Department of Chemistry and Biochemistry, 251 Nieuwland Science Hall, University of Notre Dame, Notre Dame, Indiana 46556, USA.
J Am Chem Soc. 2010 Jan 13;132(1):67-9. doi: 10.1021/ja908467y.
In vivo optical imaging shows that a fluorescent imaging probe, comprised of a near-infrared fluorophore attached to an affinity group containing two zinc(II)-dipicolylamine (Zn-DPA) units, targets prostate and mammary tumors in two different xenograft animal models. The tumor selectivity is absent with control fluorophores whose structures do not have appended Zn-DPA targeting ligands. Ex vivo biodistribution and histological analyses indicate that the probe is targeting the necrotic regions of the tumors, which is consistent with in vitro microscopy showing selective targeting of the anionic membrane surfaces of dead and dying cells.
体内光学成像显示,一种荧光成像探针由一个近红外荧光团与一个包含两个锌(II)-二吡啶甲胺(Zn-DPA)单元的亲和基团组成,可靶向两种不同异种移植动物模型中的前列腺和乳腺肿瘤。具有未附加 Zn-DPA 靶向配体的结构的对照荧光团则没有肿瘤选择性。离体生物分布和组织学分析表明,该探针靶向肿瘤的坏死区域,这与体外显微镜检查一致,表明该探针选择性地靶向死亡和垂死细胞的阴离子膜表面。