Determination of the distribution of light, optical properties, drug concentration, and tissue oxygenation in-vivo in human prostate during motexafin lutetium-mediated photodynamic therapy

被引:170
作者
Zhu, TC [1 ]
Finlay, JC [1 ]
Hahn, SM [1 ]
机构
[1] Hosp Univ Penn, Dept Radiat Oncol, Philadelphia, PA 19104 USA
关键词
PDT; in-vivo; optical properties; prostate; MLu; motexafin lutetium;
D O I
10.1016/j.jphotobiol.2004.09.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is desirable to quantify the distribution of the light fluence rate, the optical properties, the drug concentration, and the tissue oxygenation for photodynamic therapy (PDT) of prostate cancer. We have developed an integrated system to determine these quantities before and after PDT treatment using motorized probes. The optical properties (absorption (mu(a) transport scattering and effective attenuation (mu(eff)) coefficients) of cancerous human prostate were measured in-vivo using interstitial isotropic detectors. Measurements were made at 732 nm before and after motexafin lutetium (MLu) mediated PDT at different locations along each catheter. The light fluence rate distribution was also measured along the catheters during PDT. Diffuse absorption spectroscopy measurement using a white light source allows extrapolation of the distribution of oxygen saturation NOD, total blood volume ([Hb](t)), and MLu concentration. The distribution of drug concentration was also studied using fluorescence from a single optical fiber, and was found to be in good agreement with the values determined by absorption spectroscopy. This study shows significant inter- and intra-prostatic variations in the tissue optical properties and MLu drug distribution, suggesting that a real-time dosimetry measurement and feedback system for monitoring these values during treatment should be considered in future PDT studies. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:231 / 241
页数:11
相关论文
共 42 条
[1]   OPTICAL-PROPERTIES OF EXPERIMENTAL PROSTATE TUMORS INVIVO [J].
ARNFIELD, MR ;
CHAPMAN, JD ;
TULIP, J ;
FENNING, MC ;
MCPHEE, MS .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1993, 57 (02) :306-311
[2]   Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies [J].
Baas, P ;
Murrer, L ;
Zoetmulder, FAN ;
Stewart, FA ;
Ris, HB ;
vanZandwijk, N ;
Peterse, JL ;
Rutgers, EJT .
BRITISH JOURNAL OF CANCER, 1997, 76 (06) :819-826
[3]  
CATALONA WJ, 1996, LANCET, V347, P883
[4]  
Chang SC, 1996, INT J CANCER, V67, P555
[5]  
Chang SC, 1997, PROSTATE, V32, P89, DOI 10.1002/(SICI)1097-0045(19970701)32:2<89::AID-PROS3>3.0.CO
[6]  
2-A
[7]  
Chen Q, 2002, PHOTOCHEM PHOTOBIOL, V76, P438, DOI 10.1562/0031-8655(2002)076<0438:PSINCP>2.0.CO
[8]  
2
[9]   Changes in in vivo optical properties and light distributions in normal canine prostate during photodynamic therapy [J].
Chen, Q ;
Wilson, BC ;
Shetty, SD ;
Patterson, MS ;
Cerny, JC ;
Hetzel, FW .
RADIATION RESEARCH, 1997, 147 (01) :86-91
[10]   Role of interstitial radiotherapy in the management of clinically organ-confined prostate cancer: The jury is still out [J].
DAmico, AV ;
Coleman, CN .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (01) :304-315