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铜-60和铜-61的高纯度生产及潜在应用

High purity production and potential applications of copper-60 and copper-61.

作者信息

McCarthy D W, Bass L A, Cutler P D, Shefer R E, Klinkowstein R E, Herrero P, Lewis J S, Cutler C S, Anderson C J, Welch M J

机构信息

Mallinckrodt Institute of Radiology, Washington University School of Medicine, Division of Radiological Sciences, St. Louis, Missouri 63110, USA.

出版信息

Nucl Med Biol. 1999 May;26(4):351-8. doi: 10.1016/s0969-8051(98)00113-9.

Abstract

Previously we described the high yield production of 64Cu using a target system designed specifically for low energy, biomedical cyclotrons. In this study, the use of this target system for the production of 60Cu and 61Cu is described and the utility of these isotopes in the labeling of biomolecules for tumor and hypoxia imaging is demonstrated. 60Cu and 61Cu were produced by the 60Ni(p,n)60Cu, 61Ni(p,n)61Cu, and 60Ni(d,n)61Cu nuclear reactions. The nickel target (>99% enriched or natural nickel) was plated onto a gold disk as described previously (54-225 microm thickness) and irradiated (14.7 MeV proton beam and 8.1 MeV deuteron beam). The copper isotopes were separated from the nickel via ion exchange chromatography and the radioisotopic purity was assessed by gamma spectroscopy. Yields of up to 865 mCi of 60Cu have been achieved using enriched 60Ni. 61Cu has been produced with a maximum yield of 144 mCi using enriched 61Ni and 72 mCi using enriched 60Ni. Specific activities (using enriched material) ranged from 80 to 300 mCi/microg Cu for 60Cu and from 20 to 81 mCi/microg Cu for 61Cu. Bombardments of natural Ni targets were performed using both protons and deuterons. Yields and radioisotopic impurities were determined and compared with that for enriched materials. 60Cu was used to radiolabel diacetyl-bis(N4-methylthiosemicarbazone), ATSM. 60Cu-ATSM was injected into rats that had an occluded left anterior descending coronary artery. Uptake of 60Cu-ATSM in the hypoxic region of the heart was visualized clearly using autoradiography. In addition, 60Cu-ATSM was injected into dogs and excellent images of the heart and heart walls were obtained using positron emission tomography (PET). 61Cu was labeled to 1,4,8,11-tetraazacyclotetradecane-N,N',N",N"'-tetraacetic acid-octreotide (TETA-octreotide) and the PET images of tumor-bearing rats were obtained up to 2 h postinjection. After decay of the 61Cu, the same rat was injected with 64Cu-TETA-octreotide and the images were compared. The tumor images obtained using 61Cu were found to be superior to those using 64Cu as predicted based on the larger abundance of positrons emitted by 61Cu vs. 64Cu.

摘要

此前我们描述了使用专门为低能量生物医学回旋加速器设计的靶系统高产率生产64Cu的方法。在本研究中,描述了使用该靶系统生产60Cu和61Cu的情况,并证明了这些同位素在标记用于肿瘤和缺氧成像的生物分子中的效用。60Cu和61Cu通过60Ni(p,n)60Cu、61Ni(p,n)61Cu和60Ni(d,n)61Cu核反应产生。如前所述(厚度为54 - 225微米),将镍靶(富集度>99%或天然镍)镀在金盘上并进行辐照(14.7 MeV质子束和8.1 MeV氘核束)。通过离子交换色谱法从镍中分离出铜同位素,并通过伽马能谱法评估放射性同位素纯度。使用富集的60Ni已实现高达865 mCi的60Cu产量。使用富集的61Ni生产61Cu的最大产量为144 mCi,使用富集的60Ni时为72 mCi。(使用富集材料时)60Cu的比活度范围为80至300 mCi/μg Cu,61Cu的比活度范围为20至81 mCi/μg Cu。使用质子和氘核轰击天然镍靶。测定了产量和放射性同位素杂质,并与富集材料的情况进行比较。60Cu用于放射性标记双乙酰 - 双(N4 - 甲基硫代半卡巴腙),即ATSM。将60Cu - ATSM注入左前降支冠状动脉闭塞的大鼠体内。使用放射自显影清楚地观察到心脏缺氧区域对60Cu - ATSM的摄取。此外,将60Cu - ATSM注入狗体内,并使用正电子发射断层扫描(PET)获得了心脏和心脏壁的优质图像。61Cu标记到1,4,8,11 - 四氮杂环十四烷 - N,N',N",N"'- 四乙酸 - 奥曲肽(TETA - 奥曲肽)上,并在注射后长达2小时获得荷瘤大鼠的PET图像。61Cu衰变后,向同一只大鼠注射64Cu - TETA - 奥曲肽并比较图像。发现使用61Cu获得的肿瘤图像优于使用64Cu获得的图像,这与基于61Cu比64Cu发射的正电子丰度更高所预测的情况一致。

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