- Author:
Rui MA
1
;
Jie LIU
;
Yun-tao JIANG
;
Zheng LIU
;
Zi-sheng TANG
;
Dong-xia YE
;
Jin ZENG
;
Zheng-wei HUANG
Author Information
- Publication Type:Journal Article
- MeSH: Actinomyces; growth & development; Algorithms; Biofilms; growth & development; Biological Transport; Dental Plaque; microbiology; Dextrans; pharmacokinetics; Diffusion; Fluorescent Dyes; pharmacokinetics; Fusobacterium nucleatum; growth & development; Macromolecular Substances; pharmacokinetics; Microscopy, Confocal; Models, Biological; Molecular Probe Techniques; Streptococcus mutans; growth & development; Streptococcus sanguis; growth & development
- From: International Journal of Oral Science 2010;2(4):190-197
- CountryChina
- Language:English
-
Abstract:
AIMThe purpose of this study was to develop a mathematical model to quantitatively describe the passive transport of macromolecules within dental biofilms.
METHODOLOGYFluorescently labeled dextrans with different molecular mass (3 kD, 10 kD, 40 kD, 70 kD, 2000 kD) were used as a series of diffusion probes. Streptococcus mutans, Streptococcus sanguinis, Actinomyces naeslundii and Fusobacterium nucleatum were used as inocula for biofilm formation. The diffusion processes of different probes through the in vitro biofilm were recorded with a confocal laser microscope.
RESULTSMathematical function of biofilm penetration was constructed on the basis of the inverse problem method. Based on this function, not only the relationship between average concentration of steady-state and molecule weights can be analyzed, but also that between penetrative time and molecule weights.
CONCLUSIONThis can be used to predict the effective concentration and the penetrative time of anti-biofilm medicines that can diffuse through oral biofilm. Furthermore, an improved model for large molecule is proposed by considering the exchange time at the upper boundary of the dental biofilm.