Modified poly-L-lysine for use as a clearing agent in pretargeted radioimmunotherapy

IF 4.4 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Chiara Timperanza, Anna Gustafsson-Lutz, Tom Bäck, Damian J. Green, Sture Lindegren, Emma Aneheim
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引用次数: 0

Abstract

Background

Pretargeted radioimmunotherapy of cancer has the potential to increase tumor specific uptake of activity when compared with conventional radioimmunotherapy. This is especially true in radioimmunotherapy with nuclides that exhibit a relatively short half-life. When administering antibody-based pretargeting molecules systemically, the antibodies often show a relatively slow clearance from the blood. Therefore, the use of a clearing agent is advantageous to remove unbound pretargeting molecules from the circulation, facilitating a reduction in the nonspecific radiation exposure to normal tissue while maximizing the dose delivered to the tumors.

Results

In the current study, two types of poly-L-lysine based clearing agents were produced for two different pretargeting systems: (strept)avidin/biotin and Tetrazine/Transcyclooctene. Poly-L-lysine was used as scaffold for production of clearing agents. The polymer is available in multiple sizes and can readily be modified with several functional groups, allowing different pretargeting strategies to be used. In vivo evaluation of the biotin-functionalized poly-L-lysine clearing agent, 110 repeating units, resulted in a decrease in blood concentration of the Iodine-125 labeled pretargeting agent of 50%, circa 23 h after injection, compared to controls. Two sizes, 68 and 143 repeating units, of the tetrazine-functionalized poly-L-lysine clearing agent were also evaluated, which at 23 h after injection decreased the blood concentration of the Iodine-125 labeled pretargeting agent to 58 and 38% respectively.

Conclusion

The straightforward synthesis of poly-L-lysine based clearing agents makes kit preparation possible and these agents show good potential for further evaluation, especially within the Tetrazine/Transcyclooctene pretargeting system where no liver or kidney accumulation was observed.

将改性聚 L-赖氨酸用作放射免疫疗法前的清除剂。
背景:与传统的放射免疫疗法相比,癌症的预靶向放射免疫疗法有可能增加肿瘤对活性的特异性吸收。在使用半衰期相对较短的核素进行放射免疫治疗时尤其如此。在全身使用基于抗体的预靶向分子时,抗体在血液中的清除速度通常相对较慢。因此,使用清除剂有利于从血液循环中清除未结合的预靶向分子,从而减少正常组织受到的非特异性辐射照射,同时最大限度地提高肿瘤的照射剂量:在本研究中,针对两种不同的前靶向系统:(链)阿维丁/生物素和四嗪/反式环辛烯,制备了两种基于聚-L-赖氨酸的清除剂。聚 L-赖氨酸被用作生产清除剂的支架。这种聚合物有多种规格,可随时用多种官能团进行修饰,从而可采用不同的预靶向策略。对生物素功能化聚 L-赖氨酸清除剂(110 个重复单位)进行体内评估后发现,与对照组相比,碘-125 标记的预靶向剂在注射后 23 小时左右的血药浓度降低了 50%。此外,还对四嗪功能化聚-L-赖氨酸清除剂的两种规格(68 和 143 个重复单元)进行了评估,结果显示,在注射后 23 小时,碘-125 标记的预靶制剂的血药浓度分别降低了 58% 和 38%:基于聚 L-赖氨酸的清除剂的直接合成使试剂盒的制备成为可能,这些清除剂显示出进一步评估的良好潜力,特别是在四嗪/反式环辛烯预靶向系统中,没有观察到肝脏或肾脏的蓄积。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
8.70%
发文量
30
审稿时长
5 weeks
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