Application of Three Compounds Extracted from Cynodon dactylon against Streptococcus mutans Biofilm Formation to Prevent Oral Diseases

Streptococcus mutans bacteria form a biofilm called plaque that causes oral diseases, including tooth decay. Therefore, inhibition of biofilm formation is essential to maintaining good oral health. The health and nutritional benefits of Cynodon dactylon are well documented, but very little is known about its use to treat against oral diseases. The aim of this study was to detect the adhesion strength of the S. mutans bacterial biofilm in 100 cases in the Rajshahi region and evaluate the inhibitory activity of different compound extracts of C. dactylon on the S. mutans bacterial biofilm by determining the composition of isolated compounds using phytochemical analysis. Nuclear magnetic resonance (NMR) spectroscopy confirmed that three specific compounds from C. dactylon were discovered in this study: 3,7,11,15 tetramethyl hexadec-2-4dien 1-o1, compound 3,7,11,15 tetramethylhexadec-2-en-1-o1 from phytol derivatives, and stigmasterol. Results indicated that the compound of 3,7,11,15-tetramethyl-hexadec-2-en-1-ol exhibited higher antibiofilm activities on S. mutans than those of the other compound extracts. A lower level of minimum inhibitory concentration was exposed by 3, 7, 11,15 tetramethyl hexadeca-2-en-1-o1 (T2) on S. mutans at 12.5 mL. In this case, the compound of 3,7,11,15 tetramethyl hexadec 2en-1-o1 was used, and patients showed a mean value and standard error reduced from 3.42 ± 0.21 to 0.33 ± 0.06 nm. The maximum inhibition was (80.10%) in the case of patient no. 17, with a value of p < 0.05 found for S. mutans to which 12.5 μL/mL ethyl acetate extract was applied. From these findings, it may be concluded that C. dactylon extracts can be incorporated into various oral preparations to prevent tooth decay.


Introduction
Microbial biofilms are intricate bacterial colonies in the environment and the human body. Oral infectious diseases are the biggest problems of dental health care and are intimately related to microbial colonization and the development of pathogenic biofilms such as pulp infection, tooth decay (dental caries), periodontitis, induced wound infection, peri-implantitis, and tooth staining [1][2][3][4]. More than 3.5 billion people are affected by oral disorders, which significantly lower the quality of life, particularly in many low-and middle-income nations [1,[5][6][7][8][9]. Dental plaque has been recognized as a biofilm in recent years [10]. Oral biofilm is the three-dimensional arrangement of various microorganisms residing in the mouth cavity. All tissues and surfaces in the mouth cavity can be adhered to by bacterial biofilms. Human tooth decay and the inflammatory degeneration of the alveolar bone are caused by oral biofilms [11]. If the biofilm remains untreated, it can and allergic effects [26] and is used as a rejuvenator for wound healing [27]. Plants like C. dactylon contain a large number of chemicals like organic compounds, e.g., alkaloids, flavonoids, glycosides, ß-sitosterol, and carotene, stigmasterol, phytol, fryer phenols, etc. The antibacterial activities of C. dactylon are primarily attributed to a particular extract that contains quinines, tannins, and phenols. Phenolic aldehydes are used as a secondary metabolite that acts as a defensive mechanism against respective pathogens [26,27] and acts as a bioactive, chemotherapeutic, bactericidal, and bacteriostatic agent [28]. Thus, one of the key goals of dental practitioners, essential to maintaining excellent oral health, is control of dental plaque biofilm. This study also aimed to determine the antimicrobial and antibiofilm effectiveness of different compounds of C. dactylon against the biofilm of S. mutans because dental plaque cannot be developed without the growth of these bacteria.

Culture Media
Mitis Salivarius Base (MSB) agar and Luria Bertani (LB) media were used to selectively isolate and identify Streptococcus mutans selectively. First, 90.07 g MSB agar base powder was suspended in 1000 mL of distilled water, heated to boil it properly, and sterilized by autoclaving at 121 • C for 15 min. Next, the MSB media was cooled to 50-55 • C, 1 mL of sterile potassium tellurite solution was added, and the mixture was poured into sterile Petri plates.

Collection of Dental Plaque Samples from Patients
Dental plaque samples were collected from 100 individuals having various oral complications patients attending the outdoor Department of the Dental Unit at Rajshahi Medical College and Hospital, Bangladesh. As part of these 100 individuals, 32 children (approximately 1 to 10 years old) 41 teenagers (11 to 18 yearsrs old), and 27 adults were selected for this study as the WHO (World Health Organization) reported that 60 to 90% of children and young adults affected by dental caries have S. mutans bacterial biofilm to a greater extent than adults [29]. Therefore, among all the 100 cases, 2 (case numbers 17 and 55) were selected for further analysis. The plaques were spread on each Petri plate containing MSB selective media and incubated at 37 • C for 72 h.

