化学
放射性配体
谷氨酸羧肽酶Ⅱ
前列腺癌
体内分布
多塔
药代动力学
癌症研究
放射性核素治疗
放射化学
正电子发射断层摄影术
螯合作用
癌症
核医学
药理学
体外
生物化学
内科学
医学
有机化学
作者
Yimin Chen,Xiaojun Zhang,Ming Ni,Xi Gao,Xinlin Wang,Qiang Xie,Jinming Zhang,Mengchao Cui
标识
DOI:10.1021/acs.jmedchem.3c01475
摘要
Radioisotope-labeled prostate-specific membrane antigen (PSMA) PET tracers have gained popularity in diagnosing prostate cancer (PCa). This study aimed to improve the affinity and tumor-targeting capabilities of new PSMA tracers by increasing the number of pharmacophores that specifically bind to PSMA. Using biphenyl as a core scaffold, we investigated the relationship among spacer segments, affinity, and pharmacokinetic properties. In preclinical PET studies on mice with 22Rv1 tumors, compared with [68Ga]Ga-PSMA-11 (SUVmax = 3.37), [68Ga]Ga-PSMA-D5 (Ki = 0.15) showed higher tumor uptake (SUVmax = 3.51) and lower renal uptake (T/K = 1.84). In the first-in-human study, [68Ga]Ga-PSMA-D5 effectively detected small PCa-associated lesions and distant metastases. The advantages of [68Ga]Ga-PSMA-D5 include high tumor uptake, straightforward synthesis, and labeling, making it a promising PSMA PET tracer. Furthermore, [68Ga]Ga-PSMA-D5 contains a DOTA chelator, allowing convenient labeling with therapeutic radionuclides such as 177Lu and 225Ac, providing the potential for targeted radioligand therapy in PCa.
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