Substantivity of mouth‑rinse formulations containing cetylpyridinium chloride and O‑cymen‑5‑ol: a randomized‑crossover trial

dc.contributor.author
Aguilera, Felipe-Rodrigo
dc.contributor.author
Viñas, Miquel
dc.contributor.author
Sierra Ortigosa, Josep Maria
dc.contributor.author
Vinuesa Aumedes, Teresa
dc.contributor.author
Fernandez de Henestrosa, Antonio R.
dc.contributor.author
Furmancyk, Marta
dc.contributor.author
Trullás, Carles
dc.contributor.author
Jourdan, Eric
dc.contributor.author
Lopez-Lopez, José
dc.contributor.author
Jorba, Marta
dc.date.accessioned
2026-02-19T21:57:07Z
dc.date.available
2026-02-19T21:57:07Z
dc.date.issued
2026-02-17T09:13:29Z
dc.date.issued
2026-02-17T09:13:29Z
dc.date.issued
2022-12
dc.date.issued
2026-02-17T09:13:29Z
dc.identifier
1472-6831
dc.identifier
https://hdl.handle.net/2445/226950
dc.identifier
727885
dc.identifier
36575444
dc.identifier.uri
https://hdl.handle.net/2445/226950
dc.description.abstract
Background: The efficacy of mouth-rinses strongly depends upon their substantivity. The use of natural and nontoxic products that avoid secondary effects is gaining interest in preventive dentistry. The purpose of this study was to evaluate the substantivity of two formulations of mouth-washing solutions based on cetylpyridinium (CPC) and O-cymen-5-ol. Methods: This was a randomized, double-blind, crossover trial conducted at the Faculty of Medicine and Health Sciences of the University of Barcelona. Bacterial re-colonization was followed by live/dead (SYTOTM9 + propidium iodide) bacterial staining and measured by confocal laser scanning microscopy and fluorometry. Unstimulated saliva samples were collected from 16 healthy individuals at baseline saliva and then, at 15 min, 30 min and 1, 2, 3, and 4 h after the following mouth-rinses: (i) a single, 1-min mouth-rinse with 15 ml of placebo (negative control); (ii) a single, 1-min mouth-rinse with 15 ml of CPC (0.05%) ; (iii) a single, 1-min mouth-rinse with 15 ml of O-cymen-5-ol (0.09%); (iv) a single, 1-min mouth-rinse with 15 ml of CPC (0.05%) + O-cymen-5-ol (0.09%). Results: Proportion of dead bacteria was significantly higher for all mouthrinses during the first 15 min compared to baseline (CPC = 48.0 ± 13.9; 95% CI 40.98-56.99; p < 0.001, O-cymen-5-ol = 79.8 ± 21.0; 95% CI 67.71-91.90; p < 0.05, CPC + O-cymen-5-ol = 49.4 ± 14; 95% CI 40.98-56.99; p < 0.001 by fluorometry and 54.8 ± 23.0; 95% CI 41.50-68.06; p < 0.001, 76.3 ± 17.1; 95% CI 66.36-86.14; p < 0.001, 47.4 ± 11.9; 95% CI 40.49-54.30; p < 0.001 by confocal laser scanning microscopy, respectively). Nevertheless, after 4 h, CPC + O-cymen-5-ol was the only one that obtained significant values as measured by the two quantification methods used (80.3 ± 22.8; 95% CI 67.15-93.50; p < 0.05 and 81.4 ± 13.8; 95% CI 73.45-89.43; p < 0.05). The combined use of CPC + O-cymen-5-ol increased the substantivity of the mouthrinse with respect to mouthrinses prepared with either of the two active products alone. Conclusion: The synergistic interaction of CPC and O-cymen-5-ol prolongs their substantivity. The resulting formulation may be as effective as other antimicrobials, such as triclosan or chlorhexidine, but without their undesirable secondary effects. Thus, mouthrinsing products based on Combinations of CPC and O-cymen-5-ol may replace in the near future Triclosan and Chlorhexidine¿based mouthrinses.
dc.format
9 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
BioMed Central
dc.relation
Reproducció del document publicat a: https://doi.org/10.1186/s12903-022-02688-z
dc.relation
BMC Oral Health, 2022, vol. 22, num.1, p. 1-9
dc.rights
cc-by (c) Aguilera F-P et al., 2022
dc.rights
http://creativecommons.org/licenses/by/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Microbiota
dc.subject
Antisèptics
dc.subject
Odontologia preventiva
dc.subject
Higiene bucal
dc.subject
Microbiota
dc.subject
Antiseptics
dc.subject
Preventive dentistry
dc.subject
Oral hygiene
dc.title
Substantivity of mouth‑rinse formulations containing cetylpyridinium chloride and O‑cymen‑5‑ol: a randomized‑crossover trial
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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