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Cytotoxicity evaluation of Chlorhexidine and Blue®M applied to a human gingival fibroblast (HGF-1) and keratinocytes (NOK-SI): In vitro study.
Cunha, Giovanni; D'Angieri Saugo, Gustavo; Gabrielli, Marisa Aparecida Cabrini; Barbeiro, Camila de Oliveira; de Almeida, Luciana Yamamoto; Bufalino, Andréia; Pereira-Filho, Valfrido Antônio.
Afiliación
  • Cunha G; Department of Diagnosis and Surgery, Division of Oral and Maxillofacial Surgery, São Paulo State University (Unesp), School of Dentistry, Araraquara, Brazil; Private Practice. Louveira, Brazil. Electronic address: giovanni.cunha@unesp.br.
  • D'Angieri Saugo G; Private Practice.
  • Gabrielli MAC; Department of Diagnosis and Surgery, Division of Oral and Maxillofacial Surgery, São Paulo State University (Unesp), School of Dentistry, Araraquara, Brazil.
  • Barbeiro CO; Oral Medicine, Department of Diagnosis and Surgery, São Paulo State University (Unesp), School of Dentistry, Araraquara, SP, Brazil.
  • de Almeida LY; Oral Medicine, Department of Diagnosis and Surgery, São Paulo State University (Unesp), School of Dentistry, Araraquara, SP, Brazil.
  • Bufalino A; Department of Diagnosis and Surgery, São Paulo State University (Unesp), School of Dentistry, Araraquara, SP, Brazil.
  • Pereira-Filho VA; Department of Diagnosis and Surgery, Division of Oral and Maxillofacial Surgery, São Paulo State University (Unesp), School of Dentistry, Araraquara, Brazil.
J Stomatol Oral Maxillofac Surg ; : 101923, 2024 May 28.
Article en En | MEDLINE | ID: mdl-38815722
ABSTRACT
Chlorhexidine (CHX) is a prime choice to control the oral microbiota. However, it's a chemical agent leading to side effects such as teeth strains, taste disturbance, and desquamation of oral mucosa. Alternatively, the lactoferrin and oxygen-based Blue®M has been introduced as an alternative to the CHX, not disturbing tissue repair. Therefore, the study aimed to evaluate the effects of Blue®M and CHX on oral human fibroblasts (HGF-1) and keratinocytes (NOK-SI). Cell cultures using HGF-1 and NOK-SI evaluated cell proliferation, cell cycle, apoptosis and necrosis, and migration. In the dose-effect test, Blue®M reduced the HGF-1 sample in a 4-fold concentration than CHX (CHX 173.07 ±10.27; Blue®M 43.86 ±3.04). The proliferation test revealed an eightfold reduction of the sample for CHX, while for Blue®M, the proliferation rate was eighteen times lower. The apoptosis and necrosis rates increased by 25% (p<0.0001) for HGF-1 for both substances. In NOK-SI, the apoptosis rates increased by 10% (p=0.02) and 15% (p=0.001) for CHX and Blue®M, respectively. Furthermore, the fibroblast had a lower capacity for wound closure in the Scratch Assay (monolayer cell migration) for Blue®M. Despite the limitations of this in vitro study, the results of the lactoferrin and oxygen-based Blue®M demonstrated cytotoxicity in doses over the Minimum inhibitory concentration and Minimum bactericidal concentration for Oral fibroblasts (HGF- 1) and Keratinocytes (NOK-SI).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Stomatol Oral Maxillofac Surg Año: 2024 Tipo del documento: Article Pais de publicación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Stomatol Oral Maxillofac Surg Año: 2024 Tipo del documento: Article Pais de publicación: Francia