验证同时纯化和配制多肽放射性药物的尺寸排除法。

IF 4.4 Q1 CHEMISTRY, INORGANIC & NUCLEAR EJNMMI Radiopharmacy and Chemistry Pub Date : 2024-03-21 DOI:10.1186/s41181-024-00254-2
Sebastian Martin, Lennard Wendlinger, Alexandra Litvinenko, Radmila Faizova, Margret Schottelius
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引用次数: 0

摘要

背景:在临床常规和临床前研究中,放射性金属标记肽放射性药物最终纯化的既定标准程序是基于滤芯的反相(RP)固相萃取(SPE)。这种方法可以快速定量地将放射性标记肽从亲水性杂质中分离出来,而且易于集成到自动合成程序中。然而,从 RP 滤芯中洗脱产品时必须使用有机溶剂,而且产品回收率有时会受到限制。因此,我们研究了一种基于市售尺寸排阻滤芯的替代纯化方法:由于大多数多肽放射性药物的分子量大于 1 kDa,因此使用分子尺寸截止值为 700 Da 的 Sephadex G10 滤芯来最终纯化各种 68Ga、64Cu 和 99mTc 标记的实验性多肽放射性核素以及临床相关配体 PSMA-617。实验结果(放射化学纯度(RCP,由 ITLC 测定)、从固体支持物中的回收率)与相应的标准 RP-SPE 方法进行了比较。一般来说,未反应的 68Ga、64Cu 和 99mTc 盐在 G10 滤芯上的保留率为:68Ga 和 99mTc 在指定洗脱体积(1.2 mL)内为定量,64Cu 为 99.6%。即使洗脱量增加到 1.5-2 mL,洗脱出的 68Ga 和 99mTc 放射肽的 RCP 也大于 99%。对于分子量≥ 2 kDa 的所有肽段,在分别调整洗脱体积后,G10 滤芯的产物回收率始终大于 85%。68Ga]Ga-PSMA-617 的产品回收率最低(67%,1.2 mL 至 84%,2 mL)。最终产品溶液的 pH 值与体积有关(1.2 mL:pH 6.3;1.5 mL:pH 5.9;2 mL:pH 5.5)。值得注意的是,G10 滤芯可重复使用多达 20 次而不影响性能,而且在自动放射合成程序中成功实施了该方法:总的来说,在生理盐水中进行尺寸排阻纯化可在 10-12 分钟内获得放射化学纯度极佳(> 99%)的所有多肽放射性药物。虽然产品回收率略低于传统的 SPE 纯化法,但这种方法的优点是完全避免了有机溶剂,是一种经济高效、易于实施的自动化放射性示踪剂合成纯化方法。
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Validation of a size exclusion method for concomitant purification and formulation of peptide radiopharmaceuticals

Background

Both in clinical routine and in preclinical research, the established standard procedure for the final purification of radiometal-labeled peptide radiopharmaceuticals is cartridge-based reversed-phase (RP) solid phase extraction (SPE). It allows the rapid and quantitative separation of the radiolabeled peptide from hydrophilic impurities and easy integration into automated synthesis procedures. However, product elution from RP cartridges necessitates the use of organic solvents and product recovery is sometimes limited. Thus, an alternative purification method based on commercially available size exclusion cartridges was investigated.

Results

Since most peptide radiopharmaceuticals have a molecular weight > 1 kDa, Sephadex G10 cartridges with a molecular size cut-off of 700 Da were used for the final purification of a broad palette of 68Ga-, 64Cu- and 99mTc-labeled experimental peptide radiotracers as well as the clinically relevant ligand PSMA-617. Results (radiochemical purity (RCP, determined by ITLC), recovery from the solid support) were compared to the respective standard RP-SPE method. Generally, retention of unreacted 68Ga, 64Cu and 99mTc salts on the G10 cartridges was quantitative up to the specified elution volume (1.2 mL) for 68Ga and 99mTc and 99.6% for 64Cu. Even at increased elution volumes of 1.5-2 mL, RCPs of the eluted 68Ga- and 99mTc -radiopeptides were > 99%. For all peptides with a molecular weight ≥ 2 kDa, product recovery from the G10 cartridges was consistently > 85% upon respective adjustment of the elution volume. Product recovery was lowest for [68Ga]Ga-PSMA-617 (67%, 1.2 mL to 84%, 2 mL). The pH of the final product solution was found to be volume-dependent (1.2 mL: pH 6.3; 1.5 mL: pH 5.9; 2 mL: pH 5.5). Notably, the G10 cartridges were reused up to 20 times without compromising performance, and implementation of the method in an automated radiosynthesis procedure was successful.

Conclusions

Overall, size exclusion purification yielded all peptide radiopharmaceuticals in excellent radiochemical purities (> 99%) in saline within 10–12 min. Although product recovery is marginally inferior to classical SPE purifications, this method has the advantage of completely avoiding organic solvents and representing a cost-effective, easy-to-implement purification approach for automated radiotracer synthesis.

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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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