化学
前列腺癌
联苯
Pet成像
癌症
前列腺
癌症研究
正电子发射断层摄影术
纳米技术
神经科学
内科学
有机化学
医学
材料科学
生物
作者
Yimin Chen,Haonan Yu,Wanjia Liu,Ming Wang,Xinlin Wang,Xiaojun Zhang,Jinming Zhang,Shaobo Yao,Mengchao Cui
标识
DOI:10.1021/acs.jmedchem.5c01166
摘要
Prostate cancer (PCa) diagnosis faces challenges with current imaging tracers in sensitivity and contrast. We developed a biphenyl-trimeric PSMA-targeted theranostic system to address these challenges. A suite of trimeric PSMA probes ( PSMA-T0 – T6 ) was synthesized using a biphenyl scaffold and variable linkers, showing exceptional PSMA affinity ( K i = 0.11–0.60 nM). Preclinical studies demonstrated that [ 68 Ga]Ga- PSMA-T3 provided superior tumor uptake (SUV max 1.16 vs 0.61) and tumor-to-background ratios (TBR 26.82 vs 19.89) over [ 68 Ga]Ga- PSMA-11 in 22Rv1 tumor-bearing mice. The optical counterpart, ICG-conjugated PSMA-T6, prolonged tumor retention with high tumor-to-muscle ratio (T/M = 7.3 at 24 h) and remarkable ex vivo specificity (T/M = 41.9). In first-in-human PET studies, [ 68 Ga]Ga- PSMA-T3 showed comparable and enhanced detection rates of primary and metastatic lesions, particularly in liver and bone metastases, with higher TBR values than [ 68 Ga]Ga- PSMA-11 . Our biphenyl-trimeric PSMA platform demonstrates translational potential for enhanced diagnostic sensitivity and intraoperative management of PCa.
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