• 치위생과학회지
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• 제17권4호
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• pp.283-289
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• 2017

DUWL에 형성한 바이오필름을 효율적으로 제거할 수 있는 새로운 소독제는 개발되어야 하며, 실험실에서 소독제의 효과를 확인하기 위해 DUWL 바이오필름 시료는 필요하다. 이 연구의 목적은 well plate를 사용하여 간단하고 재현 가능한 DUWL 바이오필름 모델을 개발하는 것이다. 사용중인 4대의 DUWL에서 배출된 1 L의 물을 여과지에 여과시켜 세균을 얻었다. 여과지를 PBS (pH 7.4) 용액 20 ml에 현탁시킨 후, 현탁액을 R2A 액체배지에 접종하고 $25^{\circ}C$에서 10일 동안 배양하였다. 10일 배양한 세균 배양액을 $-70^{\circ}C$에 보관하였고 매 실험에 사용하였다. 세균배양액을 R2A 배지에서 5일 동안 회분 배양하였다. 12-well plate에 회분 배양한 세균 배양액과 멸균한 폴리우레탄 튜빙 조각을 넣고 정체된 상태로 $25^{\circ}C$에서 바이오필름을 형성시켰다. R2A 액체배지는 2일마다 2 ml씩 교체해주었다. 폴리우레탄 내형성된 바이오필름의 축적량을 확인하기 위해 폴리우레탄 튜빙 조각을 내면에서 수집한 바이오필름을 R2A 고체배지에 도말하였다. 도말한 R2A 고체배지는 $25^{\circ}C$에서 7일 배양하고 $CFU/cm^2$를 계산하였다. 그리고 바이오필름의 두께와 구성 세균의 형태 및 분포를 확인하기 위해 CLSM과 SEM을 사용하였다. 4일 동안 배양시킨 바이오필름의 평균 축적량은 $1.15{\times}10^7CFU/cm^2$였다. 바이오필름은 구균, 짧은 길이의 간균, 그리고 중간길이의 간균을 포함하고 있었고 폴리우레탄 튜빙 내면에 넓게 분포하고 있었다. 바이오필름두께는 위치에 따라 차이가 있지만 $2{\mu}m{\sim}7{\mu}m$였다. 이 연구에서 제작된 DUWL 바이오필름 model은 DUWL에서 수집된 모든 세균을 사용하여 세균의 다양성을 확보했고 또한 실험실에서 쉽게 구할 수 있는 well-plate를 사용했기 때문에 비용 효율적이고 재현이 간단하다. 본 연구의 DUWL 바이오필름 모델은 새로운 소독방법의 개발하는 데 유용하게 사용될 수 있다.

• 대한소아치과학회지
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• 제43권3호
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• pp.306-312
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• 2016

치아우식은 Streptococcus mutans와 S. sobrinus가 주요 원인균이며, 이를 예방하기 위해서 구강 청결제를 사용한다. 그러나 구강청결제의 부작용 및 해로움으로 인하여 소아에게 권장하기에 주위를 요한다. 전기 분해수는 물을 전극을 통해서 전류를 흘려주어 생성되는 용액으로 항균력을 갖는다. 본 연구에서는 전기 분해수를 구강 청결제 대용으로 사용하기 위해서 치아 우식원성 세균 및 바이오 필름에 대한 항균력을 조사하였다. 염화나트륨이 포함된 증류수를 백금전극을 이용하여 전기 분해수를 생성하였다. 전기분해 수소수의 물리화학적 성분을 분석하고 S. mutans 및 S. sobrinus 배양액을 원심분리하여 세균을 얻고 전기 분해수, 알코올 및 불소가 포함된 구강 청결제를 처리하고 살아있는 세균 수를 배양을 통해서 조사하였다. 또한 치아우식균의 바이오 필름을 형성시킨 후, 전기 분해수 및 구강 청결제를 처리하여 바이오 필름 제거능을 크리스탈 바이올렛 염색을 이용하여 분석하고, 바이오 필름 내 살아있는 세균수의 양은 배양을 통하여 분석하였다. 전기분해수는 높은 농도의 자유염소 (free chlorine)을 포함하고 중성 페하를 보였다. 전기 분해수는 유의하게 S. mutans 및 S. sobrinus에 대해서 항균력을 보였으며, 이 세균들의 바이오 필름 제거능 및 바이오 필름 내 세균에 대해서도 항균력을 보였다. 전기 분해수는 부유세균에 대해서 알코올이 포함된 구강청결제보다 약한 항균력을 보였지만, 바이오 필름 세균에 대해서는 더 강한 항균력을 나타냈다. 이러한 결과를 바탕으로 중성 전기 분해수는 치아우식 예방을 위한 기존 구강 청결제의 대체 용액으로 사용이 가능할 것으로 사료된다.

