Fluid-driven interfacial instabilities and turbulence in bacterial biofilms.

Biofilms are thin layers of bacteria embedded within a slime matrix that live on surfaces. They are ubiquitous in nature and responsible for many medical and dental infections, industrial fouling and are also evident in ancient fossils. A biofilm structure is shaped by growth, detachment and response to mechanical forces acting on them. The main contribution to biofilm versatility in response to physical forces is the matrix that provides a platform for the bacteria to grow. The interaction between biofilm structure and hydrodynamics remains a fundamental question concerning biofilm dynamics. Here, we document the appearance of ripples and wrinkles in biofilms grown from three species of bacteria when subjected to high-velocity fluid flows. Linear stability analysis suggested that the ripples were Kelvin-Helmholtz Instabilities. The analysis also predicted a strong dependence of the instability formation on biofilm viscosity explaining the different surface corrugations observed. Turbulence through Kelvin-Helmholtz instabilities occurring at the interface demonstrated that the biofilm flows like a viscous liquid under high flow velocities applied within milliseconds. Biofilm fluid-like behavior may have important implications for our understanding of how fluid flow influences biofilm biology since turbulence will likely disrupt metabolite and signal gradients as well as community stratification.

In Vitro Comparison of the Area of Biofilm Removal by the Quad Stream Nozzle Versus a Traditional Oral Irrigator Standard Nozzle.

The objective of this in vitro study was to compare the area of oral biofilm removal by the Philips Sonicare Quad Stream (PSQS) nozzle (used on a Philips® Sonicare® Power Flosser) and a traditional oral irrigator with a standard nozzle (TOIS) when used per the directions for use (DFU) instructions for both devices.

In Vitro Biofilm Removal From Human Enamel Using a Philips® Sonicare® Power Flosser.

The objective of this in vitro study was to quantify the removal of dental biofilm from human enamel surfaces after treatment with the Philips® Sonicare® Power Flosser. Dental biofilms were grown from pooled human saliva on human enamel disks for 4 days, according to an established academic model.* The biofilms (n = 6) were treated with the Philips Sonicare Power Flosser for 3 seconds using the Quad Stream nozzle. To quantify the number of bacteria before treatment, the biofilm volume was measured using optical coherence tomography (OCT) and the bacterial cell density was determined from untreated control samples (n = 6) using confocal laser scanning microscopy (CLSM). After treatment the number of remaining bacteria were counted using CLSM. Additionally, scanning electron microscope (SEM) images were recorded. While before treatment 0.2-mm thick dense biofilms were present, after treatment only scattered groups of bacteria remained (Figure 1 through Figure 4). Quantitative analysis showed 99.96% removal for the Quad Stream nozzle. The Philips Sonicare Power Flosser oral irrigator with Quad Stream nozzle removed over 99.9% of the bacteria in this established laboratory model of dental biofilm.

Power Flossing Removes Biofilm From Model Periodontal Pockets In Vitro and Shifts the Microbiome During Biofilm Regrowth.

The Philips® Sonicare® Power Flosser (PSPF) is highly effective in reducing gum disease. Next to effective supragingival cleaning, this may be partially driven by subgingival cleaning. This in vitro study aimed to assess the effectiveness of the PSPF in removing biofilm from a model periodontal pocket up to 6 mm deep and to investigate the taxonomic composition of biofilm regrown after use of the PSPF.

Insights into blue light accelerated tooth whitening.

