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首页> 外文期刊>Biological & pharmaceutical bulletin >In vivo evaluation of a radiogallium-labeled bifunctional radiopharmaceutical, Ga-DOTA-MN2, for hypoxic tumor imaging
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In vivo evaluation of a radiogallium-labeled bifunctional radiopharmaceutical, Ga-DOTA-MN2, for hypoxic tumor imaging

机译:放射性镓标记的双功能放射性药物Ga-DOTA-MN2的体内评估,用于低氧肿瘤成像

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On the basis of the findings obtained by X-ray crystallography of Ga-DOTA chelates and the drug design concept of bifunctional radiopharmaceuticals, we previously designed and synthesized a radiogallium-labeled DOTA chelate containing two metronidazole moieties, ~(67)Ga-DOTA-MN2, for hypoxic tumor imaging. As expected, ~(67)Ga-DOTA-MN2 exhibited high in vivo stability, although two carboxyl groups in the DOTA skeleton were conjugated with metronidazole moieties. In this study, we evaluated ~(67/68)Ga- DOTA-MN2 as a nuclear imaging agent for hypoxic tumors. ~(67)Ga-labeling of DOTA-MN2 with ~(67)GaCl_3 was achieved with high radiochemical yield (>85%) by 1-min of microwave irradiation (50W). The pharmacokinetics of ~(67)Ga-DOTA-MN2 were examined in FM3A tumor-bearing mice, and compared with those of ~(67)Ga-DOTA-MN1 containing one metronidazole unit and ~(67)Ga-DOTA. Upon administration, ~(67)Ga-DOTA-MN2 exhibited higher accumulation in the implanted tumors than ~(67)Ga-DOTA. Tumor-to-blood ratios of ~(67)Ga-DOTA-MN2 were about two-fold higher than those of ~(67)Ga-DOTA-MN1. Autoradiographic analysis showed the heterogeneous localization of ~(67)Ga-DOTA-MN2 in the tumors, which corresponds to hypoxic regions suggested by well-established hypoxia marker drug, pimonidazole. Furthermore, in positron emission tomography (PET) study, the tumors of mice administered ~(68)Ga-labeled DOTA-MN2 were clearly imaged by small-animal PET at 1 h after administration. This study demonstrates the potential usefulness of ~(67/68)Ga-DOTA-MN2 as a nuclear imaging agent for hypoxic tumors and suggests that two functional moieties, such as metronidazole, can be conjugated to radiogallium-DOTA chelate without reducing the complex stability. The present findings provide useful information about the chemical design of radiogallium-labeled radiopharmaceuticals for PET and single photon emission computed tomography (SPECT) studies.
机译:根据Ga-DOTA螯合物的X射线晶体学发现和双功能放射性药物的药物设计概念,我们先前设计并合成了含有两个甲硝唑部分〜(67)Ga-DOTA-的放射性镓标记的DOTA螯合物。 MN2,用于缺氧肿瘤成像。如预期的那样,〜(67)Ga-DOTA-MN2表现出高的体内稳定性,尽管DOTA骨架中的两个羧基与甲硝唑部分共轭。在这项研究中,我们评估了〜(67/68)Ga-DOTA-MN2作为低氧肿瘤的核显像剂。通过微波辐射(50W)1分钟,以〜(67)GaCl_3〜(67)Ga标记DOTA-MN2,放射化学收率高(> 85%)。在携带FM3A肿瘤的小鼠中检查〜(67)Ga-DOTA-MN2的药代动力学,并与含有一个甲硝唑单元和〜(67)Ga-DOTA的〜(67)Ga-DOTA-MN1进行比较。给药后,〜(67)Ga-DOTA-MN2在植入的肿瘤中比〜(67)Ga-DOTA表现出更高的积累。 〜(67)Ga-DOTA-MN2的肿瘤血比约为〜(67)Ga-DOTA-MN1的两倍。放射自显影分析显示〜(67)Ga-DOTA-MN2在肿瘤中的异质定位,这与完善的缺氧标记药物pimonidazole提示的低氧区域相对应。此外,在正电子发射断层扫描(PET)研究中,在给药后1小时,通过小动物PET清晰地拍摄了〜(68)Ga标记的DOTA-MN2小鼠的肿瘤。这项研究表明〜(67/68)Ga-DOTA-MN2作为低氧性肿瘤的核显像剂的潜在用途,并表明可以将两个功能部分(如甲硝唑)与放射性镓-DOTA螯合物结合,而不会降低复杂的稳定性。本发现提供了有关用于PET和单光子发射计算机断层扫描(SPECT)研究的放射性镓标记的放射性药物的化学设计的有用信息。

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