Afsoon Asadollahi¹, Ali Taghavi¹, Hossein Eslami¹, Marzyeh Aghazadeh², Elham Zeinalzadeh³ and Hossein Samadi Kafil⁴*

¹Department of Oral and Maxillofacial Medicine, Faculty of Dentistry, Tabriz University of Medical Sciences, Tabriz, Iran.

²Infectious Diseases and Tropical Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

³Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

⁴Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

*Corresponding Author E-mail: Kafilhs@tbzmed.ac.ir

DOI : https://dx.doi.org/10.13005/bpj/1004

Abstract

Because of increase in antibiotic resistance, finding alternative treatments for controlling infections in oral cavity is critical. In this study we aimed to compare use of halite with CO2 laser radiation for controlling infections by S.aureus and P.aeruginosa. Staphilococcus aureus (ATCC 29213) and Pseudomonas aeruginosa (ATCC 27853) were used as standard strains. The effect of CO2 Laser was evaluated 5, 10, and 15 seconds after exposure to the standard suspension of bacterium with energy density of 12.5 J/cm2 at a distance of 17mm.  halite (Chlorhexidine digluconate 0.05%, Cetylpyridinium chloride (CPC) 0.05% and Zinc lactate 0.14%) was examined in the same condition. The average number of microbes was lower in the Halita group than CO2 laser group before 15 second (P-value <0.001). But after 15 second, No growth observed in CO2 laser group in contrary with Halita group (P-value and lt;0.001). Average time for complete infection removal for Halita was 60 second and for CO2 laser was 15 seconds. findings of the present study showed that CO2 laser radiation is valuable tools for infection control in oral cavity infections. Also halite was successful for infection remove after 60 seconds. Using CO2 laser radiation in combination of halita mouthwash can help for complete eradication of infections from oral cavity.

Keywords

halita; Co2 laser; chlorohexidine; Cetylpyridinium chloride; Infection control

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Copy the following to cite this article: Asadollahi A, Taghavi A, Eslami H, Aghazadeh M, Zeinalzadeh E, Kafil H. S. Comparing Antimicrobial Effect of CO2 Laser with Halita in Oral Infection Control. Biomed Pharmacol J 2016;9(2).

Copy the following to cite this URL: Asadollahi A, Taghavi A, Eslami H, Aghazadeh M, Zeinalzadeh E, Kafil H. S. Comparing Antimicrobial Effect of CO2 Laser with Halita in Oral Infection Control. Biomed Pharmacol J 2016;9(2). Available from: http://biomedpharmajournal.org/?p=7949

Introduction

Oral cavity infections are one of the most important medical problems and increasing drug resistance infections causes hardships in their treatment (1). Because of increase in antibiotic resistance, finding alternative treatments is critical. Use of these alternative methods especially against infections such as Staphylococcus aureus (S. aureus) and Pseudomonas aeruginosa (P. aeruginosa) is very important. The most important infections by these microbes are angular cheilitis, bacterial sialoadenitis in salivary glands in patients with septic arthritis of joints, necrotizing ulcerative gingivitis lesions (NUG), pneumonia and chronic suppurative otitis media (2). Also these infections can play role as a source of heart valve endocarditis (3). Another common problem by these microbes in oral cavity is inflammation around the implant which can causes destroy of supportive bone of implant (peri implantitis) (4). Microbial biofilm is the main pathogenesis mechanism of these microorganisms (5). It shows importance of biofilm remove for infection control of oral pathogens. In implant failures, biofilm remove and infection control is too important and several therapeutic methods are developed to control these infections (6-7). Mechanical debridement is the most common method to remove biofilms from implants, especially by set of plastic court to avoid the scratch on the surface of implant (5), but this method is unable to remove bacteria from all porous of implant. Use of chlorhexidine gluconate (CHG) or different antibiotics (such as tetracycline) is another common way for infection control in these patients (8). Several studies indicated usefulness of Chlorhexidine in the infection control and treatment of peri-implantitis infections (9). But chlorohexidine has some adverse effects such as Brown teeth, changes in sense of taste, increased mass production and ulceration of the mucous (10). Cetylpyridinium chloride (CPC) is a Quaternary ammonium compound used as mouthwash with wide range of antimicrobial effect (11). Halita is a combination of CHG, CPC and lactate to reduce adverse effect of each component and synergy effect for treatment of bacterial infections. There are several studies on anti fungal and anti enterococci effect of halite but no study against S. aureus and P. aeruginosa.

