• 제목/요약/키워드: Fluorescence

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HPLC와 Fluorescence Derivatization 기법을 이용한 극미량 NDMA의 수질분석 (Trace-level Determination of N-nitrosodimethylamine(NDMA) in Water Samples using a High-Performance Liquid Chromatography with Fluorescence Derivatization)

  • 차우석;;;최희철
    • 대한환경공학회지
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    • 제28권2호
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    • pp.223-228
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    • 2006
  • 본 연구에서는 fluorescence derivatization 기법과 HPLC를 이용하여 수중에 nanograms per liter로 존재하는 극미량 N-nitrosodimethylamine(NDMA)를 분석하고자 하였다. 이를 위해 먼저 다양한 조건 하에서의 fluorescence intensity를 측정함으로써 derivatization 기법을 최적화하였는데, fluorescence detector의 excitation/emission wavelength는 340 nm(excitation)과 530 nm(emission)에서, denitrosation 후 용액의 pH는 9-12의 범위에서, 그리고 dansyl chloride의 농도는 330-500 mg/L 범위에서, 최대 fluorescence intensity를 보여주였다. 용매추출을 통한 수질 시료의 분석에서, 표준농도와 검출농도의 차이는, 저농도(10-200 ng/L) 범위에서 12-162%, 고농도(100-1000 ng/L) 범위에서 6-23%를 보여, 저농도 범위에서 더 많은 차이가 나는 것으로 나타났으나, 두 농도 범위 모두 표준농도와 검출농도의 평균 대비율이 1에 매우 근접해 있어, 수십에서 수백 nanograms NDMA per liter의 분석이 가능함을 보여주었다. 하수처리장 처리수에 주입한 NDMA의 분석에서도 다른 물질에 의한 간섭없이 정확한 농도 검출이 가능했는데, 이는 목적물질을 선별적으로 분석해내는 derivatization 과정에 의한 것으로 나타났다. HPLC와 fluorescence derivatization 기법을 이용한 NDMA의 분석은 상수 및 하수를 사용하는 다양한 실험 연구에서 NDMA를 분석하는 방법으로 효과적으로 사용될 수 있을 것이다.

레이저 형광법을 이용한 인접면 우식증 탐지효과 (DETECTION OF PROXIMAL CARIES USING LASER FLUORESCENCE)

  • 모경희;윤정훈;김수관;이상호
    • 대한소아치과학회지
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    • 제31권2호
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    • pp.323-330
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    • 2004
  • 본 연구는 레이저 형광을 치아의 인접면에 적용하여 임상에서 초기 인접면 우식증의 감별에 레이저의 이용가능성을 평가하는데 그 목적이 있다. 염료와 레이저 형광법의 인접면 우식증 탐지효과를 평가하기 위해 조선대학교 소아치과에 내원한 아동 중 유구치의 탈락이 없으며 인접면의 수복치료를 받지 않은 $3{\sim}9$세 사이의 어린이 30명을 대상으로 하였으며, 시진, 교익 방사선사진, 레이저 형광법, 염료와 레이저 형광법을 이용해 관찰한 결과를 비교하여 다음과 같은 결과를 얻었다. 1. 인접면 우식증의 교익 방사선 사진검사와 시진, 레이저 형광법, 염료와 레이저 형광법 사이에서 모두 높은 상관 관계(r=0.725-0.911)를 보였다(p<0.05). 2. 인접면 우식증의 교익 방사선사진 검사와 각 검사법간의 일치도(kappa치)는 각각 시진이 0.451 레이저 형광법이 0.683, 염료와 레이저 형광법이 0.772로 가장 일치도가 높았다. 이상의 결과를 종합해 보면 교익 방사선사진 검사법과 염료와 레이저 형광법 검사 수치의 상관관계가 진단학적 일치도가 높아 레이저 형광법이 향후 교익방사선 사진 검사법을 대치 할 수 있는 인접면 우식증 검사법으로 사료된다.

