Dental caries remains one of the most prevalent chronic diseases in humans, and it is an important cause of oral pain and dental loss, which lead to school and work absenteeism, affecting individuals’ daily activities, and emotional stability.1 Dental caries is caused by specific pathogenic microorganisms that metabolize carbohydrates ingested to form acids, deficient oral hygiene habits, and high-sugar diets.2
Growing evidence indicates that one-step incomplete excavation seems suitable to treat deep caries lesions.3 The partial removal of carious tissue and the subsequent restoration of the dental element are sufficient to reduce the caries microbiota.4 Protocols for ultraconservative caries removal, such as Carisolv™5 and Papacarie™,6 have been used as an alternative method for complementing the effects of manual excavation, thus reducing cariogenic microbiota.
Several studies have shown that oral bacteria are susceptible to antimicrobial photodynamic therapy (aPDT).7,8 aPDT has recently been studied as a coadjuvant therapy against microorganisms of dental caries, which suggests that it might be useful as adjunctive therapy to current deep carious lesion.9–14 Therefore, the aim of this study was to perform a systematic review and meta-analysis to evaluate the effect of aPDT as a coadjuvant therapy in reducing microorganisms in deep carious lesions.
This systematic review was registered in the PROSPERO database (PROSPERO registry number: CRD42015029891) and was conducted following the PRISMA statements.15
Is aPDT an effective coadjuvant therapy to reduce microorganisms in deep carious lesions?
Strategy for Identification and Selection of the Studies
A broad search for articles was conducted, and only articles published before March 29, 2016, were considered for review. The selection process is described in Fig. 1. The following databases were used: Pubmed, Web of Science (WOS), Scopus, Cochrane Library, and Lilacs. The gray literature was also consulted trough Opensigle. The MeSH terms “Photochemotherapy” and “Dental caries” were used. MeSH synonyms, related terms, and free terms were included. These keywords were selected from DeCS—Health Sciences Descriptors developed and from the Medical Subject Headings (MeSH) of the US National Library of Medicine. The terms were combined to refine the search results (the combination of these search descriptors is shown in Table 1). The titles and abstracts of the identified articles were independently evaluated by two researchers (POO and LAA) to determine whether they met the inclusion criteria for the review. The electronic search was supplemented by a manual search of the reference list from the included articles.
Electronic database used and search strategy.
|PubMed||#1 (“Photochemotherapy” [MeSH Terms] OR “Photochemotherapy” [Title/Abstract] OR “Photodynamic Therapies” [Title/Abstract] OR “Photodynamic Therapy” [Title/Abstract] OR “TFD” [Title/Abstract])|
|#2 (“Dental Caries” [MeSH Terms] OR “Dental Caries” [Title/Abstract] OR “Dental Decay” [Title/Abstract] OR “Carious Dentin” [Title/Abstract] OR “Carious Dentins” [Title/Abstract])|
|#1 and #2|
|Scopus||(TITLE-ABS-KEY (Photochemotherapy) OR TITLE-ABS-KEY (Photodynamic Therapies) OR TITLE-ABS-KEY (Photodynamic Therapy OR TITLE-ABS-KEY (TFD))|
|(TITLE-ABS-KEY (Dental Caries) OR TITLE-ABS-KEY (Dental Decay) OR TITLE-ABS-KEY (Carious Dentin) OR TITLE-ABS-KEY (Carious Dentins))|
|#1 and #2|
|WOS||#1 TS=(“Photochemotherapy” OR “Photodynamic Therapies” OR “Photodynamic Therapy” OR “TFD”)|
|#2 TS=(“Dental Caries” “OR “Dental Decay” OR “Carious Dentin” OR “Carious Dentins”)|
|#1 and #2|
|Lilacs||(ab:(Photochemotherapy)) OR (ab:(Photodynamic Therapies)) OR (ab:(Photodynamic Therapy)) OR (ab:(TFD)) AND (ab:(Dental Caries)) OR (ab:(Dental Decay)) OR (ab:(Carious Dentin)) OR (ab:(Carious Dentins))|
|Cochrane Library||#1 (Dental Caries:ti,ab,kw or Dental Decay:ti,ab,kw or Carious Dentin:ti,ab,kw or Carious Dentins:ti,ab,kw)|
|#2 (Photochemotherapy:ti,ab,kw or Photodynamic Therapy:ti,ab,kw or Photodynamic Therapies:ti,ab,kw or TFD:ti,ab,kw)|
|#1 and #2|
The publications were selected if they were in vivo clinical studies. There was no restriction on language. The inclusion criteria outlines articles according to the population, intervention, comparisons, and outcomes (PICOS) as follows:
Population (P): Healthy humans who were not taking any medication that could affect the results of the study.
