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In vitro and In vivo Activity of a New N-Oxide Derivative for Acne Vulgaris Treatment.
Delgado, Ivone Leila Lima; Scarim, Cauê Benito; Fernandes, Felipe Hugo Alencar; Barbieri, Karina Pereira; Polesi, Marisa Campos; Pavan, Aline Renata; Chiba, Diego Eidy; Salgado, Hérida Regina Nunes; Carlos, Iracilda Zeppone; Corrêa, Marcos Antonio; de Andrade, Cleverton Roberto; Dos Santos, Jean Leandro.
Afiliación
  • Delgado ILL; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Scarim CB; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Fernandes FHA; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Barbieri KP; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Polesi MC; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Pavan AR; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Chiba DE; Institute of Chemistry, São Paulo State University (UNESP), Francisco Degni 55, Araraquara, 14800060, Brazil.
  • Salgado HRN; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Carlos IZ; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Corrêa MA; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • de Andrade CR; School of Pharmaceutical Sciences, São Paulo State University (UNESP), Rod. Araraquara-Jaú, Araraquara, 14800-903, Brazil.
  • Dos Santos JL; School of Dentistry, São Paulo State University (UNESP), R. Humaitá 1680, Araraquara, 14801-385, Brazil.
Med Chem ; 2024 Jul 30.
Article en En | MEDLINE | ID: mdl-39082171
ABSTRACT

INTRODUCTION:

Furoxan and benzofuroxan are compounds containing an N-oxide function, known for their diverse pharmacological properties, including antimicrobial and antiinflammatory effects. This study aimed to investigate these activities using an in-house library of N-oxide compounds.

METHOD:

Twenty compounds were tested against both Gram-positive and Gram-negative bacteria, including Cutibacterium acnes (C. acnes), a microorganism implicated in the development of acne vulgaris. One compound, (E)-4-(3-((2-(3-hydroxybenzoyl)hydrazone)methyl)phenoxy)-3- (phenylsulfonyl)-1,2,5-oxadiazol-2-N-oxide (compound 15), exhibited selective antimicrobial activity against C. acnes, with a Minimum Inhibitory Concentration (MIC) value of 2 µg/mL. Indirect measurement of Nitric Oxide (NO) release showed that compound 15 and isosorbide dinitrate, when treated with L-cysteine, produced nitrite levels of 20.1% and 9.95%, respectively. Using a NO scavenger (PTIO) in combination with compound 15 in a culture of C. acnes resulted in reduced antimicrobial activity, indicating that NO release is part of its mechanism of action. Cytotoxicity assessments using murine macrophages showed cellular viability above 70% at concentrations up to 0.78 µg/mL.

RESULTS:

Measurements of Interleukin-1 beta (IL1-ß) and Tumor Necrosis Factor-alpha (TNF-α) indicated that compound 15 did not reduce the levels of these pro-inflammatory cytokines. Sustained NO production by inducible Nitric Oxide Synthase (iNOS) in macrophages or neutrophils has been found to be involved in the inflammatory process in acne vulgaris and lead to toxicity in surrounding tissues. Nitrite levels in the supernatant of murine macrophages were found to be decreased at a concentration of 0.78 µg/mL of compound 15, indicating an anti-inflammatory effect. In vivo studies were conducted using Balb/c nude mice inoculated subcutaneously with C. acnes. Cream and gel formulations of compound 15 were applied to treat the animals, along with commercially available anti-acne drugs, for 14 days. Animals treated with a cream base containing 5% of compound 15 exhibited less acanthosis with mild inflammatory infiltration compared to other groups, highlighting its anti-inflammatory properties.

CONCLUSION:

Similar results were observed in the benzoyl peroxide group, demonstrating that compound 15 presented comparable anti-inflammatory activity to the FDA-approved drug. These promising results suggest that compound 15 has a dual mechanism of action, with selective antimicrobial activity against C. acnes and notable anti-inflammatory properties, making it a potential prototype for developing new treatments for acne vulgaris.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Med Chem Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Med Chem Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Países Bajos