A "dose on demand" Biomarker Generator for automated production of [18F]F- and [18F]FDG

被引:28
作者
Awasthi, V. [1 ]
Watson, J. [2 ]
Gali, H. [1 ]
Matlock, G. [1 ]
McFarland, A. [2 ]
Bailey, J. [2 ]
Anzellotti, A. [2 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Coll Pharm, Dept Pharmaceut Sci, Oklahoma City, OK 73117 USA
[2] ABT Mol Imaging, Louisville, TN 37777 USA
关键词
Cyclotron; FDG; PET; F-18-FDG PET;
D O I
10.1016/j.apradiso.2014.02.015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The University of Oklahoma-College of Pharmacy has installed the first Biomarker Generator (BG75) comprising a self-shielded 7.5-MeV proton beam positive ion cyclotron and an aseptic automated chemistry production and quality control module for production of [F-18]F- and clinical [F-18]FDG. Performance, reliability, and safety of the system for the production of "dose on demand" were tested over several months. No-carrier-added [F-18]F- was obtained through the O-18(p,n)F-18 nuclear reaction by irradiation (20-40 min) of a > 95% enriched [O-18]H2O target (280 mu l) with a 7.5-MeV proton beam (3.5-5.0 mu A). Automated quality control tests were performed on each dose. The HPLC-based analytical methods were validated against USP methods of quality control. [18F]FDG produced by BG75 was tested in a mouse tumor model implanted with H441 human lung adenocarcinoma cells. After initial installment and optimization, the [18F]F- production has been consistent since March 2011 with a maximum production of 400 to 450 mCi in a day. The average yield is 0.61 mCi/min and 0.92 mCi/min at 3.8 mu A and 5 mu A, respectively. The current target window has held up for over 25 weeks against >400 bombardment cycles. [F-18]FDG production has been consistent since June 2012 with an average of six doses/day in an automated synthesis mode (RCY approximate to 50%). The release criteria included USP-specified limits for pH, residual solvents (acetonitrile/ethanol), kryptofix, radiochemical purity/identity, and filter integrity test. The entire automated operation generated minimal radiation exposure hazard to the operator and environment. As expected, [F-18]FDG produced by BG75 was found to delineate tumor volume in a mouse model of xenograft tumor. In summary, production and quality control of [F-18]FDG dose on demand" have been accomplished in an automated and safe manner by the first Biomarker Generator. The implementation of a cGMP quality system is under way towards the ANDA submission and first clinical use of [F-18]FDG produced by BG75. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:167 / 175
页数:9
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