Moerlein S M, Gaehle G G, Lechner K R, Bera R K, Welch M J
Edward Mallinckrodt Institute of Radiology, Washington University School of Medicine, St Louis, MO 63110.
Appl Radiat Isot. 1993 Sep;44(9):1213-8. doi: 10.1016/0969-8043(93)90067-k.
Because [15O]butanol is the radiopharmaceutical of choice for PET studies of cerebral perfusion and neurological activation, we have developed a microprocessor-controlled radiosynthetic system for the preparation of this radiotracer in up to ten batches at a time. An IBM-compatible minicomputer was programmed to direct the reaction of molecular [15O]oxygen with tri-(n-butyl)borane bound to alumina, followed by purification of product [15O]butanol via solid phase extraction with C18 Sep-Paks and sterile filtration. Routine batch yields of over 150 mCi were achieved with a preparation turn-around time of 6.0 min. The final product had high radiochemical purity, low chemical impurity, and was sterile and apyrogenic. This radiopharmaceutical production system is reliable and suitable for tracer production in clinical PET imaging centers.
由于[15O]丁醇是用于脑灌注和神经激活PET研究的首选放射性药物,我们开发了一种微处理器控制的放射性合成系统,可一次制备多达十批这种放射性示踪剂。对一台IBM兼容小型计算机进行编程,以指导分子[15O]氧与结合在氧化铝上的三(正丁基)硼烷的反应,然后通过用C18 Sep-Pak进行固相萃取和无菌过滤来纯化产物[15O]丁醇。常规批产量超过150 mCi,制备周转时间为6.0分钟。最终产品具有高放射化学纯度、低化学杂质,并且无菌、无热原。这种放射性药物生产系统可靠,适用于临床PET成像中心的示踪剂生产。