Table 1 . Studies Using TBO as PS .
Author/Year | Type | Bacteria | Groups | PS | Wavelength | Results |
Gergova et al19 2015 | In vitro | Enterococcus faecalis and other gram-positive cocci | 1) Control group; 2) Laser group; 3) PDT; 4) Different chemical substances; 5) Different solution | TBO 0.1 mg/mL |
660 nm P: 100 mW T: 5 min |
The PDT with FotoSan, hydrogen peroxide, and all tested types of iontophoresis all showed strong disinfection potential with very small, insignificant differences. |
Muhammad et al20 2014 |
In vitro | Enterococcus faecalis, Streptococcus salivarius, Porphyromonas gingivalis and Prevotella intermedia bacteria | 1) Aseptim Plus® photo-activated (LED) disinfection system; 2) Group by a 650 nm diode laser and toluidine blue as photosensitizer; 3) Control group, by ultrasonic irrigation (PUI) using EDTA 17% and NaOCl 2.6% solutions | TBO 15 μg/mL |
650 nm P: 60 mW T: 120 s |
There was no statistically significant difference between results obtained from groups treated by Aseptim Plus® and diode laser. |
Tennert et al212014 | In vitro | Clinical isolate of E. faecalis | 1) PDT group; 2) NaOCl; ) NaOCl-PDT group |
TBO 13-15 mg/mL |
635 nm P:100 mW T: 120 s |
Antimicrobial treatment of root canals caused a significant reduction of bacterial load in all groups. |
Pinheiro et al222014 | In vitro | Enterococcus faecalis | 1) Manual instrumentation; 2) Rotary instrumentation; (Toluidine blue O/laser, fuchsin/halogen light and fuchsin/LED) |
TBO 0.005% |
660 nm P: 100 mW T: 60 s |
It may be concluded that both rotary and manual instrumentation reduced E. faecalis. PDT can be used as an adjuvant to conventional endodontic treatment. |
Schiffner et al23 2014 |
In vitro | E. faecalis with mixed aerobic or anaerobic microbial populations | 1) Untreated; 2) NaCl alone; 3) PAD (PS plus irradiation) for 60 s; 4) The PS alone; 5) Irradiation for 60 s alone. | TBO not mentioned |
632-644 nm P: 200 mW T: 60 s |
The bactericidal activity of PAD appears to be enhanced by serum proteins in vitro, but is limited to bacteria present within the root canal. |
Hecker et al24 2013 |
In vitro | E. faecalis | 1) Disinfection with NaOCl (0.5%, 1.0% or 3.0% for 30 or 60 or 600 s); 2) Disinfection with NaOCl (as above) followed by application of neutralizing solution; 3) Disinfection with the PACT 200 system. | TBO not mentioned |
635 nm P: 200 mW T: 4 or 6 min |
The antibacterial PDT system did not achieve sufficient disinfection. |
Bago et al25 2013 |
In vitro | E. faecalis | 1) Diode laser irradiation (2 W; 3, 9, and 20 s); 2) PAD (100 mW, 60 s); 3) PAD with 3D Endoprobe (100 mW, 60 s); 4) 30-gauge syringe irrigation with NaOCl (60 s); 5) sonic agitation of NaOCl with the EndoActivator system (60 s); 6) 30-gauge syringe irrigation with NaCl (60 s). | TBO 155 μg/ mL |
660 nm P:100 mW T: 60 s |
The PAD and EndoActivator system were more successful in reducing the root canal infection than the diode laser and NaOCl syringe irrigation alone. |
Yao et al262012 | In vitro | Enterococcus faecalis |
Energy dose ranging from 0.5 to 5.5 J. 50 or 100 mW, irradiation time 5 to 55 s. part II: PAD therapy; 5.25% NaOCl irrigation and saline |
TBO 12.7 μg/mL |
635 nm P: 100 mW E: 0.5 to 5.5J |
PAD could decrease E. faecalis in root canals effectively, but was no more effective than 5.25% NaOCl. |
Vaziri et al27 2012 | In vitro | E. faecalis | 1) Sodium hypochlorite (NaOCl) irrigation; 2) Diode laser plus 2.5% NaOCl; 3) PDT; 4) 2.5% NaOCl plus PDT; 5) Chlorhexidine irrigation; 6) Control groups | TBO 15 μg/mL |
625 nm 200 mw/cm2 60 s |
Combination of PDT and 2.5% NaOCl achieved maximum reduction in recovered viable bacteria, no viable bacteria was observed after treatment of PDT + 2.5% NaOCl. |
