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Cytotoxic effects of different mouthwash solutions on primary human articular chondrocytes and normal human articular cartilage - an in vitro study.
Cai, Xiaoyu; Venkatesan, Jagadeesh K; Schmitt, Gertrud; Reda, Bashar; Cucchiarini, Magali; Hannig, Matthias; Madry, Henning.
Afiliação
  • Cai X; Center of Experimental Orthopaedics, Saarland University, 66421, Homburg, Germany.
  • Venkatesan JK; Department of Spine Surgery, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
  • Schmitt G; Center of Experimental Orthopaedics, Saarland University, 66421, Homburg, Germany.
  • Reda B; Center of Experimental Orthopaedics, Saarland University, 66421, Homburg, Germany.
  • Cucchiarini M; Clinic of Operative Dentistry, Periodontology and Preventive Dentistry, University Hospital, Saarland University, 66421, Homburg, Germany.
  • Hannig M; Center of Experimental Orthopaedics, Saarland University, 66421, Homburg, Germany.
  • Madry H; Clinic of Operative Dentistry, Periodontology and Preventive Dentistry, University Hospital, Saarland University, 66421, Homburg, Germany.
Clin Oral Investig ; 27(9): 4987-5000, 2023 Sep.
Article em En | MEDLINE | ID: mdl-37329464
ABSTRACT

OBJECTIVES:

To compare the cytotoxicity of octenidine dihydrochloride and chlorhexidine gluconate at different concentrations on primary human articular chondrocytes and cartilage. MATERIALS AND

METHODS:

Primary cultures of human normal adult articular chondrocytes were exposed to octenidine dihydrochloride (0.001562%, 0.003125%, 0.00625%, 0.0125%, 0.025%, 0.05%, and 0.1%), chlorhexidine gluconate (0.003125%, 0.00625%, 0.0125%, 0.025%, 0.05%, 0.1%, and 0.2%), and control (Dulbecco's modified Eagle medium or phosphate-buffered saline) for 30 s. Normal human articular cartilage explants were exposed to octenidine dihydrochloride (0.1% versus control) and chlorhexidine gluconate (0.1% versus control) for 30 s. The viability of human articular chondrocytes was measured by Trypan blue staining, Cell Proliferation Reagent WST-1, and Live/Dead staining. The proliferation of human chondrocytes was measured using the Cell Proliferation Reagent WST-1. The viability of human articular cartilage explants was measured by using Live/Dead staining.

RESULTS:

Octenidine dihydrochloride and chlorhexidine gluconate exposure decreased cell viability and proliferation in a dose-dependent manner in primary human articular chondrocytes. Octenidine dihydrochloride and chlorhexidine gluconate exposure decreased cell viability in human articular cartilage explant cultures.

CONCLUSION:

The degree of toxicity varied between octenidine dihydrochloride and chlorhexidine gluconate, with chlorhexidine gluconate being less toxic than octenidine dihydrochloride at the same concentration. Additionally, both octenidine dihydrochloride and chlorhexidine gluconate evaluation had cytotoxic effects on human articular cartilage. Therefore, dosing for the antimicrobial mouthwash ingredients administration would ideally be determined to remain below IC50. CLINICAL RELEVANCE These data support the in vitro safety of antimicrobial mouthwashes on primary adult human articular chondrocytes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cartilagem Articular / Anti-Infecciosos / Antineoplásicos Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cartilagem Articular / Anti-Infecciosos / Antineoplásicos Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article