体内分布
化学
高效液相色谱法
肽
显像剂
多塔
放射化学
Pet成像
药理学
核医学
生物化学
色谱法
体内
正电子发射断层摄影术
体外
螯合作用
医学
生物技术
生物
有机化学
作者
Naeimeh Amraee,Behrouz Alirezaour,Mohammad Hosntalab,Asghar Hadadi,Hassan Yousefnia
出处
期刊:Current Radiopharmaceuticals
[Bentham Science]
日期:2024-02-22
卷期号:17
标识
DOI:10.2174/0118744710246897240209070005
摘要
Background: In this study, [64Cu]Cu-NODAGA-RGD-BBN was prepared and its preclinical assessments were evaluated for PET imaging of GRPR overexpressing tumors. background: Among the 64Cu peptide-based radiopharmaceuticals, targeting of GRPRs, somatostatin receptors (SSTRs), and integrins αvβ3, have received the most attention Methods: NODAGA-RGD-BBN heterodimer peptide was successfully labeled with cyclotronproduced copper-64 at optimized conditions. The radiochemical purity of the radiotracer was checked by HPLC and RTLC methods. The stability of the radiolabeled compound was assessed in PBS (4°C) and in human blood serum (37°C). Binding affinity and internalization of [64Cu]Cu-NODAGA-RGD-BBN were studied on PC3, LNCaP, and CHO cell lines. The biodistribution of the radiotracer was evaluated in normal and tumor-bearing mice. Results: [64Cu]Cu-NODAGA-RGD-BBN was prepared with radiochemical purity >99 ± 0.7% (HPLC/ITLC) and specific activity of 18.5 ± 2.2 TBq/mmol. The radiotracer showed high stability in PBS (95 ± 1.05%) and in human blood serum (96 ± 1.24%) and, high affinity to the GRP expressing tumor cells. [64Cu]Cu-NODAGA-RGD-BBN showed hydrophilic (log p = -1.14) and agonistic nature. The biodistribution and imaging studies demonstrated high uptake at the tumor site at all intervals post-injection and 3-4 h post-injection can be considered an appropriate time of imaging. method: NODAGA-RGD-BBN heterodimer peptide was successfully labelled with cyclotron-produced copper-64 at optimized conditions. The radiochemical purity of the radiotracer was checked by HPLC and RTLC methods. The stability of the radiolabeled compound was assessed in PBS (4 °C) and in human blood serum (37 °C). Binding affinity and internalization of [64Cu]Cu-NODAGA-RGD-BBN were studied on PC3, LNCaP and CHO cell lines. The biodistribution of the radiotracer was evaluated in normal and tumor-bearing mice. Conclusion: The results indicated that [64Cu]Cu-NODAGA-RGD-BBN radiolabeled heterodimer peptide can be considered as a high-potential agent for PET imaging of GRPRoverexpressing tumors.
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