Intervention (I): Treatment of deep carious lesions.
Comparison (C): Group treated with aPDT and group treated without aPDT; and/or comparison before and after aPDT.
Outcome (O): microorganism count.
Study design (S): clinical studies.
Duplicate articles, literature reviews, records out of the proposed theme, case reports, in vitro studies, dissertations, thesis, or monographs, and studies with animals were excluded.
Initially, two of the authors (POO and LAA) selected the studies by title and abstracts according to the previously described search strategy (PICOS criteria). To evaluate agreement between authors, 10% of the publications were randomly selected and had their classification compared, and then a Kappa statistic of 0.97 was determined. Only articles that matched the inclusion criteria were accepted. Articles appearing in more than one database were considered only once (Fig. 1). Subsequently, the full texts of the potentially eligible studies were completely accessed and the PICOS criteria were applied again. Any disagreement was discussed and solved by consensus or discussion with the third review author. After the inclusion of the abstracts that fulfilled the selection criteria and verification of eligibility by reading the complete articles, the articles were submitted to verify the quality assessment and risk of bias.
Assessment of Risk of Bias in Included Studies
We used the Cochrane Collaboration’s tool for assessing risk of bias.16 The following domains were assessed: generation of allocation sequence, allocation concealment, blinding of participants and outcome assessors, incomplete outcome data, and selective outcome reporting. Each domain was classified as having low (+), high (−), or uncertain (?) risk of bias. The authors also included studies with no description of inclusion and exclusion criteria as a possible risk of bias.
The data from the included papers were compiled. Data extraction was conducted independently by two reviewers (LAA and POO) by completely reading the articles and considering the categories and variables. We considered the following clinical parameters: sample/number of teeth, age, dentition/teeth, groups assessed, irradiation location, and removal of photosensitizer (PS) before irradiation. We also evaluated the aPDT parameters: PS type, concentration, and preirradiation time, active laser media, laser wavelength (nm), energy (J), dose (), power (mW), irradiance (), spot size (), and duration of irradiation (min).
A meta-analysis was also performed to combine comparable results. The outcome was presented in all studies as continuous data. For the meta-analysis, we extracted the mean and the standard deviation (Log ). Subgroups were established prior to the overall analysis of the outcome according to the evaluated microorganism(s) as follows: 1) total viable microorganisms counts; 2) mutans streptococci counts; and 3) Lactobacillus spp. counts.
A fixed effect model was used for the meta-analysis. The weighted standard mean differences before and after aPDT were performed using the inverse-variance meta-analysis. Publication bias was assessed using a funnel plot. The was used to assess statistical heterogeneity between studies, where values of 25%, 50%, and 75% indicated low, medium, and high-heterogeneity, respectively.17 The meta-analysis calculation and Forest plots creations were performed with RevMan 5.3. In the Forest plots, negative values in the mean difference represent an increase in microorganism count.
Search and Selection of Articles
A flow diagram of the search strategy is presented in Fig. 1. Initially, the search resulted in 227 published studies: 40 from PubMed, 4 from Cochrane, 71 from Scopus, 63 from LILACS, 49 from WOS, and 0 from Opensigle. Seventy-five records were excluded because they were duplicated. The analysis of the titles and abstracts resulted in the exclusion of 146 of the published studies, leaving 6 for full text reading. The references of the six remaining articles were hand searched and more three articles were selected. This resulted in a total of nine articles selected for reading in full. After access to the complete file, three records were excluded because one was a literature review, another because it was outside of the proposed theme, and the last was an in vitro study, thus leaving only six articles.
Quality Assessment of Risk of Bias
Figure 2 demonstrates the evaluation of the inner methodological risk of bias, according to the Cochrane Collaboration’s tool for assessing risk of bias. Melo et al.’s13 study presented the best classification. In general, the results and exclusion criteria were well described in all selected papers. The risk of bias was more frequent in allocation, randomization, and sample size calculation.
