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具有高体内稳定性和骨蓄积性的211At和131I标记的双膦酸盐。

211At- and 131I-labeled bisphosphonates with high in vivo stability and bone accumulation.

作者信息

Larsen R H, Murud K M, Akabani G, Hoff P, Bruland O S, Zalutsky M R

机构信息

Department of Chemistry, University of Oslo, Norway.

出版信息

J Nucl Med. 1999 Jul;40(7):1197-203.

Abstract

UNLABELLED

Bisphosphonates were synthesized for use as carriers for astatine and iodine radioisotopes to target bone neoplasms.

METHODS

Radiohalogenated activated esters were coupled to the amino group in the side chain of the bisphosphonate. The bisphosphonate 3-amino-1-hydroxypropylidene bisphosphonate was combined with four different acylation agents: N-succinimidyl 3-[211At]astatobenzoate, N-succinimidyl 3-[131I]iodobenzoate, N-succinimidyl-5-[211At]astato-3-pyridinecarboxylate and N-succinimidyl-5-[131I]iodo-5-pyridinecarboxylate. The products, 3-[131I]iodobenzamide-N-3-hydroxypropylidene-3,3-bisphosphonate (IBPB), 3-[211At]astato-benzamide-N-3-hydroxypropylidene-3,3-bisphosphonat e (ABPB), 5-[131I]iodopyridine-3-amide-N-3-hydroxypropylidene-3,3-bisphospho nate (IPPB) and 5-[211At]astatopyridine-3-amide-N-3-hydroxypropylidene-3,3-bisphos phonate (APPB), were injected intravenously into Balb/c mice. MIRD and Monte Carlo methods were used on the basis of cumulated activity calculated from biodistribution data to estimate dose to organs and bone segments.

RESULTS

All 131I- and 211At-labeled analogs were strongly incorporated into osseous tissue and retained there at stable levels, while a rapid clearance from blood was observed. The bone uptake was found to be similar for 211At- and 131I-labeled bisphosphonate when compared in paired label experiments. Bone uptake and bone-to-tissue ratios were better for IBPB compared with IPPB, and ABPB compared with APPB. All four compounds appeared to be highly resistant to in vivo dehalogenation as indicated by low uptake of 131I/211At in the thyroid gland and stomach. According to dosimetric estimates, the bone surface-to-bone marrow ratio was three times higher with 211At than with 131I.

CONCLUSION

Both the beta-particle- and alpha-particle-emitting compounds showed high in vivo stability and excellent affinity for osseous tissue. Further preclinical evaluation is therefore warranted.

摘要

未标记

双膦酸盐被合成用作砹和碘放射性同位素的载体,以靶向骨肿瘤。

方法

将放射性卤代活化酯与双膦酸盐侧链中的氨基偶联。双膦酸盐3-氨基-1-羟基亚丙基双膦酸盐与四种不同的酰化剂结合:N-琥珀酰亚胺基3-[211At]砹苯甲酸酯、N-琥珀酰亚胺基3-[131I]碘苯甲酸酯、N-琥珀酰亚胺基-5-[211At]砹-3-吡啶羧酸酯和N-琥珀酰亚胺基-5-[131I]碘-5-吡啶羧酸酯。产物3-[131I]碘苯甲酰胺-N-3-羟基亚丙基-3,3-双膦酸盐(IBPB)、3-[211At]砹苯甲酰胺-N-3-羟基亚丙基-3,3-双膦酸盐(ABPB)、5-[131I]碘吡啶-3-酰胺-N-3-羟基亚丙基-3,3-双膦酸盐(IPPB)和5-[211At]砹吡啶-3-酰胺-N-3-羟基亚丙基-3,3-双膦酸盐(APPB)静脉注射到Balb/c小鼠体内。基于从生物分布数据计算的累积活度,使用MIRD和蒙特卡罗方法来估计器官和骨段的剂量。

结果

所有131I和211At标记的类似物都强烈掺入骨组织并在那里保持稳定水平,同时观察到从血液中快速清除。在配对标记实验中比较时,发现211At和131I标记的双膦酸盐的骨摄取相似。与IPPB相比,IBPB的骨摄取和骨与组织的比率更好,与APPB相比,ABPB的骨摄取和骨与组织的比率更好。如甲状腺和胃中131I/211At的低摄取所示,所有四种化合物似乎对体内脱卤具有高度抗性。根据剂量学估计,211At的骨表面与骨髓的比率比131I高两倍。

结论

发射β粒子和α粒子的化合物在体内均表现出高稳定性和对骨组织的优异亲和力。因此有必要进行进一步的临床前评估。

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