• 대한소아치과학회지
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• 제36권3호
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• pp.358-366
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• 2009

유산균이 위장관과 구강건강에 probiotics로서 긍정적인 영향을 미치고 있음이 보고되고 있다. 이에 시판되는 유산균 발효유 5종과 우유를 선택하여 우식유발 원인균인 S. mutans에 대한 증식억제 및 biofilm 형성에 미치는 영향을 평가하고, 발효유의 산도, 완충능, 산생성능, 칼슘과 인의 함량을 측정하였다. 유산균 발효유에 S. mutans를 주입한 후 생균수를 측정한 결과 모든 발효유의 %가 증가함에 따라 S. mutans 수가 감소했으나 우유에서는 변화가 없었다. 10% 유산균 발효유에 S. mutans를 주입한 후 biofilm 형성 정도를 측정한 결과 액티브 GG, 불가리스는 biofilm 형성이 감소하였고, 이오는 유의한 변화가 없었으며, 투티, 에이스, 우유는 증가하였다(P<0.05). 유산균 발효유 및 우유의 산도를 측정한 결과 이오(3.48${\pm}$0.01), 투티(3.67${\pm}$0.02), 에이스(3.71${\pm}$0.02), 액티브 GG(4.04${\pm}$0.02), 불가리스(4.19${\pm}$0.02) 순으로 나타났다. 유산균 발효유의 산생성능을 평가한 결과 불가리스가 가장 높은 산생성능을 보였으며 액티브 GG, 에이스, 투티, 이오, 우유 순으로 산도 하강 경향을 나타냈다. 이상의 결과는 유산균 발효유가 초기산도 및 산생성능 측정 결과 우식유발 가능성이 있음을 나타냈다. 그러나 유산균 발효유 중에서 농후발효유가 우식유발균인 S. mutans를 억제하였고 biofilm 형성을 감소시켜 긍정적인 효과를 가지고 있음을 알 수 있었다.

• Journal of Periodontal and Implant Science
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• 제43권2호
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• pp.72-78
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• 2013

Purpose: The purpose of this study was to compare the phototoxic effects of blue light exposure on periodontal pathogens in both planktonic and biofilm cultures. Methods: Strains of Aggregatibacter actinomycetemcomitans, Fusobacterium nucleatum, and Porphyromonas gingivalis, in planktonic or biofilm states, were exposed to visible light at wavelengths of 400.520 nm. A quartz-tungsten-halogen lamp at a power density of $500mW/cm^2$ was used for the light source. Each sample was exposed to 15, 30, 60, 90, or 120 seconds of each bacterial strain in the planktonic or biofilm state. Confocal scanning laser microscopy (CSLM) was used to observe the distribution of live/dead bacterial cells in biofilms. After light exposure, the bacterial killing rates were calculated from colony forming unit (CFU) counts. Results: CLSM images that were obtained from biofilms showed a mixture of dead and live bacterial cells extending to a depth of $30-45{\mu}m$. Obvious differences in the live-to-dead bacterial cell ratio were found in P. gingivalis biofilm according to light exposure time. In the planktonic state, almost all bacteria were killed with 60 seconds of light exposure to F. nucleatum (99.1%) and with 15 seconds to P. gingivalis (100%). In the biofilm state, however, only the CFU of P. gingivalis demonstrated a decreasing tendency with increasing light exposure time, and there was a lower efficacy of phototoxicity to P. gingivalis as biofilm than in the planktonic state. Conclusions: Blue light exposure using a dental halogen curing unit is effective in reducing periodontal pathogens in the planktonic state. It is recommended that an adjunctive exogenous photosensitizer be used and that pathogens be exposed to visible light for clinical antimicrobial periodontal therapy.

