Radioiodination and preliminary in vivo investigation of the alkaloid cryptolepine

Q. Salako , S.Y.S. Ablordeppey , D. Dwuma-Badu , J.R. Thornback
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引用次数: 4

Abstract

In this paper we report the successful labelling of cryptolepine with 131I using the chloramine T method. Quality control by ITLC of the labelled product showed 80% labelling but when the mixture was equilibrated with some amberlite (Cl) anion resin to exchange the excess free iodide, the radiochemical purity was raised to >90%. Preliminary biodistribution in a rat did not show specific localisation of the tracer; rather, rapid clearance from the blood was indicated. It appears that its main excretory pathway is the hepatobiliary tract despite its relatively small molecular weight of 365. Also, despite i.v. administration, an appreciable 8% uptake was found in the stomach at 1 h post injection, indicating the process of enterohepatic reflux. These findings may have some bearings on the antimicrobial property of the plant.

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隐平生物碱的放射碘化及体内初步研究
本文报道用氯胺T法成功地用131I标记隐tolepine。标记产物的ITLC质量控制显示标记率为80%,但当混合物与一些琥珀石(Cl−)阴离子树脂平衡以交换多余的游离碘时,放射化学纯度提高到90%。在大鼠体内的初步生物分布未显示示踪剂的特异性定位;更确切地说,是血液中的快速清除。尽管其相对较小的分子量为365,但其主要排泄途径似乎是肝胆道。此外,尽管静脉给药,注射后1小时胃中仍有8%的明显摄取,表明肠肝反流的过程。这些发现可能对该植物的抗菌特性有一定的影响。
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