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Toxicity of chlorhexidine on odontoblast-like cells
Lessa, Fernanda Campos Rosetti; Aranha, Andreza Maria Fabio; Nogueira, Indri; Giro, Elisa Maria Aparecida; Hebling, Josimeri; Costa, Carlos Alberto de Souza.
  • Lessa, Fernanda Campos Rosetti; Araraquara Dental School. São Paulo State University. Department of Orthodontics and Pediatric Dentistry. Pediatric Dentistry. Araraquara. BR
  • Aranha, Andreza Maria Fabio; Araraquara Dental School. São Paulo State University. Department of Orthodontics and Pediatric Dentistry. Pediatric Dentistry. Araraquara. BR
  • Nogueira, Indri; Araraquara Dental School. São Paulo State University. Department of Orthodontics and Pediatric Dentistry. Pediatric Dentistry. Araraquara. BR
  • Giro, Elisa Maria Aparecida; Araraquara Dental School. São Paulo State University. Department of Orthodontics and Pediatric Dentistry. Pediatric Dentistry. Araraquara. BR
  • Hebling, Josimeri; Araraquara Dental School. São Paulo State University. Department of Orthodontics and Pediatric Dentistry. Pediatric Dentistry. Araraquara. BR
  • Costa, Carlos Alberto de Souza; Araraquara Dental School. São Paulo State University. Department of Physiology and Pathology. Pathology. Araraquara. BR
J. appl. oral sci ; 18(1): 50-58, Jan.-Feb. 2010. tab, ilus
Article in English | LILACS | ID: lil-545027
ABSTRACT
Chlorhexidine gluconate (CHX) is recommended for a number of clinical procedures and it has been pointed out as a potential cavity cleanser to be applied before adhesive restoration of dental cavities.

OBJECTIVE:

As CHX may diffuse through the dentinal tubules to reach a monolayer of odontoblasts that underlies the dentin substrate, this study evaluated the cytotoxic effects of different concentrations of CHX on cultured odontoblast-like cells (MDPC-23). MATERIAL AND

METHODS:

Cells were cultured and exposed to CHX solutions at concentrations of 0.06 percent, 0.12 percent, 0.2 percent, 1 percent and 2 percent. Pure culture medium (á-MEM) and 3 percent hydrogen peroxide were used as negative and positive control, respectively. After exposing the cultured cells to the controls and CHX solutions for 60 s, 2 h or 60 s with a 24-h recovery period, cell metabolism (MTT assay) and total protein concentration were evaluated. Cell morphology was assessed under scanning electron microscopy. CHX had a dose-dependent toxic effect on the MDPC-23 cells.

RESULTS:

Statistically significant difference was observed when the cells were exposed to CHX in all periods (p<0.05). Significant difference was also determined for all CHX concentrations (p<0.05). The 60-s exposure time was the least cytotoxic (p<0.05), while exposure to CHX for 60 s with a 24-h recovery period was the most toxic to the cells (p<0.05).

CONCLUSION:

Regardless of the exposure time, all CHX concentrations had a high direct cytotoxic effect to cultured MDPC-23 cells.
Subject(s)

Full text: Available Index: LILACS (Americas) Main subject: Chlorhexidine / Anti-Infective Agents, Local / Odontoblasts Limits: Humans Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2010 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Araraquara Dental School/BR

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Full text: Available Index: LILACS (Americas) Main subject: Chlorhexidine / Anti-Infective Agents, Local / Odontoblasts Limits: Humans Language: English Journal: J. appl. oral sci Journal subject: Dentistry Year: 2010 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Araraquara Dental School/BR