• 치위생과학회지
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• 제12권6호
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• pp.545-557
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• 2012

Dental caries is biofilm induced disease throughout life and is recognized significant oral health problem. This article reviewed new trends in dental caries management by risk assessment, including history, protocol/guideline, and collaborated model. Dental caries prevention and treatment according to caries management by risk assessment (CAMBRA) model is patient-centered, risk-based, evidence-based practice. Team approach is necessary and clinician need to integrate science, practice and product. Dental hygienist take a important role in implementing CAMBRA. CAMBRA model could be incorporated into clinical dental hygiene education based on dental hygiene process of care as standard of dental hygiene practice and education. Dentist and dental hygienist able to provide scientific and ethical care managing dental caries by risk assessment.

• Journal of Microbiology and Biotechnology
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• 제23권8호
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• pp.1070-1075
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• 2013

Streptococcus mutans is the primary etiological agent of dental caries. The antimicrobial peptide $\small{D}$-Nal-Pac-525 was designed by replacing the tryptophans of the Trp-rich peptide Pac-525 with $\small{D}$-${\beta}$-naphthyalanines. To assess the effect of $\small{D}$-Nal-Pac-525 on cariogenic bacteria, the activity of $\small{D}$-Nal-Pac-525 on the growth of S. mutans and its biofilm formation were examined. $\small{D}$-Nal-Pac-525 showed robust antimicrobial activity against S. mutans (minimum inhibitory concentration of 4 ${\mu}g/ml$). Using scanning electron microscopy and transmission electron microscopy, it was shown that $\small{D}$-Nal-Pac-525 caused morphological changes and damaged the cell membrane of S. mutans. $\small{D}$-Nal-Pac-525 inhibited biofilm formation of S. mutans at 2 ${\mu}g/ml$. The results of this study suggest that $\small{D}$-Nal-Pac-525 has great potential for clinical application as a dental caries-preventing agent.

• 치위생과학회지
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• 제24권1호
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• pp.54-61
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• 2024

Background: The Korean name for Angelica gigas Nakai (AGN) is Cham-dang-gui, which grows naturally or is cultivated, and its dried roots are used in traditional herbal medicines. The AGN root exert various pharmacological effects. Despite the various pharmacological effects of the AGN root, there are no reports on its anti-oral microbial effects. The purpose of this study was to reveal the anti-oral microbial effect and the microbial and biochemical changes in oral microorganisms according to the concentration of the ethanol extract of AGN (EAGN) root, and to confirm the possibility of using EAGN as a plant-derived functional substance for controlling oral infectious microorganisms. Methods: Disk diffusion test, growth measurement, biofilm formation assay, and measurements of acid production and buffering capacity were performed to confirm the antibacterial effect of EAGN. Results: EAGN showed anti-oral bacterial effects against Streptococcus mutans and Aggregatibacter actinomycetemcomitans at all concentrations, with S. mutans showing a more susceptible effect at concentrations above 5.0 mg/ml and A. actinomycetemcomitans at 3.75 mg/ml. EAGN treatment significantly reduced A. actinomycetemcomitans growth at all concentrations tested. Biofilm formation was significantly reduced at concentrations above 3.75 mg/ml for S. mutans and 2.5 mg/ml for A. actinomycetemcomitans. Acid production in S. mutans and A. actinomycetemcomitans was significantly increased by treatment with EAGN, and the buffering capacities of S. mutans and A. actinomycetemcomitans increased from an EAGN concentration of 3.75 mg/ml and above. Conclusion: EAGN showed anti-oral bacterial effects against both S. mutans and A. actinomycetemcomitans at concentrations above 3.75 mg/ml, which were thought to be related to the inhibition of their growth and biofilm formation. Therefore, EAGN can be used as a safe functional substance derived from medicinal plants owing to its antibacterial effects against S. mutans and A. actinomycetemcomitans.

