In vivo determination of the absorption and scattering spectra of the human prostate during photodynamic therapy

被引:18
作者
Finlay, JC [1 ]
Zhu, TC [1 ]
Dimofte, A [1 ]
Stripp, D [1 ]
Malkowicz, SB [1 ]
Whittington, R [1 ]
Miles, J [1 ]
Glatstein, E [1 ]
Hahn, SM [1 ]
机构
[1] Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
来源
OPTICAL METHODS FOR TUMOR TREATMENT AND DETECTION: MECHANISMS AND TECHNIQUES IN PHOTODYNAMIC THERAPY XIII | 2004年 / 5315卷
关键词
photodynamic therapy; motexafin lutetiurn; in-vivo light dosimetry; tissue optical properties; diffusion theory; diffuse reflectance;
D O I
10.1117/12.528968
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A continuing challenge in photodynamic therapy is the accurate in vivo determination of the optical properties of the tissue being treated. We have developed a method for characterizing the absorption and scattering spectra of prostate tissue undergoing PDT treatment. Our current prostate treatment protocol involves interstitial illumination of the organ via cylindrical diffusing optical fibers (CDFs) inserted into the prostate through clear catheters. We employ one of these catheters to insert an isotropic white light point source into the prostate. An isotropic detection fiber connected to a spectrograph is inserted into a second catheter a known distance away. The detector is moved along the catheter by a computer-controlled step motor, acquiring diffuse light spectra at 2 mm intervals along its path. We model the fluence rate as a function of wavelength and distance along the detector's path using an infinite medium diffusion theory model whose free parameters are the absorption coefficient La at each wavelength and two variables A and b which characterize the reduced scattering spectrum of the form mu'(s) = Alambda(-b). We analyze our spectroscopic data using a nonlinear fitting algorithm to determine A, b, and mu(a) at each wavelength independently; no prior knowledge of the absorption spectrum or of the sample's constituent absorbers is required. We have tested this method in tissue simulating phantoms composed of intralipid and the photosensitizer motexafin lutetium (MLu). The MLu absorption spectrum recovered from the phantoms agrees with that measured in clear solution, and mu(a) at the MLu absorption peak varies linearly with concentration. The mu'(s) spectrum reported by the fit is in agreement with the known scattering coefficient of intralipid. We have applied this algorithm to spectroscopic data from human patients sensitized with MLu (2 mg kg(-1)) acquired before and after PDT. Before PDT, the absorption spectra we measure include the characteristic MLu absorption peak. Using our phantom data as a calibration, we have determined the pre-treatment MLu concentration to be approximately 2 to 8 mg kg(-1). After PDT, the concentration is reduced to 1 to 2.5 mg kg(-1), an indication of photobleaching induced by irradiation. In addition, absorption features corresponding to the oxygenated and deoxygenated forms of hemoglobin indicate a reduction in tissue oxygenation during treatment.
引用
收藏
页码:132 / 142
页数:11
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