Formation of S. mutans Bacterial Biofilm by Microtiter Plate and Microtiter Spectrophotometric Biofilm Production Methods
The biofilm assay was performed following the O'Toole protocol with slight changes [30]. Briefly, four to five mL liquid LB medium was taken to each test tube, and a single colony of S. mutans was added and incubated at 37 • C for 24 h at 120 rpm. The overnight culture was diluted at 1:100 into fresh LB medium for biofilm assays. Then, the cultures were distributed in flat-bottom 96-well polystyrene microtiter plates in triplicate at 200 µL per well (Figure 1). Two other strains named Pseudomonas aeruginosa and Escherichia coli were selected for control samples in this study for biofilm formation. P. aeruginosa is a Gram-negative aerobic non-spore-forming rod and E. coli is a facultative Gram-negative rodshaped bacterium. These two bacteria were collected from the stock bacterial culture of the molecular pathology laboratory of the Institute of Biological Sciences, Rajshahi University. The microtiter plate was incubated at 37 • C for 24 h. After incubation, planktonic cells were aspirated and washed three times with sterile saline (0.9%). The biofilms were fixed with 99% methanol for 15 min and were stained with 200 µL of 0.1% crystal violet for 15 min. The excess crystal violet was drained and biofilms were washed thrice with tap water and air dried. Finally, the adherent cell-bound crystal violet was dissolved by adding 200 µL of 33% glacial acetic acid to each well, and biofilms were quantified using a microplate reader at OD 595 .

Collection and Preparation of Cynodon dactylon
Cynodon dactylon was collected from the Botanical Garden of Rajshahi University campus, Rajshahi, Bangladesh, and my supervisor confirmed the conformity of collected plants. C. dactylon was thoroughly washed with tap water, rinsed with distilled water, and air dried in a shady place. Finally, it was pulverized to fine powder using a grinding machine. Ethyl acetate was added with the pulverized C. dactylon and filtrated using Whatman 0.45 μm filter paper. The filtrated crude extracts were dried and stored for further use.

Isolation and Purification of Compounds from C. dactylon
This study was conducted at the Insect Biotechnology and Molecular Pathology Laboratory, Institute of Biological Sciences, Rajshahi University, and Rajshahi Dental College. The compounds were isolated and purified using column chromatographic techniques, following the protocol described in the flow chart ( Figure 2). The dry columns were prepared with silica gel and solvents such as n-hexane, acetone, ethyl acetate, etc., were used. The extracted compounds were identified using gas chromatography-mass spectrometry (GC-MS) analysis, and structure determination was conducted by using nuclear magnetic resonance (NMR) analysis. Here, we provide the spectral data of 1H NMR and C-13 NMR spectroscopy with the chemical structure of the compound of 3,7,11,15 tetramethyl hexadec-2,4 dien 1-o1, 3,7,11,15 tetramethyl hexadec 2en-1-o1 from phytol derivatives, and stigmasterol according to Ahmed et al. [31] as well as Subavathy and Thilaga [32].

Collection and Preparation of Cynodon dactylon
Cynodon dactylon was collected from the Botanical Garden of Rajshahi University campus, Rajshahi, Bangladesh, and my supervisor confirmed the conformity of collected plants. C. dactylon was thoroughly washed with tap water, rinsed with distilled water, and air dried in a shady place. Finally, it was pulverized to fine powder using a grinding machine. Ethyl acetate was added with the pulverized C. dactylon and filtrated using Whatman 0.45 µm filter paper. The filtrated crude extracts were dried and stored for further use.

Isolation and Purification of Compounds from C. dactylon
This study was conducted at the Insect Biotechnology and Molecular Pathology Laboratory, Institute of Biological Sciences, Rajshahi University, and Rajshahi Dental College. The compounds were isolated and purified using column chromatographic techniques, following the protocol described in the flow chart ( Figure 2). The dry columns were prepared with silica gel and solvents such as n-hexane, acetone, ethyl acetate, etc., were used. The extracted compounds were identified using gas chromatography-mass spectrometry (GC-MS) analysis, and structure determination was conducted by using nuclear magnetic resonance (NMR) analysis. Here, we provide the spectral data of 1H NMR and C-13 NMR spectroscopy with the chemical structure of the compound of 3,7,11,15 tetramethyl hexadec-2,4 dien 1-o1, 3,7,11,15 tetramethyl hexadec 2en-1-o1 from phytol derivatives, and stigmasterol according to Ahmed et al. [31] as well as Subavathy and Thilaga [32].

Collection and Preparation of Cynodon dactylon
Cynodon dactylon was collected from the Botanical Garden of Rajshahi Univer campus, Rajshahi, Bangladesh, and my supervisor confirmed the conformity of collec plants. C. dactylon was thoroughly washed with tap water, rinsed with distilled water, a air dried in a shady place. Finally, it was pulverized to fine powder using a grind machine. Ethyl acetate was added with the pulverized C. dactylon and filtrated us Whatman 0.45 μm filter paper. The filtrated crude extracts were dried and stored further use.

Isolation and Purification of Compounds from C. dactylon
This study was conducted at the Insect Biotechnology and Molecular Pathol Laboratory, Institute of Biological Sciences, Rajshahi University, and Rajshahi Den College. The compounds were isolated and purified using column chromatograp techniques, following the protocol described in the flow chart ( Figure 2). The dry colum were prepared with silica gel and solvents such as n-hexane, acetone, ethyl acetate, e were used. The extracted compounds were identified using gas chromatography-m spectrometry (GC-MS) analysis, and structure determination was conducted by us nuclear magnetic resonance (NMR) analysis. Here, we provide the spectral data of NMR and C-13 NMR spectroscopy with the chemical structure of the compound 3,7,11,15 tetramethyl hexadec-2,4 dien 1-o1, 3,7,11,15 tetramethyl hexadec 2en-1-o1 fr phytol derivatives, and stigmasterol according to Ahmed et al. [31] as well as Subava and Thilaga [32].