Data extraction from the selected articles is described in Table 2. In the included articles, the sample size ranged from 10 to 90 teeth. Of the six selected articles, only Longo et al.11 did not provide the patient age. One article12 did not describe the type of teeth used. Three articles9,10,13 used permanent teeth, another11 used primary and permanent molars, and only one of the selected articles used primary molars.14 Five articles9–12,14 used the same teeth after manual excavation and compared before (control) and immediately after aPDT (experimental). Only Melo et al.13 performed a randomized, controlled, intraindividual comparison (split-mouth), with two groups (intervention and control).
Characteristics of the included studies.
|Author/year||Type of study||Sample/number of teeth||Age||Dentition/teeth||Groups evaluated||Outcome|
|Borges et al., 2010||Case–control||5/20||19 to 36 years||Permanent /WD||1. Without TBO and without light2. With TBO alone3. With aPDT alone4. With TBO plus aPDT||The association of TBO and aPDT was effective in killing oral microorganisms present in carious dentin lesions|
|Guglielmi et al., 2011||Case–control||23/26||8 to 25 years||Permanent /molars||In the same teeth, they were compared before and immediately after aPDT mediated by MB||aPDT may be an appropriate approach for the treatment of deep carious lesions using minimally invasive procedures|
|Longo et al., 2012||Case–control||10/12||Children and adults||Primary and permanent/molars||In the same teeth, they were compared before and immediately after aPDT mediated by AlClPc liposomal solution||aPDT protocol mediated by cationic liposomes containing AlClPc is safety for clinical application and is efficient in the reduction of bacterial load in caries lesions|
|Araújo et al., 2015||Case–control||WD/10||3 to 9 years||WD/Molars||Using the same teeth, the following groups were assessed:1. Untreated superficial dentin2. Untreated deep dentin3. aPDT-treated deep dentin directly irradiated4. aPDT-treated superficial dentin5. aPDT-treated deep dentin not directly irradiated||Although aPDT may not affect the number of S. mutans DNA copies immediately after the treatment, clear reduction of the number of CFU was found|
|Melo et al., 2015||Single blind, randomized, controlled, split-mouth, clinical trial||45/90||Above 18 years||Permanent /posterior teeth||1. Control group: 0.89% NaCl2. Experimental group: aPDT mediated by TBO||aPDT significantly reduced viable counts of all tested microorganisms|
|Steiner-Oliveira et al., 2015||Clinical trial||32/WD||5 to 7 years||Primary/molars||1. Control: 2% chlorhexidine;2. Group LEDTB:aPDT with LED (LED) mediated by TBO;3. Group LMB: aPDT with laser mediated by MB||Independent of the treatment, a significant reduction in microorganisms was found for universal bacteria|
The data collected from the six selected studies regarding the aPDT parameters are summarized in Table 3. The laser wavelength (nm) used ranged between 500 and 800 and the diameter of the spot the laser focused on varied between 2.8 and . The output power ranged between 40 and 260 mW and the duration of irradiation ranged between 1 and 10 min. Melo et al.13 did not describe the irradiation duration. The PSs used included toluidine blue (TBO), methylene blue (MB), and aluminum-chloride-phthalocyanine (AlClPc). Guglielmi et al.10 and Araújo et al.12 used MB as the PS in their studies. TBO was used as PS in studies by Borges et al.,9 and Melo et al.13 Longo et al.11 used AlClPc, whereas Steiner-Oliveira et al.14 evaluated two PSs (TBO and MB). Guglielmi et al.10 and Longo et al.11 used only one group treated with aPDT, whereas Borges et al.,9 Araújo et al.,12 Melo et al.,13 and Steiner-Oliveira et al.14 divided the sample into different groups receiving different treatment alternatives: aPDT with TBO, PDT with MB, and chlorhexidine (Table 2).
aPDT parameters in the selected studies.
