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基于纳米氧化铈-聚酰胺纳米纤维(68)Ge/(68)Ga 发生器用于制备(68)Ga 标记的环 RGD 二聚体作为肿瘤成像的潜在 PET 放射性示踪剂的实用性。

The practicality of nanoceria-PAN-based (68)Ge/(68)Ga generator toward preparation of (68)Ga-labeled cyclic RGD dimer as a potential PET radiotracer for tumor imaging.

机构信息

Radiopharmaceuticals Division, Bhabha Atomic Research Centre, Mumbai, India.

出版信息

Cancer Biother Radiopharm. 2013 Feb;28(1):77-83. doi: 10.1089/cbr.2012.1252. Epub 2012 Sep 11.

Abstract

Cyclic RGD (Arg-Gly-Asp) peptides radiolabeled with (68)Ga have great potential for the early tumor detection and noninvasive monitoring of tumor metastasis and therapeutic response. Herein, the preparation of (68)Ga-labeled DOTA-Ec(RGDfK) (DOTA=1,4,7,10-tetraazacylododecane-1,4,7,10-tetracetic acid; E=Glutamic acid; R=Arginine; G=Glycine; D=Aspartic acid; f=phenyl alanine; K=lysine) using (68)Ga directly eluted from a nanoceria-polyacrylonitrile (CeO(2)-PAN)-based (68)Ge/(68)Ga generator developed in-house was reported. The (68)Ga complex of DOTA-Ec(RGDfK) was synthesized with >98% radiochemical purity by incubating 20 μg of the conjugate with (68)GaCl(3) (74-111 MBq) in acetate buffer (pH 3.5-4.0) at 90°C for 10 minutes. The complex exhibited excellent in vitro stability in 0.1 M EDTA solution at room temperature upto 1 hour studied (radiochemical purity: 98.0%). The biological efficacy of the radiolabeled conjugate was studied in C57/BL6 mice bearing melanoma tumors. The results of the biodistribution studies revealed significant tumor uptake (4.14±0.54%ID/g) within 10 minutes postinjection (p.i.), which increased further to 4.61±0.31%ID/g at 30 minutes p.i. The tumor-to-blood ratio was found to increase from 1.75±0.42 at 10 minutes p.i. to 2.25±0.20 at 60 minutes p.i., whereas the tumor-to-liver and tumor-to-muscle ratio between the same time points increased from 2.71±0.76 to 3.31±0.84 and 5.37±1.08 to 8.97±1.32, respectively. The study successfully demonstrated the preparation of (68)Ga-DOTA-Ec(RGDfK) as a potential positron-emission tomography radiotracer for possible use in tumor imaging by using (68)Ga eluted from a reliable, easy-to-handle (68)Ge/(68)Ga generator developed in-house, without any postelution purification of (68)Ga.

摘要

用(68)Ga 直接标记从内部开发的基于纳米氧化铈-聚丙烯腈(CeO2-PAN)的(68)Ge/(68)Ga 发生器洗脱的(68)Ga 标记环肽(Arg-Gly-Asp)[c(RGDfK)](2)(DOTA=1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸;E=谷氨酸;R=精氨酸;G=甘氨酸;D=天冬氨酸;f=苯丙氨酸;K=赖氨酸),制备(68)Ga 标记的 DOTA-E[c(RGDfK)](2)(DOTA=1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸;E=谷氨酸;R=精氨酸;G=甘氨酸;D=天冬氨酸;f=苯丙氨酸;K=赖氨酸),该报告已发表。(68)Ga 络合物的 DOTA-E[c(RGDfK)](2)通过在 90°C 下用(68)GaCl3(74-111MBq)在醋酸盐缓冲液(pH3.5-4.0)中孵育 20μg 缀合物 10 分钟来合成,具有>98%的放射化学纯度。该络合物在室温下在 0.1M EDTA 溶液中具有出色的体外稳定性,在 1 小时的研究中(放射化学纯度:98.0%)。在携带黑色素瘤的 C57 / BL6 小鼠中研究了放射性标记缀合物的生物学功效。生物分布研究的结果表明,在注射后 10 分钟内(p.i.),肿瘤摄取显著(4.14±0.54%ID/g),在 30 分钟 p.i.时进一步增加至 4.61±0.31%ID/g。肿瘤与血液的比率从 10 分钟 p.i.时的 1.75±0.42 增加到 60 分钟 p.i.时的 2.25±0.20,而同一时间点的肿瘤与肝脏和肿瘤与肌肉的比率分别从 2.71±0.76 增加到 3.31±0.84 和 5.37±1.08 增加到 8.97±1.32。该研究成功地证明了(68)Ga-DOTA-E[c(RGDfK)](2)的制备,作为一种潜在的正电子发射断层扫描放射性示踪剂,可用于使用从内部开发的可靠,易于处理的(68)Ge/(68)Ga 发生器洗脱的(68)Ga 进行肿瘤成像,而无需对(68)Ga 进行任何洗脱后纯化。

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