Rhemium-186-monoaminemonoamidedithiol-conjugated bisphosphonate derivatives for bone pain palliation

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• 作者：Kazuma Ogawa ; Takahiro Mukai ; Yasushi Arano ; Akira Otaka ; Masashi Ueda ; Tomoya Uehara ; Yasuhiro Magata ; Kazuyuki Hashimoto and Hideo Saji
• 关键词：Rhenium-186 ; Monoaminemonoamidedithiols ; Bisphosphonate ; Bone ; Palliation
• 刊名：Nuclear Medicine and Biology
• 出版年：2006
• 出版时间：May 2006
• 年：2006
• 卷：33
• 期：4
• 页码：513-520
• 全文大小：277 K

文摘

To develop a radiopharmaceutical for the palliation of painful bone metastases based on the concept of bifunctional radiopharmaceuticals, we synthesized a bisphosphonate derivative labeled with rhenium-186 (¹⁸⁶Re) that contains a hydroxyl group at the central carbon of its bisphosphonate structure, we attached a stable ¹⁸⁶Re-MAMA chelate to the amino group of a 4-amino butylidene-bisphosphonate derivative [N-[2-[[4-[(4-hydroxy-4,4-diphosphonobutyl)amino]-4-oxobutyl]-2-thioethylamino]acetyl]-2-aminoethanethiolate] oxorhenium (V) (¹⁸⁶Re-MAMA-HBP) and we investigated the effect of a hydroxyl group at the central carbon of its bisphosphonate structure on affinity for hydroxyapatite and on biodistribution by conducting a comparative study with [N-[2-[[3-(3,3-diphosphonopropylcarbamoyl)propyl]-2-thioethylamino]acetyl]-2-aminoethanethiolate] oxorhenium (V) (¹⁸⁶Re-MAMA-BP). The precursor of ¹⁸⁶Re-MAMA-HBP, trityl (Tr)-MAMA-HBP, was obtained by coupling a Tr-MAMA derivative to 4-amino-1-hydroxybutylidene-1,1-bisphosphonate. ¹⁸⁶Re-MAMA-HBP was prepared by a reaction with ¹⁸⁶ReO₄⁻ and SnCl₂ in citrate buffer after the deprotection of the Tr groups of Tr-MAMA-HBP. After reversed-phase high-performance liquid chromatography, ¹⁸⁶Re-MAMA-HBP had a radiochemical purity of over 95 % . Compared with ¹⁸⁶Re-MAMA-BP, ¹⁸⁶Re-MAMA-HBP showed a greater affinity for hydroxyapatite beads in vitro and accumulated a significantly higher level in the femur in vivo. Thus, the introduction of a hydroxyl group into ¹⁸⁶Re complex-conjugated bisphosphonates would be effective in enhancing accumulation in bones. These findings provide useful information on the design of bone-seeking therapeutic radiopharmaceuticals.