2021
DOI: 10.1186/s12903-021-01502-6
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Tooth mousse containing casein phosphopeptide-amorphous calcium phosphate prevents biofilm formation of Streptococcus mutans

Abstract: Background Streptococcus mutans is a common cariogenic bacterium in the oral cavity involved in plaque formation. Casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) has been introduced into tooth mousse to encourage remineralization of dental enamel. The aim of this research was to study the effect of tooth mousse containing CPP-ACP (GC Tooth Mousse®) or CPP-ACP with 0.2% fluoride (CPP-ACPF; GC Tooth Mousse Plus®; GCP) on S. mutans planktonic growth and biofilm formation. … Show more

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Cited by 27 publications
(22 citation statements)
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“…SYPRO Ruby stain labels most classes of proteins and is used to stain proteins in the extracellular matrices of bacterial biofilms. The washed biofilms were stained with 100 µL of the FilmTracer SYPRO Ruby biofilm matrix stain (Invitrogen, Molecular Probes, Eugene, OR, USA) for 30 min at room temperature followed by several washes with DDW [39]. The fluorescence intensity of the stained biofilms was measured in the M200 Tecan microplate reader with an excitation at 450 nm and an emission at 610 nm.…”
Section: Filmtracer Sypro Ruby Biofilm Matrix Stainmentioning
confidence: 99%
“…SYPRO Ruby stain labels most classes of proteins and is used to stain proteins in the extracellular matrices of bacterial biofilms. The washed biofilms were stained with 100 µL of the FilmTracer SYPRO Ruby biofilm matrix stain (Invitrogen, Molecular Probes, Eugene, OR, USA) for 30 min at room temperature followed by several washes with DDW [39]. The fluorescence intensity of the stained biofilms was measured in the M200 Tecan microplate reader with an excitation at 450 nm and an emission at 610 nm.…”
Section: Filmtracer Sypro Ruby Biofilm Matrix Stainmentioning
confidence: 99%
“…At various time intervals, 200 µL of each sample in triplicates were transferred to transparent flat-bottom 96-well plates (Corning Incorporated, Kennebunk, ME, USA), and the OD 600nm was measured in a Tecan Infinite M200 microplate reader (Tecan Trading AG, Männedorf, Switzerland). In parallel, 100 µL of each sample in triplicates were transferred to µ-clear flat-bottomed 96-well white plates (Greiner Bio-One GmbH, Frickenhausen, Germany) to which 100 µL of the BacTiter Glo bacterial viability reagent (Promega Corporation, Madison, WI, USA) were added to measure the bacterial ATP content [ 126 ]. After a 10 min incubation at room temperature, the luminescence intensity was measured using the Tecan Infinite M200 microplate reader.…”
Section: Methodsmentioning
confidence: 99%
“…The working solutions were used fresh. For planktonic growth, the bacteria were incubated in BHI, while for biofilm formation BHI was supplemented with sucrose to a 2% final concentration (BHIS) [ 33 ]. The diluted EGCG solutions in BHI/BHIS were filtrated through a filtration device with a pore size of 0.22 μm before use to remove any precipitates.…”
Section: Methodsmentioning
confidence: 99%
“…Untreated and EGCG-treated planktonic S. mutans after 2 h incubation were fixed in 4% glutaraldehyde (MERCK, Darmstadt, Germany) in DDW for 2 h and then washed in DDW and let dry. Thereafter, the samples were coated with iridium and visualized using a Magellan 400 L High Resolution Scanning Electron Microscope (HR-SEM) at 10,000×–50,000× magnifications [ 33 ].…”
Section: Methodsmentioning
confidence: 99%