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使用单个13X分子筛柱进行试剂捕集、放射性标记和选择性纯化,用于正电子发射断层显像(PET)成像的[11C]棕榈酸的合成。

Synthesis of [11C]palmitic acid for PET imaging using a single molecular sieve 13X cartridge for reagent trapping, radiolabeling and selective purification.

作者信息

Amor-Coarasa Alejandro, Kelly James M, Babich John W

机构信息

Radiopharmaceutical Sciences, Department of Radiology, Weill Cornell Medical College, Belfer Research Building, Room 1600, 413 East 69th Street, New York, NY 10021.

Radiopharmaceutical Sciences, Department of Radiology, Weill Cornell Medical College, Belfer Research Building, Room 1600, 413 East 69th Street, New York, NY 10021.

出版信息

Nucl Med Biol. 2015 Aug;42(8):685-90. doi: 10.1016/j.nucmedbio.2015.03.008. Epub 2015 Apr 9.

Abstract

INTRODUCTION

Radiolabeled fatty acids are valuable metabolic tracers for PET imaging. Carbon-11 is widely used in clinical PET studies due to the prevalence of facile techniques enabling the incorporation of [(11)C]CO2 and [(11)C]CH3 into molecules and a short half-life (20.4 min) that translates into low patient dose. However, the short half-life considerably limits the time for radiosynthesis. Furthermore, the majority of the syntheses of [(11)C]palmitic acid in common use employ high starting [(11)C]CO2 activities and/or expensive equipment.

METHODS

[(11)C]CO2 was trapped with greater than 99.99% efficiency by a three stage cartridge packed with molecular sieve 13X, 100-120 mesh. The labeling of n-pentadecylmagnesium bromide took place in 5 min in the cartridge, and the [(11)C]palmitic acid product was selectively eluted in ethanol following alkaline and acidic washes of the column.

RESULTS

The system reliably produced more than 925 MBq (25 mCi) of [(11)C]palmitic acid suitable for human use from 7.4 GBq (200 mCi) of [(11)C]CO2 in 8 min from end-of-bombardment.

CONCLUSIONS

We have exploited the properties of the inexpensive molecular sieve 13X to develop a miniature, disposable and leak tight "gas capture" system for the rapid labeling and purification of [(11)C]fatty acids in good yield and >99% radiochemical purity. The rapidity of the synthesis and purification allows small [(11)C]CO2 starting activities to be used, and with no requirement for expensive synthesis equipment or facilities, the system can be implemented in any radiopharmaceutical center.

摘要

引言

放射性标记脂肪酸是用于正电子发射断层扫描(PET)成像的重要代谢示踪剂。碳-11由于能够将[(11)C]CO₂和[(11)C]CH₃掺入分子的简便技术的普及以及短半衰期(20.4分钟)从而使患者剂量较低,因此广泛应用于临床PET研究。然而,短半衰期极大地限制了放射性合成的时间。此外,常用的[(11)C]棕榈酸的大多数合成方法都采用高起始[(11)C]CO₂活度和/或昂贵的设备。

方法

[(11)C]CO₂被填充有100-120目13X分子筛的三级柱以大于99.99%的效率捕获。正十五烷基溴化镁的标记在柱中5分钟内完成,[(11)C]棕榈酸产物在柱经过碱性和酸性洗涤后在乙醇中被选择性洗脱。

结果

该系统从轰击结束起8分钟内,能可靠地从7.4GBq(200mCi)的[(11)C]CO₂中生产出超过925MBq(25mCi)适合人体使用的[(11)C]棕榈酸。

结论

我们利用廉价的13X分子筛的特性开发了一种微型、一次性且不漏气的“气体捕获”系统,用于以高收率和>99%的放射化学纯度快速标记和纯化[(11)C]脂肪酸。合成和纯化的快速性使得可以使用少量的[(11)C]CO₂起始活度,并且由于不需要昂贵的合成设备或设施,该系统可在任何放射性药物中心实施。

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