Antimicrobial Activity of a Formulation of Libidibia ferrea L. against Microorganisms of the Dental Biofilm

This study aimed to evaluate the antimicrobial activity of the extract of Libidibia ferrea L. (228.022-INPA) and a mouthwash formulation against microorganisms of the dental biofilm. The extract of Libidibia ferrea L. was prepared and formulated with an alcohol-free mouthwash. The Minimum Inhibitory Concentration—MIC was determined by microdilution and cell viability was evaluated through fluorescence. The MICs for the extract were 4.375 µg/mL (Streptococcus mutans), 3.750 µg/mL (Streptococcus oralis), 4.375 µg/mL (Lactobacillus casei). In contrast, for the mouthwash, the MICs were 6.000 µg/mL (bacteriostatic against Streptococcus mutans and bactericidal against Streptococcus oralis). In 1.250 µg/mL of the extract, the number of viable cells measured by fluorescence tests was 16.47% and 14.12% for Streptococcus mutans and Lactobacillus casei, respectively. For the mouthwash (1.000 µg/mL), 20.60% of viable cells for Streptococcus mutans, and 9.60% for Lactobacillus casei were observed. It can be concluded that the extract and its mouthwash containig Libidibia ferrea L. showed antibacterial activity against microorganisms from the dental biofilm.


Introduction
Dental biofilm is formed in an orderly manner, possessing a diversified and How to cite this paper: de Oliveira Marreiro, R., Bandeira, M.F.C.L., Toda, C., Sampaio, F.C., de Souza, T.P., Venâncio Advances in Microbiology, 10, 434-442. https://doi.org/10.4236/aim.2020.109032 complex microbial composition that, over time, remains relatively stable, known as microbial homeostasis. The tangle of various synergistic and antagonistic interactions leads to microbial interdependencies providing resilience to the biofilm so that changes in competitiveness among oral microorganisms can lead to the dysbiosis occurrence, and this has a vital role in the development of diseases such as caries and periodontal disease [1].
The variety of natural products is an important source in the search for bioactive compounds. Plants have a wide range of secondary metabolites relevant to drug discovery for various diseases and infections by microorganisms [2].
In Brazil, medicinal plants are evidenced as an incalculable cultural heritage and represent an essential resource for the health of the population. The Amazon stands out for having high biodiversity, popular and traditional knowledge of medicinal plants, making natural products the basis for disease prevention and treatment [3] [4] [5].
Several types of research using Amazonian flora plants have been carried out to prove their efficacy as an antibacterial agent on microorganisms of dental biofilm [6] [7] [8].
Libidibia ferrea is a plant species widely used in folk medicine, popularly known as "Juca" or "ironwood". Currently, the scientific name for this species is Libidibia ferrea (Mart. Ex Tul.) L.P. Queiroz var. ferrea, whose basionym is Caesalpinia ferrea Mart. ex Tul. (Caesalpiniaceae). It is a species of the Leguminosae family, one of the largest among the dicotyledons, found in Brazil's tropical regions, especially in the North and Northeast [9]. To verify the chemical compounds of the hydroalcoholic extract of L. ferrea, studies on the phytochemical profile indicated the presence of flavonoids, saponins, steroids, tannins, and coumarins that have a high antioxidant and enzymatic potential [10].
In addition, through chromatographic and spectrophotometric analysis of phenolic compounds from fruits of Libidibia ferrea Martius it was observed that its main constituents are hydrolyzable tannins (gallic acid and ellagic acid). Performing the qualitative analysis, the separation and identification of these markers was verified and the quantitative analysis of the phenolic compounds allowed their quantification by ultraviolet/visible [11]. The present study evaluated the antimicrobial activity of the extract and a mouthwash formulation from Libidibia ferrea L. extract on microorganisms in the oral cavity.

Mouthwash formulation
The botanical species Libidibia ferrea L. The preparation of the Libidibia ferrea L. mouthwash followed the methodology proposed by [12], being defined as the concentration of 1% of the extract of Libidibia ferrea L. in the mouthwash solution. The other components were: sodium benzoate (0.06 g), saccharin (0.03 g), glycerin (0.8 ml), 80% tween (0.08 ml), 20% tween (0.08 ml), oil of mint (0.08 mL) and distilled water (20 mL). Evaluation of the minimum inhibitory concentration (MIC) of the extract and mouthwash of Libidibia ferrea L. The microorganisms used were: Streptococcus mutans (ATCC25175), Streptococcus oralis (ATCC10557), Streptococcus salivarius (ATCC7073) and Lactobacillus casei (ATCC7469), provided by the laboratory of the National Institute for Health Quality Control of the Oswaldo Cruz Foundation (Rio de Janeiro).