Recently uses of different laser systems have been developed for infection control and treatment of peri-implantitis. They are recommended to be used in combination with the traditional tools and therapies. Developing these methods have several advantages such as deep penetration and complete removal of microorganisms. In this study we aimed to compare use of halite with CO2 laser for controlling infections by S.aureus and P.aeruginosa.

Materials and methods

All standard strains containing Staphilococcus aureus (ATCC 29213) and Pseudomonas aeruginosa (ATCC 27853) were collected from Iranian national Microbial collection (PTCC.irost.org). To evaluate antimicrobial effect each strain were cultured in  the liquid medium of Brain Heart Infusion (BHI) (Merck KGaA, Darmstadt, Germany) . Antimicrobial test were done according to previously described (9, 12). In brief, overnight culture of strains were provided by culture at 37 ° C in optional anaerobic conditions to logarithmic phase of bacteria. For getting logarithmic phase, strains were subcultured and their optimal density (OD) were obtained by spectrophotometry (620nm, OD=0.6). Organisms of logarithmic phase were centrifuged for 15 minutes at g 3000 and the liquid surface was removed. The pellet was washed using sterile phosphate buffer saline (PBS) for 2 or 3 times. Sterile buffer was added and the final concentration of cell suspension (approximately CFU / ml) was prepared. For laser experience, 1 microliter of prepared strains suspension were poured in 1.5 mL eppendorf tubes, then the CO2 laser radiation was assessed for every 5, 10 and15 seconds at final intervals of 24 hours and 48 hours. For CO2 laser radiation, wavelength of 10.6 μm and energy density of 12.5 J / cm2 through the tapered humeral head and lack of focus with 5 mm diameter were used at distance of 17mm. All experiences were done in triplicate and suspensions were diluted and were spread at Brain hear infusion agar plates. After 24 hour incubation at 35-37° C their effect were subjected by colony counting.

Halita is the combination of Chlorhexidine digluconate 0.05%, Cetylpyridinium chloride (CPC) 0.05% and Zinc lactate 0.14% prolongs the antiseptic action of the two components for greater bacterial control and reduction of malodorous gas production. For antimicrobial evaluation of halita, 9ml of commercially available solution of halita was added to 1 ml of each microbial suspension (approximately CFU / ml). For time intervals, after every 5, 10, 15 and 60 seconds of exposure, solutions were subjected for culturing in Brain heart infusion agar plates. All plates were incubated 24 at 37 ° C and their bactericidal effect was evaluated colonies counting. (13).

Descriptive analysis were used for statistical analysis and Kruskal-Wallis test was used by SPSS ver 17 (IBM, United States) because of Non-normal distribution of data.

Results

Colony count of stains after treatment with Halita and CO2 laser are presented in Table 1. The main differences are shown in 5 and 10 second intervals. However, CO2 laser and Halita showed completely different manner on infection removal. The average number of S. aureus was lower in the Halita group than CO2 laser group before 15 second (P-value <0.001). But after 15 second, No growth observed in CO2 laser group in contrary with Halita group (P-value <0.001). The same results were obtained after extending incubation time to 48 hours. Average time for complete infection removal for Halita was 60 second and for CO2 laser was 15 seconds (Table 1).

Table 1: Antimicrobial effect of Halita and CO2 laser against Staphylococcus aureus and Pseudomonas aeruginosa in different time intervals.

Time intervals (seconds)	Pseudomonas aeruginosa		Staphylococcus aureus
	CO2 laser	Halita	CO2 laser	Halita
5 sec	10000/0±1600/0	3.7 ±1.2	1246/67±1501/11	104.3± 48.5
10 sec	5533/3±503/3	11.6 ± 4.7	8400/0±1708/80	56.8± 23.4
15 sec	0	8.5± 2.9	0	55.9± 17.3
30 sec	0	7.4± 3.1	0	20± 9.4
60 sec	0	0	0	1.5±.46

 

Discussion

Findings of the present study indicated that CO2 laser successfully reduced bacterial count after short time intervals. This method significantly increased bacteria after 15 seconds which can be used as a conventional method for oral infection control. For halita required time was 60 seconds for complete removal effect. However this time is enough when patient use it as mouthwash but by considering its low penetration power and infection conditions, CO2 laser seems to be more effective for control of these infections. S. aureus and P. aeruginosa bacteria play important roles in development of various diseases such as peri implantitis in the oral cavity. These bacteria are important in other sites of the body and can cause range of infections (14-16).

