A targeted low molecular weight near-infrared fluorescent probe for prostate cancer

被引:58
|
作者
Liu, Tiancheng [1 ]
Wu, Lisa Y. [1 ]
Hopkins, Mark R. [1 ]
Choi, Joseph K. [1 ]
Berkman, Clifford E. [1 ,2 ]
机构
[1] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
[2] Canc Targeted Technol, Woodinville, WA 98072 USA
基金
美国国家卫生研究院;
关键词
Tumor-targeting; Near-infrared imaging; PSMA; Cy5.5; conjugate; GLUTAMATE-CARBOXYPEPTIDASE-II; MEMBRANE ANTIGEN; PRECLINICAL EVALUATION; PHOTODYNAMIC THERAPY; MONOCLONAL-ANTIBODY; SOLID TUMORS; INHIBITORS; J591; INTERNALIZATION; EXPRESSION;
D O I
10.1016/j.bmcl.2010.09.057
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Prostate-specific membrane antigen (PSMA) remains an active target for imaging and therapeutic applications for prostate cancer. Although radionuclide-based imaging is generally more sensitive and also has been deeply explored, near-infrared fluorescence imaging agents are simple to prepare and compatible with long-term storage conditions. In the present study, a near-infrared fluorescent imaging probe (Cy5.5-CTT-54.2) has been developed by chemical conjugation of Cy5.5N-hydroxysuccinimide ester (Cy5.5-NHS) with a potent PSMA inhibitor CTT-54.2 (IC(50) = 144 nM). The probe displays a highly potency (IC(50) = 0.55 nM) against PSMA and has demonstrated successful application for specifically labeling PSMA-positive prostate cancer cells in both two and three-dimensional cell culture conditions. These results suggest that the potent, near-infrared Cy5.5-PSMA inhibitor conjugate may be useful for the detection of prostate tumor cells by optical in vivo imaging. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7124 / 7126
页数:3
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