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Porphyromonas gingivalis가 일부 구강미생물의 형광 발현에 미치는 영향 (Red fluorescence of oral bacteria interacting with Porphyromonas gingivalis)

  • 김세연;우동협;이민아;김지수;이정하;정승화
    • Journal of Korean Academy of Oral Health
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    • 제41권1호
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    • pp.22-27
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    • 2017
  • Objectives: Dental plaque is composed of 700 bacterial species. It is known that some oral microorganisms produce porphyrin, and thus, they emit red fluorescence when illuminated with blue light at a specific wavelength of <410 nm. Porphyromonas gingivalis belongs to the genus Porphyromonas, which is characterized by the production of porphyrin. The aim of this study was to evaluate red fluorescence emission of some oral microorganisms interacting with P. gingivalis. Methods: Five bacterial strains (P. gingivalis, Streptococcus mutans, Lactobacillus casei, Actinomyces naeslundii, and Fusobacterium nucleatum) were used for this study. Tryptic soy agar medium supplemented with hemin, vitamin K3, and sheep blood was used as a growth medium. The fluorescence emission of bacterial colonies was evaluated under 405 nm-wavelength blue light using a Quantitative Light-induced Fluorescence Digital (QLF-D) camera system. Each bacterium was cultured alone and co-cultured in close proximity with P. gingivalis. The red/green (R/G) ratio of fluorescence image was calculated and the differences of R/G ratio according to each growth condition were compared using the Mann-Whitney test (P<0.05). Results: Single cultured S. mutans, L. casei and A. naeslundii colonies emitted red fluorescence (R/G ratio=$2.15{\pm}0.06$, $4.31{\pm}0.17$, $5.52{\pm}1.29$, respectively). Fusobacterium nucleatum colonies emitted green fluorescence (R/G ratio=$1.36{\pm}0.06$). The R/G ratios of A. naeslundii and F. nucleatum were increased when P. gingivalis was co-cultured with each bacterium (P<0.05). In contrast, the R/G ratios of S. mutans and L. casei were decreased when P. gingivalis was co-cultured with each bacterium (P=0.002, 0.003). Conclusions: This study confirmed that P. gingivalis could affect the red fluorescence of other oral bacteria under 405 nm-wavelength blue light. Our findings concluded that P. gingivalis has an important role for red fluorescence emission of dental biofilm.

Fluorescence in situ hybridization (FISH)를 이용하여 분석한 Bleomycin에 의한 사람 림프구의 염색체 재배열 (Chromosome Rearrangements Detected by Fluorescence in situ Hybridization in Human Lymphocyte Exposed to Bleomycin)

  • 손은희;정경인;정해원
    • 한국환경성돌연변이발암원학회지
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    • 제17권1호
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    • pp.12-16
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    • 1997
  • Chromosome rearrangement induced by bleomycin were identified by fluorescence in situ hybridization with probe for chromosome 4. The frequency of color junctions, translocations, dicentric and acenttic fragments increased with bleomycin dose. Different types of balanced translocation and dicentric were scored and compared. The frequency of cells exhibiting multiple aberration was higher compared to that of cells exposed to Gamma radiation suggesting that effect of bleomycin might be similar to that of high LET radiation.

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Preparation of a Fluoroionophore Based on Porphyrin-Crown Ether

  • Shin, Eun Ju;Jung, Hyun-Suk
    • Journal of Photoscience
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    • 제11권2호
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    • pp.83-87
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    • 2004
  • A porphyrin compound containing a crown ether moiety (Por-Crown) and its zinc complex (ZnPor-Crown) have been prepared and the effect of the addition of alkali metal on their fluorescence has been investigated. As alkali metal cations were added, the absorption and fluorescence maxima did not change. However, the absorbance and intensity of fluorescence increased dramatically. Among the alkali metal cations tested, addition of K$^{+}$ and Cs$^{+}$ showed strongest enhancement of absorbance and fluorescence intensity of Por-Crown and ZnPor-Crown.own.

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Synthesis of Fluorescent Thiophene-derivatized Pentytiptycenes and Their Aggregate Behaviors

  • 송진우
    • 통합자연과학논문집
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    • 제3권1호
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    • pp.28-32
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    • 2010
  • Thiophene-derivatized pentiptycenes were synthesized and characterized by NMR and UV-Vis spectroscopy. Aggregation behavior of thiophene-derivatized pentiptycenes was monitored by the measurement of fluorescence. Fluorescence intensities for the thiophene-derivatized pentiptycenes and thiophene-derivatized pentiptycenes aggregates were compared. There is no shift in the maximum of the emission wavelength. In the range of water fraction between 20% and 40%, the emission intensity of thiophene-derivatized pentiptycene aggregates remains almost identical. Fluorescence efficiency incresaed by about 5 times higher when the thiophene-derivatized pentiptycenes forms the aggregates in solution.

