángeles Alvelais-Palacios, J. A. Almeida-Pérez, Javier Bogdanchikova, Nina Pestryakov, Alexey Almanza-Reyes, Horacio Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial |
title | Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial |
title_full | Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial |
title_fullStr | Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial |
title_full_unstemmed | Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial |
title_short | Evaluation of the Efficacy and Safety of Silver Nanoparticles in the Treatment of Non-Neurological and Neurological Distemper in Dogs: A Randomized Clinical Trial |
title_sort | evaluation of the efficacy and safety of silver nanoparticles in the treatment of non-neurological and neurological distemper in dogs: a randomized clinical trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694365/ https://www.ncbi.nlm.nih.gov/pubmed/36366427 http://dx.doi.org/10.3390/v14112329 |
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