A hyperspectral fluorescence lifetime probe for skin cancer diagnosis

被引:73
作者
De Beule, P. A. A. [1 ]
Dunsby, C. [1 ]
Galletly, N. P. [2 ]
Stamp, G. W. [2 ]
Chu, A. C. [3 ]
Anand, U. [4 ]
Anand, P. [4 ]
Benham, C. D. [5 ]
Naylor, A. [5 ]
French, P. M. W. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Phys, London SW7 2AZ, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Histopathol, London W12 0NN, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Dermatol, London W12 0NN, England
[4] Univ London Imperial Coll Sci Technol & Med, Dept Neurosci & Mental Hlth, London W12 0NN, England
[5] GlaxoSmithKline, Harlow CM19 5AW, Essex, England
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1063/1.2818785
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
The autofluorescence of biological tissue can be exploited for the detection and diagnosis of disease but, to date, its complex nature and relatively weak signal levels have impeded its widespread application in biology and medicine. We present here a portable instrument designed for the in situ simultaneous measurement of autofluorescence emission spectra and temporal decay profiles, permitting the analysis of complex fluorescence signals. This hyperspectral fluorescence lifetime probe utilizes two ultrafast lasers operating at 355 and 440 nm that can excite autofluorescence from many different biomolecules present in skin tissue including keratin, collagen, nicotinamide adenine dinucleotide (phosphate), and flavins. The instrument incorporates an optical fiber probe to provide sample illumination and fluorescence collection over a millimeter-sized area. We present a description of the system, including spectral and temporal characterizations, and report the preliminary application of this instrument to a study of recently resected (<2 h) ex vivo skin lesions, illustrating its potential for skin cancer detection and diagnosis. (C) 2007 American Institute of Physics.
引用
收藏
页数:7
相关论文
共 40 条
[11]   Spectrally resolved time-correlated single photon counting: a novel approach for characterization of endogenous fluorescence in isolated cardiac myocytes [J].
Chorvat, D., Jr. ;
Chorvatova, A. .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2006, 36 (01) :73-83
[12]   CROSS-LINKING IN COLLAGEN AND ELASTIN [J].
EYRE, DR ;
PAZ, MA ;
GALLOP, PM .
ANNUAL REVIEW OF BIOCHEMISTRY, 1984, 53 :717-748
[13]   Time-domain laser-induced fluorescence spectroscopy apparatus for clinical diagnostics [J].
Fang, QY ;
Papaioannou, T ;
Jo, JA ;
Vaitha, R ;
Shastry, K ;
Marcu, L .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2004, 75 (01) :151-162
[14]   FLUORESCENCE DECAY STUDIES OF REDUCED NICOTINAMIDE ADENINE-DINUCLEOTIDE IN SOLUTION AND BOUND TO LIVER ALCOHOL-DEHYDROGENASE [J].
GAFNI, A ;
BRAND, L .
BIOCHEMISTRY, 1976, 15 (15) :3165-3171
[15]  
Gupta PK, 1997, LASER SURG MED, V21, P417, DOI 10.1002/(SICI)1096-9101(1997)21:5<417::AID-LSM2>3.0.CO
[16]  
2-T
[17]   INSITU DIFFERENTIATION BETWEEN NEVI AND MALIGNANT MELANOMAS BY FLUORESCENCE MEASUREMENTS [J].
LOHMANN, W ;
NILLES, M ;
BODEKER, RH .
NATURWISSENSCHAFTEN, 1991, 78 (10) :456-457
[18]   In vivo detection of macrophages in a rabbit atherosclerotic model by time-resolved laser-induced fluorescence spectroscopy [J].
Marcu, L ;
Fang, QY ;
Jo, JA ;
Papaioannou, T ;
Dorafshar, A ;
Reil, T ;
Qiao, JH ;
Baker, JD ;
Freischlag, JA ;
Fishbein, MC .
ATHEROSCLEROSIS, 2005, 181 (02) :295-303
[19]   Fluorescence lifetime spectroscopy of glioblastoma multiforme [J].
Marcu, L ;
Jo, JA ;
Butte, PV ;
Yong, WH ;
Pikul, BK ;
Black, KL ;
Thompson, RC .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 2004, 80 (01) :98-103
[20]  
MARCU L, 2000, P SOC PHOTO-OPT INS, V1, P93