Predictions of mathematical models of tissue oxygenation and generation of singlet oxygen during photodynamic therapy

被引:15
作者
Yuan, J
MahamaRelue, PA
Fournier, RL
Hampton, JA
机构
[1] UNIV TOLEDO,DEPT BIOENGN,TOLEDO,OH 43606
[2] MED COLL OHIO,DEPT PATHOL,TOLEDO,OH 43614
[3] MED COLL OHIO,DEPT UROL,TOLEDO,OH 43614
关键词
D O I
10.2307/3579524
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Photodynamic therapy (PDT) is a relatively new protocol for cancer treatment which has recently been approved for limited clinical use. Traditionally, the success of treatment with PDT has been compared on the basis of total light delivery, Using the mathematical model of Henning et al. (Radiat. Res. 142, 221-226, 1995), we have determined that when oxygen is not depleted from the tissue, the concentration of singlet oxygen that is generated is directly proportional to the product of the light fluence rate (Phi) and the concentration of the photosensitizer (C-s). Therefore, Phi C-s is an appropriate parameter for comparing the potential success of PDT protocols under these conditions. For a treatment of time t, the observed photodynamic effect resulting from singlet oxygen exposure should be directly related to Phi C(s)t. For high Phi C-s, the model predicts that oxygen depletion occurs within the tumor tissue. As a result, the photodynamic effect is no longer proportional to Phi C(s)t. We have expanded the model of Henning et al. to include the changes in oxygen concentration which occur within the capillary as blood flows through the tissue, Our new predictions with the mathematical model for optimal PDT treatment conditions are significantly different from those predicted by the previous models, Predictions of the model are given using parameters relevant for treatment of solid tumors with Photofrin(R). (C) 1997 bg Radiation Research Society.
引用
收藏
页码:386 / 394
页数:9
相关论文
共 26 条
[1]   PHOTOBLEACHING OF PHOTOFRIN-II AS A MEANS OF ELIMINATING SKIN PHOTOSENSITIVITY [J].
BOYLE, DG ;
POTTER, WR .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 46 (06) :997-1001
[2]   OXYGEN DEPENDENCY OF TUMOR-CELL KILLING INVITRO BY LIGHT-ACTIVATED PHOTOFRIN-II [J].
CHAPMAN, JD ;
STOBBE, CC ;
ARNFIELD, MR ;
SANTUS, R ;
LEE, J ;
MCPHEE, MS .
RADIATION RESEARCH, 1991, 126 (01) :73-79
[3]   THE EFFECT OF LIGHT FLUENCE RATE IN PHOTODYNAMIC THERAPY OF NORMAL RAT-BRAIN [J].
CHEN, Q ;
CHOPP, M ;
DERESKI, MO ;
WILSON, BC ;
PATTERSON, MS ;
SCHREIBER, A ;
HETZEL, FW .
RADIATION RESEARCH, 1992, 132 (01) :120-123
[4]   DOSE-DEPENDENT METABOLIC RESPONSE OF MAMMARY-CARCINOMA TO PHOTODYNAMIC THERAPY [J].
CHOPP, M ;
HETZEL, FW ;
JIANG, Q .
RADIATION RESEARCH, 1990, 121 (03) :288-294
[5]   MORPHOLOGIC AND HEMODYNAMIC COMPARISON OF TUMOR AND HEALING NORMAL TISSUE MICROVASCULATURE [J].
DEWHIRST, MW ;
TSO, CY ;
OLIVER, R ;
GUSTAFSON, CS ;
SECOMB, TW ;
GROSS, JF .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1989, 17 (01) :91-99
[6]  
FOSTER TH, 1995, P SOC PHOTO-OPT INS, V2392, P141, DOI 10.1117/12.208183
[7]   OXYGEN-CONSUMPTION AND DIFFUSION EFFECTS IN PHOTODYNAMIC THERAPY [J].
FOSTER, TH ;
MURANT, RS ;
BRYANT, RG ;
KNOX, RS ;
GIBSON, SL ;
HILF, R .
RADIATION RESEARCH, 1991, 126 (03) :296-303
[8]   DOSIMETRY IN PHOTODYNAMIC THERAPY - OXYGEN AND THE CRITICAL IMPORTANCE OF CAPILLARY DENSITY [J].
FOSTER, TH ;
GAO, L .
RADIATION RESEARCH, 1992, 130 (03) :379-383
[9]  
FOSTER TH, 1992, SPIE, V1645, P104
[10]  
FOURNIER RL, 1995, BASIC CONCEPTS BIOME, P115