Autofluorescence Detection Method for Dental Plaque Bacteria Detection and Classification: Example of <i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i<
The use of fluorescence spectroscopy for plaque detection is a fast and effective way to monitor oral health. At present, there is no uniform specification for the design of the excitation light source of related products for generating fluorescence. To carry out experiments on dental plaque, the fl...
Ausführliche Beschreibung
Autor*in: |
Yung-Jhe Yan [verfasserIn] Bo-Wen Wang [verfasserIn] Chih-Man Yang [verfasserIn] Ching-Yi Wu [verfasserIn] Mang Ou-Yang [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Übergeordnetes Werk: |
In: Dentistry Journal - MDPI AG, 2013, 9(2021), 7, p 74 |
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Übergeordnetes Werk: |
volume:9 ; year:2021 ; number:7, p 74 |
Links: |
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DOI / URN: |
10.3390/dj9070074 |
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Katalog-ID: |
DOAJ030407850 |
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10.3390/dj9070074 doi (DE-627)DOAJ030407850 (DE-599)DOAJ7ab008f4bc74455bb971d2408639acee DE-627 ger DE-627 rakwb eng RK1-715 Yung-Jhe Yan verfasserin aut Autofluorescence Detection Method for Dental Plaque Bacteria Detection and Classification: Example of <i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i< 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The use of fluorescence spectroscopy for plaque detection is a fast and effective way to monitor oral health. At present, there is no uniform specification for the design of the excitation light source of related products for generating fluorescence. To carry out experiments on dental plaque, the fluorescence spectra of three different bacterial species (<i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i<) were measured by hyperspectral imaging microscopy (HIM). Three critical issues were found in the experiments. One issue was the unwanted spectrum generated from a mercury line source; two four-order low-pass filters were evaluated for eliminating the unwanted spectrum and meet the experimental requirements. The second issue was the red fluorescence generated from the microscope slide made of borosilicate glass; this could affect the observation of the red fluorescence from the bacteria; quartz microscope slides were found to reduce the fluorescence intensity by about 2 dB compared with the borosilicate slide. The third issue of photobleaching in the fluorescence of the <i<Porphyromonas gingivalis</i< was studied. This study proposes a method of classifying three bacteria based on the spectral intensity ratios (510/635 and 500/635 nm) under the 405 nm excitation light was proposed in this study. The sensitivity and specificity of the classification were approximately 99% and 99%, respectively. plaque detection dental plaque autofluorescence <i<Porphyromonas gingivalis</i< <i<Aggregatibacter actinomycetemcomitans</i< <i<Streptococcus mutans</i< Dentistry Bo-Wen Wang verfasserin aut Chih-Man Yang verfasserin aut Ching-Yi Wu verfasserin aut Mang Ou-Yang verfasserin aut In Dentistry Journal MDPI AG, 2013 9(2021), 7, p 74 (DE-627)726120650 (DE-600)2681351-8 23046767 nnns volume:9 year:2021 number:7, p 74 https://doi.org/10.3390/dj9070074 kostenfrei https://doaj.org/article/7ab008f4bc74455bb971d2408639acee kostenfrei https://www.mdpi.com/2304-6767/9/7/74 kostenfrei https://doaj.org/toc/2304-6767 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 9 2021 7, p 74 |
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RK1-715 Autofluorescence Detection Method for Dental Plaque Bacteria Detection and Classification: Example of <i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i< plaque detection dental plaque autofluorescence <i<Porphyromonas gingivalis</i< <i<Aggregatibacter actinomycetemcomitans</i< <i<Streptococcus mutans</i< |
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autofluorescence detection method for dental plaque bacteria detection and classification: example of <i<porphyromonas gingivalis</i<, <i<aggregatibacter actinomycetemcomitans</i<, and <i<streptococcus mutans</i< |
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Autofluorescence Detection Method for Dental Plaque Bacteria Detection and Classification: Example of <i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i< |
abstract |