|Author/year||Wavelength (nm)||PS (concentration)/preirradiation time||Removal of PS before irradiation||Irradiation time||Irradiation location||Light source||Energy (J)||Dose (J /cm2)||Output power (mW)||Irradiance (mW/cm2)||Spot (mm2)|
|Borges et al., 2010||620 to 660 predominant wavelength of 638.8||TBO () produced by Sigma Chemicals, Poole, UK/5 min||WD||10 min||WD||Red light-emitting diode (Laserbeam, Rio de Janeiro, RJ, Brazil)||WD||94||40||WD||9.5 with a diffused beam at 2.0 mm of working distance|
|Guglielmi et al., 2011||660||produced by Formula and Ação, São Paulo, Brazil/5 min||WD||90 s||Single point in the center of each cavity||Diode laser (InGaAIP)||9||320||100||WD||2.8|
|Longo et al., 2012||660||AlClPc liposomal solution/5 min||Excess removed with water||3 min||WD||Red Laser (MM Optics, São Carlos, São Paulo, Brazil)||WD||180||40||250||4|
|Araújo et al., 2015||500 to 800||MB () produced by Aptivalux, Belo Horizonte, Brazil/5 min||WD||1 min (fractionated with an interval of 20 s between two applications of 30 s)||WD||Halogen light curing unit emitting a white light (Curing Light 3 M Espe®, 3 M Espe, USA)||WD||WD||260||WD||WD|
|Melo et al., 2015||TBO () () produced by Sigma, St. Louis, MO, USA/5 min||Removed with autoclaved distilled water 30 s||WD||2.0 mm from the cavity floor||Red light-emitting diode (MM Optics, São Carlos, São Paulo, Brazil)||WD||94||150||WD||Connected to an optical fiber ()|
|Steiner-Oliveira et al., 2015||LEDTB-630 LMB-660||LEDTB-TBO LMB-MB (0.01%) (Chimiolux® Hyrofarma, Belo Horizonte, Minas Gerais, Brazil)/5 min||The PS was removed after irradiation (washed out with water and dried with a sterile cotton pellet)||LEDTB-1 min LMB-90 s||WD||LEDTB-Red LED light source (MM Optics, São Carlos, São Paulo, Brazil) LMB-Red low power LASER light source (Photon Lase III—DMC, São Carlos, São Paulo, Brazil)||9||LEDTB−30 LMB-320||100||WD||WD|
According to the information described in Table 4, we concluded that most studies performed the collection of deep dentin, except Araújo et al.,12 which completed the collection of both deep dentin and shallow dentin as well. Regarding the form of collection, most authors used manual resource diggers. Guglielmi et al.10 and Steiner-Oliveira et al.14 differed by using a micropunch.
Microbiological methods of the selected studies.
|Author/year||Instrument collection||Local dentin collection||Volume of dentin||Transport||Repeat||Dispersion||Technique||Culture media/incubation|
|Streptococcus||Mutans streptococci||Lactobacillus||Total microorganisms|
|Borges et al., 2010||Hand excavator||Deep||By weighing||WD||Triplicate||Tubes with 3 sterile glass beads, agitated for 1 min in a Disrupter||CFU||MSA + S / 48 H / 37 deg/0%||MSA + B / 48 H / 37 deg / 10%||Rogosa agar / 48H / 37 deg / 10%||Blood Agar / 48H / 37 deg / 10%|
|Guglielmi et al., 2011||Micropunch||Deep||1 mm of diameter, depths of 0.5 mm/average weights of 0.059 mg||VMGA III||Triplicate||2 min in a vortex||CFU||—||MSA + S + B / 48H / 37 deg / Candle jar||Rogosa agar / 48H / 37 deg||Brucella blood agar /7 Days/anaerobic cabinet.|
|Longo et al., 2012||Hand excavator||Deep||Sufficient to cover the surface of the active portion of the excavator||BHI||Triplicate||Plastic tubes stirred in vortex for 1 min||CFU||—||—||—||BHI agar/48 H/37 deg|
|Araújo et al., 2015||Dentin spoon n 17||Deep and shallow||WD||Immediate processing for CFU/Placed in Eppendorf tubes and stored at until used for qPCR||Triplicate for CFU/Duplicate for qPCR||Eppendorf tubes containing 1 ml of sterile distilled water, vortexed ()||CFU and qPCR only for S. mutans species||MSA—48H/37 deg/ Candle jar||—||Rogosa agar/48H/37 deg/Candle jar||BHI agar/48H/37 deg/Candle jar|
|Melo et al., 2015||Sterile binangle discoid spoon||Deep||By weighing||WD||Triplicate||Glass beads were added to tubes following agitation for 1 min in a cell disruptor||CFU||—||MSA + B + S 37°C, 5% 48 h||Rogosa agar 37°C/5% /48 h||Blood Agar/37°C/5% /48 h|
