Fully Automated Methods for [18F]FDG and [18F]-NaF Productions Using Explora FDG4: Validation and Reliability of Multi-Subsequent Preparations for Clinical Applications.

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
E. Awad, H. Ali, James Lamb, E. Al‐Momani
{"title":"Fully Automated Methods for [18F]FDG and [18F]-NaF Productions Using Explora FDG4: Validation and Reliability of Multi-Subsequent Preparations for Clinical Applications.","authors":"E. Awad, H. Ali, James Lamb, E. Al‐Momani","doi":"10.2174/1874471015666220518115244","DOIUrl":null,"url":null,"abstract":"BACKGROUND The worldwide usage of [18F]-sodium fluoride in clinical applications increase the interest of the facility of its production. The development of a new automated method for multi-preparations of [18F]-NaF and [18F]FDG on an Explora FDG4 module is described. Explora FDG4 is one of the most widely used synthesizers for FDG production in daily routine use and specifically designed to run up to four different productions with single module. Therefore, slight modifications were carried out in order to increase the potential of the synthesizer to perform more radiopharmaceuticals. METHODS A fully automated method for multi-preparations of [18F]-NaF and [18F]FDG using Explora FDG4 was performed. Slight modifications of the Explora's hardware and software configuration were applied. A new elution vial for NaF preparation was installed and connected to the free position to MVP1. Quality control was carried-out using the standard analytical methods that applied for GMP production. RESULTS This modification successfully provides preparation of [18F]-NaF without affecting the daily FDG production using one set preparation. [18F]-NaF was obtained in a high radiochemical yield (>90%, n=100) in 10 min total preparation time. The quality control results for both obtained products FDG (RCP >95%) and NaF (RCP >98%)showed that the radiopharmaceuticals were in compliance with USP and Ph.Eur. specifications and compatible with clinical applications. CONCLUSION A rapid and simple method for multi preparations of [18F]-NaF and [18F]FDG using single Explora module was designed. Yet, the chemistry module has the potential to generate more radiopharmaceuticals to decrease the cost of preparation of [18F]-NaF comparing with the cassette-based synthesizers, reducing radiation exposure resulted by manual preparations and increase the reproducibility of [18F]-NaF preparation.","PeriodicalId":10991,"journal":{"name":"Current radiopharmaceuticals","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2022-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current radiopharmaceuticals","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/1874471015666220518115244","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND The worldwide usage of [18F]-sodium fluoride in clinical applications increase the interest of the facility of its production. The development of a new automated method for multi-preparations of [18F]-NaF and [18F]FDG on an Explora FDG4 module is described. Explora FDG4 is one of the most widely used synthesizers for FDG production in daily routine use and specifically designed to run up to four different productions with single module. Therefore, slight modifications were carried out in order to increase the potential of the synthesizer to perform more radiopharmaceuticals. METHODS A fully automated method for multi-preparations of [18F]-NaF and [18F]FDG using Explora FDG4 was performed. Slight modifications of the Explora's hardware and software configuration were applied. A new elution vial for NaF preparation was installed and connected to the free position to MVP1. Quality control was carried-out using the standard analytical methods that applied for GMP production. RESULTS This modification successfully provides preparation of [18F]-NaF without affecting the daily FDG production using one set preparation. [18F]-NaF was obtained in a high radiochemical yield (>90%, n=100) in 10 min total preparation time. The quality control results for both obtained products FDG (RCP >95%) and NaF (RCP >98%)showed that the radiopharmaceuticals were in compliance with USP and Ph.Eur. specifications and compatible with clinical applications. CONCLUSION A rapid and simple method for multi preparations of [18F]-NaF and [18F]FDG using single Explora module was designed. Yet, the chemistry module has the potential to generate more radiopharmaceuticals to decrease the cost of preparation of [18F]-NaF comparing with the cassette-based synthesizers, reducing radiation exposure resulted by manual preparations and increase the reproducibility of [18F]-NaF preparation.
使用Explora FDG4生产[18F]FDG和[18F]-NaF的全自动方法:临床应用多后续制剂的验证和可靠性。
[18F]-氟化钠在世界范围内的临床应用增加了对其生产设施的兴趣。本文介绍了在Explora FDG4模块上开发的一种新的自动化方法,用于多种制备[18F]-NaF和[18F]FDG。explorora FDG4是在日常使用中最广泛使用的FDG生产合成器之一,专门设计用于运行多达四个不同的生产与单个模块。因此,进行了轻微的修改,以增加合成器的潜力,以执行更多的放射性药物。方法采用Explora FDG4全自动制备[18F]-NaF和[18F]FDG。对探索者的硬件和软件配置进行了轻微的修改。安装了一个新的NaF制备洗脱瓶,并连接到MVP1的自由位置。质量控制采用GMP生产标准的分析方法进行。结果该修饰成功地制备了[18F]-NaF,而不影响每天的FDG产量。[18F]-NaF在10 min的总制备时间内获得了很高的放射化学产率(>90%,n=100)。所得产品FDG (RCP >95%)和NaF (RCP >98%)的质量控制结果表明,两种放射性药物均符合USP和Ph.Eur标准。规格和兼容临床应用。结论设计了一种快速简便的用单个explore模块制备[18F]-NaF和[18F]FDG的方法。然而,与盒式合成器相比,化学模块有潜力产生更多的放射性药物,以降低[18F]-NaF的制备成本,减少手工制备造成的辐射暴露,提高[18F]-NaF制备的可重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Current radiopharmaceuticals
Current radiopharmaceuticals PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
4.30%
发文量
43
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信