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开发一种使用回旋加速器生产的 Ga68 来制备临床和研究用 Ga68 示踪剂的通用方法。

Towards a General Method for Using Cyclotron-Produced Ga68 to Manufacture Clinical and Research Ga68 Tracers.

机构信息

Department of Medicinal Chemistry, College of Pharmacy, University of Michigan, 1301 Catherine St. 2276 Medical Science I, Ann Arbor, MI 48109, USA.

Division of Nuclear Medicine, Department of Radiology, University of Michigan, 1301 Catherine St. 2276 Medical Science I, Ann Arbor, MI 48109, USA.

出版信息

Molecules. 2024 Nov 19;29(22):5457. doi: 10.3390/molecules29225457.

Abstract

The success of multiple nuclear medicine radiotherapeutics in treating cancer requires an increased supply of companion diagnostic imaging agents radiolabeled with gallium-68. Cyclotron production addresses the need for access to gallium-68 and has been validated for use with commercially produced sterile kits. For novel research tracers undergoing translational studies (IND or RDRC), developing and purchasing sterile kits is time- and cost-prohibitive. An on-cassette labeling method with terminal filtration allows non-sterile kits to be fabricated in-house, simplifying workflow and allowing multiple PET imaging agents to be evaluated using the same kit (i.e., parts, reagents, and timelist) with minimal variation. Using modified GE gallium chloride cassettes, four diverse clinically relevant tracers (DOTA-TOC, FAPI-04, pentixafor, and PSMA-11) were radiolabeled with gallium-68 to evaluate the approach using DOTA and HBED-CC chelator types. The tracers were all formulated according to established FDA-approved formulations and sterile-filtered using a PVDF membrane. The automated procedure is robust, tolerating DOTA and HBED-CC chelators, and can be used to screen numerous gallium-68 agents for rapid translation to clinical use.

摘要

多种核医学放射治疗癌症的成功需要更多用镓-68 标记的伴随诊断成像剂。回旋加速器生产满足了对镓-68 的需求,并已通过使用商业生产的无菌试剂盒进行了验证。对于正在进行转化研究的新型研究示踪剂(IND 或 RDRC),开发和购买无菌试剂盒在时间和成本上都是不可行的。采用终端过滤的盒式标记方法可以在内部制造非无菌试剂盒,简化工作流程,并允许使用相同的试剂盒(即零件、试剂和时间表)评估多种 PET 成像剂,变化最小。使用改良的通用电气镓氯化物试剂盒,用镓-68 标记了四种不同的临床相关示踪剂(DOTA-TOC、FAPI-04、pentixafor 和 PSMA-11),以评估使用 DOTA 和 HBED-CC 螯合剂类型的方法。所有示踪剂均根据已建立的 FDA 批准的配方进行配制,并使用 PVDF 膜进行无菌过滤。自动化程序稳健,可耐受 DOTA 和 HBED-CC 螯合剂,并可用于筛选大量镓-68 试剂,以快速转化为临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeca/11597648/b1029b9af1df/molecules-29-05457-g001.jpg

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