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新型锝-氮化物和锝-氧化物配合物与4-甲氧基-苯丙氨酸二硫代氨基甲酸盐用于肿瘤成像的放射性标记及生物学评价

Radiolabeling and Biological Evaluation of Novel Tc-Nitrido and Tc-Oxo Complexes with 4-Methoxy--Phenylalanine Dithiocarbamate for Tumor Imaging.

作者信息

Yin Guangxing, Ruan Qing, Jiang Yuhao, Zhang Junbo

机构信息

Key Laboratory of Radiopharmaceuticals of Ministry of Education, NMPA (National Medical Products Administration) Key Laboratory for Research and Evaluation of Radiopharmaceuticals, College of Chemistry, Beijing Normal University, Beijing 100875, China.

出版信息

Pharmaceutics. 2022 Oct 15;14(10):2196. doi: 10.3390/pharmaceutics14102196.

Abstract

To develop novel radiolabeled amino acid tumor imaging agents, 4-methoxy-L-phenylalanine dithiocarbamate (MOPADTC) was synthesized successfully, and two kinds of 99mTc-labeled complexes ([99mTc]TcN-MOPADTC and [99mTc]TcO-MOPADTC) with high radiochemical purities (RCP > 95%) were obtained. The in vitro stability and partition coefficient were determined, and the results show that both of these complexes have good in vitro stability; [99mTc]TcO-MOPADTC is hydrophilic, while [99mTc]TcN-MOPADTC is slightly lipophilic. The biodistribution of [99mTc]TcN-MOPADTC and [99mTc]TcO-MOPADTC in mice bearing S180 tumors shows that the tumor uptake and tumor/muscle ratio of [99mTc]TcO-MOPADTC were higher than the tumor uptake and tumor/muscle ratio of [99mTc]TcN-MOPADTC. In addition, the tumor retention of [99mTc]TcO-MOPADTC is better than the tumor retention of [99mTc]TcN-MOPADTC. A competitive inhibition assay was performed, and the results indicate that [99mTc]TcO-MOPADTC may enter cells primarily via the L-alanine/L-serine/L-cysteine (ASC) system. Single-photon emission computed tomography (SPECT) imaging of [99mTc]TcO-MOPADTC shows obvious accumulation in tumor sites, suggesting that [99mTc]TcO-MOPADTC is a novel potential tumor-imaging agent.

摘要

为开发新型放射性标记氨基酸肿瘤显像剂,成功合成了4-甲氧基-L-苯丙氨酸二硫代氨基甲酸盐(MOPADTC),并获得了两种放射化学纯度高(RCP>95%)的99mTc标记配合物([99mTc]TcN-MOPADTC和[99mTc]TcO-MOPADTC)。测定了其体外稳定性和分配系数,结果表明这两种配合物均具有良好的体外稳定性;[99mTc]TcO-MOPADTC具有亲水性,而[99mTc]TcN-MOPADTC具有轻微的亲脂性。[99mTc]TcN-MOPADTC和[99mTc]TcO-MOPADTC在荷S180肿瘤小鼠体内的生物分布表明,[99mTc]TcO-MOPADTC的肿瘤摄取及肿瘤/肌肉比值高于[99mTc]TcN-MOPADTC的肿瘤摄取及肿瘤/肌肉比值。此外,[99mTc]TcO-MOPADTC的肿瘤滞留性优于[99mTc]TcN-MOPADTC。进行了竞争抑制试验,结果表明[99mTc]TcO-MOPADTC可能主要通过L-丙氨酸/L-丝氨酸/L-半胱氨酸(ASC)系统进入细胞。[99mTc]TcO-MOPADTC的单光子发射计算机断层扫描(SPECT)成像显示在肿瘤部位有明显积聚,表明[99mTc]TcO-MOPADTC是一种新型潜在的肿瘤显像剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2e/9607073/4fb267e40eb3/pharmaceutics-14-02196-g001.jpg

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