Antibiofilm activity of promethazine, deferiprone, and Manuka honey in an ex vivo wound model

Author:

Guedes Gláucia Morgana de Melo12,Freitas Alyne Soares1,Pinheiro Rodrigo Machado1,Pereira Vinicius Carvalho1,Melgarejo Carliane Melo Alves1,de Araujo Emanuela Silva1,Ribeiro Késia Veras Costa1,Bandeira Silviane Praciano2,Cordeiro Rossana de Aguiar2,Rocha Marcos Fábio Gadelha23,Sidrim José Júlio Costa2,Castelo-Branco Débora de Souza Collares Maia12ORCID

Affiliation:

1. Department of Pathology & Legal Medicine, Postgraduate Program in Medical Microbiology, Group of Applied Medical Microbiology, Federal University of Ceará , Rua Coronel Nunes de Melo, 1315 - Rodolfo Teófilo - CEP 60430-275, Fortaleza, Ceará , Brazil

2. Department of Pathology & Legal Medicine, Postgraduate Program in Medical Microbiology, Specialized Medical Mycology Center, Federal University of Ceará , Rua Coronel, Nunes de Melo, 1315 - Rodolfo Teófilo - CEP 60430-275, Fortaleza, Ceará , Brazil

3. Postgraduate Program in Veterinary Sciences, School of Veterinary, State University of Ceará , Avenida Dr. Silas Munguba, 1700 – Itaperi – CEP 60714-903, Fortaleza, Ceará , Brazil

Abstract

Abstract This study evaluated the antibiofilm activity of promethazine, deferiprone, and Manuka honey against Staphylococcus aureus and Pseudomonas aeruginosa in vitro and ex vivo in a wound model on porcine skin. The minimum inhibitory concentrations (MICs) and the effects of the compounds on biofilms were evaluated. Then, counting colony-forming units (CFUs) and confocal microscopy were performed on biofilms cultivated on porcine skin for evaluation of the compounds. For promethazine, MICs ranging from 97.66 to 781.25 µg/ml and minimum biofilm eradication concentration (MBEC) values ranging from 195.31 to 1562.5 µg/ml were found. In addition to reducing the biomass of both species’ biofilms. As for deferiprone, the MICs were 512 and >1024 µg/ml, the MBECs were ≥1024 µg/ml, and it reduced the biomass of biofilms. Manuka honey had MICs of 10%–40%, MBECs of 20 to >40% and reduced the biomass of S. aureus biofilms only. Concerning the analyses in the ex vivo model, the compounds reduced (P < .05) CFU counts for both bacterial species, altering the biofilm architecture. The action of the compounds on biofilms in in vitro and ex vivo tests raises the possibility of using them against biofilm-associated wounds. However, further studies are needed to characterize the mechanisms of action and their effectiveness on biofilms in vivo.

Funder

National Council for Scientific and Technological Development

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology

Reference44 articles.

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