OBJECTIVE: To test the hypotheses that blue light accelerates whitening through either (1) direct photobleaching or (2) photon-assisted oxidation using sequential longitudinal bleaching. METHODS: Thirty extracted human tooth samples having natural life accumulated color were divided over five groups: A. 9h light + 10h 6% H2O2 gel + 6h light & 6% H2O2 combined; B. 9h 6% H2O2 gel + 10h light + 6h light & 6% H2O2 combined; C. 11 h light & 6% H2O2 combined; D. 8.45h 25 %H2O2 gel + 10h of light only + 6h light & 25% H2O2 combined E. 10.45 h light & 25 %H2O2 combined. Blue light (456nm) was used at 190 mW/cm2. Color change (ΔE) was measured over time, and reported after 48h color stabilization. RESULTS: Groups A, B and D reached saturation in the first phase (at 9h) at a ΔE of 4.3 ± 0.7, 4.9 ± 1.3 and 10.9 ± 2.2, respectively. Groups C and E achieved in the same time a significantly higher ΔE of 14.2 ± 1.7 and 15.6 ± 1.9, respectively. Subsequently adding the opposite single modality to groups A, B and D for 10h did reach an end stage at 8.1 ± 1.3, 8.8 ± 1.8 and 10.8 ± 1.4 ΔE, respectively. The final 6h treatment combining light and H2O2 showed in these groups a statistically significant step in ΔE reaching 12.9 ± 1.4, 10.7 ± 2.5 and 15.3 ± 1.7, respectively. CONCLUSIONS: Blue light significantly increases bleaching rate and final achievable ΔE.This sequential whitening study provides a first indication that this enhanced bleaching is the result of the hypothesized light mechanisms acting in parallel to hydrogen peroxide bleaching. CLINICAL SIGNIFICANCE: This study shows that blue light can accelerate whitening, within the limits of an in-vitro model. The findings help the clinician explain to their patients that in light accelerated whitening the light not merely accelerates the bleaching process, but that it attacks more stain compounds than peroxide alone does.

In vitro and in vivo antimicrobial activity of covalently coupled quaternary ammonium silane coatings on silicone rubber.

Biomaterial-centered infection is a dreaded complication associated with the use of biomedical implants. In this paper, the antimicrobial activity of silicone rubber with a covalently coupled 3-(trimethoxysilyl)-propyldimethyloctadecylammonium chloride (QAS) coating was studied in vitro and in vivo. Gram-positive Staphylococcus aureus ATCC 12600, Staphylococcus epidermidis HBH, 102, and Gram-negative Esherichia coli O2K2 and Pseudomonas aeruginos AK1 were seeded on silicone rubber with and without QAS-coating, in the absence or presence of adsorbed human plasma proteins. The viability of the adherent bacteria was determined using a live/dead fluorescent stain and a confocal laser scanning microscope. The coating reduced the viability of adherent staphylococci from 90% to 0%), and of Gram-negative bacteria from 90% to 25% while the presencc of adsorbed plasma proteins had little influence. The biomaterials were also subcutaneously implanted in rats for 3 or 7 days, while pre- or postoperatively seeded with S. aureus ATCC 12600. Preoperative seeding resulted in infection of 7 out of 8 silicone rubber implants against 1 out of 8 QAS-coated silicone rubber implants. Postoperative seeding resulted in similar infection incidences on both implant types, but the numbers of adhering bacteria were 70% lower on QAS-coated silicone rubber. In conclusion, QAS-coated silicone rubber shows antimicrobial properties against adhering bacteria, both in vitro and in vivo.

Positively charged biomaterials exert antimicrobial effects on gram-negative bacilli in rats.

Biomaterial-centered infection is a much-dreaded complication associated with the use of biomedical implants. Although positively charged biomaterial surfaces stimulate bacterial adhesion, it has been suggested that surface growth of adhering Gram-negative bacilli is inhibited on positively charged surfaces. In the present paper, we determined the infection rate of differently charged poly(methacrylates) in rats. To this end, 2 x 10(6)/cm(2) Escherichia coli O2K2 or 2 x 10(4)/cm(2) Pseudomonas aeruginosa AK1 were seeded on glass discs coated with three differently charged poly(methacrylates) coatings in a parallel plate flow chamber. Three rats received six subcutaneous discs (two discs of each charge variant) seeded with E. coli, while three other rats received discs seeded with P. aeruginosa. The numbers of viable bacteria on the surfaces were determined 48h after implantation. On 50% of all positively charged discs viable E. coli were absent, while the negatively charged discs were all colonized by E. coli. P. aeruginosa, however, were isolated from both positively and negatively charged discs. Probably, P. aeruginosa can circumvent the antimicrobial effect of the positive charge through the formation of extracellular polysaccharides.