• Restorative Dentistry and Endodontics
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• 제41권2호
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• pp.91-97
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• 2016

Objectives: The purpose of this ex vivo study was to compare the antifungal activity of a synthetic peptide consisting of 15 amino acids at the C-terminus of human ${\beta}$-defensin 3 (HBD3-C15) with calcium hydroxide (CH) and Nystatin (Nys) against Candida albicans (C. albicans) biofilm. Materials and Methods: C. albicans were grown on cover glass bottom dishes or human dentin disks for 48 hr, and then treated with HBD3-C15 (0, 12.5, 25, 50, 100, 150, 200, and $300{\mu}g/mL$), CH ($100{\mu}g/mL$), and Nys ($20{\mu}g/mL$) for 7 days at $37^{\circ}C$. On cover glass, live and dead cells in the biomass were measured by the FilmTracer Biofilm viability assay, and observed by confocal laser scanning microscopy (CLSM). On dentin, normal, diminished and ruptured cells were observed by field-emission scanning electron microscopy (FE-SEM). The results were subjected to a two-tailed t-test, a one way analysis variance and a post hoc test at a significance level of p = 0.05. Results: C. albicans survival on dentin was inhibited by HBD3-C15 in a dose-dependent manner. There were fewer aggregations of C. albicans in the groups of Nys and HBD3-C15 (${\geq}100{\mu}g/mL$). CLSM showed C. albicans survival was reduced by HBD3-C15 in a dose dependent manner. Nys and HBD3-C15 (${\geq}100{\mu}g/mL$) showed significant fungicidal activity compared to CH group (p < 0.05). Conclusions: Synthetic HBD3-C15 peptide (${\geq}100{\mu}g/mL$) and Nys exhibited significantly higher antifungal activity than CH against C. albicans by inhibiting cell survival and biofilm.

• Journal of Periodontal and Implant Science
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• 제49권5호
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• pp.319-329
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• 2019

Purpose: Direct application of atmospheric-pressure plasma jets (APPJs) has been established as an effective method of microbial decontamination. This study aimed to investigate the bactericidal effect of direct application of an APPJ using helium gas (He-APPJ) on Porphyromonas gingivalis biofilms on sandblasted and acid-etched (SLA) titanium discs. Methods: On the SLA discs covered by P. gingivalis biofilms, an APPJ with helium (He) as a discharge gas was applied at 3 different time intervals (0, 3, and 5 minutes). To evaluate the effect of the plasma itself, the He gas-only group was used as the control group. The bactericidal effect of the He-APPJ was determined by the number of colony-forming units. Bacterial viability was observed by confocal laser scanning microscopy (CLSM), and bacterial morphology was examined by scanning electron microscopy (SEM). Results: As the plasma treatment time increased, the amount of P. gingivalis decreased, and the difference was statistically significant. In the SEM images, compared to the control group, the bacterial biofilm structure on SLA discs treated by the He-APPJ for more than 3 minutes was destroyed. In addition, the CLSM images showed consistent results. Even in sites distant from the area of direct He-APPJ exposure, decontamination effects were observed in both SEM and CLSM images. Conclusions: He-APPJ application was effective in removing P. gingivalis biofilm on SLA titanium discs in an in vitro experiment.

• International Journal of Oral Biology
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• 제43권3호
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• pp.123-127
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• 2018

Polyphenon 60 refers to the mixture of catechins present in green tea. The aim of this study was to investigate the antimicrobial activities of polyphenon 60 against 4 strains of Streptococcus mutans and 2 strains of Streptococcus sorbrinus, which are the major causative bacteria of dental caries. The minimum bactericidal concentration (MBC) values of polyphenon 60 for S. mutans and S. sobrinus were determined and the effect of biofilm formation inhibition of that was evaluated. The MBC value of polyphenon 60 against the bacterial strains was 2.5 mg/ml except for one particular strain, S. mutans KCOM 1128 for which the value was 1.25 mg/ml. The results of biofilm formation inhibition assay revealed that polyphenon 60 inhibited biofilm formation more than 90% at a concentration of 2.5 mg/ml. It was apparent that polyphenon exhibited biofilm formation inhibition activity along with bactericidal effect against S. mutans and S. sobrinus. Therefore, it is proposed that polyphenon 60 as one of the components of bactericidal agents could be useful in developing oral hygiene products, toothpaste or gargling solution.