|Steiner-Oliveira et al., 2015||Micropunch||Deep||1 mm of diameter, depths of 0.5 mm||Placed in microtubes containing of TE buffer and stored at until use||Duplicate||Vortex||qPCR for total bacteria and species: S. mutans, S. sobrinus, L. casei, F. nucleatum, A. rimae||—||—||—||—|
With respect to the volume of dentin collected, Borges et al.9 and Melo et al.13 quantified this volume by weight. Araújo et al.12 did not provide this information. Guglielmi et al.10 mentioned an average weight, whereas Longo et al.11 described the collected dentin only as a volume sufficient to cover the surface of the active portion of the excavator. Steiner-Oliveira et al.14 and Guglielmi et al.10 reported doing the dentin collection using a micropunch and gave details on the diameter and penetration of the instrument, but only Guglielmi et al.10 measured the average weight of the dentin.
In most studies, the gold standard method for detecting the antimicrobial effect of aPDT—the conventional culture method by CFU—was used. Borges et al.9 evaluated colonies of mutans streptococci, total streptococci, lactobacilli, and total microorganisms. Guglielmi et al.10 and Melo et al.13 did not take a count Streptococcus, Araújo et al.12 did not evaluate colonies of mutans streptococci, and Longo et al.11 determined only the total viable bacteria. Araújo and coworkers12 used the real-time PCR to detect Streptococcus mutans species, and Steiner-Oliveira et al.14 also used the real-time PCR to assess the total bacteria and five specific species (S. mutans, Streptococcus sobrinus, Lactobacillus casei, Fusobacterium nucleatum, and Atopobium rimae). The studies that used the CFU method were run in triplicate, while the ones that choose PCR performed in duplicate
As described in Table 5, all studies observed CFU reduction for all kinds of microorganisms evaluated by this method. However, Araújo et al.12 also used the real-time PCR analyses and showed that the S. mutans DNA did not reduce after aPDT, whereas Steiner-Oliveira et al.14 demonstrated that aPDT evaluated by real-time PCR analyses reduced the total number of total bacteria, S. mutans, S. sobrinus, F. nucleatum, A. rimae after each treatment, but did not reduce S. sobrinus.
Microbiologic results for the selected studies.
|Total microorganisms||Lactobacillus||Streptococcus||Mutans streptococci||S. mutans||S. sobrinus||F. nucleatum||A. rimae||L. casei|
|Borges et al., 2010||Yes/—||No||Yes/—||No||Yes/—||Yes||Yes/—||Yes||—||—||—||—||—||—||—||—||—||—|
|Guglielmi et al., 2011||Yes/0.91||Yes||Yes/0.93||Yes||—||—||Yes/1.38||Yes||—||—||—||—||—||—||—||—||—||—|
|Longo et al., 2012||Yes/0.82||Yes||—||—||—||—||—||—||—||—||—||—||—||—||—||—||—||—|
|Araújo et al., 2015||Yes/1.90||Yes||Yes/2.16||Yes||Yes/2.19||Yes||—||—||No||No||—||—||—||—||—||—||—||—|
|Melo et al., 2015||Yes/1.07||Yes||Yes/1.69||Yes||—||—||Yes/1.08||Yes||—||—||—||—||—||—||—||—||—||—|
|Steiner-Oliveira et al., 2015||Yes||Yes||—||—||—||—||—||—||Yes||Yes||No||No||Yes||Yes||Yes||Yes||Yes||Yes|
Two articles were not included in the meta-analysis: one article9 due the fact that there was missing data, and we did not achieve contact with the authors, and the other14 only used real-time PCR to analyze the microorganism reduction. The four included studies evaluated the total viable bacteria count.10–13 Three studies10,12,13 evaluated Lactobacillus spp. counts and two studies10,13 evaluated mutans streptococci counts. Forest plots are presented in Fig. 2. The studies showed low heterogeneity in the total viable bacteria counts analysis and in the mutans streptococci counts analysis (). The Forest plots (Fig. 3) demonstrated that all of the meta-analyses presented a significant difference before and after aPDT. For the total viable bacteria count analyses, mean difference and 95% confidence interval was 1.32 [1.13, 1.51]; (). Mean difference and 95% confidence interval for mutans streptococci counts were 1.63 [1.05, 2.20]; () and were 1.50 [1.22, 1.79]; () for Lactobacillus spp.
