Photophysics and photochemistry of photodynamic therapy: fundamental aspects

被引:667
作者
Plaetzer, K. [1 ]
Krammer, B. [1 ]
Berlanda, J. [1 ]
Berr, F. [2 ,3 ]
Kiesslich, T. [2 ,3 ]
机构
[1] Salzburg Univ, Dept Mol Biol, A-5020 Salzburg, Austria
[2] Paracelsus Med Univ, Univ Hosp Internal Med 1, A-5020 Salzburg, Austria
[3] SALK, A-5020 Salzburg, Austria
关键词
Photodynamic therapy; Photophysics; Photochemistry; Photosensitizer; Singlet oxygen; SULFONATED MESO-TETRAPHENYLPORPHINES; SINGLET OXYGEN; IN-VIVO; 5-AMINOLEVULINIC ACID; PROTOPORPHYRIN-IX; PHTHALOCYANINE TETRASULFONATE; FLUORESCENCE; CELLS; LIGHT; PHOTOSENSITIZERS;
D O I
10.1007/s10103-008-0539-1
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Photodynamic therapy (PDT) is a treatment modality for cancer and various other diseases. The clinical protocol covers the illumination of target cells (or tissue), which have been loaded with a photoactive drug (photosensitizer). In this review we describe the photophysical and primary photochemical processes that occur during PDT. Interaction of light with tissue results in attenuation of the incident light energy due to reflectance, absorption, scattering, and refraction. Refraction and reflection are reduced by perpendicular light application, whereas absorption can be minimized by the choice of a photosensitizer that absorbs in the far red region of the electromagnetic spectrum. Interaction of light and the photosensitizer can result in degradation, modification or relocalization of the drug, which differently affect the effectiveness of PDT. Photodynamic therapy itself, however, employs the light-induced chemical reactions of the activated photosensitizer (triplet state), resulting in the production of various reactive oxygen species, amongst them singlet oxygen as the primary photochemical product. Based on these considerations, the properties of an ideal photosensitizer for PDT are discussed. According to the clinical experience with PDT, it is proposed that the innovative concept of PDT is most successfully implemented into the mainstream of anticancer therapies by following an application-, i.e. tumor-centered approach with a focus on the actual clinical requirements of the respective tumor type.
引用
收藏
页码:259 / 268
页数:10
相关论文
共 70 条
[1]   Photosensitizers in clinical PDT [J].
Allison, Ron R. ;
Downie, Gordon H. ;
Cuenca, Rosa ;
Hu, Xin-Hua ;
Childs, Carter J. H. ;
Sibata, Claudio H. .
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2004, 1 (01) :27-42
[2]   THE OPTICS OF HUMAN-SKIN [J].
ANDERSON, RR ;
PARRISH, JA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1981, 77 (01) :13-19
[3]  
[Anonymous], 2003, Introduction to Biophotonics
[4]  
Aveline B.M., 2001, PHOTODYNAMIC THERAPY, P17
[5]  
Bagdonas S, 2000, PHOTOCHEM PHOTOBIOL, V72, P186, DOI 10.1562/0031-8655(2000)072<0186:POAAIP>2.0.CO
[6]  
2
[7]  
Ball DJ, 1999, PHOTOCHEM PHOTOBIOL, V69, P390, DOI 10.1562/0031-8655(1999)069<0390:ACSOTC>2.3.CO
[8]  
2
[9]   INTRACELLULAR-LOCALIZATION OF SULFONATED MESO-TETRAPHENYLPORPHINES IN A HUMAN CARCINOMA CELL-LINE [J].
BERG, K ;
WESTERN, A ;
BOMMER, JC ;
MOAN, J .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1990, 52 (03) :481-487
[10]   LIGHT-INDUCED RELOCALIZATION OF SULFONATED MESO-TETRAPHENYLPORPHINES IN NHIK 3025 CELLS AND EFFECTS OF DOSE FRACTIONATION [J].
BERG, K ;
MADSLIEN, K ;
BOMMER, JC ;
OFTEBRO, R ;
WINKELMAN, JW ;
MOAN, J .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1991, 53 (02) :203-210