A novel approach to a bifunctional photosensitizer for tumor imaging and phototherapy

被引:85
作者
Chen, YH
Gryshuk, A
Achilefu, S
Ohulchansky, T
Potter, W
Zhong, TX
Morgan, J
Chance, B
Prasad, PN
Henderson, BW
Oseroff, A
Pandey, RK [1 ]
机构
[1] Roswell Pk Canc Inst, PDT Ctr, Buffalo, NY 14263 USA
[2] Roswell Pk Canc Inst, Dept Dermatol, Buffalo, NY 14263 USA
[3] Washington Univ, Sch Med, Dept Radiol, St Louis, MO 63110 USA
[4] SUNY Buffalo, Dept Chem, Buffalo, NY 14221 USA
[5] Univ Penn, Dept Biophys, Philadelphia, PA 19104 USA
关键词
D O I
10.1021/bc050177o
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Optical imaging has attracted a great attention for studying molecular recognitions because minute fluorescent tracers can be detected in homogeneous and heterogeneous media with existing laboratory instruments. In our preliminary study, a clinically relevant photosensitizer (HPPH, a chlorophyll-a analog) was linked with a cyanine dye (with required photophysical characteristics but limited tumor selectivity), and the resulting conjugate was found to be an efficient tumor imaging (fluorescence imaging) and photosensitizing agent. Compared to HPPH, the presence of the cyanine dye moiety in the conjugate produced a significantly higher uptake in tumor than skin. At a therapeutic/imaging dose, the conjugate did not show any significant skin phototoxicity, a major drawback associated with most of the porphyrin-based photosensitizers. These results suggest that tumor-avid porphyrin-based compounds can be used as "vehicles" to deliver the desired fluorescent agent(s) to tumor. The development of tumor imaging or improved photodynamic therapy agent(s) by itself represents an important step, but a dual function agent (fluorescence imaging and photodynamic therapy) provides the potential for tumor detection and targeted photodynamic therapy, combining two modalities into a single cost-effective "see and treat" approach.
引用
收藏
页码:1264 / 1274
页数:11
相关论文
共 54 条
[1]   Synthesis, in vitro receptor binding, and in vivo evaluation of fluorescein and carbocyanine peptide-based optical contrast agents [J].
Achilefu, S ;
Jimenez, HN ;
Dorshow, RB ;
Bugaj, JE ;
Webb, EG ;
Wilhelm, RR ;
Rajagopalan, R ;
Johler, J ;
Erion, JL .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (10) :2003-2015
[2]   Metal complexes as photo- and radiosensitizers [J].
Ali, H ;
van Lier, JE .
CHEMICAL REVIEWS, 1999, 99 (09) :2379-2450
[3]   PHOTOSENSITIZED DESTRUCTION OF HUMAN BLADDER-CARCINOMA CELLS TREATED WITH CHLORIN E6-CONJUGATED MICROSPHERES [J].
BACHOR, R ;
SHEA, CR ;
GILLIES, R ;
HASAN, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) :1580-1584
[4]   Receptor-targeted optical imaging of tumors with near-infrared fluorescent ligands [J].
Becker, A ;
Hessenius, C ;
Licha, K ;
Ebert, B ;
Sukowski, U ;
Semmler, W ;
Wiedenmann, B ;
Grötzinger, C .
NATURE BIOTECHNOLOGY, 2001, 19 (04) :327-331
[5]  
Bellnier DA, 2003, CANCER RES, V63, P1806
[6]  
BELLNIER DA, 1995, PHOTOCHEM PHOTOBIOL, V62, P896
[7]   An assay for the quantitation of Photofrin(R) in tissues and fluids [J].
Bellnier, DA ;
Greco, WR ;
Parsons, JC ;
Oseroff, AR ;
Kuebler, A ;
Dougherty, TJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (02) :237-244
[8]   POTENTIATION OF PHOTODYNAMIC THERAPY IN MICE WITH RECOMBINANT HUMAN TUMOR-NECROSIS-FACTOR-ALPHA [J].
BELLNIER, DA .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1991, 8 (02) :203-210
[9]  
CHANCE B, 1979, J BIOL CHEM, V254, P4764
[10]   Synthesis and photosensitizing efficacy of isomerically pure bacteriopurpurinimides [J].
Chen, YH ;
Sumlin, A ;
Morgan, J ;
Gryshuk, A ;
Oseroff, A ;
Henderson, BW ;
Dougherty, TJ ;
Pandey, RK .
JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (20) :4814-4817