Time-resolved fluorescence imaging in biology and medicine

被引:203
作者
Cubeddu, R
Comelli, D
D'Andrea, C
Taroni, P
Valentini, G
机构
[1] Politecn Milan, INFM, Dipartimento Fis, I-20133 Milan, Italy
[2] CNR, IFN, I-20133 Milan, Italy
关键词
D O I
10.1088/0022-3727/35/9/201
中图分类号
O59 [应用物理学];
学科分类号
摘要
Fluorescence lifetime imaging is a rather new and effective tool that can be used to study complex biological samples, either at microscopic or macroscopic levels. The map of the fluorescence lifetime allows one to discriminate amongst different fluorophores and to achieve valuable insights into the behaviour of emitting molecules, leading to information like local pH, oxygen concentration in cells, etc. Moreover, the distribution in space of any fluorescent marker achievable with this technique can be exploited for diagnostic purposes in medicine. After a brief introduction on the motivations for applying fluorescence lifetime imaging in biology and medicine, the basic principles of this technique will be addressed. Then, the two possible implementations of fluorescence lifetime imaging (i.e. the frequency domain and the time domain methods) will be presented. For this purpose, special attention will be devoted to practical aspects of image acquisition and processing, especially for what concerns the time domain method. Then, the analysis of the state-of-the-art systems will include a brief discussion on new concepts that have recently been introduced in this research field. Finally, two interesting applications of fluorescence lifetime imaging will be presented. The former refers to skin tumour detection and has been successfully applied in a preliminary clinical trial, the latter regards DNA chips reading and has been tested only at laboratory level, yet it has produced promising results for its future implementation in commercial systems.
引用
收藏
页码:R61 / R76
页数:16
相关论文
共 116 条
[1]  
Ackroyd R, 2001, PHOTOCHEM PHOTOBIOL, V74, P656, DOI 10.1562/0031-8655(2001)074<0656:THOPAP>2.0.CO
[2]  
2
[3]   Kinetic fluorescence studies of 5-aminolaevulinic acid-induced protoporphyrin IX accumulation in basal cell carcinomas [J].
af Klinteberg, C ;
Enejder, AMK ;
Wang, I ;
Andersson-Engels, S ;
Svanberg, S ;
Svanberg, K .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1999, 49 (2-3) :120-128
[4]   FLUORESCENCE LIFETIME DISTRIBUTIONS IN PROTEINS [J].
ALCALA, JR ;
GRATTON, E ;
PRENDERGAST, FG .
BIOPHYSICAL JOURNAL, 1987, 51 (04) :597-604
[5]  
Andersson-Engels S, 2000, LASER SURG MED, V26, P76, DOI 10.1002/(SICI)1096-9101(2000)26:1<76::AID-LSM11>3.0.CO
[6]  
2-4
[7]  
ANDREONI A, 1981, LASERS APPL, P286
[8]   RATIOING FLUOROMETER PROBE FOR LOCALIZING CARCINOMA INSITU IN BRONCHI OF THE LUNG [J].
BALCHUM, OJ ;
PROFIO, AE ;
RAZUM, N .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 46 (05) :887-891
[9]   CHARACTERIZATION OF THE FLUORESCENT MORPHOLOGICAL STRUCTURES IN HUMAN ARTERIAL-WALL USING ULTRAVIOLET-EXCITED MICROSPECTROFLUORIMETRY [J].
BARAGA, JJ ;
RAVA, RP ;
FITZMAURICE, M ;
TONG, LL ;
TARONI, P ;
KITTRELL, C ;
FELD, MS .
ATHEROSCLEROSIS, 1991, 88 (01) :1-14
[10]   HIGH CONTRAST FLUORESCENCE IMAGING USING 2-WAVELENGTH LASER EXCITATION AND IMAGE-PROCESSING [J].
BAUMGARTNER, R ;
UNSOLD, E .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1987, 1 (01) :130-132