The use of fluorescence spectroscopy for plaque detection is a fast and effective way to monitor oral health. At present, there is no uniform specification for the design of the excitation light source of related products for generating fluorescence. To carry out experiments on dental plaque, the fluorescence spectra of three different bacterial species (<i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i<) were measured by hyperspectral imaging microscopy (HIM). Three critical issues were found in the experiments. One issue was the unwanted spectrum generated from a mercury line source; two four-order low-pass filters were evaluated for eliminating the unwanted spectrum and meet the experimental requirements. The second issue was the red fluorescence generated from the microscope slide made of borosilicate glass; this could affect the observation of the red fluorescence from the bacteria; quartz microscope slides were found to reduce the fluorescence intensity by about 2 dB compared with the borosilicate slide. The third issue of photobleaching in the fluorescence of the <i<Porphyromonas gingivalis</i< was studied. This study proposes a method of classifying three bacteria based on the spectral intensity ratios (510/635 and 500/635 nm) under the 405 nm excitation light was proposed in this study. The sensitivity and specificity of the classification were approximately 99% and 99%, respectively. |
abstractGer |
The use of fluorescence spectroscopy for plaque detection is a fast and effective way to monitor oral health. At present, there is no uniform specification for the design of the excitation light source of related products for generating fluorescence. To carry out experiments on dental plaque, the fluorescence spectra of three different bacterial species (<i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i<) were measured by hyperspectral imaging microscopy (HIM). Three critical issues were found in the experiments. One issue was the unwanted spectrum generated from a mercury line source; two four-order low-pass filters were evaluated for eliminating the unwanted spectrum and meet the experimental requirements. The second issue was the red fluorescence generated from the microscope slide made of borosilicate glass; this could affect the observation of the red fluorescence from the bacteria; quartz microscope slides were found to reduce the fluorescence intensity by about 2 dB compared with the borosilicate slide. The third issue of photobleaching in the fluorescence of the <i<Porphyromonas gingivalis</i< was studied. This study proposes a method of classifying three bacteria based on the spectral intensity ratios (510/635 and 500/635 nm) under the 405 nm excitation light was proposed in this study. The sensitivity and specificity of the classification were approximately 99% and 99%, respectively. |
abstract_unstemmed |
The use of fluorescence spectroscopy for plaque detection is a fast and effective way to monitor oral health. At present, there is no uniform specification for the design of the excitation light source of related products for generating fluorescence. To carry out experiments on dental plaque, the fluorescence spectra of three different bacterial species (<i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i<) were measured by hyperspectral imaging microscopy (HIM). Three critical issues were found in the experiments. One issue was the unwanted spectrum generated from a mercury line source; two four-order low-pass filters were evaluated for eliminating the unwanted spectrum and meet the experimental requirements. The second issue was the red fluorescence generated from the microscope slide made of borosilicate glass; this could affect the observation of the red fluorescence from the bacteria; quartz microscope slides were found to reduce the fluorescence intensity by about 2 dB compared with the borosilicate slide. The third issue of photobleaching in the fluorescence of the <i<Porphyromonas gingivalis</i< was studied. This study proposes a method of classifying three bacteria based on the spectral intensity ratios (510/635 and 500/635 nm) under the 405 nm excitation light was proposed in this study. The sensitivity and specificity of the classification were approximately 99% and 99%, respectively. |
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Autofluorescence Detection Method for Dental Plaque Bacteria Detection and Classification: Example of <i<Porphyromonas gingivalis</i<, <i<Aggregatibacter actinomycetemcomitans</i<, and <i<Streptococcus mutans</i< |
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The third issue of photobleaching in the fluorescence of the <i<Porphyromonas gingivalis</i< was studied. This study proposes a method of classifying three bacteria based on the spectral intensity ratios (510/635 and 500/635 nm) under the 405 nm excitation light was proposed in this study. 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