Prevention of S. mutans Biofilm Using Different Compounds Extracted from C. dactylon
Biofilms were produced from bacteria grown on MSB medium using a microplatebased system in an in vitro model, which detected the adhesion strength of the biofilm developed by S. mutans in the 100 studied samples. Case 17, a 9-year-old, had the greatest adhesive forces with the underlying substratum of LB media (4.12 ± 0.31), while case 55, a 35-year-old, had the greatest adhesive forces of S. mutans bacterial biofilm with the substratum of LB media with the mean value 4.32 ± 0.19. Therefore, these two cases were selected to observe the inhibitory effects of the three compounds derived from ethyl acetate extract. Minimum inhibitory concentration (MIC) of the extracts was determined using a broth dilution technique as described by Adikwu et al. [28]. Twofold serial dilutions of the extracts were prepared by adding 5 mL of 100 mg/mL of the extract into a test tube containing 5 mL of nutrient broth and mixed vigorously, thus producing a solution containing 50 mg/mL of the extract. The process continued serially up to the fifth test tube and the last 5 mL was discarded, leaving equal volume in the tubes, hence producing the following concentrations: 50, 25 and 12.5 mg/mL. McFarland standards of test organisms were introduced into the disc and incubated at 37 • C for 24 h.

Statistical Analysis
All the information is stated as mean ± SE (standard error) of the mean. Statistical analysis was performed using SPSS software (version 16). The significance of differences and comparisons among the mean values were determined by Duncan's multiple range tests (DMRT) as well as the p-value reached from the DMRT test at a 1% level (p < 0.01). The isolated compound was determined using nuclear magnetic resonance (NMR) spectroscopy and the microtiter spectrophotometric biofilm method measured the adhesion strength (nanometer).

Microbiological Investigation
Dental plaques and saliva samples were collected from patients from the dental unit of Rajshahi Medical College and Hospital, spread on an MSB (mitis salivarius bacitracin) medium, and inoculated with long-chain purple-colored Streptococcus mutans bacterial colonies. The isolates showed Gram-positive Cocci in chains with hard, raised, convex pale blue colonies with a frosty glass appearance ( Figure 3).

Prevention of S. mutans Biofilm Using Different Compounds Extracted from C. dactylon
Biofilms were produced from bacteria grown on MSB medium using a microplatebased system in an in vitro model, which detected the adhesion strength of the biofilm developed by S. mutans in the 100 studied samples. Case 17, a 9-year-old, had the greatest adhesive forces with the underlying substratum of LB media (4.12 ± 0.31), while case 55, a 35-year-old, had the greatest adhesive forces of S. mutans bacterial biofilm with the substratum of LB media with the mean value 4.32 ± 0.19. Therefore, these two cases were selected to observe the inhibitory effects of the three compounds derived from ethyl acetate extract. Minimum inhibitory concentration (MIC) of the extracts was determined using a broth dilution technique as described by Adikwu et al. [28]. Twofold serial dilutions of the extracts were prepared by adding 5 mL of 100 mg/mL of the extract into a test tube containing 5 mL of nutrient broth and mixed vigorously, thus producing a solution containing 50 mg/mL of the extract. The process continued serially up to the fifth test tube and the last 5 mL was discarded, leaving equal volume in the tubes, hence producing the following concentrations: 50, 25 and 12.5 mg/mL. McFarland standards of test organisms were introduced into the disc and incubated at 37 °C for 24 h.

Statistical Analysis
All the information is stated as mean ± SE (standard error) of the mean. Statistical analysis was performed using SPSS software (version 16). The significance of differences and comparisons among the mean values were determined by Duncan's multiple range tests (DMRT) as well as the p-value reached from the DMRT test at a 1% level (p < 0.01). The isolated compound was determined using nuclear magnetic resonance (NMR) spectroscopy and the microtiter spectrophotometric biofilm method measured the adhesion strength (nanometer).

Microbiological Investigation
Dental plaques and saliva samples were collected from patients from the dental unit of Rajshahi Medical College and Hospital, spread on an MSB (mitis salivarius bacitracin) medium, and inoculated with long-chain purple-colored Streptococcus mutans bacterial colonies. The isolates showed Gram-positive Cocci in chains with hard, raised, convex pale blue colonies with a frosty glass appearance ( Figure 3).

Extraction of Compounds from C. dactylon
The crude extract of C. dactylon and purified products were run through thin-layer chromatography. After finishing this procedure, several compound bands are visualized on the TLC plate after being eluted with a mixture of two solvents sprayed with vanillinsulfuric acid reagents. These compounds were run through on the TLC plate to obtain specific bands of the molecules. The compounds' names were confirmed by the spectral data of 1H NMR and C-13 NMR spectroscopy. The chemical structures of the three compounds were compared by gas chromatography-mass spectrometry (GC-MS) analysis. The results are displayed in Figures 4 and 5, respectively.