Meire et al282012 | In vitro | E. faecalis | 1) aPDT (Denfotex Helbo system); 2) Er:YAG laser irradiation (2940 nm, 50 mJ or 100 mJ, 15 Hz, 40 s); 3) Er:YAG laser irradiation (2940 nm, 100 mJ, 15 Hz, 40 s); 4) Nd:YAG laser irradiation (1064 nm, 2 W, 15 Hz, 40 s); 5) immersion in 2.5% (w/v) NaOCl for 1 min; 6) immersion in 2.5% (w/v) NaOCl for 5 min; 7) immersion in 2.5% (w/v) NaOCl for 10 min; immersion in 2.5% (w/v) NaOCl for 30 min in control group; 8) NaOCl 0.25% + Er:YAG | TBO 12.7 mg /mL |
635 nm P: 100 mw T: 10 s |
The use of both commercial aPDT systems resulted in a weak reduction in the number of E. faecalis cells. |
Poggio et al29 2011 |
In vitro | Enterococcus faecalis, Streptococcus mutans and Streptococcus sanguis strains | 1) Teeth treated with PAD (FotoSan system); 2) teeth treated with PAD and with 5% NaOCl solution; 3) teeth irrigated with TBO; 4) teeth treated with PAD for longer time (FotoSan system);5) teeth irrigated with 5% NaOCl solution (positive control). |
TBO 100 μg/mL |
628 nm P:1 w T: 30 or 90 s |
PAD applied for a longer time (in respect to manufacturer’s instructions) or PAD associated to 5% NaOCl showed the significantly higher antibacterial effects. |
Rios et al30 2011 |
In vitro | E. faecalis |
Five experimental groups and three control groups: 1) NaOCl; 2) toluidine blue O (TBO); (3) light: canals were filled with sterile saline; (4) TBO/light; (5) NaOCl/TBO/light |
TBO low viscosity |
635 nm 30 s |
PDT using TBO and a LED lamp has the potential to be used as an adjunctive antimicrobial procedure in conventional endodontic therapy. |
Schlafer et al312010 | In vitro | Escherichia coli, Candida albicans, Enterococcus faecalis, Fusobacterium nucleatum, and Streptococcus intermedius | 1) T−L−, No TBO, no light (negative control treatment); 2) T+L−, TBO, no light; 3) T−L+, no TBO irradiation; 4) T+L+, TBO + irradiation |
TBO 100 µg/mL |
628 nm 30 s |
PAD yielded significant reductions in the viable counts of all organisms in planktonic suspension. |
Souza et al32 2010 |
In vitro | E. faecalis |
1) MB/NaOCl (PDT with MB and NaOCl as the irrigant), 2) TB/NaOCl (PDT with TBO and NaOCl as the irrigant), 3) MB/NaCl (PDT with MB and NaCl as the irrigant), 4) TB/NaCl (PDT with TBO and NaCl as the irrigant) |
MB 15 µg/mL |
660 nm 40 mW T: 4 min |
These in vitro results suggest that PDT with either MB or TBO may not exert a significant supplemental effect to instrumentation/irrigation procedures. |
Meire et al33 2009 |
In vitro | E. faecalis |
1) Nd:YAG laser 2) KTP laser 3) PAD treatment 4) NaOCl solution 5) positive control |
TBO 12.7 mg /mL |
635 nm P:100 mW T: 150 s Energy: 15 J |
In aqueous suspension, PAD and NaOCl resulted in a significant reduction in the number of E. faecalis. |
Bergmans et al342008 | In vitro | Streptococcus anginosus, E. faecalis or Fusobacterium nucleatum |
1) PAD 2) Laser 3) Dye 4) Positive control |
TBO 12.7 mg/mL |
635 nm P:100 mW T: 150 s |
Treatment of root canals with PAD (15 J) caused a significant reduction of the bacterial load, resulting in a 93.8% kill of S. anginosus (P<0.0001), a 88.4% kill of E. faecalis. |
Fonseca et al352008 | In vitro | E. faecalis | 1) Control group and 2) test group | TBO 0.0125% |
660 nm P: 50 mW |
The mean decrease in CFU/mL was 99.9% in the test group. |
Bonsor et al36 2006 |
In vivo | Fusobacterium nucleatum, Prevotella intermedia, Streptococcus intermedius and Peptostreptococcus micros | A microbiological sample of the canal was taken on accessing the canal, after conventional endodontic therapy, and finally |
TBO |
635 nm 60 s at 100 mW |
The PAD system offers a means of destroying bacteria remaining after using conventional irrigants in endodontic therapy. |