Fukuda H, Matsuzawa T, Tada M, Takahashi T, Ishiwata K, Yamada K, Abe Y, Yoshioka S, Sato T, Ido T
Eur J Nucl Med. 1986;11(11):444-8. doi: 10.1007/BF00261007.
We prepared 2-deoxy-2-[18F]fluoro-D-galactose as a potential radiopharmaceutical for liver imaging and for the assessment by positron emission tomography of regional metabolic function of the liver. In biodistribution studies of rats, the liver uptake of the compound was very high, almost reaching a plateau (6.33% dose/g) at 30 min and remaining constant until 120 min. This high uptake was reduced by simultaneous administration of D-galactose, but D-glucose had no effect. The compound was much less concentrated in the liver that had been damaged by CCl4 treatment. Positron imaging of a rabbit liver showed a remarkable uptake of the compound with a high liver-to-blood ratio. The high concentration in the liver was also reduced by the administration of D-galactose. These data suggest that the compound was trapped in the liver by a metabolic process and could be used for the measurement by positron emission tomography of galactose metabolism in the liver.
我们制备了2-脱氧-2-[¹⁸F]氟-D-半乳糖,作为一种潜在的放射性药物用于肝脏成像以及通过正电子发射断层扫描评估肝脏区域代谢功能。在大鼠的生物分布研究中,该化合物在肝脏中的摄取量非常高,在30分钟时几乎达到平台期(6.33%剂量/克),并一直保持到120分钟。同时给予D-半乳糖可降低这种高摄取,但D-葡萄糖则无此作用。该化合物在经四氯化碳处理而受损的肝脏中的浓度要低得多。对兔肝脏进行的正电子成像显示该化合物有显著摄取,肝脏与血液的比值很高。给予D-半乳糖也会降低肝脏中的高浓度。这些数据表明该化合物通过代谢过程被肝脏捕获,可用于通过正电子发射断层扫描测量肝脏中的半乳糖代谢。