Kim Young-Seok, Lee Eun-Song, Kwon Ho-Keun, Kim Baek-Il
Department of Preventive Dentistry and Public Oral Health, BK 21 Plus Project, Yonsei University College of Dentistry, 50 Yonsei-ro, Seodaemun-gu, Seoul, Republic of Korea.
Department of Preventive Dentistry and Public Oral Health, BK 21 Plus Project, Yonsei University College of Dentistry, 50 Yonsei-ro, Seodaemun-gu, Seoul, Republic of Korea.
J Dent. 2014 Jun;42(6):691-6. doi: 10.1016/j.jdent.2014.03.006. Epub 2014 Mar 19.
The aim of this study was to investigate whether Quantitative Light-induced Fluorescence-Digital (QLF-D) could monitor the degree of maturation of dental microcosm biofilms by observing the red fluorescence emitted from the biofilms.
Dental microcosm the biofilms were grown on bovine enamel discs. They were initiated from human saliva, and then grown in 0.5% sucrose growth media for 10 days. On days 1, 2, 3, 7, and 10 after the inoculation, fluorescence images of the biofilms were captured using the QLF-D and the red fluorescence intensity was quantified by calculating the red/green ratio (R/G value). Total and aciduric bacteria within the biofilms were counted, and the degree of demineralization was evaluated by measuring the percentage of surface microhardness change (ΔVHN) and lesion depth in the enamel.
The R/G values of the biofilms assessed by the QLF-D increased significantly over time up to 7 days after inoculation (p<0.0001). The R/G values showed significant positive correlations with the total bacterial CFUs (r=0.74, p=0.001), aciduric bacterial CFUs (r=0.85, p=0.001), ΔVHN (r=0.65, p=0.001), and lesion depth in the enamel (r=0.82, p=0.001) according to the maturation time.
The red fluorescence detected by the QLF-D increased according to biofilm maturation and was significantly associated with the cariogenicity of the biofilm. Therefore, this device could be used to monitor the degree of biofilm maturation by observing the red fluorescence emitted from cariogenic biofilms.
The QLF-D enables the detection of a mature dental plaque and monitoring of its cariogenic status by observing the plaque fluorescence non-destructively, in real time.
本研究旨在通过观察生物膜发出的红色荧光,探讨定量光诱导荧光数字成像(QLF-D)能否监测牙菌斑生物膜的成熟程度。
牙菌斑生物膜在牛牙釉质盘上生长。从人唾液开始接种,然后在0.5%蔗糖生长培养基中培养10天。接种后第1、2、3、7和10天,使用QLF-D采集生物膜的荧光图像,并通过计算红/绿比(R/G值)对红色荧光强度进行定量。计数生物膜内的总细菌和耐酸细菌,并通过测量釉质表面显微硬度变化百分比(ΔVHN)和病变深度来评估脱矿程度。
接种后7天内,通过QLF-D评估的生物膜R/G值随时间显著增加(p<0.0001)。根据成熟时间,R/G值与总细菌菌落形成单位(CFUs)(r=0.74,p=0.001)、耐酸细菌CFUs(r=0.85,p=0.001)、ΔVHN(r=0.65,p=0.001)和釉质病变深度(r=0.82,p=0.001)呈显著正相关。
QLF-D检测到的红色荧光随生物膜成熟而增加,且与生物膜的致龋性显著相关。因此,该设备可通过观察致龋生物膜发出的红色荧光来监测生物膜的成熟程度。
QLF-D能够通过实时、无损地观察菌斑荧光来检测成熟牙菌斑并监测其致龋状态。