细菌显像剂18F-FDS的合成及动物显像应用研究
投稿时间:2015-08-03  修订日期:2015-09-06  点此下载全文
引用本文:邢海群,朱文佳,蔡炯,张迎强,要少波,霍力,李方.细菌显像剂18F-FDS的合成及动物显像应用研究[J].医学研究杂志,2016,45(1):51-54
DOI: 10.11969/j.issn.1673-548X.2016.01.013
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作者单位E-mail
邢海群 100730 中国医学科学院北京协和医院核医学科  
朱文佳 100730 中国医学科学院北京协和医院核医学科  
蔡炯 100730 中国医学科学院北京协和医院核医学科  
张迎强 100730 中国医学科学院北京协和医院核医学科  
要少波 100730 中国医学科学院北京协和医院核医学科  
霍力 100730 中国医学科学院北京协和医院核医学科  
李方 100730 中国医学科学院北京协和医院核医学科 jiongcai@sina.com 
基金项目:国家自然科学基金资助项目(面上项目)(81571712)
中文摘要:目的 探讨细菌显像剂2-脱氧-2-氟山梨醇(2-deoxy-2-[18F]-fluorosorbitol, 18F-FDS)的合成过程、正常小鼠显像并计算内照射剂量,比较小鼠模型中大肠杆菌感染病灶及肿瘤病灶对FDS的摄取情况。方法 18F-FDS由氟多功能模块经"一锅法"由PET常用显像剂2-氟-2脱氧葡萄糖(18F-fluorodeoxyglucose, 18F-FDG)经NaBH4还原制备;实验组感染小鼠及荷瘤鼠尾静脉注射18F-FDS后60min进行microPET显像,通过Inveron Research软件测量病灶靶/本底比值;对照组注射18F-FDG,同样方法测量病灶靶/本底比值进行对照分析。结果 18F-FDS放化收率为80%±5%(n=8,未进行时间衰减校正),合成时间25min,放化纯度>99%。正常小鼠尾静脉注射18F-FDS后microPET显像提示示踪剂从泌尿系统排泄;背景组织肺及脑内的非特异性放射性摄取较低;大肠杆菌感染小鼠microPET显像,感染灶有较高的感染灶/肌肉比值,荷瘤鼠显像示18F-FDS肿瘤组织靶/本底比值明显低于18F-FDG。结论 18F-FDS放化合成方法操作简单,收率高,细菌感染灶有特异性摄取,在分辨感染和肿瘤上具有应用前景。
中文关键词:感染  18F-FDS  大肠杆菌  肿瘤  放化标记
 
Radiosynthesis of Infection Tracer 18F-FDS and Animal Imaging
Abstract:Objective To synthesis 18F-FDS from 18F-FDG, calculate internal radiation dose in normal mice imaging, look for the difference of FDS accumulated in E.coli infection mouse model and in tumor lesions. Methods 18F-FDS was synthesized on multifunctional synthesis module from 18F-FDG with sodium borohydride reduction by 'One-pot reaction'. In test group, 18F-FDS was injected into infection mice model and tumor mice model via tail vein for microPET imaging after 60min. T/B values of 18F-FDS were measured and analyzed by Inveron Research software. 18F-FDG was injected into model mice in control group and T/B values were measured as describe above for comparison. Results It took 25 min to complete 18F-FDS synthesis. The radiochemical yield and radiochemistry purity of 18F-FDS was 80%±5%, and over 99% respectively. MicroPET imaging data with normal mouse suggested that 18F-FDS was cleared from kidneys. The nonspecific uptake of 18F-FDS in background tissue such as lung, brain was very low. MicroPET imaging data showed that E. coli infected loci in mouse model had high T/B ratio, while tumor lesions had much lower T/B ratio. Conclusion 18F-FDS is easy to be prepared with high yield and can be used to trace bacteria infected loci specifically. It is a promising radiotracer for differentiated diagnosis of bacteria infection from tumor.
keywords:Infection  18F-FDS  E.coli  Tumor  Radiolabeling
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