Extraction of Compounds from C. dactylon
The crude extract of C. dactylon and purified products were run through thin-layer chromatography. After finishing this procedure, several compound bands are visualized on the TLC plate after being eluted with a mixture of two solvents sprayed with vanillinsulfuric acid reagents. These compounds were run through on the TLC plate to obtain specific bands of the molecules. The compounds' names were confirmed by the spectral data of 1H NMR and C-13 NMR spectroscopy. The chemical structures of the three compounds were compared by gas chromatography-mass spectrometry (GC-MS) analysis. The results are displayed in Figures 4 and 5, respectively.  tetramethylhexadec-2,4 dien-1-o1, (B) single band for 3, 7, 11, 15 tetramethylhexadec-2-en-1-o1, and (C) single band for stigmasterol which was confirmed by 1 H nuclear magnetic resonance (NMR) and C-13 NMR spectrometry at the Department of Microbiology, Jahangirnagar University, Bangladesh. Figure 5 shows that each lane contains several brands expressing a mixture of several compounds. These compounds were further run through TLC to obtain the specific brands of the molecules. Figure 5 displays the three compounds obtained from the ethyl acetate extract of C. dactylon-3, 7,11,15 tetramethylhexdec-2,4 dien-1-o1 ( Figure 5A) as a dark blue color, 3,7,11,15 tetramethylhexadec-2en-1-o1 from phytol derivatives ( Figure  5B) as a light blue color, and stigmasterol ( Figure 5C) as a green color-after being subjected to the solvent system in n-hexane:acetone (7:2) sprayed with a vanillin-sulfuric acid reagent.
The isolated compounds were subjected to several analyses, including different spectroscopic analyses such as 1 H nuclear magnetic resonance (NMR) and C-13 NMR spectroscopy, accomplished by utilizing Bruker 600 and 400 MHz instruments and

Extraction of Compounds from C. dactylon
The crude extract of C. dactylon and purified products were run through thin-layer chromatography. After finishing this procedure, several compound bands are visualized on the TLC plate after being eluted with a mixture of two solvents sprayed with vanillinsulfuric acid reagents. These compounds were run through on the TLC plate to obtain specific bands of the molecules. The compounds' names were confirmed by the spectral data of 1H NMR and C-13 NMR spectroscopy. The chemical structures of the three compounds were compared by gas chromatography-mass spectrometry (GC-MS) analysis. The results are displayed in Figures 4 and 5, respectively.  tetramethylhexadec-2,4 dien-1-o1, (B) single band for 3, 7, 11, 15 tetramethylhexadec-2-en-1-o1, and (C) single band for stigmasterol which was confirmed by 1 H nuclear magnetic resonance (NMR) and C-13 NMR spectrometry at the Department of Microbiology, Jahangirnagar University, Bangladesh. Figure 5 shows that each lane contains several brands expressing a mixture of several compounds. These compounds were further run through TLC to obtain the specific brands of the molecules. Figure 5 displays the three compounds obtained from the ethyl acetate extract of C. dactylon-3, 7,11,15 tetramethylhexdec-2,4 dien-1-o1 ( Figure 5A) as a dark blue color, 3,7,11,15 tetramethylhexadec-2en-1-o1 from phytol derivatives ( Figure  5B) as a light blue color, and stigmasterol ( Figure 5C) as a green color-after being subjected to the solvent system in n-hexane:acetone (7:2) sprayed with a vanillin-sulfuric acid reagent.
The isolated compounds were subjected to several analyses, including different spectroscopic analyses such as 1 H nuclear magnetic resonance (NMR) and C-13 NMR spectroscopy, accomplished by utilizing Bruker 600 and 400 MHz instruments and tetramethylhexadec-2,4 dien-1-o1, (B) single band for 3, 7, 11, 15 tetramethylhexadec-2-en-1-o1, and (C) single band for stigmasterol which was confirmed by 1 H nuclear magnetic resonance (NMR) and C-13 NMR spectrometry at the Department of Microbiology, Jahangirnagar University, Bangladesh. Figure 5 shows that each lane contains several brands expressing a mixture of several compounds. These compounds were further run through TLC to obtain the specific brands of the molecules. Figure 5 displays the three compounds obtained from the ethyl acetate extract of C. dactylon-3, 7,11,15 tetramethylhexdec-2,4 dien-1-o1 ( Figure 5A) as a dark blue color, 3,7,11,15 tetramethylhexadec-2en-1-o1 from phytol derivatives ( Figure 5B) as a light blue color, and stigmasterol ( Figure 5C) as a green color-after being subjected to the solvent system in n-hexane:acetone (7:2) sprayed with a vanillin-sulfuric acid reagent.
The isolated compounds were subjected to several analyses, including different spectroscopic analyses such as 1 H nuclear magnetic resonance (NMR) and C-13 NMR spectroscopy, accomplished by utilizing Bruker 600 and 400 MHz instruments and reported in CDCl3, recorded on a Bruken advance 11,400 NMR spectrometer at the Department of Microbiology, Jahangirnagar University, Bangladesh. CDCl3 is a trichloromethane (chloroform) molecule in which the hydrogen has been replaced by its isotope deuterium and is commonly used as the solvent in proton NMR. NMR signals are analyzed with respect to two characteristics such as intensity and frequency (megahertz (MHz) are usually used for the measurement of absolute frequencies); all of the data are presented in Figures 6-8. After completion of structure determination by NMR spectroscopy, it was confirmed that the active compounds were 3,7,11,15 tetramethyl hexadec-2,4 dien 1-o1 (T 1 ), 3,7,11,15 tetram-ethyl hexadec 2en-1-o1 (T 2 ) from phytol derivatives, and stigmasterol (T 3 ) following the standard protocol of Ahmed et al. [31] as well as that of Subavathy and Thilaga [32] by gas chromatography-mass spectrometry (GC-MS) analysis.

