An in vitro diagnosis of oral premalignant lesion using time-resolved fluorescence spectroscopy under UV excitation-a pilot study

被引:5
作者
Kanniyappan, Udayakumar [1 ]
Prakasarao, Aruna [1 ]
Dornadula, Koteeswaran [2 ]
Singaravelu, Ganesan [1 ]
机构
[1] Anna Univ, Dept Med Phys, Chennai 600025, Tamil Nadu, India
[2] Meenakshi Ammal Dent Coll & Hosp, Dept Oral Med & Radiol, Chennai 600095, Tamil Nadu, India
关键词
Fluorescence; Fluorescence lifetime; Premalignant tissue; Discriminant analysis; NATIVE FLUORESCENCE; TISSUES; AUTOFLUORESCENCE; CARCINOMA; MICROSCOPY; LIFETIMES; CANCER; STATE; CELLS; NADH;
D O I
10.1016/j.pdpdt.2016.02.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In spite of rapid advancement in cancer treatment, early diagnosis of cancer and medicable precursors are still the finest approach towards the assurance of patient lives and enhancement in the quality of their life. In this regard, the present study deals with the time-resolved fluorescence spectroscopy of normal and premalignant oral tissues under UV excitations (280 nm and 310 nm). The decay kinetics at 350 nm emission of normal tissues exhibit higher fluorescence lifetime than that of premalignant tissues and subsequent statistical analysis shows that the data were statistically significant. Further, the decay kinetics at 450 nm emission for normal and premalignant oral tissues was obtained. Subsequently, statistical analysis revealed that except fast component, rest of the component lifetimes and fractional amplitudes were not statistically significant. An attempt has also been made to explore the better statistical tool to discriminate premalignant tissues from normal ones at 350 nm emission. Among stepwise linear discriminant analysis (SLDA) and receiver operator characteristics (ROC), the former discriminates premalignant from normal tissues with 86.7% specificity and 93.3% sensitivity. Hence, fluorescence lifetime spectroscopy at 350 nm emission opens a new avenue for early detection of oral cancer. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:18 / 24
页数:7
相关论文
共 33 条
  • [1] Origin of Tryptophan Fluorescence Lifetimes Part 1. Fluorescence Lifetimes Origin of Tryptophan Free in Solution
    Albani, J. R.
    [J]. JOURNAL OF FLUORESCENCE, 2014, 24 (01) : 93 - 104
  • [2] ALFANO R R, 1988, Journal of Tumor Marker Oncology, V3, P165
  • [3] [Anonymous], DIG ENDOSC
  • [4] BANERJEE S, 1989, Indian Journal of Cancer, V26, P21
  • [5] Bedard N., 2013, BIOMED OPT EXP, P4
  • [6] Separating NADH and NADPH fluorescence in live cells and tissues using FLIM
    Blacker, Thomas S.
    Mann, Zoe F.
    Gale, Jonathan E.
    Ziegler, Mathias
    Bain, Angus J.
    Szabadkai, Gyorgy
    Duchen, Michael R.
    [J]. NATURE COMMUNICATIONS, 2014, 5
  • [7] In vivo time-resolved autofluorescence measurements to test for glycation of human skin
    Blackwell, Jennifer
    Katika, Kamal M.
    Pilon, Laurent
    Dipple, Katrina M.
    Levin, Seymour R.
    Nouvong, Aksone
    [J]. JOURNAL OF BIOMEDICAL OPTICS, 2008, 13 (01)
  • [8] Intraoperative delineation of primary brain tumors using time-resolved fluorescence spectroscopy
    Butte, Pramod V.
    Fang, Qiyin
    Jo, Javier A.
    Yong, William H.
    Pikul, Brian K.
    Black, Keith L.
    Marcu, Laura
    [J]. JOURNAL OF BIOMEDICAL OPTICS, 2010, 15 (02)
  • [9] Time-resolved autofluorescence spectroscopy for classifying normal and premalignant oral tissues
    Chen, HM
    Chiang, CP
    You, C
    Hsiao, TC
    Wang, CY
    [J]. LASERS IN SURGERY AND MEDICINE, 2005, 37 (01) : 37 - 45
  • [10] Raman mapping of oral tissues for cancer diagnosis
    Daniel, Amuthachelvi
    Prakasarao, Aruna
    David, Balu
    Joseph, Leena
    Krishna, C. Murali
    Koteeswaran, D.
    Ganesan, Singaravelu
    [J]. JOURNAL OF RAMAN SPECTROSCOPY, 2014, 45 (07) : 541 - 549