Synthesis and evaluation of 111In-labeled tetrapeptide-based compounds as single-photon emission computed tomography imaging probes targeting granzyme B

被引:0
|
作者
Kazuta, Nobuki [1 ]
Watanabe, Hiroyuki [1 ]
Ono, Masahiro [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Patho Funct Bioanal, Kyoto, Japan
[2] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Patho Funct Bioanal, 46 29 Yoshida Shimoadachi cho,Sakyo ku, Kyoto 6068501, Japan
关键词
In-111; granzyme B; immune checkpoint inhibitor (ICI); single-photon emission computed tomography (SPECT); CARBONIC ANHYDRASE-IX; PHARMACOKINETICS; RADIOLIGAND; INHIBITORS; CANCER;
D O I
10.1002/jlcr.4045
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Granzyme B is an attractive target as a biomarker for contributing to improve the treatment with immune checkpoint inhibitor (ICI). In this study, we designed novel In-111-labeled granzyme B-targeting single-photon emission computed tomography (SPECT) imaging probes, [In-111]IDT and [In-111]IDAT. Nonradioactive In-labeled granzyme B-targeting compounds ([In-nat]IDT, [In-nat]IDAT) showed the affinity for recombinant mouse granzyme B. [In-111]IDT and [In-111]IDAT were obtained with moderate radiochemical yield and high stability in mouse plasma (>95%). In a biodistribution experiment using tumor-bearing mice, [In-111]IDT and [In-111]IDAT showed moderate accumulation in tumor. Ex vivo autoradiography (ARG) indicated that the accumulation of radioactivity in tumor was correlated to expression of granzyme B confirmed by the immunohistochemical staining. These results indicated that [In-111]IDT and [In-111]IDAT showed the basic properties as granzyme B-targeting SPECT probes.
引用
收藏
页码:298 / 307
页数:10
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