Spectral Analysis of the Compounds from C. dactylon
The three isolated compounds from the ethyl acetate extract of C. dactylon are shown in Figure 6. Analysis of the ChemDraw spectrum of the phytol derivative compound (3, 7, 11, 15 ttramethylhexadeca-2-4 dien 1-01) showed six olefinic protons at δ 5.15, 5.03, and 5.96 and 5.03, 5.70, and 4.97, corboxic acid at 11.0 ppm as the primary amine proton, and δ 2.0 generally disposed the methyl proton at δ 1.33 as a singlet. Figure 7 shows the analysis of the phytol derivative compound 3, 7, 11, 15 tetramethyhexadeca 2-en-1-o1; six olefinic protons were revealed, similar to compound 3, 7, 11, 15 tetramethyhexadeca-2-4 dien 1-o1, and two methyl protons were observed at δ 3.23 and 3.24.  The 1H and C-13 NMR spectra of these two compounds are presumed to indicate all peaks present in these two compounds of phytol derivatives with some impurities. In the case of Figure 8, we revealed that the C-13 NMR spectrum of stigmasterol showed recognizable signals at 19.064, 40.543, 121.321, 129.341, 138.404, and 140.943 ppm. Finally, the nomenclature of these above three compounds was confirmed by comparing it with some data obtained from a previous study conducted by Ahmed et al. [31] as well as Subavathy and Thilaga [32] using gas chromatography-mass spectrometry (GC-MS) analysis. The main compound is 3, 7, 11, 15-tetramethyl-headeca-2-en-1-o1 (
The 1H and C-13 NMR spectra of these two compounds are presumed to indicate all peaks present in these two compounds of phytol derivatives with some impurities. In the case of Figure 8, we revealed that the C-13 NMR spectrum of stigmasterol showed

Patient Status with Dental Plaque and Oral Hygienic Grounds for Biofilm Formation
For biofilm formation, 100 cases were enumerated and their dental plaque and oral hygienic conditions were observed. Among these 100 cases, there were females 44 and 56 males (Appendix A). All the patients' ages were divided into six groups. So, among these 100 patients, 28 were 5 to 10 years old, 23 were 11 to 16 years old, 17 were 17 to 22 years old, 14 were 23 to 28 years old, 10 were 29 to 34 years old, and 8 were 35 to 40 years old. In terms of dental plaque, mild, moderate, and severe scores were obtained. This study included patients with different oral hygiene agreements such as good, average, and poor. Of the patients, 10 cases (case numbers 4, 17, 24, 33, 55, 63, 68, 80, and 93) had severe plaque; approximately 38 cases had moderate plaque, and the rest of cases (52) had mild plaque. Finally, the nomenclature of these above three compounds was confirmed by comparing it with some data obtained from a previous study conducted by Ahmed et al. [31] as well as Subavathy and Thilaga [32] using gas chromatography-mass spectrometry (GC-MS) analysis. The main compound is 3, 7, 11, 15-tetramethyl-headeca-2-en-1-o1 (Table 1).

Patient Status with Dental Plaque and Oral Hygienic Grounds for Biofilm Formation
For biofilm formation, 100 cases were enumerated and their dental plaque and oral hygienic conditions were observed. Among these 100 cases, there were females 44 and 56 males (Appendix A). All the patients' ages were divided into six groups. So, among these 100 patients, 28 were 5 to 10 years old, 23 were 11 to 16 years old, 17 were 17 to 22 years old, 14 were 23 to 28 years old, 10 were 29 to 34 years old, and 8 were 35 to 40 years old. In terms of dental plaque, mild, moderate, and severe scores were obtained. This study included patients with different oral hygiene agreements such as good, average, and poor. Of the patients, 10 cases (case numbers 4, 17, 24, 33, 55, 63, 68, 80, and 93) had severe plaque; approximately 38 cases had moderate plaque, and the rest of cases (52) had mild plaque.
The majority of patients (61%) had good oral hygiene, while 31% had average and 8% had poor oral hygiene. The poor-oral-hygiene patients had allocated case numbers 4, 7, 17, 33, 55, 63, 68, and 80 (Appendix A). Case number 17 was a 9 year-old-male patient; on the other hand, case number 55 was a 35-year-old female patient (Appendix A).

Biofilm Formation of Dental Plaque-Causing Bacteria
The adhesion strength of S. mutans bacterial biofilm was quantified for all 100 cases and the results are displayed in Figure 9. The results showed that the biofilm formation of all the patients was divided into three groups: weak, moderate, and strong. The biofilm formation ranges from 0.5 to 2.0 nm for the weak group, 2.0 to 3.5 nm for the moderate group, and 3.5 to 5.0 nm for the strong group (Table 2). Among the 100 patients, 54 (54%) were in the weak group, 34 (34%) were in the moderate group, and 12 (12%) were in the strong group for biofilm formation. The mean value of biofilm formation was 3.97 ± 0.46 for the strong group, followed by 2.79 ± 0.31 for the moderate group and 1.41 ± 0.53 for the weak group, showing significant differences ( Table 2). The results show that patient numbers 17 and 55 were confirmed to have presented the highest level of biofilm formation and strong biofilm formation, respectively. Patient number 17 exhibited the highest level (4.48 ± 0.42 nm) of biofilm formation. Patient number 55 showed 4.32 ± 0.65 nm ( Figure 9). Thus, patients 17 and 55 were selected for biofilm formation. Finally, the nomenclature of these above three compounds was confirmed by comparing it with some data obtained from a previous study conducted by Ahmed et al. [31] as well as Subavathy and Thilaga [32] using gas chromatography-mass spectrometry (GC-MS) analysis. The main compound is 3, 7, 11, 15-tetramethyl-headeca-2-en-1-o1 (Table 1).

