Adaptation of the 18FDG Module for the Preparation of a Sodium Fluoride [18F] Injection Solution in Agreement with the United States (USP 32) and European Pharmacopeia (PhEur 6)

T. Martínez , B. Cordero , S. Medín , A. Sánchez Salmón
{"title":"Adaptation of the 18FDG Module for the Preparation of a Sodium Fluoride [18F] Injection Solution in Agreement with the United States (USP 32) and European Pharmacopeia (PhEur 6)","authors":"T. Martínez ,&nbsp;B. Cordero ,&nbsp;S. Medín ,&nbsp;A. Sánchez Salmón","doi":"10.1016/j.remngl.2011.02.004","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To establish an automated procedure for the preparation of sodium fluoride <sup>18</sup>F injection using the resources available in our laboratory for the preparation of <sup>18</sup>FDG and to analyze the repercussion of the conditioning column of the fluoride ion entrapment on the characteristics of the final product.</p></div><div><h3>Material and method</h3><p>The sequence of an <sup>18</sup>FDG synthesis module prepared so that it traps the fluoride ion from the cyclotron in ion-exchange resin diluted with 0.9% sodium chloride. The final solution was dosified and sterilized in a final vial in an automatized dispensing module. Three different column conditioning protocols within the process were tested. Quality controls were run according to USP 32 and EurPh 6, adding control of ethanol levels of residual solvent and quality controls of the solution at 8<!--> <!-->h post-preparation.</p></div><div><h3>Results</h3><p>Activation of the resin cartridges with ethanol and water was the chosen procedure, with fluoride ion trapping &gt;95% and pH around 7. Ethanol levels were &lt;5000<!--> <!-->ppm. Quality controls at 8<!--> <!-->h indicated that the solution was in compliance with the USP 32 and EurPh 6 specifications.</p></div><div><h3>Conclusion</h3><p>This is an easy, low-cost, reliable automated method for sodium fluoride preparation in PET facilities with existing equipment for <sup>18</sup>FDG synthesis and quality control.</p></div>","PeriodicalId":101111,"journal":{"name":"Revista Espa?ola de Medicina Nuclear (English Edition)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2011-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.remngl.2011.02.004","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista Espa?ola de Medicina Nuclear (English Edition)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1578200X11000210","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

Objective

To establish an automated procedure for the preparation of sodium fluoride 18F injection using the resources available in our laboratory for the preparation of 18FDG and to analyze the repercussion of the conditioning column of the fluoride ion entrapment on the characteristics of the final product.

Material and method

The sequence of an 18FDG synthesis module prepared so that it traps the fluoride ion from the cyclotron in ion-exchange resin diluted with 0.9% sodium chloride. The final solution was dosified and sterilized in a final vial in an automatized dispensing module. Three different column conditioning protocols within the process were tested. Quality controls were run according to USP 32 and EurPh 6, adding control of ethanol levels of residual solvent and quality controls of the solution at 8 h post-preparation.

Results

Activation of the resin cartridges with ethanol and water was the chosen procedure, with fluoride ion trapping >95% and pH around 7. Ethanol levels were <5000 ppm. Quality controls at 8 h indicated that the solution was in compliance with the USP 32 and EurPh 6 specifications.

Conclusion

This is an easy, low-cost, reliable automated method for sodium fluoride preparation in PET facilities with existing equipment for 18FDG synthesis and quality control.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
根据与美国(USP 32)和欧洲药典(PhEur 6)的协议,调整18FDG模块用于制备氟化钠[18F]注射溶液
目的利用实验室现有的18FDG制备资源,建立氟化钠18F注射液的自动化制备工艺,并分析氟离子包封调节柱对最终产品特性的影响。材料和方法制备了18FDG合成模块的序列,该模块可以在0.9%氯化钠稀释的离子交换树脂中捕获回旋加速器中的氟离子。最终溶液在自动配药模块中的最终小瓶中进行剂量和灭菌。在此过程中测试了三种不同的柱调节方案。按照USP 32和EurPh 6进行质量控制,添加乙醇残留量控制和制备后8 h溶液质量控制。结果树脂筒采用乙醇和水活化,氟化物离子捕获率为95%,pH值为7左右。乙醇浓度为5000ppm。8小时的质量控制表明该溶液符合USP 32和EurPh 6规范。结论利用现有的18FDG合成及质量控制设备,在PET设施中制备氟化钠是一种简便、低成本、可靠的自动化方法。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Asymmetrically increased uptake in upper extremities on 99mTc-MDP bone scintigraphy caused by intra-arterial injection: Different uptake patterns in three cases 99mTc-MIBI SPECT in the Study of Lymphoma of the Brain Tracheostomy Cannula as a Cause of False Positive in the Body Scan with 131I in the Follow-up of Differentiated Thyroid Cancer Lipomatous Hypertrophy of the Interatrial Septum. Findings in the 18F-FDG PET/CT Scan; MRI Bone Marrow Scintigraphy for the Evaluation of a Mediastinic Nodule in a Patient with Chronic Hematopoietic Disorder
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1