Solubilization by $\beta$-Cyclodextrin: A Fluorescence Quenching Study

  • Panda, M.;Mishra, A.K.
    • Journal of Photoscience
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    • 제9권3호
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    • pp.75-79
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    • 2002
  • Solubility of carbon tetrachloride ($CCl_4$) in water increases appreciably in presence of $\beta$-cyclodextrin ($\beta$CD). $CCl_4$ is a very good quencher of 1-naphthol (1ROH) fluorescence. By studying the quenching of fluorescence of 1ROH included in $\beta$CD cavity, it was found that there is an increase in the availability of $CCl_4$ around $\beta$CD in the aqueous medium. This could help to rationalize the enhanced solubility of $CCl_4$.

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Excimer Fluorescence Quenching of Poly (styrene-co-acrylic acid)-Eu Complex by Simple Hydrocarbons in Tetrahydrofuran Solutions

  • Park, Doo-Hee;Kim, Kang-Jin
    • Bulletin of the Korean Chemical Society
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    • 제7권1호
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    • pp.42-45
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    • 1986
  • Quenching of excimer fluorescence from polystyrene-acrylic acid copolymers containing $Eu^{3+}$ has been studied in tetrahydrofuran solution using simple aromatic hydrocarbons as quenchers under steady-state conditions. Aromatic hydrocarbons quenched collisionally the excimer fluorescence and their rate constants of quenching were determined. The magnitude of quenching constant is interpreted in terms of the cube root of the molar volume of quencher. Cycloalkanes were not effective in quenching the excimer fluorescence possibly due to different solubility characteristics from aromatic hydrocarbons.

Intramolecular Excimer Formation Processes of 1,3-Dipyrenylpropane in Silicate Sol-Gel

  • 권미수;이윤희;안병태;이민영
    • Bulletin of the Korean Chemical Society
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    • 제17권2호
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    • pp.158-162
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    • 1996
  • The steady-state emission and fluorescence lifetimes of 1,3-dipyrenylpropane were measured in silicate sol-gel and xerogel matrices. In sol solution, the fluorescence emission spectra of monomer and excimer resemble those in hydrocarbon solvents. In gel and xerogel condition, however, the fluorescence spectra exhibit significant change, largely confirming the intramolecular motions in gel pores are influenced by microviscosity. The rate constants for intramolecular excimer formation were obtained from the measured fluorescence lifetimes and the rate processes for excimer forming in silicate sol-gel are described by a simple kinetic scheme.

Effects of Iron, Chelators and Nitrate Concentration on in vivo Fluorescence and Nitrate Reductase of the Red Tide Organism Amphidinium carterae

  • Yang, Sung-Ryull;Song, Hwan-Seok;Pae, Se-Jin;Huh, Sung-Hoi
    • Journal of the korean society of oceanography
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    • 제34권1호
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    • pp.49-57
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    • 1999
  • A red tide organism, Amphidinium carterae was incubated under different iron/chelator and nitrate concentrations to investigate the factors controlling the growth. The chelation capacity played a critical role in regulating the nitrate reductase (NR) activity and in vivo fluorescence of this organism. However, there was a significant difference between the NR activity and in vivo fluorescence in response to trace metals and chelator treatments. In vivo fluorescence was the highest in FeEDTA 10 ${\mu}$M treatments and the lowest in DTPA 10 ${\mu}$M treatments. This indicates that the availability of the trace metal is important in regulating the in vivo fluorescence of this photosynthetic microalgae In contrast, NR activity showed the highest values in trace metal enriched treatments, and trace metal + DTPA treatments showed fairly high NR activities. This suggests that DTPA treatment did not hinder the NR activity as much as it did in vivo fluorescence. In vivo fluorescence and NR activity increased with nitrate concentration of up to 50 ${\mu}$M and remained relatively constant or the rate of increase decreased above that concentration, indicating that initial nitrate concentration of higher than a certain level would not accelerate the growth of A. carterae. Further investigation is needed to elucidate the reason for the difference in timing sequence between the NR and in vivo fluorescence in response to different metal treatments and chelation capacity.

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