Patient Status with Dental Plaque and Oral Hygienic Grounds for Biofilm Formation
For biofilm formation, 100 cases were enumerated and their dental plaque and oral hygienic conditions were observed. Among these 100 cases, there were females 44 and 56 males (Appendix A). All the patients' ages were divided into six groups. So, among these 100 patients, 28 were 5 to 10 years old, 23 were 11 to 16 years old, 17 were 17 to 22 years old, 14 were 23 to 28 years old, 10 were 29 to 34 years old, and 8 were 35 to 40 years old. In terms of dental plaque, mild, moderate, and severe scores were obtained. This study included patients with different oral hygiene agreements such as good, average, and poor. Of the patients, 10 cases (case numbers 4, 17, 24, 33, 55, 63, 68, 80, and 93) had severe plaque; approximately 38 cases had moderate plaque, and the rest of cases (52) had mild plaque.
The majority of patients (61%) had good oral hygiene, while 31% had average and 8% had poor oral hygiene. The poor-oral-hygiene patients had allocated case numbers 4, 7, 17, 33, 55, 63, 68, and 80 (Appendix A). Case number 17 was a 9 year-old-male patient; on the other hand, case number 55 was a 35-year-old female patient (Appendix A).

Biofilm Formation of Dental Plaque-Causing Bacteria
The adhesion strength of S. mutans bacterial biofilm was quantified for all 100 cases and the results are displayed in Figure 9. The results showed that the biofilm formation of all the patients was divided into three groups: weak, moderate, and strong. The biofilm formation ranges from 0.5 to 2.0 nm for the weak group, 2.0 to 3.5 nm for the moderate group, and 3.5 to 5.0 nm for the strong group (Table 2). Among the 100 patients, 54 (54%) were in the weak group, 34 (34%) were in the moderate group, and 12 (12%) were in the strong group for biofilm formation. The mean value of biofilm formation was 3.97 ± 0.46 for the strong group, followed by 2.79 ± 0.31 for the moderate group and 1.41 ± 0.53 for the weak group, showing significant differences ( Table 2). The results show that patient numbers 17 and 55 were confirmed to have presented the highest level of biofilm formation and strong biofilm formation, respectively. Patient number 17 exhibited the highest level (4.48 ± 0.42 nm) of biofilm formation. Patient number 55 showed 4.32 ± 0.65 nm (Figure 9). Thus, patients 17 and 55 were selected for biofilm formation.  Finally, the nomenclature of these above three compounds was confirmed by comparing it with some data obtained from a previous study conducted by Ahmed et al. [31] as well as Subavathy and Thilaga [32] using gas chromatography-mass spectrometry (GC-MS) analysis. The main compound is 3, 7, 11, 15-tetramethyl-headeca-2-en-1-o1 (Table 1).

Patient Status with Dental Plaque and Oral Hygienic Grounds for Biofilm Formation
For biofilm formation, 100 cases were enumerated and their dental plaque and oral hygienic conditions were observed. Among these 100 cases, there were females 44 and 56 males (Appendix A). All the patients' ages were divided into six groups. So, among these 100 patients, 28 were 5 to 10 years old, 23 were 11 to 16 years old, 17 were 17 to 22 years old, 14 were 23 to 28 years old, 10 were 29 to 34 years old, and 8 were 35 to 40 years old. In terms of dental plaque, mild, moderate, and severe scores were obtained. This study included patients with different oral hygiene agreements such as good, average, and poor. Of the patients, 10 cases (case numbers 4, 17, 24, 33, 55, 63, 68, 80, and 93) had severe plaque; approximately 38 cases had moderate plaque, and the rest of cases (52) had mild plaque.
The majority of patients (61%) had good oral hygiene, while 31% had average and 8% had poor oral hygiene. The poor-oral-hygiene patients had allocated case numbers 4, 7, 17, 33, 55, 63, 68, and 80 (Appendix A). Case number 17 was a 9 year-old-male patient; on the other hand, case number 55 was a 35-year-old female patient (Appendix A).

Biofilm Formation of Dental Plaque-Causing Bacteria
The adhesion strength of S. mutans bacterial biofilm was quantified for all 100 cases and the results are displayed in Figure 9. The results showed that the biofilm formation of all the patients was divided into three groups: weak, moderate, and strong. The biofilm formation ranges from 0.5 to 2.0 nm for the weak group, 2.0 to 3.5 nm for the moderate group, and 3.5 to 5.0 nm for the strong group (Table 2). Among the 100 patients, 54 (54%) were in the weak group, 34 (34%) were in the moderate group, and 12 (12%) were in the strong group for biofilm formation. The mean value of biofilm formation was 3.97 ± 0.46 for the strong group, followed by 2.79 ± 0.31 for the moderate group and 1.41 ± 0.53 for the weak group, showing significant differences ( Table 2). The results show that patient numbers 17 and 55 were confirmed to have presented the highest level of biofilm formation and strong biofilm formation, respectively. Patient number 17 exhibited the highest level (4.48 ± 0.42 nm) of biofilm formation. Patient number 55 showed 4.32 ± 0.65 nm (Figure 9). Thus, patients 17 and 55 were selected for biofilm formation. The majority of patients (61%) had good oral hygiene, while 31% had average and 8% had poor oral hygiene. The poor-oral-hygiene patients had allocated case numbers 4, 7, 17, 33, 55, 63, 68, and 80 (Appendix A). Case number 17 was a 9 year-old-male patient; on the other hand, case number 55 was a 35-year-old female patient (Appendix A).