Bacterial biofilm production and surfaceadhesion are the key pathogenic factors in pathogenesis of peri implantitis and the inflammation process concluded to destruction of soft and hard tissue around the implant (17). Colonization of bacteria such as S. aureus and P. aeruginosa in the failed implants is the most important problem; this problem will be emphasized when isolate is resistance to different antibiotics. Therefore, treatment of peri implantitis should be associated with the infection control and prevention of disease progression (18).

Laser optimization including optimized wavelength and energy output level is important and excessive radiation can damage the materials of the surface due to high temperature (19). In the present study we used optimal laser wavelength and energy output for less possible damage and high efficacy against microbes. According to our finding this power can successfully remove all microbes after 15 second of radiation.

aureus is the major responsible pathogen for angular chilitis, sialoadenitis in salivary glands while it is the most common bacteria involved in bacterial septic arthritis TMJ joints that previously had arthritis (1). P aeruginosa has critical role in the development of Necrotizing Ulcerative Gingivitis (NUG) associated with chronic suppurative otitis media, and pneumonia (1).

In an experience by Hauser- Grspach et al, demonstrated that CO2 laser with low energy (2100 j/cm) reduce the number of Porphyromonas gingivalis and Streptococcus sanguis bacteria which from the surfaces of zirconia discs (20). Kato et al used CO2 laser 286 and 245 j / cm² against S.sanguis and P.gingivalis and results showed acceptable infection control (21). The results of this study showed that 100% of S. aureus and P. aeruginosa were killed 15 seconds after CO2 laser radiation which is consistent with the results of the previous studies another experiences demonstrated the antibacterial effects of CO2 against Streptococcus and Actinomyces species (22). In a study with energy density of 7.5 and 12.5 j/cm², 99.9% of P. gingivalis bacteria and more than 99% of A. actinomycetemcomitans bacteria were killed successfully (23). There is no study on effect of halita against S.aureus and P. aeruginosa but its main components are Chlorohexidine with demonstrated antimicrobial effect. Several studies demonstrated antimicrobial effect of chlorohexidine and Cetylpyridinium chloride. Albequerque et al demonstrated anti-staphylococcus effect of chlorohexidine and Cetylpyridinium chloride (24). Also, a study by witt et al. demonstrated synergy effect of Cetylpyridinium chloride against microbes and plaque formation (25). Findings of the present study showed effective time of 1 minute for complete microbial remove in S. aureus and P. aeruginosa infections.

In conclusion findings of the present study showed that CO2 laser radiation is valuable tools for infection control in oral cavity infections. Also halite was successful for infection remove after 60 seconds. Using CO2 laser radiation in combination of halita mouthwash can help for complete eradication of infections from oral cavity.

Acknowledgments

This study was supported by Drug Applied Research Center, Tabriz University of Medical Sciences. Present study was done as dissertation of Dr Afsoon Asadollahi and Experiences were done in Microbiology Laboratory of Drug Applied Research Center and Laser Laboratory of Faculty of Dentistry.

