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Synthesis and evaluation of [68Ga]Ga-/[177Lu]Lu-PSMA-SCN as a novel prostate-specific membrane antigen-targeting agent for theranostics
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Ling-er LI1, Xin GAO1, Xiu-shuang YUAN1, Xue-li QIU2, Jiang WU3, Lu-lu ZHANG3, Hong-yi HUANG1, Si-qi ZHANG1, Feng WANG3, Ying-zi ZHANG2, *, Kuan HU1, *
Acta Pharmaceutica Sinica | 2025, 60(10) : 3120 - 3130
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Acta Pharmaceutica Sinica | 2025, 60(10): 3120-3130
• Original Articles •
Synthesis and evaluation of [68Ga]Ga-/[177Lu]Lu-PSMA-SCN as a novel prostate-specific membrane antigen-targeting agent for theranostics
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Ling-er LI1, Xin GAO1, Xiu-shuang YUAN1, Xue-li QIU2, Jiang WU3, Lu-lu ZHANG3, Hong-yi HUANG1, Si-qi ZHANG1, Feng WANG3, Ying-zi ZHANG2, *, Kuan HU1, *
Affiliations
  • 1State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
  • 2Department of Orthopedics, the Second Affiliated Hospital of Soochow University, Suzhou 215031, China
  • 3Department of Nuclear Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing 211166, China
Published: 2025-10-12 doi: 10.16438/j.0513-4870.2025-0802
Outline
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Metastatic castration-resistant prostate cancer (mCRPC) is an advanced stage of prostate cancer. It is resistant to first-line prostate cancer treatments and poses a significant threat to men's health. The prostate-specific membrane antigen (PSMA)-targeting radiopharmaceutical [177Lu]Lu-PSMA-617 has been approved by the FDA in 2022 to treat PSMA-positive patients with mCRPC, demonstrating significant clinical benefits on patients. In this work, we introduced a chelator, p-SCN-Bn-DOTA, instead of DOTA for radiolabeling and constructed the radioligand, PSMA-SCN, and systematically evaluated its diagnostic and therapeutic performance in prostate cancer. Both molecular docking and cellular competitive inhibition assays indicated that the introduction of p-SCN-Bn-DOTA enhanced the binding affinity of PSMA-SCN for the target protein PSMA compared to PSMA-617. For diagnosis, [68Ga]Ga-PSMA-SCN was used to evaluate the tumor imaging capability and in vivo metabolic profiling by microPET/CT. Quantitative analysis of microPET images shows higher tumor uptake of [68Ga]Ga-PSMA-SCN [(46.27 ± 0.45) and (31.15 ± 0.21)%ID·g-1] than that of [68Ga]Ga-PSMA-617 [(16.8 ± 0.98) and (13.38 ± 1.44)%ID·g-1] in LNCaP and RM-1 (PSMA+) tumor-bearing mouse models, respectively. [68Ga]Ga-PSMA-SCN also has faster clearance rates in non-targeted organs. The possible reason is that the introduction of p-SCN-Bn-DOTA improves the affinity of PSMA-SCN to the targeting protein and has no significant effect on pharmacokinetic metabolism. For therapeutics, [177Lu]Lu-PSMA-SCN was used in the treatment of tumor-bearing mice to assess its inhibitory effect on tumor growth, and the results demonstrated a favorable safety profile. These results confirm that PSMA-SCN has significant advantages in the theranostics of prostate cancer in comparison with PSMA-617. In conclusion, both theoretical analysis and biological evaluation of the PSMA-targeting molecule PSMA-SCN confirm its potential value for the diagnosis and treatment of prostate cancer. All experimental procedures involving animals were conducted in strict accordance with the ethical guidelines of the Institute of Materia Medica, Chinese Academy of Medical Sciences (ethics approval No. 00002217).

prostate cancer  /  prostate-specific membrane antigen  /  PET  /  gallium-68  /  lutetium-177  /  theranostics
李灵珥, 高新, 袁秀双, 邱学力, 吴江, 张露露, 黄宏怡, 张思琪, 王峰, 张应子, 胡宽. 新型前列腺特异性膜抗原靶向诊疗一体化分子[68Ga]Ga-/[177Lu]Lu-PSMA-SCN的制备与评价. 药学学报, 2025 , 60 (10) : 3120 -3130 . DOI: 10.16438/j.0513-4870.2025-0802
Ling-er LI, Xin GAO, Xiu-shuang YUAN, Xue-li QIU, Jiang WU, Lu-lu ZHANG, Hong-yi HUANG, Si-qi ZHANG, Feng WANG, Ying-zi ZHANG, Kuan HU. Synthesis and evaluation of [68Ga]Ga-/[177Lu]Lu-PSMA-SCN as a novel prostate-specific membrane antigen-targeting agent for theranostics[J]. Acta Pharmaceutica Sinica, 2025 , 60 (10) : 3120 -3130 . DOI: 10.16438/j.0513-4870.2025-0802
Year 2025 volume 60 Issue 10
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87
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doi: 10.16438/j.0513-4870.2025-0802
  • Receive Date:2025-07-11
  • Online Date:2026-09-20
  • Published:2025-10-12
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  • Received:2025-07-11
  • Revised:2025-08-11
Affiliations
    1State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China
    2Department of Orthopedics, the Second Affiliated Hospital of Soochow University, Suzhou 215031, China
    3Department of Nuclear Medicine, Nanjing First Hospital, Nanjing Medical University, Nanjing 211166, China
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表12种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
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Percentage of
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属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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