The microorganisms were reactivated in BHI (Brain Heart Infusion-DIFCO) nutrient agar broth, in 10 × 150 mm test tubes, incubated at 37˚C for 24 hours in aerophilic, for S. oralis, S. salivarius, and L. casei, and in microaerophilia for S. mutans. The entire procedure was performed in a laminar flow hood. Aliquots of the bacteria were removed with a sterile platinum loop of 5 mm in diameter and inoculated in 5 mL of sterile BHI broth in 10 × 150 mm test tubes. The suspensions were vortexed until they became homogeneous. The inoculum was standardized using the McFarland # 0.5 scale to provide a 10 8 CFU/mL standard.
The antimicrobial activity of the Libidibia ferrea L. extract and mouthwash was determined according to the Minimum Inhibitory Concentration (MIC) methodology in microdilution proposed by [13] [14], adapted by [8]. The 0.12% chlorhexidine digluconate was used as a positive control. 96-hole microplates ("U" shaped) were used so that each well had a final volume of 100 µL. On the plaque, the columns were distributed in the numbers 1 to 12 and the lines in the letters "A" to "H". The juca extract and rinse were distributed in the wells to contain the different concentrations of the test substances. The dilution system was controlled by the volume of the test products, occupying wells 2 to 11. In the same wells, a standard volume of inoculum (20 µL) was added, and the final volume was supplemented with the medium.
Column 01 represented the sterility of the test substance, rinse or extract + medium without bacteria. Column 12 represented the viability of the bacteria, medium + inoculum, without test product. Line G represented the vehicle (negative control) and line H the 0.12% chlorhexidine digluconate (positive control). A single microplate was used for each microorganism, and the jucá rinse was tested on lines A, B, and C and jucá extract on lines E, F, and G.
After filling all wells, the microplates were sealed with parafilm and incubated at 370 C for 24 hours, in aerophilic for S. oralis, L. casei and S. salivarius, and in microaerophilia for S. mutans. After the incubation period, 30 µL of resazurin reagent prepared in aqueous solution (0.01%, 10 mg diluted in 100 mL) were included in the wells. The plates were again incubated for 30 minutes. The absence of color change in the holes was interpreted as a microorganism sensitive to the tested solution. To verify the minimum inhibitory concentration activity (MIC), when possible, 100 µL were removed from the wells referring to the mouthwash/juca extract in different concentrations (lines C and G, respectively), sown in Petri dishes with BHI agar and incubated at 37˚C in aerophilia and microaerophilic, according to the microorganism tested, for 24 hours to confirm the presence of viable bacteria.
Cell viability analysis by fluorescence technique The cell viability activity of the 0.6% extract and the 1% Libidibia ferrea L.
mouthwash were determined according to the fluorescence methodology proposed by [15] against S. mutans (UA 159-2-ATCC 700610) and L. casei (ATCC7469). Solutions were prepared for the extract, and the mouthwash established as Mother Solution (extract /mouthwash + BHI medium in the proportion of 1:1).
The cell viability test required MIC to be performed as described in the previous topic. The MICs of the extract and mouthwash solutions were determined in different concentrations. From the result of the MICs of the extract and the jucá mouthwash, the observation of cell viability of these concentrations was re-evaluated by reading fluorescence through the LIVE/DEAD® BacLight™ Bacterial Viability Kit L13152 (Molecular Probes, Eugene, United States). In this system, viable cells without damage to the cell wall are stained green (Component A: SYTO 9), and red (Component B: propidium iodide) are the cells with damage to the cell membrane. Bacterial suspensions were prepared to construct the standard curve, through known concentrations of viable bacteria and dead cells. Two falcon® tubes containing 3 mL of BHI broth with the reactivated bacteria were centrifuged for 15 minutes, after which the supernatant was removed, and the precipitate was resuspended with 240 µL of NaCl and homogenized in the Vortex®. Then 4.8 mL of NaCl was added to the tube representing live bacteria, and in the other tube representing the dead cells, 4.8 mL of 70% isopropyl alcohol was added. The two tubes were incubated at room temperature for 60 minutes with shaking every 15 minutes. They were again centrifuged for another 15 minutes, and the supernatant removed and the precipitate resuspended with 2.4 mL of NaCl.
