2013
DOI: 10.1590/s1806-83242013000100004
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Biofilm biomass disruption by natural substances with potential for endodontic use

Abstract: This study evaluated the in vitro effects of four natural substances on the biomass of bacterial biofilms to assess their potential use as root canal irrigants. The following substances and their combinations were tested: 0.2% farnesol; 5% xylitol; 20% xylitol; 0.2% farnesol and 5% xylitol; 0.2% farnesol, 5% xylitol, and 0.1% lactoferrin; 5% xylitol and 0.1% lactoferrin; and 20 mM salicylic acid. The crystal violet assay was used to evaluate the effects of these substances on the biomass of biofilms formed by … Show more

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Cited by 28 publications
(16 citation statements)
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“…The broad‐spectrum antimicrobial activity of LF has been explored in detail to assess its effect on other bacterial species. Alves, Silva, Rôças, and Siqueira () found that application of 0.2% tt‐farnesol, 5% xylitol, and 0.1% LF significantly reduced the biofilm mass formed by Enterococcus faecalis and Staphylococcus epidermidis (bacteria commonly reside in the apical root canal system of teeth with primary or post‐treatment apical periodontitis). This agent has also been used in endodontics as a root canal irrigant to combat pathological biofilms (Alves et al., ).…”
Section: Effect Of Lf On Periodontal Pathogensmentioning
confidence: 99%
“…The broad‐spectrum antimicrobial activity of LF has been explored in detail to assess its effect on other bacterial species. Alves, Silva, Rôças, and Siqueira () found that application of 0.2% tt‐farnesol, 5% xylitol, and 0.1% LF significantly reduced the biofilm mass formed by Enterococcus faecalis and Staphylococcus epidermidis (bacteria commonly reside in the apical root canal system of teeth with primary or post‐treatment apical periodontitis). This agent has also been used in endodontics as a root canal irrigant to combat pathological biofilms (Alves et al., ).…”
Section: Effect Of Lf On Periodontal Pathogensmentioning
confidence: 99%
“…Biofilm biomass was visualized and quantified by a crystal violet binding assay as previously described (17,18 Plates were overturned and air-dried, and the dye bound to the adherent cells was solubilized with 150 µL of 95% ethanol for 5 min. For quantification of biofilm biomass remaining after exposure to the test solutions, absorbance of the crystal violet solution was measured using an ELISA reader model 680 (Bio-Rad Laboratories, Hercules, CA, USA) at a wavelength of 590 nm.…”
Section: Crystal Violet Assaymentioning
confidence: 99%
“…Although, the poor correlation between the biofilm biomass reduction, metabolic activities and cellular viability remains a major limitation of this method because of the non-selective staining of the biofilm matrix including viable and dead cells as well [53]. Therefore, results obtained from the crystal violet assay must be combined with other multi-parametric techniques such as intracellular ATP, ATP/protein ratio, live/dead cell discrimination and selective visualization of the biomass matrix [54][55][56].…”
Section: Discussionmentioning
confidence: 99%