Photodynamic inactivation of planktonic cultures of Streptococcus mutans using erythrosine irradiated by LED

Authors

  • Maria Ângela Lacerda Rangel Esper UNESP – Univ Estadual Paulista - Institute of Science and Technology, São José dos Campos - Department of Restorative Dentistry, - São Paulo State University – UNESP - São José dos Campos, São Paulo, Brazil. http://orcid.org/0000-0001-5218-9173
  • Junia Oliveira Barbosa UNESP – Univ Estadual Paulista - Institute of Science and Technology, São José dos Campos - Department of Biosciences and Oral Diagnosis - São José dos Campos - São Paulo - Brazil. http://orcid.org/0000-0002-1481-7631
  • Janaína de Araújo Alvarenga UNESP – Univ Estadual Paulista - Institute of Science and Technology, São José dos Campos - Department of Biosciences and Oral Diagnosis - São José dos Campos - São Paulo - Brazil. http://orcid.org/0000-0002-9103-0621
  • Juliana Campos Junqueira UNESP – Univ Estadual Paulista - Institute of Science and Technology, São José dos Campos - Department of Biosciences and Oral Diagnosis - São José dos Campos - São Paulo - Brazil. http://orcid.org/0000-0001-6646-6856
  • Alessandra nara de Souza Rastelli UNESP – Univ Estadual Paulista - Department of Restorative Dentistry, Araraquara, São Paulo - Brazil. http://orcid.org/0000-0002-6768-2670
  • Sérgio Eduardo de Paiva Gonçalves UNESP – Univ Estadual Paulista - Institute of Science and Technology, São José dos Campos - Department of Restorative Dentistry, - São Paulo State University – UNESP - São José dos Campos, São Paulo, Brazil. http://orcid.org/0000-0003-1796-0393

DOI:

https://doi.org/10.14295/bds.2020.v23i2.1857

Abstract

Objective: The aim of this in vitro study was to evaluate the efficacy of photodynamic inactivation (PDI) with erythrosine (E), using a light-emitting diode (LED) on planktonic cultures of Streptococcus mutans. Material and Methods: A Streptococcus mutans strain (UA 159) was used to prepare the suspensions containing 107 cells/mL, which was tested under different experimental conditions: a) LED irradiation in the presence of erythrosine as a photosensitizer (E+L+); b) LED irradiation only (P-L+); c) treatment with erythrosine only (E+L-); and d) no LED irradiation or photosensitizer (P) treatment, which served as a control group (P-L-). After treatment, strains were seeded onto MSBS agar for determination of the number of colony-forming units (CFU/mL). Results: The results were submitted to analysis of variance and the Tukey test (p < 0.05). No reduction in the number of CFU/mL was observed in the treatment group with erythrosine (E+L+) when compared to the control (P-L-). Conclusion: PDI using erythrosine did not reduce the number of CFUs per millimeter within the parameters in this study.

KEYWORDS

Erythrosine; Decay; Photodynamic inactivation; Light-emitting diode.

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Published

2020-03-31

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Clinical or Laboratorial Research Manuscript