Ly Jimmy, Ha Noel S, Cheung Shilin, van Dam R Michael
Department of Bioengineering, Henry Samueli School of Engineering and Applied Science, University of California Los Angeles, 420 Westwood Plaza, Los Angeles, CA, 90095-7227, USA.
Crump Institute for Molecular Imaging and Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California Los Angeles, 650 Charles E Young Dr., Los Angeles, CA, 90095-8352, USA.
Anal Bioanal Chem. 2018 Mar;410(9):2423-2436. doi: 10.1007/s00216-018-0924-y. Epub 2018 Feb 22.
Miniaturized synthesis of positron emission tomography (PET) tracers is poised to offer numerous advantages including reduced tracer production costs and increased availability of diverse tracers. While many steps of the tracer production process have been miniaturized, there has been relatively little development of microscale systems for the quality control (QC) testing process that is required by regulatory agencies to ensure purity, identity, and biological safety of the radiotracer before use in human subjects. Every batch must be tested, and in contrast with ordinary pharmaceuticals, the whole set of tests of radiopharmaceuticals must be completed within a short-period of time to minimize losses due to radioactive decay. By replacing conventional techniques with microscale analytical ones, it may be possible to significantly reduce instrument cost, conserve lab space, shorten analysis times, and streamline this aspect of PET tracer production. We focus in this work on miniaturizing the subset of QC tests for chemical identity and purity. These tests generally require high-resolution chromatographic separation prior to detection to enable the approach to be applied to many different tracers (and their impurities), and have not yet, to the best of our knowledge, been tackled in microfluidic systems. Toward this end, we previously explored the feasibility of using the technique of capillary electrophoresis (CE) as a replacement for the "gold standard" approach of using high-performance liquid chromatography (HPLC) since CE offers similar separating power, flexibility, and sensitivity, but can readily be implemented in a microchip format. Using a conventional CE system, we previously demonstrated the successful separation of non-radioactive version of a clinical PET tracer, 3'-deoxy-3'-fluorothymidine (FLT), from its known by-products, and the separation of the PET tracer 1-(2'-deoxy-2'-fluoro-β-D-arabinofuranosyl)-cytosine (D-FAC) from its α-isomer, with sensitivity nearly as good as HPLC. Building on this feasibility study, in this paper, we describe the first effort to miniaturize the chemical identity and purity tests by using microchip electrophoresis (MCE). The fully automated proof-of-concept system comprises a chip for sample injection, a separation capillary, and an optical detection chip. Using the same model compound (FLT and its known by-products), we demonstrate that samples can be injected, separated, and detected, and show the potential to match the performance of HPLC. Addition of a radiation detector in the future would enable analysis of radiochemical identity and purity in the same device. We envision that eventually this MCE method could be combined with other miniaturized QC tests into a compact integrated system for automated routine QC testing of radiopharmaceuticals in the future. Graphical abstract Miniaturized quality control (QC) testing of batches of radiopharmaceuticals via microfluidic analysis. The proof-of-concept hybrid microchip electrophoresis (MCE) device demonstrated the feasibility of achieving comparable performance to conventional analytical instruments (HPLC or CE) for chemical purity testing.
正电子发射断层扫描(PET)示踪剂的小型化合成有望带来诸多优势,包括降低示踪剂生产成本以及增加多种示踪剂的可得性。虽然示踪剂生产过程的许多步骤已实现小型化,但用于质量控制(QC)测试过程的微尺度系统的开发相对较少,而监管机构要求进行该测试以确保放射性示踪剂在用于人体受试者之前的纯度、同一性和生物安全性。每一批次都必须进行测试,与普通药品不同的是,放射性药物的整套测试必须在短时间内完成,以尽量减少放射性衰变造成的损失。通过用微尺度分析技术取代传统技术,有可能显著降低仪器成本、节省实验室空间、缩短分析时间并简化PET示踪剂生产的这一方面。我们在这项工作中专注于将化学同一性和纯度的QC测试子集小型化。这些测试通常需要在检测之前进行高分辨率色谱分离,以使该方法能够应用于许多不同的示踪剂(及其杂质),据我们所知,微流控系统尚未解决这一问题。为此,我们之前探索了使用毛细管电泳(CE)技术替代使用高效液相色谱(HPLC)的“金标准”方法的可行性,因为CE具有相似的分离能力、灵活性和灵敏度,但可以很容易地以微芯片形式实现。使用传统的CE系统,我们之前证明了成功地将临床PET示踪剂3'-脱氧-3'-氟胸苷(FLT)的非放射性版本与其已知副产物分离,以及将PET示踪剂1-(2'-脱氧-2'-氟-β-D-阿拉伯呋喃糖基)-胞嘧啶(D-FAC)与其α-异构体分离,灵敏度几乎与HPLC相当。基于这项可行性研究,在本文中,我们描述了首次通过使用微芯片电泳(MCE)将化学同一性和纯度测试小型化的努力。全自动化的概念验证系统包括一个用于样品注入的芯片、一根分离毛细管和一个光学检测芯片。使用相同的模型化合物(FLT及其已知副产物),我们证明了样品可以被注入、分离和检测,并显示出与HPLC性能相匹配的潜力。未来添加一个辐射探测器将能够在同一设备中分析放射化学同一性和纯度。我们设想最终这种MCE方法可以与其他小型化的QC测试结合成一个紧凑的集成系统,用于未来放射性药物的自动化常规QC测试。图形摘要 通过微流控分析对批次放射性药物进行小型化质量控制(QC)测试。概念验证混合微芯片电泳(MCE)装置证明了在化学纯度测试中实现与传统分析仪器(HPLC或CE)相当性能的可行性。