Exploring the association between a standardized extract of pequi peels (Caryocar brasiliense Cambess) and blue light as a photodynamic therapy for treating superficial wounds

Author:

Diniz Luiza Alves12ORCID,Ferreira Luiza de Almeida Queiroz12ORCID,Ribeiro Rafaela de Brito1,de Jesus Sarah Luiza Galvão1,Anestino Thales Augusto3,Caldeira Alisson Samuel Portes45,Souto Giovanna Ribeiro26,de Avelar Gleide Fernandes7,Amaral Flávio Almeida8,Ferreira Marcus Vinícius Lucas1,Madeira Mila Fernandes Moreira3,Braga Fernão Castro4,Diniz Ivana Márcia Alves12

Affiliation:

1. Department of Restorative Dentistry, School of Dentistry Universidade Federal de Minas Gerais Belo Horizonte Brazil

2. LASER Biotechnologies, School of Dentistry Universidade Federal de Minas Gerais Belo Horizonte Brazil

3. Department of Microbiology, Biological Sciences Institute Universidade Federal de Minas Gerais Belo Horizonte Brazil

4. Department of Pharmaceutical Sciences, Faculty of Pharmacy Universidade Federal de Minas Gerais Belo Horizonte Brazil

5. Vice Directorate of Research René Rachou Institute—Fiocruz Minas Belo Horizonte Brazil

6. Department of Dentistry Pontifícia Universidade Católica de Minas Gerais Belo Horizonte Brazil

7. Department of Morphology, Biological Sciences Institute Universidade Federal de Minas Gerais Belo Horizonte Brazil

8. Department of Biochemistry and Immunology, Biological Sciences Institute Universidade Federal de Minas Gerais Belo Horizonte Brazil

Abstract

AbstractNatural products derived from plants can be used as photosensitizers for antimicrobial photodynamic therapy (aPDT) combining key therapeutic strategies for tissue repair while controlling microorganisms' growth. We investigated a standardized extract of pequi peels (Caryocar brasiliense Cambess) as a brownish natural photosensitizer for aPDT using blue light. Three concentrations of the pequi extract (PE; 10, 30, or 90 μg/mL) were tested solely or associated with blue laser (445 nm, 100 mW, 138 J/cm2, 6 J, 60 s). In vitro, we quantified reactive oxygen species (ROS), assessed skin keratinocytes (HaCat) viability and migration, and aPDT antimicrobial activity on Streptococcus or Staphylococcus strains. In vivo, we assessed wound closure for the most active concentration disclosed by the in vitro assay (30 μg/mL). Upon aPDT treatments, ROS were significantly increased in cell monolayers regardless of PE concentration. PE at low doses stimulates epithelial cells. Although PE stimulated cellular migration, aPDT was moderately cytotoxic to skin keratinocytes, particularly at the highest concentration. The antimicrobial activity was observed for PE at the lowest concentration (10 μg/mL) and mostly at PE 10 μg/mL and 30 μg/mL when used as aPDT photosensitizers. aPDT with PE 30 μg/mL presents antimicrobial activity without compromising the initial phases of skin repair.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado de Minas Gerais

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,General Medicine,Biochemistry

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