Bacterial cell patterns were prepared by proportions of known concentrations of viable bacteria: dead cells with 0:100 (0 viable bacteria per 100 dead cells); 20:80; 50:50; 80:20 and 100:0, respectively. 96-well plates of black color for luminosity control (Greiner-Bio-One) were used to construct the standard curves. The proportions of concentration of live bacteria and dead cells were placed in wells A1 to A5. In wells B1 to B5, 100 µL of the aliquots of the MIC result were placed, considering two concentrations ahead and two after. Equal volumes of SYTO9 and Propidium Iodide were mixed in a miniature vortex/mixer (Thomas Scientific, New Jersey, USA) that reaches a speed of 2.800 rpm for 3 minutes. A volume of 30 μL of the mixture was added to the fluorescence plate. The wells were then incubated in the dark and at room temperature for 15 min. The reading was performed by fluorescence intensity through the multi-mode microplate reader (FLUORStar Optima, BMGLab Tech, Germany) under an excitation filter of 485 nm and emission with 520 and 620 nm to detect green and red respectively. The results obtained were tabulated and presented through a descriptive analysis [16].

Results and Discussion
The evaluation of the antibacterial activity of the Libidibia ferrea L. extract and mouthwash against strains of Streptococcus mutans, Streptococcus oralis, Streptococcus salivarius, and Lactobacillus casei, using the microdilution test in microplate showed that the extract of Libidibia ferrea L. to 0.6% showed bactericidal antibacterial activity against S. mutans, S. oralis and L. casei at concentrations of 4.375 µg/mL; 3.750 µg/ml; 4.375 µg/mL, respectively. This result reinforces the study by [17] in which they proposed a formulation of a mouthwash using Juca extract, concluding that this product is viable. Considering the good results achieved in the study about the antimicrobial activity against S. mutans, and S. oralis. Regarding S. salivarius, there was no activity of extract and formulation.
The juca mouthwash showed bacteriostatic activity against S. mutans and bactericide for S. oralis at a concentration of 6.000 µg/mL for both. However, against L. casei, no inhibitory activity was observed. Sterility checks of the test product + medium were performed on the four plates used to assess MIC, in column 1; in column 12, the viability of the inoculum + medium, with a more It must be pointed out that the CBM did not coincide with the MICs, concerning the fluorescence results, which may be due to the performance of two methodologies with different readings, being the most accurate fluorescence technique, since the reading is performed with the use of a reader such as flow cytometer, spectrofluorometer, microplate reader and Optrode, a fiber-based spectroscopic system and not only visual [18]. It is a quick alternative to standard culture-based tests, using fluorescent dyes, which includes the evaluation of membrane potential and its integrity. It has advantages such as the quantification of cell death directly, in almost real-time, and not retrospectively from the knowledge of the colonies formed [18] [19] [20]. Besides, this seems to be the best proven and appropriate method for biofilm research [21].
The MIC test used was based on a colorimetric methodology and, therefore, the turbidity in which the method is compared to the standards generally of the Macfarland 0.5 scale is not able to give a standardized number of CFU for all strains. Therefore, reading is subjective. It also makes it difficult to compare different bacterial species as they have different optical densities [22]. Studies carried out to compare different techniques associated with inoculum standardization have shown that this standardization has a good correlation in the CFU count. However, it is not configured as a precision technique, as its reliability depends on subjective factors, such as training the observer, for example, adding uncertainties to the method [23].
In light of the above limitations, more robust techniques are necessary. According to the study by [21], the assessment of colony-forming units is not in- The non-activity verified against S. salivarius seems to be a satisfactory result considering that this microorganism represents one of the first ones in the initial colonization in the mucosa and the formation of biofilm [24]. Still, both the extract and the mouthwash was effective against L. casei, S. oralis, and S. mutans, the latter being considered the main bacterial species involved in the formation of the biofilm. Together, S. mutans and Lactobacillus, are particularly useful in the process of transforming sugar into acid thanks to the ability to be acidophilic bacteria [25] [26].
According to [27], the control of the growth of Streptococcus mutans causes a significant reduction in the formation of biofilm in the teeth. Its control can be adequately done by chemical and mechanical means. [28], emphasize the importance of therapeutic indications as a low cost and alternative method for the control of biofilm, which opens the way for research with products derived from medicinal plants.
Numerous studies such as [5] [17] [29] and [30], have already evaluated the antimicrobial activity of plant extracts from the Amazon in order to bring alternatives of chemical agents of natural origin for the control of dental biofilm and thus favor the maintenance of oral health.
Based on the results of the methodology used, it was possible to conclude that the Libidibia ferrea L. mouthwash showed antibacterial activity against the biofilm microorganisms tested.