Biofilm Formation of Dental Plaque-Causing Bacteria
The adhesion strength of S. mutans bacterial biofilm was quantified for all 100 cases and the results are displayed in Figure 9. The results showed that the biofilm formation of all the patients was divided into three groups: weak, moderate, and strong. The biofilm formation ranges from 0.5 to 2.0 nm for the weak group, 2.0 to 3.5 nm for the moderate group, and 3.5 to 5.0 nm for the strong group (Table 2). Among the 100 patients, 54 (54%) were in the weak group, 34 (34%) were in the moderate group, and 12 (12%) were in the strong group for biofilm formation. The mean value of biofilm formation was 3.97 ± 0.46 for the strong group, followed by 2.79 ± 0.31 for the moderate group and 1.41 ± 0.53 for the weak group, showing significant differences ( Table 2). The results show that patient numbers 17 and 55 were confirmed to have presented the highest level of biofilm formation and strong biofilm formation, respectively. Patient number 17 exhibited the highest level (4.48 ± 0.42 nm) of biofilm formation. Patient number 55 showed 4.32 ± 0.65 nm ( Figure 9). Thus, patients 17 and 55 were selected for biofilm formation.
The results were compared with the control (without adding any compounds) and are demonstrated in Figure 10. The results showed that all three compounds possess antimicrobial activities against S. mutans, E. coli, and P. aeruginosa bacterial biofilm or dental plaque. The utmost motion showed evidence of Streptococcus mutans for 12.5 µL of the extract. Compound 3, 7, 11, 15-tetramethyl-hexadeca-2-en-1-ol (T 2 ) was confirmed to possess peak antimicrobial properties in favor of the escalation of reticence on top of the biofilm of Streptococcus mutans along with the other compounds of Cynodon dactylon. The compound 3, 7, 11, 15 tetramethyl hexadec 2en-1-o1 (T 2 ) showed a maximum inhibition of 3.42 ± 0.21 nm for case No. 17 ( Figure 10A) and 3.07 ± 0.14 nm for case No. 55 ( Figure 10B) in Streptococcus mutans. On the other hand, the compound stigmasterol (T 3 ) showed a minimum inhibition of 0.33 ± 0.06 nm in case No. 55 in E. coli ( Figure 10B).

Effect of the Plant Extracts on the Growth of Biofilm Formation
After extracting the compounds from C. dactylon, the three compounds were applied for minimum inhibitory concentration (MIC), as denoted in Table 3. The results show that dilutions of the three compounds derived from ethyl acetate extract (3, 7, 11,15 tetramethyl hexadeca-2,4 dien1-o1 (T1), 3, 7, 11,15 tetramethyl hexadeca-2-en-1-o1 (T2), and stigmasterol (T3)) can inhibit the segregates on the biofilm produced by three bacteria viz. P. aeruginosa, E. coli, and S. mutans. A lower minimum inhibitory concentration was exposed by 3, 7, 11,15 tetramethyl hexadeca-2-en-1-o1 (T2) on S. mutans at 12.5 μL/mL. The results were compared with the control (without adding any compounds) and are demonstrated in Figure 10. The results showed that all three compounds possess    The percentages (%) of growth of biofilm formation were calculated after the inhibition of bacterial growth. The results are displayed in Table 4. Among the compounds, 3, 7, 11, 15 tetramethylhexdec-2-en-1-01 (T 2 ) has the highest antibiofilm and antimicrobial activities against all bacterial species. The maximum inhibition was 80.10% for case number 17 and 79.74% for case number 55 (Table 4). Investigations across the three compounds of ethyl acetate have shown that 12.5 µL of ethyl acetate demonstrates maximum antimicrobial activity. the extract. Compound 3, 7, 11, 15-tetramethyl-hexadeca-2-en-1-ol (T2) was confirmed to possess peak antimicrobial properties in favor of the escalation of reticence on top of the biofilm of Streptococcus mutans along with the other compounds of Cynodon dactylon. The compound 3, 7, 11, 15 tetramethyl hexadec 2en-1-o1 (T2) showed a maximum inhibition of 3.42 ± 0.21 nm for case No. 17 ( Figure 10A) and 3.07 ± 0.14 nm for case No. 55 ( Figure 10B) in Streptococcus mutans. On the other hand, the compound stigmasterol (T3) showed a minimum inhibition of 0.33 ± 0.06 nm in case No. 55 in E. coli ( Figure 10B). The percentages (%) of growth of biofilm formation were calculated after the inhibition of bacterial growth. The results are displayed in Table 4. Among the compounds, 3, 7, 11, 15 tetramethylhexdec-2-en-1-01 (T2) has the highest antibiofilm and

