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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
来源:
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.
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页码:298 / 307
页数:10
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