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131I标记4-碘-L-苯丙氨酸的合成及生物分布研究

Studies on Synthesis and Biodistribution of 131I-labeled 4-iodine-L-phenylalanine

  • 摘要: L型氨基酸转运蛋白(LAT1)作为癌症显像与治疗的靶点,是目前癌症研究的热点之一。本研究以4-硼-L-苯丙氨酸(BPA)为反应物,采用水相一步放射取代反应合成131I标记的4-碘-L-苯丙氨酸(131IPA)示踪剂,并进行肿瘤诊断研究的初步评估。结果显示,所合成的131IPA放射化学纯度(RCP)为96.33%,放射化学产率(RCY)达到92%±0.3%。非小细胞肺癌A549细胞对131IPA的摄取量在3 h达到最高;而胶质瘤GL261细胞对其的摄取量在8 h达到峰值。在小鼠体内131IPA主要通过肝、肾代谢及排泄,24 h后体内几乎无残留。此外,小动物活体成像显示2~12 h内131IPA在A549肿瘤模型中具有高的摄取量和较长的停留时间,在原位GL261肿瘤模型中2 h可观察到131IPA透过血脑屏障到达脑肿瘤,8 h及12 h成像显示其有较好的脑肿瘤特异性,靶本比为T/M≈3.4。

     

    Abstract: L-type amino acid transporter protein(LAT1) is one of the hotspots in cancer research as a target for cancer visualization and therapy. In this study, 131I-labeled 4-iodo-L-phenylalanine(131IPA) tracer was synthesized by aqueous-phase one-step radiosubstitution reaction using 4-boron-L-phenylalanine(BPA) as a reactant and initially evaluated for tumor diagnostic studies. The results showed that the radiochemical purity(RCP) of the synthesized 131IPA was 96.33%, and the radiochemical yield(RCY) reached 92±0.3%. The intake of 131IPA in non-small-cell lung cancer A549 cells reached the highest value at 3 h; whereas the intake in glioma GL261 cell to peak value was at 8 h. In mice, 131IPA was mainly metabolized and excreted through the liver and kidney, with almost no residue in the body after 24 h. In addition, in vivo imaging in small animals showed that 131IPA had high intake and long residence time in A549 tumor model from 2 to 12 h. In the in situ GL261 tumor model, 131IPA could be observed to reach brain tumors through the blood-brain barrier at 2 h. Imagings at 8 h and 12 h showed better brain tumor specificity, with a target-to-benefit ratio of T/M≈3.4.

     

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