Discussions
Dental plaque samples were collected from 100 individuals with various oral complications patients attending the outdoor department of the dental unit at Rajshahi Medical College and Hospital, Rajshahi, Bangladesh. Cynodon dactylon was collected, pulverized, isolated, and purified using column chromatographic techniques; subsequently, biofilms were produced from bacteria grown on MSB medium using a microplate-based system in an in vitro model, which detected the adhesion strength of the biofilm developed by S. mutans in the 100 studied samples. It was also revealed that, among these 100 cases, patients with very poor oral hygiene had been suffering from spontaneous bleeding and severe gum diseases and had severe dental plaque, which badly affected most of the teeth of the oral cavity. This study also revealed that the patients had different levels of oral hygiene, such as good, average, and poor. A majority of the patients (61%) had good oral hygiene, while 31% had average and 8% had poor oral hygiene. An almost similar result was found in several experiments where gingivitis was dominant in children, teenagers, and adults, and a maximum of 80% of the global residents experienced mild to moderate gingivitis [33]. There were 242 (48.9%) male and 253 (51.1%) female participants, and most (20.2%) of the participants were six years old [34]. Out of the 100 cases, two (case numbers 17 and 55) were chosen for further analysis because they both had severe plaque scores and poor oral hygiene conditions and showed strong biofilm formation. All the results summarize that patients 17 and 55 had strong biofilm formation. Patient number 17 exhibited the highest level (4.48 ± 0.42 nm) of S. mutans biofilm formation. Patient number 55 showed a biofilm formation level of 4.32 ± 0.65 nm. Thus, patients 17 and 55 were selected for biofilm formation.
Among the compounds, 3,7,11,15 tetramethylhexdec-2-en-1-01 has the highest antibiofilm and antimicrobial activities against all bacterial species. The maximum inhibition was 80.10% with a p-value < 0.05 in case number 17 and 53.74% in case number 55. Similarly, Sharma and Singh [35] have shown that C. dactylon possesses a synergistic effect against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus coagulasse, and Enterococcus faecalis. C. dactylon and other extracts of tested medicinal plants have a broad spectrum of antibacterial activity against a panel of bacteria that cause the most prevalent bacterial illnesses. Investigations across three compounds of ethyl acetate showed that a lower minimum inhibitory concentration was exposed by 3, 7, 11,15 tetramethyl hexadeca-2-en-1-o1 (T2) on S. mutans at 12.5 µL/mL. This study agrees with other studies. Adikwu et al. [28] reported that organisms exhibited smaller MIC when exposed to extracts of Psidium guajava: an MIC of 3.125 mg/mL was found using methanol extract. Zayed et al. [13] stated that minimum biofilm inhibitory concentrations of alcoholic green tea extracts were in the range of 3.1 to 12.5 mg/mL. Among the compounds,3, 7, 11, 15 tetramethylhexdec-2-en-1-01 (T2) has the highest antibiofilm and antimicrobial activities against all bacterial species. The maximum inhibition was 80.10% in case number 17 and 79.74% inhibition in case number 55. The present experiment is similar to the study of Shekar et al. [36]; they showed 75.54% inhibition of S. mutans bacteria. Nallathambi and Bhargavan [37] recorded the existence of bioactive compounds in the moist extract of C. dactylon by using a gas chromatograph and a mass spectrometer with a quadruple double-focusing mass analyzer and detected eight compounds which included Alanine, 9, 12-octadecadienoic acid, n-Hexadecenoic acid, oleic acid, 3-octyl-methyl-ester trans, phytoderivatives and coumarine, 3-(2-4-dinitrophenyl), etc. The compounds of phytol derivates are used due to their antimicrobial, anticancer, antiinflammatory, antioxidant, and diuretic properties [23]. Here, antimicrobial activity was assessed for bacterial growth of inhibition. Sharma and Singh [35] found that S. sanguis and S. mitis were the most susceptible bacteria to all plant extracts as compared to S. mutans and Enterococci. The reported plant extract showed significant activity against the investigated microbial strain. The present study was similar to that of Sharma and Singh [35]. Similarly, Nalini and Prakasham [38] noticed that C. dactylon extract exhibits the simplicity of a zone of hydrolysis, making the process easy, effective, and rapid for the screening of a large number of microorganisms. It was also reported that the extracts of selected species contain a good potential antimicrobial component that can be utilized to prepare potent drugs for treating dental problems and Streptococcus-related health.

Conclusions
The present study was conducted to identify the effect of compounds isolated from C. dactylon on the inhibition of S. mutans biofilm isolated from dental plaque samples. Three compounds named 3,7,11,15 tetramethylhexadec-2,4 dien-1-o1,3,7,11, 15 tetramethylhexadec-2-en-1-o1, and stigmasterol were extracted. The extracts of C. dactylon showed a notable excellent inhibitory impact against particular bacteria strains, including Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. The inhibitory activity of these three compounds was evaluated, and the findings demonstrated that 12.5 µL of ethyl acetate extract compound 3,7,11, 15 tetramethyl hexadec-2-en-1-o1 showed the highest antibiofilm activities with an 80.10% growth of inhibition (p < 0.05) in case of patient number 17. C. dactylon is shown to have surprising health benefits and antibacterial properties. Based on the findings of this study, it could be included that C. dactylon possesses several vital antibacterial components that could be very useful in the creation of strong medicines for the treatment of medical conditions. To popularize C. dactylon for medicinal purposes, more research is needed.

Data Availability Statement:
The data used in this study are available from the corresponding author upon reasonable request.

Acknowledgments:
We gratefully acknowledge Wahedul Islam, Entomology and Insect Biotechnology Laboratory, Institute of Biological Sciences, University of Rajshahi, Bangladesh, for his help and the Director of the same institute for providing laboratory facilities necessary for the completion of this work.

Conflicts of Interest:
The authors declare no conflict of interest.