aPDT has been gaining attention in research on alternative antimicrobial approaches, and studies have shown that aPDT has such properties.18,12,19 aPDT is effective in killing oral microorganisms present in dentine caries that are produced in situ and in vitro and may be useful in minimally invasive dentistry.20,21 Assuming that the in vitro and in situ techniques are effective, we suggest the following question: Is aPDT an effective coadjuvant therapy to reduce microorganisms in deep carious lesions? To answer this question, a systematic review and meta-analysis were carried out.
Systematic reviews and meta-analyses are important tools and are commonly used for scientific evidence of health practices. They are likely to be used with increasing frequency as current initiatives to share clinical trial data gain momentum and may be particularly important in reviewing controversial therapeutic areas.15 These types of studies also provide possible recommendations for future studies, evaluate the applied research methods, and provide a summary of evidence related to a specific intervention strategy.
Our systematic review and meta-analysis of the included studies clearly supported the hypothesis that aPDT is an effective coadjuvant tool in reducing microorganisms in the treatment of deep carious lesions. A significant reduction in microorganism counts was observed in all analysis, which highlights this method as a useful minimally invasive tool for dental clinicians.
The included studies used different clinical protocols. Longo et al.,11 Araújo et al.,12 and Steiner-Oliveira et al.14 did not describe the location point where the irradiation was carried out. Araújo et al.12 held a 1-min irradiation, divided into two irradiations of 30 s. However, it is not described whether or not irradiation was performed at a single point or two points in the cavity. The same author made an analysis of superficial and deep dentin, but the result when comparing to control was statistically different when the dentin was directly irradiated or not directly irradiated. Thus, it is suggested that new studies should evaluate if the irradiation at more than one point in the cavity results in a greater reduction of microorganisms or, if a single point of irradiation in the cavity is enough. The single irradiation point would be very beneficial, especially for treatment of primary teeth in pediatrics, because the shorter the chair time, the better. Furthermore, three of the six studies did not mention the removal of excess PS. Longo et al.11 and Melo et al.13 removed the excess before the irradiation, whereas Steiner-Oliveira et al.14 carried out the irradiation first, followed by the removal of PS excess.
In some studies, the reported data were confusing. Longo et al.11 used adults and children in their sample, however, they did not report the findings in each age group separately. Araújo et al.12 used a sample of children aged from 3 to 9-years old, however, it was not clear what type of teeth were studied since the children in this age group can present deciduous or permanent molars. This lack of information in both studies can raise questions such as what kind of teeth is aPDT more effective for, deciduous or permanent? Could the primary dentition respond to the treatment differently than the permanent dentition, and thus have different results? Based on these questions, we recommend future studies to confirm or refute these hypotheses.
The six evaluated studies presented potential risk of bias. Only Melo et al.13 followed all checklist recommendations reported by the CONSORT statement (consolidated standards of reporting trials).22 Only three studies supported their findings on sample size calculation.10,13,14 From the six selected and analyzed studies, four underwent randomization.9,11,13,14 Regarding the blinding of participants (single blind), Longo et al.,11 Melo et al.,13 and Steiner-Oliveira et al.14 followed this CONSORT recommendation for conducting microbiology analyses using blind counting of codified labeled samples (double blind) ensuring the absence of biased results.
From analyzing the aPDT parameters, we observed that the authors used different parameters, such as PS, light source, and dosimetry. Borges et al.9 and Melo et al.,13 used red light-emitting diode (LED) as a light source. Steiner-Oliveira et al.14 also used LED as a light source but only in the group of PS TBO (LEDTB). The light source is selected according to the type of PSs. In terms of costs, LED present advantages when compared with the laser sources. A difference in irradiation time was also used. However, all studies achieved positive results in reducing bacteria even while using different application times. This observation suggests that a protocol with a shorter exposure period would be highly advantageous. In the case of pediatric care, this would be a wonderful advantage as shortened chair time is a priority.
