Glu-Urea-Lys Scaffold Functionalized Superparamagnetic Iron Oxide Nanoparticles Targeting PSMA for In Vivo Molecular MRI of Prostate Cancer

被引:5
作者
Zhou, Wei [1 ]
Huang, Jiandong [1 ]
Xiao, Qingwei [1 ]
Hu, Shunmin [1 ]
Li, Shijia [1 ]
Zheng, Jie [1 ]
Du, Zhiyun [1 ]
Peng, Jiangling [1 ]
Chen, Huixiong [1 ,2 ]
机构
[1] Guangdong Univ Technol, Sch Biomed & Pharmaceut Sci, 100 Waihuanxi Rd, Guangzhou 510006, Peoples R China
[2] Paris Descartes Univ, Lab Pharmacol & Toxicol Chem & Biochem, UMR 8601, CNRS, F-75006 Paris, France
基金
中国国家自然科学基金;
关键词
prostate cancer; PSMA; molecular imaging; MRI contrast agent; SPIONs; MEMBRANE ANTIGEN PSMA; INHIBITORS; LIGANDS; CONTRAST; THERAPY; WEIGHT; PROBES; AGENTS; SPIONS;
D O I
10.3390/pharmaceutics14102051
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The prostate specific membrane antigen (PSMA), extensively overexpressed on prostate cancer (PCa) cell surface, has been validated as a diagnostic biomarker for PCa. However, insufficient attention has been paid to the development of PSMA-specific probes loaded with small chemical molecules for the in vivo molecular imaging of PCa. In this study, we innovatively labelled superparamagnetic iron oxide nanoparticles with a PSMA-targeting Glu-Urea-Lys scaffold. An optimized synthetic route was developed to offer a physiochemically stable probe. The probe demonstrated high binding affinity (0.38 +/- 0.08 mu g(Fe)/mL) and binding specificity to PSMA expressed on prostate cancer cell surface in vitro. In a xenograft PCa mouse model, significant negative contrast of the implanted prostate cancer xenograft could be specifically observed by MRI 6 h after tail vein injection of the tracer (Fe, 20 mg/kg), exhibiting its potential to exclusively enhance magnetic resonance detection of PCa.
引用
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页数:21
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