连接器
化学
内化
药代动力学
放射性配体
前列腺癌
药效学
放射合成
药理学
体内
癌症研究
多塔
体外
生物化学
脚手架
BETA(编程语言)
体内分布
配体(生物化学)
联动装置(软件)
敌手
生物物理学
结构-活动关系
唾液腺
癌症
谷氨酸羧肽酶Ⅱ
受体
Pet成像
肿瘤细胞
作者
Xin Gao,Yuan Miao,Linger Li,Dong Dai,Hongyi Huang,Quan Zuo,Jiang Wu,Can Liu,Feng Wang,Shufen Zhang,Rui Wang,Kuan Hu
标识
DOI:10.1021/acs.jmedchem.5c02821
摘要
[ 18 F]PSMA-1007 is widely used for prostate cancer imaging, but suffers from nonspecific accumulation in healthy tissues. Our previous work demonstrated that linker manipulation with beta 3 (β 3 )-amino acid effectively reduces salivary gland accumulation and enhances tumor uptake of PSMA-617. Here, we redesigned the scaffold of [ 18 F]PSMA-1007 by incorporating β 3 -amino acid linker and a DOTA chelator, yielding PSMA-HK9. Preclinical evaluations showed that [ 68 Ga]Ga-PSMA-HK9 demonstrated enhanced binding affinity, significantly reduced uptake in kidneys and salivary glands, and increased tumor uptake compared with the 68 Ga-labeled analog of [ 18 F]PSMA-1007. A first-in-human study further characterized the in vivo pharmacokinetics of [ 68 Ga]Ga-PSMA-HK9, revealing a trend toward higher tumor uptake compared with [ 68 Ga]Ga-PSMA-617. Therapeutically, [ 177 Lu]Lu-PSMA-HK9 demonstrated efficient cellular internalization and superior tumor inhibition compared with [ 177 Lu]Lu-PSMA-617, with acceptable safety profiles. These findings indicate the linker manipulation with β 3 -amino acid as an effective and promising strategy for optimizing the pharmacokinetics and pharmacodynamics performance of PSMA-targeted radioligands.
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