Despite the fact that the different aPDT parameters have been applied in different ways, all of the studies reached a reduction of most of the tested microorganisms, thus confirming the effectiveness of the use of aPDT as an adjunctive in the treatment of deep caries. However, among the observed reductions, some studies showed significant reductions and others did not, which may have been influenced by different parameters of aPDT. Guglielmi et al.10 and Araújo et al.12 used MB as a PS in their clinical protocol, and both placed the PS in contact with the teeth for 5 min before irradiation. Although these authors used different light sources, their results were similar.
Borges et al.9 and Melo et al.,13 in turn, used the same PS (TBO), the same light source, red LED, and the same dose of , but they used different output powers. Borges et al.9 used the output power of 40 mW, whereas Melo et al.13 used 150 mW. Thus, these different parameters used in the aPDT protocol may have influenced the difference in results for the species present in total microorganisms and for Lactobacillus. Both of them achieved reduction, however, only Melo et al.13 had a significant reduction.
Several PSs are used to achieve the antimicrobial effect during the application of aPDT, but MB and TBO have been the most commonly tested option in in vivo and in situ studies.20,23–25 In this context, it is important to analyze the absorption spectrum of the PS and the emission spectra of the light source to have an efficient photodynamic action. Guglielmi et al.10 and Steiner-Oliveira et al.,14 in one of their experimental groups, used MB and red low power LASER light source with a wavelength of 660 nm that is coincident with the absorption band of MB (610 to 660 nm).26 Araújo et al.12 also used MB, however, a halogen curing light unit was used, which emits white light that has an emission spectrum ranging between 500 and 800 nm. Melo et al.13 and Borges et al.9 used TBO and LED sources that provided the emission spectrum within the characteristic absorption range for this PS (590 to 630 nm).26 Longo et al.,11 in turn, used AlClPc and a red laser of 660 nm, which is coincident with the electromagnetic spectrum, in which the phthalocyanine group absorbs light (660 to 700 nm).26 However, Steiner-Oliveira et al.14 tested two PS s, TBO with LED and MB with a low-power laser. This study demonstrated that all therapies, including the control group, reduced the number of all tested microorganisms except for S. sobrinus, and no statistical differences were observed among the protocols. In turn, there are no differences between the LED and low-power laser parameters. For these authors, the main goal of aPDT is to perform a conservative treatment of deep caries lesions to reduce the number of microorganisms in the remaining affected dentin to avoid the need for endodontic treatment.
The preirradiation time of 5 min appears to be an important detail to reach the antibacterial effect of aPDT PS in regards to maintaining the inside bacteria, and this time enables greater absorption of light.27 Borges et al.9 showed that the use of a laser without a PS, and PS s in the absence of a light source, result in a minimal reduction in the amount of bacteria, without a significant effect on the reduction of microorganisms.
With regard to the volume of dentin analyzed, only Borges et al.9 and Melo et al.13 provided the dentin weight information. The weighing of each dentin can promote the standardization of the number of CFU/mg of dentin collected, and thus enables better comparisons. Based on this, we recommend that future studies weigh the dentin and evaluate the amount of CFU/mg of dentin that is analyzed.
Of all of the studies that used CFU as their counting method and to which we had access to the data, the study of Araújo et al.12 stood out for achieving the highest log reduction value.
