Correlation of in vivo photosensitizer fluorescence and photodynamic-therapy-induced depth of necrosis in a murine tumor model

被引:29
|
作者
Cheung, R
Solonenko, M
Busch, TM
Del Piero, F
Putt, ME
Hahn, SM
Yodh, AG
机构
[1] Univ Penn, Dept Phys & Astron, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Pathobiol, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
关键词
spectroscopy; photodynamic therapy; light-induced fluorescence; necrosis; photofrin; radiation-induced fibrosarcoma tumor; dosimetry;
D O I
10.1117/1.1560011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We compared light-induced fluorescence (LIF) to nominal injected drug dose for predicting the depth of necrosis response to photodynamic therapy (PDT) in a murine tumor model. Mice were implanted with radiation-induced fibrosarcoma (RIF) and were injected with 0, 5, or 10 mg/kg Photofrin. 630-nm I ight (30 J/cm(2), 75 mW/cm(2)) was delivered to the tumor after 24 hours. Fluorescence emission (lambda(excitation)=545 nm, lambda(emission)=628 nm) from the tumor was measured. The LIF data had less scatter than injected drug dose, and was found to be at least as good as an injected drug dose for predicting the depth of necrosis after PDT. Our observations provide further evidence that fluorescence spectroscopy can be used to quantify tissue photosensitizer uptake and to predict PDT tissue damage. (C) 2003 Society of Photo-Optical Instrumentation Engineers.
引用
收藏
页码:248 / 252
页数:5
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