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Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo
OBJECTIVE: Evaluate the effect of a multidrug solution, adopted by a referral hospital for cancer to control and treat chemotherapy-induced oral mucositis in rats. METHODS: Oral mucositis (OM) was induced by 5-Fluorouracil (5-FU), and the animals were treated with saline (n = 8, G1), 0.12% chlorhexi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213868/ https://www.ncbi.nlm.nih.gov/pubmed/37251722 http://dx.doi.org/10.1016/j.sdentj.2023.03.014 |
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author | Tolentino Limeira, Rebecca Rhuanny Lima Arrais Ribeiro, Isabella Ferreti Bonan, Paulo Rogério da Nóbrega Alves, Danielle dos Santos Ferreira, Elba Vieira Lopes da Costa, Tereza Karla Weege Nonaka, Cassiano Francisco Dantas de Medeiros, Ana Claúdia Barbosa de Sousa, Frederico Gondim Valença, Ana Maria Dias de Castro, Ricardo |
author_facet | Tolentino Limeira, Rebecca Rhuanny Lima Arrais Ribeiro, Isabella Ferreti Bonan, Paulo Rogério da Nóbrega Alves, Danielle dos Santos Ferreira, Elba Vieira Lopes da Costa, Tereza Karla Weege Nonaka, Cassiano Francisco Dantas de Medeiros, Ana Claúdia Barbosa de Sousa, Frederico Gondim Valença, Ana Maria Dias de Castro, Ricardo |
author_sort | Tolentino Limeira, Rebecca Rhuanny |
collection | PubMed |
description | OBJECTIVE: Evaluate the effect of a multidrug solution, adopted by a referral hospital for cancer to control and treat chemotherapy-induced oral mucositis in rats. METHODS: Oral mucositis (OM) was induced by 5-Fluorouracil (5-FU), and the animals were treated with saline (n = 8, G1), 0.12% chlorhexidine (n = 8, G2); and multidrug solution (n = 8, G3). The animals were submitted to clinical and histological analysis of the lesion using mucosal fragments. The animals' food consumption during treatment was also evaluated. RESULTS: Clinical improvement (p < 0.05) was observed in the groups treated with the multidrug solution and 0.12% chlorhexidine digluconate. In G2 and G3, there was a prevalence of reepithelialization covering <50% of the lesion. Evaluation of the inflammatory infiltrate indicated that the G1 treatment permitted an intense inflammatory response in all animals, yet this evaluation parameter was moderate in groups G2 and G3. The G3 group (p < 0.05) presented higher food consumption than the other groups. CONCLUSIONS: The multidrug solution improved the clinical and histological parameters of the chemotherapy-induced oral mucositis, as well as promoted an increase in food intake. |
format | Online Article Text |
id | pubmed-10213868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102138682023-05-27 Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo Tolentino Limeira, Rebecca Rhuanny Lima Arrais Ribeiro, Isabella Ferreti Bonan, Paulo Rogério da Nóbrega Alves, Danielle dos Santos Ferreira, Elba Vieira Lopes da Costa, Tereza Karla Weege Nonaka, Cassiano Francisco Dantas de Medeiros, Ana Claúdia Barbosa de Sousa, Frederico Gondim Valença, Ana Maria Dias de Castro, Ricardo Saudi Dent J Original Article OBJECTIVE: Evaluate the effect of a multidrug solution, adopted by a referral hospital for cancer to control and treat chemotherapy-induced oral mucositis in rats. METHODS: Oral mucositis (OM) was induced by 5-Fluorouracil (5-FU), and the animals were treated with saline (n = 8, G1), 0.12% chlorhexidine (n = 8, G2); and multidrug solution (n = 8, G3). The animals were submitted to clinical and histological analysis of the lesion using mucosal fragments. The animals' food consumption during treatment was also evaluated. RESULTS: Clinical improvement (p < 0.05) was observed in the groups treated with the multidrug solution and 0.12% chlorhexidine digluconate. In G2 and G3, there was a prevalence of reepithelialization covering <50% of the lesion. Evaluation of the inflammatory infiltrate indicated that the G1 treatment permitted an intense inflammatory response in all animals, yet this evaluation parameter was moderate in groups G2 and G3. The G3 group (p < 0.05) presented higher food consumption than the other groups. CONCLUSIONS: The multidrug solution improved the clinical and histological parameters of the chemotherapy-induced oral mucositis, as well as promoted an increase in food intake. Elsevier 2023-05 2023-04-05 /pmc/articles/PMC10213868/ /pubmed/37251722 http://dx.doi.org/10.1016/j.sdentj.2023.03.014 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Tolentino Limeira, Rebecca Rhuanny Lima Arrais Ribeiro, Isabella Ferreti Bonan, Paulo Rogério da Nóbrega Alves, Danielle dos Santos Ferreira, Elba Vieira Lopes da Costa, Tereza Karla Weege Nonaka, Cassiano Francisco Dantas de Medeiros, Ana Claúdia Barbosa de Sousa, Frederico Gondim Valença, Ana Maria Dias de Castro, Ricardo Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo |
title | Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo |
title_full | Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo |
title_fullStr | Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo |
title_full_unstemmed | Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo |
title_short | Effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo |
title_sort | effect of multidrug solution for the treatment of chemotherapy-induced oral mucositis in vivo |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213868/ https://www.ncbi.nlm.nih.gov/pubmed/37251722 http://dx.doi.org/10.1016/j.sdentj.2023.03.014 |
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