This systematic review has grouped the data found in the selected studies, describing the parameters of the aPDT, and the species that each of the studies assessed. It was observed that, in the studies included in this review, the vast majority of bacteria investigated were of the Gram-positive genus, which are microorganisms likely to be affected by aPDT. This can be explained on the basis of the link mechanism of cell membrane, in a function of the structural variations in their cell walls. Gram-negative bacteria have an outer membrane complex that includes two lipid bilayers that serve as a physical and functional barrier between the cells and the environment, whereas Gram-positive cells are more sensitive and have a relatively permeable thickness of membrane.28
While analyzing the aPDT parameters used in the selected studies, we observed that different culture media and atmospheres for incubating the microorganisms were used. In relation to the way samples were transported to the laboratory for CFU analyses, Guglielmi et al.10 used the VMGA III, a transport media, Longo et al.11 selected BHI medium, whereas Araújo et al.12 performed immediate processing. Borges et al.9 and Melo et al.13 did not provide this information. All specimens must be promptly transported to the laboratory for CFU counts, preferably within 2 h. If processing is delayed, specimens collected for detection of bacterial agents may be stored under specified conditions.29 Generally, transport media provide a nonnutrient source that sustains the viability of both aerobic and anaerobic organisms without allowing significant growth.30 The BHI medium, used by Longo et al.11 as a transport media, is a nutritive base that is used to cultivate a wide variety of organisms.31 This medium can overestimate the number of CFU.
Although the results of these studies are encouraging, more in vivo studies are necessary to solve doubts regarding parameters such as irradiation time and whether the use of multiple irradiation points improves the use of this therapy in clinical settings.
The authors would like to thank the authors of the selected articles for the contribution of available data from their papers. We are indebted to Sarah Vinski who revised the text for grammar and style. This manuscript is part of the first author’s dissertation. L.A.A. was supported by Carlos Chagas Filho Foundation for Research Support of Rio de Janeiro State (FAPERJ-Jovem Cientista do Nosso Estado). The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article.
Pâmela Oliveira Ornellas is an MSc student at the School of Dentistry, Fluminense Federal University, Nova Friburgo, Rio de Janeiro, Brazil. Her main topic of research interest is the effect of the antimicrobial photodynamic therapy on microorganism reduction in deep caries lesions.
Leonardo Santos Antunes is an assistant professor in endodontic clinic at Fluminense Federal University, Nova Friburgo, Rio de Janeiro, Brazil. He received his MSc degree in dentistry in 2006 and his PhD in science in 2012 at Fluminense Federal University, Niterói, Rio de Janeiro, Brazil. His research interests are basically related to the applications of photodynamic therapy in dentistry, endodontic field, and dental genetics.
Karla Bianca Fernandes da Costa Fontes received her MSc and PhD degrees in oral pathology from the Fluminense Federal University, Niterói, Rio de Janeiro, Brazil, in 2007 and 2009, respectively. Currently, she is working as an assistant professor for oral pathology and oral medicine at Fluminense Federal University, Nova Friburgo, Rio de Janeiro, Brazil. Her research interests are basically related to the applications of photodynamic therapy and laser therapy in dentistry.
Helvécio Cardoso Corrêa Póvoa is an assistant professor for microbiology at Fluminense Federal University, Nova Friburgo, Rio de Janeiro, Brazil. He received his MSc degree in microbiology in 1999 from the University State of Rio de Janeiro, Rio de Janeiro, Brazil and his PhD in patology in 2008 from Fluminense Federal University, Niterói, Rio de Janeiro, Brazil. His research interests are basically related to the applications of photodynamic therapy in microbiology.
Erika Calvano Küchler is dental researcher in pediatric dentistry at the University of São Paulo, School of Dentistry of Ribeirão Preto, São Paulo, Brazil. She received her MSc degree in pediatric dentistry in Rio de Janeiro Federal University, Rio de Janeiro, Brazil and her PhD in science in Fluminense Federal University, Niterói, Rio de Janeiro, Brazil. Her research focuses are related to molecular and clinical dental research.
Natalia Lopes Pontes Iorio received her MSc and PhD degrees in microbiology from Rio de Janeiro Federal University, Rio de Janeiro, Brazil, in 2007 and 2011, respectively. Currently, she is working as an assistant professor for microbiology at Fluminense Federal University, Nova Friburgo, Rio de Janeiro, Brazil. Her research interests are basically related to the applications of photodynamic therapy in microbiology.
Lívia Azeredo Alves Antunes received her MSc and PhD degrees in pediatric dentistry from Rio de Janeiro Federal University, Rio de Janeiro, Brazil in 2006 and 2012, respectively. Currently, she is working as an assistant professor for pediatric dentistry at Fluminense Federal University, Nova Friburgo, Rio de Janeiro, Brazil. Her research interests are related to the applications of photodynamic therapy in dentistry, minimally invasive dentistry, quality of life, and dental genetics.