A Cyanine-Bridged Somatostatin Hybrid Probe for Multimodal SSTR2 Imaging in Vitro and in Vivo: Synthesis and Evaluation

被引:6
作者
Heing-Becker, Isabelle [1 ]
Grotzinger, Carsten [2 ]
Beindorff, Nicola [3 ]
Prasad, Sonal [3 ,4 ]
Erdmann, Sarah [2 ]
Exner, Samantha [2 ]
Haag, Rainer [1 ]
Licha, Kai [1 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, Takustr 3, D-14195 Berlin, Germany
[2] Charite Univ Med Berlin, Dept Gastroenterol & Hepatol, Augustenburger Pl 1, D-13353 Berlin, Germany
[3] Charite Univ Med Berlin, BERIC Berlin Expt Radionuclide Imaging Ctr, Augustenburger Pl 1, D-13353 Berlin, Germany
[4] Charite Univ Med Berlin, Dept Nucl Med, Augustenburger Pl 1, D-13353 Berlin, Germany
关键词
cyanines; fluorescence; multimodal imaging; octreotate; SSTR2; ANALOG; FLUORESCENT; GA-68-DOTATATE; AFFINITY; CANCER; AGENTS; TATE;
D O I
10.1002/cbic.202000791
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
Multimodal imaging probes have attracted the interest of ongoing research, for example, for the surgical removal of tumors. Modular synthesis approaches allow the construction of hybrid probes consisting of a radiotracer, a fluorophore and a targeting unit. We present the synthesis of a new asymmetric bifunctional cyanine dye that can be used as a structural and functional linker for the construction of such hybrid probes. Ga-68-DOTATATE, a well-characterized radiopeptide targeting the overexpressed somatostatin receptor subtype 2 (SSTR2) in neuroendocrine tumors, was labeled with our cyanine dye, thus providing additional information along with the data obtained from the radiotracer. We tested the SSTR2-targeting and imaging properties of the resulting probe Ga-68-DOTA-ICC-TATE in vitro and in a tumor xenograft mouse model. Despite the close proximity between dye and pharmacophore, we observed a high binding affinity towards SSTR2 as well as elevated uptake in SSTR2-overexpressing tumors in the positron emission tomography (PET) scan and histological examination.
引用
收藏
页码:1307 / 1315
页数:9
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