Chloroacetamide derivatives as a promising topical treatment for fungal skin infections
The aim of this study was to evaluate the antifungal potential of 11 chloroacetamide derivatives and derivative incorporated into a film-forming system (FFS) as a potential alternative for the topical treatment of superficial and skin mycoses. The minimum inhibitory concentration (MIC) evaluation fo...
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Published in | Mycologia Vol. 111; no. 4; pp. 612 - 623 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Taylor & Francis
04.07.2019
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Abstract | The aim of this study was to evaluate the antifungal potential of 11 chloroacetamide derivatives and derivative incorporated into a film-forming system (FFS) as a potential alternative for the topical treatment of superficial and skin mycoses. The minimum inhibitory concentration (MIC) evaluation followed Clinical and Laboratory Standards Institute protocols M27-A3 (Candida) and M28-A2 (dermatophytes). Compounds 2, 3, and 4 were the most effective against Candida species (MIC range: 25-50 µg/mL) and dermatophytes (MIC range: 3.12-50 µg/mL). Compound 2 maintained its antifungal activity when incorporated in a FFS, with MIC values equivalent to the free compound. In addition, the compound does not act through complexation with ergosterol, suggesting that it may act on other targets of the fungal cell membrane. Chloroacetamide derivatives presented anti-Candida and anti-dermatophytic effectiveness. The FFS containing compound 2 has shown to be superior to traditional topical treatment of superficial and cutaneous fungal infections. It was found that these new chemical entities, with their applicability, are an excellent alternative to the topical treatment of fungal skin infections. |
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AbstractList | The aim of this study was to evaluate the antifungal potential of 11 chloroacetamide derivatives and derivative incorporated into a film-forming system (FFS) as a potential alternative for the topical treatment of superficial and skin mycoses. The minimum inhibitory concentration (MIC) evaluation followed Clinical and Laboratory Standards Institute protocols M27-A3 (
) and M28-A2 (dermatophytes). Compounds
, and
were the most effective against
species (MIC range: 25-50 µg/mL) and dermatophytes (MIC range: 3.12-50 µg/mL). Compound
maintained its antifungal activity when incorporated in a FFS, with MIC values equivalent to the free compound. In addition, the compound does not act through complexation with ergosterol, suggesting that it may act on other targets of the fungal cell membrane. Chloroacetamide derivatives presented anti-
and anti-dermatophytic effectiveness. The FFS containing compound
has shown to be superior to traditional topical treatment of superficial and cutaneous fungal infections. It was found that these new chemical entities, with their applicability, are an excellent alternative to the topical treatment of fungal skin infections. The aim of this study was to evaluate the antifungal potential of 11 chloroacetamide derivatives and derivative incorporated into a film-forming system (FFS) as a potential alternative for the topical treatment of superficial and skin mycoses. The minimum inhibitory concentration (MIC) evaluation followed Clinical and Laboratory Standards Institute protocols M27-A3 (Candida) and M28-A2 (dermatophytes). Compounds 2, 3, and 4 were the most effective against Candida species (MIC range: 25-50 µg/mL) and dermatophytes (MIC range: 3.12-50 µg/mL). Compound 2 maintained its antifungal activity when incorporated in a FFS, with MIC values equivalent to the free compound. In addition, the compound does not act through complexation with ergosterol, suggesting that it may act on other targets of the fungal cell membrane. Chloroacetamide derivatives presented anti-Candida and anti-dermatophytic effectiveness. The FFS containing compound 2 has shown to be superior to traditional topical treatment of superficial and cutaneous fungal infections. It was found that these new chemical entities, with their applicability, are an excellent alternative to the topical treatment of fungal skin infections. |
Author | Machado, Gabriella da Rosa Monte Vainstein, Marilene Henning Lopes, William Alves, Ricardo José Pippi, Bruna Bergamo, Vanessa Zafaneli Jacobus Berlitz, Simone Fuentefria, Alexandre Meneghello Lavorato, Stefânia Neiva Teixeira, Mário Lettieri Fernandes de Andrade, Saulo Clemes Külkamp Guerreiro, Irene |
Author_xml | – sequence: 1 givenname: Gabriella da Rosa Monte orcidid: 0000-0003-1950-9731 surname: Machado fullname: Machado, Gabriella da Rosa Monte email: 00237927@ufrgs.br organization: Programa de Pós Graduação em Microbiologia Agrícola e do Ambiente, Universidade Federal do Rio Grande do Sul – sequence: 2 givenname: Saulo orcidid: 0000-0003-2873-7939 surname: Fernandes de Andrade fullname: Fernandes de Andrade, Saulo organization: Programa de Pós Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul – sequence: 3 givenname: Bruna surname: Pippi fullname: Pippi, Bruna organization: Programa de Pós Graduação em Microbiologia Agrícola e do Ambiente, Universidade Federal do Rio Grande do Sul – sequence: 4 givenname: Vanessa Zafaneli surname: Bergamo fullname: Bergamo, Vanessa Zafaneli organization: Programa de Pós Graduação em Microbiologia Agrícola e do Ambiente, Universidade Federal do Rio Grande do Sul – sequence: 5 givenname: Simone surname: Jacobus Berlitz fullname: Jacobus Berlitz, Simone organization: Programa de Pós Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul – sequence: 6 givenname: William orcidid: 0000-0002-6040-3704 surname: Lopes fullname: Lopes, William organization: Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul – sequence: 7 givenname: Stefânia Neiva surname: Lavorato fullname: Lavorato, Stefânia Neiva organization: Departamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais – sequence: 8 givenname: Irene surname: Clemes Külkamp Guerreiro fullname: Clemes Külkamp Guerreiro, Irene organization: Programa de Pós Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul – sequence: 9 givenname: Marilene Henning orcidid: 0000-0001-8607-7612 surname: Vainstein fullname: Vainstein, Marilene Henning organization: Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul – sequence: 10 givenname: Mário Lettieri surname: Teixeira fullname: Teixeira, Mário Lettieri organization: Laboratório de Farmacologia, Instituto Federal Catarinense, Campus Concórdia – sequence: 11 givenname: Ricardo José surname: Alves fullname: Alves, Ricardo José organization: Departamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais – sequence: 12 givenname: Alexandre Meneghello surname: Fuentefria fullname: Fuentefria, Alexandre Meneghello organization: Programa de Pós Graduação em Ciências Farmacêuticas, Universidade Federal do Rio Grande do Sul |
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SubjectTerms | Acetamides - administration & dosage Acetamides - pharmacology Acetamides - therapeutic use Administration, Topical Antifungal Agents - therapeutic use Arthrodermataceae - drug effects Candida - drug effects Candida spp chloroacetamide derivatives Dermatomycoses - drug therapy Dermatomycoses - microbiology dermatophyte film-forming system fungal infections Humans Microbial Sensitivity Tests new chemical entities Skin - microbiology |
Title | Chloroacetamide derivatives as a promising topical treatment for fungal skin infections |
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