Refrences

1. Bialvaei AZ, Kafil HS. Colistin, Mechanisms and Prevalence of Resistance. Current Medical Research & Opinion. 2015; 31:707-721.
2. Glick M. Burket’s oral medicine, Eleventh edition .2008: pp: 81, 209, 252, And 53,301.
3. Little WJ, Miller C, Rhodus NL, Falace D. Little and falace‘s Dental management of medically compromised patient, Eight edition. 2013: pp 22.
4. Kafil HS,,Mobarez AM, Moghadam MF. Adhesion and virulence factor properties of Enterococci isolated from clinical samples in Iran. Indian J Pathol Microbiol 2013; 56(3): 238-42.
5. Kafil HS, Mobarez AM. Assessment of biofilm formation by enterococci isolates from urinary tract infections with different virulence profiles. J King Saud Univ – Sci 2015: 27 (4), 312-317.
6. Augthun M, Tinschert J, Huber A. In vitro studies on the effect of cleaning methods on different implant surfaces. J Periodontol 1998; 69(8): 857-64.
7. Parham PL, Jr., Cobb CM, French AA, Love JW, Drisko CL, et al. Effects of an air-powder abrasive system on plasma-sprayed titanium implant surfaces: an in vitro evaluation. J Oral Implantol 1989; 15(2): 78-86.
8. Ericsson I, Persson LG, Berglundh T, Edlund T,Lindhe J. The effect of antimicrobial therapy on periimplantitis lesions. An experimental study in the dog. Clin Oral Implants Res 1996; 7(4): 320-8.
9. Taghavi A, Asadollahi A, Eslami H, Attaran R, Ranjkesh MR, Kafil HS. Comparing Anti-bacterial Effect of CO 2 Laser and 0.2% Chlorhexidine Solution on Staphylococcus aureus and Pseudomonas aeruginosa: In Vitro Study. Journal of Advanced Oral Research 2016; 7:1-5.
10. Mandel ID. Antimicrobial mouthrinses: overview and update. J Am Dent Assoc 1994; 125(Suppl 2):2S-10S.
11. Quisno R, Foter MJ. Cetylpyridinium chloride: I. Germicidal properties. J Bacteriol 1946; 52:111-7.
12. Anyanwu OC, Baugh KK, Bennett SB, Johnson JM, Madlock RL, Pllard NE, Chikwem JO. Comparison of the antibacterial effectiveness of alcohl-containing and non-alcohl containing mouthwashes. Lin Uni J Sci 2011; 2(1): 7-12.
13. Witt J, Ramji N, Gibb R, Dunavent J, Flood J, Barners J. Antibacterial and antiplaque effects of an alcohl-free oral rinse with cetylpyridinium choloride(CPC). 2009. Available at: http://www.ada.org/goto/cerp.
14. Clauditz A, Resch A, Wieland KP, Peschel A, Götz F. Staphyloxanthin plays a role in the fitness of Staphylococcus aureus and its ability to cope with oxidative stress. Infection and immunity2006; 74 (8): 4950–3.
15. Balcht, Aldona & Smith, Raymond. Pseudomonas aeruginosa: Infections and Treatment. Informa Health Care 1994: 83–4.
16. Najafi K, Kafil HS, Shokrian S, et al. Virulence Genes and Antibiotic Resistance Profile of Pseudomonas aeruginosa Isolates in Northwest of Iran. Journal of pure and applied Microbiology 2015; 9: 383-9.
17. Mombelli A. Microbiology and antimicrobial therapy of peri-implantitis. Periodontol 2002; 28(1): 77-89.
18. Robert A. Weinstein.Controlling Antimicrobial Resistence: Infection control and use of Antibiotics,Emerging Infectious Disease 2001; 7(2): 188.
19. Stubinger S, Homann F, Etter C, Miskiewicz M, Wieland M, et al. Effect of Er: YAG, CO(2) and diode laser irradiation on surface properties of zirconia endosseous dental implants. Lasers Surg Med 2008; 40(3): 223-8.
20. Hauser-Gerspach I, Stubinger S,Meyer J. Bactericidal effects of different laser systems on bacteria adhered to dental implant surfaces: an in vitro study comparing zirconia with titanium. Clin Oral Implants Res 2010; 21(3): 277-83.
21. Kato T, Kusakari H, Hoshino E. Bactericidal efficacy of carbon dioxide laser against bacteria-contaminated titanium implant and subsequent cellular adhesion to irradiated area. Lasers Surg Med 1998; 23(5): 299-309.
22. Dederich DN, Pickard MA, Vaughn AS, Tulip J, Zakariasen KL. Comparative bactericidal exposures for selected oral bacteria using carbon dioxide laser radiation. Lasers Surg Med 1990; 10(6): 591-4.
23. Kojima T, Shimada K, Iwasaki H, Ito K. Inhibitory effects of a super pulsed carbon dioxide laser at low energy density on periodontopathic bacteria and lipopolysaccharide in vitro. J Periodontal Res 2005; 40(6): 469-73.
24. Jones CG. Chlorhexidine: is it still the gold standard? Periodontol 2000; 1555-62.
25. Witt J, Ramji N, Gibb R, Dunavent J, Flood J, Barnes J. Antibacterial and antiplaque effects of a novel, alcohol-free oral rinse with cetylpyridinium chloride. J Contemp Dent Pract 2005; 6(1):1-9.

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