Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms. / Rabe, Per; Twetman, Svante; Kinnby, Bertil; Svensäter, Gunnel; Davies, Julia R.

In: The Open Dentistry Journal, Vol. 9, 2015, p. 106-11.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rabe, P, Twetman, S, Kinnby, B, Svensäter, G & Davies, JR 2015, 'Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms', The Open Dentistry Journal, vol. 9, pp. 106-11. https://doi.org/10.2174/1874210601509010106

APA

Rabe, P., Twetman, S., Kinnby, B., Svensäter, G., & Davies, J. R. (2015). Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms. The Open Dentistry Journal, 9, 106-11. https://doi.org/10.2174/1874210601509010106

Vancouver

Rabe P, Twetman S, Kinnby B, Svensäter G, Davies JR. Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms. The Open Dentistry Journal. 2015;9:106-11. https://doi.org/10.2174/1874210601509010106

Author

Rabe, Per ; Twetman, Svante ; Kinnby, Bertil ; Svensäter, Gunnel ; Davies, Julia R. / Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms. In: The Open Dentistry Journal. 2015 ; Vol. 9. pp. 106-11.

Bibtex

@article{9fd07705069040bba8a8005c51e4802b,
title = "Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms",
abstract = "OBJECTIVE: To develop a model in which to investigate the architecture of plaque biofilms formed on enamel surfaces in vivo and to compare the effects of anti-microbial agents of relevance for caries on biofilm vitality. Materials and Methodology : Enamel discs mounted on healing abutments in the pre-molar region were worn by three subjects for 7 days. Control discs were removed before subjects rinsed with 0.1% chlorhexidine digluconate (CHX) or 0.2% sodium fluoride (NaF) for 1 minute. Biofilms were stained with Baclight Live/Dead and z-stacks of images created using confocal scanning laser micoscopy. The levels of vital and dead/damaged bacteria in the biofilms, assessed as the proportion of green and red pixels respectively, were analysed using ImageTrak({\textregistered}) software. Results : The subjects showed individual differences in biofilm architecture. The thickness of the biofilms varied from 28-96µm although cell density was always the greatest in the middle layers. In control biofilms, the overall levels of vitality were high (71-98%) especially in the area closest to the enamel interface. Rinsing with either CHX or NaF caused a similar reduction in overall vitality. CHX exerted an effect throughout the biofilm, particularly on the surface of cell clusters whereas NaF caused cell damage/death mainly in the middle to lower biofilm layers. Conclusion : We describe a model that allows the formation of mature, undisturbed oral biofilms on human enamel surfaces in vivo and show that CHX and NaF have a similar effect on overall vitality but differ in their sites of action.",
author = "Per Rabe and Svante Twetman and Bertil Kinnby and Gunnel Svens{\"a}ter and Davies, {Julia R}",
year = "2015",
doi = "10.2174/1874210601509010106",
language = "English",
volume = "9",
pages = "106--11",
journal = "The Open Dentistry Journal",
issn = "1874-2106",
publisher = "Bentham Open",

}

RIS

TY - JOUR

T1 - Effect of fluoride and chlorhexidine digluconate mouthrinses on plaque biofilms

AU - Rabe, Per

AU - Twetman, Svante

AU - Kinnby, Bertil

AU - Svensäter, Gunnel

AU - Davies, Julia R

PY - 2015

Y1 - 2015

N2 - OBJECTIVE: To develop a model in which to investigate the architecture of plaque biofilms formed on enamel surfaces in vivo and to compare the effects of anti-microbial agents of relevance for caries on biofilm vitality. Materials and Methodology : Enamel discs mounted on healing abutments in the pre-molar region were worn by three subjects for 7 days. Control discs were removed before subjects rinsed with 0.1% chlorhexidine digluconate (CHX) or 0.2% sodium fluoride (NaF) for 1 minute. Biofilms were stained with Baclight Live/Dead and z-stacks of images created using confocal scanning laser micoscopy. The levels of vital and dead/damaged bacteria in the biofilms, assessed as the proportion of green and red pixels respectively, were analysed using ImageTrak(®) software. Results : The subjects showed individual differences in biofilm architecture. The thickness of the biofilms varied from 28-96µm although cell density was always the greatest in the middle layers. In control biofilms, the overall levels of vitality were high (71-98%) especially in the area closest to the enamel interface. Rinsing with either CHX or NaF caused a similar reduction in overall vitality. CHX exerted an effect throughout the biofilm, particularly on the surface of cell clusters whereas NaF caused cell damage/death mainly in the middle to lower biofilm layers. Conclusion : We describe a model that allows the formation of mature, undisturbed oral biofilms on human enamel surfaces in vivo and show that CHX and NaF have a similar effect on overall vitality but differ in their sites of action.

AB - OBJECTIVE: To develop a model in which to investigate the architecture of plaque biofilms formed on enamel surfaces in vivo and to compare the effects of anti-microbial agents of relevance for caries on biofilm vitality. Materials and Methodology : Enamel discs mounted on healing abutments in the pre-molar region were worn by three subjects for 7 days. Control discs were removed before subjects rinsed with 0.1% chlorhexidine digluconate (CHX) or 0.2% sodium fluoride (NaF) for 1 minute. Biofilms were stained with Baclight Live/Dead and z-stacks of images created using confocal scanning laser micoscopy. The levels of vital and dead/damaged bacteria in the biofilms, assessed as the proportion of green and red pixels respectively, were analysed using ImageTrak(®) software. Results : The subjects showed individual differences in biofilm architecture. The thickness of the biofilms varied from 28-96µm although cell density was always the greatest in the middle layers. In control biofilms, the overall levels of vitality were high (71-98%) especially in the area closest to the enamel interface. Rinsing with either CHX or NaF caused a similar reduction in overall vitality. CHX exerted an effect throughout the biofilm, particularly on the surface of cell clusters whereas NaF caused cell damage/death mainly in the middle to lower biofilm layers. Conclusion : We describe a model that allows the formation of mature, undisturbed oral biofilms on human enamel surfaces in vivo and show that CHX and NaF have a similar effect on overall vitality but differ in their sites of action.

U2 - 10.2174/1874210601509010106

DO - 10.2174/1874210601509010106

M3 - Journal article

C2 - 25870718

VL - 9

SP - 106

EP - 111

JO - The Open Dentistry Journal

JF - The Open Dentistry Journal

SN - 1874-2106

ER -

ID: 156561498