Plasma deactivation of oral bacteria seeded on hydroxyapatite disks as tooth enamel analogue.

PURPOSE To study the plasma treatment effects on deactivation of oral bacteria seeded on a tooth enamel analogue. METHODS A non-thermal atmospheric pressure argon plasma brush was used to treat two different Gram-positive oral bacteria including Lactobacillus acidophilus (L. acidophilus) and Streptococcus mutans (S. mutans). The bacteria were seeded on hydroxyapatite (HA) disks used as tooth enamel analogue with three initial bacterial seeding concentrations: a low inoculum concentration between 2.1 x 10(8) and 2.4 x 10(8) cfu/mL, a medium inoculum concentration between 9.8x10(8) and 2.4 x 10(9) cfu/mL, and a high inoculum concentration between 1.7 x 10(10) and 3.5 x 10(10) cfu/mL. The bacterial survivability upon plasma exposure was examined in terms of plasma exposure time and oxygen addition into the plasmas. SEM was performed to examine bacterial morphological changes after plasma exposure. RESULTS The experimental data indicated that a 13-second plasma exposure time completely killed all the bacteria when initial bacterial seeding density on HA surfaces was less than 6.9 x 10(6) cfu/cm2 for L. acidophilus and 1.7 x 10(7) cfu/cm2 for S. mutans, which resulted from low initial seeding inoculum concentration between 2.1 x 10(8) and 2.4 x 10(8) cfu/mL. Plasma exposure of the bacteria at higher initial bacterial seeding density obtained with high initial seeding inoculum concentration, however, only resulted in approximately 1.5 to 2 log reduction and approximately 2 to 2.5 log reduction for L. acidophilus and S. mutans, respectively. It was also noted that oxygen addition into the argon plasma brush did not affect the plasma deactivation effectiveness. SEM images showed that plasma deactivation mainly occurred with the top layer bacteria, while shadowing effects from the resulting bacterial debris reduced the plasma deactivation of the underlying bacteria.

[1]  P. Webster,et al.  Research Article In Vitro Antimicrobial Effect of a Cold Plasma Jet against , 2022 .

[2]  A. McBain,et al.  Bacteriological effects of a Lactobacillus reuteri probiotic on in vitro oral biofilms. , 2011, Archives of oral biology.

[3]  A. Schubert,et al.  Removing Biofilms from Microstructured Titanium Ex Vivo: A Novel Approach Using Atmospheric Plasma Technology , 2011, PloS one.

[4]  A. Mustapha,et al.  Oral bacterial deactivation using a low-temperature atmospheric argon plasma brush. , 2011, Journal of dentistry.

[5]  A. Yanguas-Gil,et al.  Inactivation of Bacteria and Biomolecules by Low-Pressure Plasma Discharges , 2010 .

[6]  A. Schubert,et al.  Killing of adherent oral microbes by a non-thermal atmospheric plasma jet , 2010 .

[7]  Gregory Fridman,et al.  Physical and biological mechanisms of direct plasma interaction with living tissue , 2009 .

[8]  S. Reuter,et al.  Spatially resolved diagnostics on a microscale atmospheric pressure plasma jet , 2008 .

[9]  M. Gundersen,et al.  Low Energy Nanosecond Pulsed Plasma Sterilization for Endodontic Applications , 2008, 2008 IEEE International Power Modulators and High-Voltage Conference.

[10]  Mounir Laroussi,et al.  Arc-Free Atmospheric Pressure Cold Plasma Jets: A Review , 2007 .

[11]  Boris Rubinsky,et al.  Irreversible Electroporation in Medicine , 2007, Technology in cancer research & treatment.

[12]  D. Beighton,et al.  Assessment of the Ozone-Mediated Killing of Bacteria in Infected Dentine Associated with Non-Cavitated Occlusal Carious Lesions , 2007, Caries Research.

[13]  James L. Walsh,et al.  Probing bactericidal mechanisms induced by cold atmospheric plasmas with Escherichia coli mutants , 2007 .

[14]  F. Hsieh,et al.  Bacterial Deactivation Using a Low Temperature Argon Atmospheric Plasma Brush with Oxygen Addition , 2007 .

[15]  F. Hsieh,et al.  Bacterial inactivation using a low-temperature atmospheric plasma brush sustained with argon gas. , 2007, Journal of biomedical materials research. Part B, Applied biomaterials.

[16]  G. Georghiou,et al.  Bactericidal Action of the Reactive Species Produced by Gas-Discharge Nonthermal Plasma at Atmospheric Pressure: A Review , 2006, IEEE Transactions on Plasma Science.

[17]  Bin Liu,et al.  Killing of S. mutans Bacteria Using a Plasma Needle at Atmospheric Pressure , 2006, IEEE Transactions on Plasma Science.

[18]  B. Saoudi,et al.  Bacterial spore inactivation by atmospheric-pressure plasmas in the presence or absence of UV photons as obtained with the same gas mixture , 2006 .

[19]  Daniel Palanker,et al.  Plasma-mediated transfection of RPE , 2006, SPIE BiOS.

[20]  Mounir Laroussi,et al.  Room-temperature atmospheric pressure plasma plume for biomedical applications , 2005 .

[21]  R. Walraven,et al.  Plasma treatment of dental cavities: a feasibility study , 2004, IEEE Transactions on Plasma Science.

[22]  J. Featherstone,et al.  The Continuum of Dental Caries—Evidence for a Dynamic Disease Process , 2004, Journal of dental research.

[23]  Eva Stoffels,et al.  Plasma needle: a non-destructive atmospheric plasma source for fine surface treatment of (bio)materials , 2002 .

[24]  W. Bowen,et al.  In situ studies of pellicle formation on hydroxyapatite discs. , 2000, Archives of oral biology.

[25]  J. Roth,et al.  An overview of research using the one atmosphere uniform glow discharge plasma (OAUGDP) for sterilization of surfaces and materials , 2000 .

[26]  Erich E. Kunhardt,et al.  Generation of large-volume, atmospheric-pressure, nonequilibrium plasmas , 2000 .

[27]  K. Schoenbach,et al.  Direct current high-pressure glow discharges , 1999 .

[28]  C. Laux,et al.  Experimental investigation of atmospheric pressure nonequilibrium plasma chemistry , 1997 .

[29]  W. Loesche Role of Streptococcus mutans in human dental decay. , 1986, Microbiological reviews.

[30]  P. Jay Lactobacillus Acidophilus and Dental Caries. , 1938, American journal of public health and the nation's health.