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用于CT26肿瘤细胞上过表达叶酸受体的正电子发射断层扫描成像的Ga-HBED-CC-EDBE-叶酸的合成与评价

Synthesis and evaluation of Ga-HBED-CC-EDBE-folate for positron-emission tomography imaging of overexpressed folate receptors on CT26 tumor cells.

作者信息

Choi Pyeong Seok, Lee Jun Young, Park Jeong Hoon, Kim Sang Wook

机构信息

Department of Advanced Materials Chemistry, Dongguk University, Gyeongju, Republic of Korea.

Radiation Instrumentation Research Division, Korea Atomic Energy Research Institute, Jeongeup, Republic of Korea.

出版信息

J Labelled Comp Radiopharm. 2018 Jan;61(1):4-10. doi: 10.1002/jlcr.3563. Epub 2017 Dec 29.

Abstract

The Ga is a positron-emitting radionuclide that can be combined with bifunctional chelating agents and bioactive substances for use as positron-emission tomography (PET) diagnostic agents. The HBED-CC is an acyclic chelating agent that is rapidly labeled with Ga under mild conditions. To target cancer cells, bioactive substances can be conjugated to the carboxyl terminus of HBED-CC. Because folic acid strongly binds to folate receptors that are overexpressed on the surfaces of many types of cancer cells, it was coupled with HBED-CC through a small polyethylene glycol-based linker (EDBE) to generate an active, receptor-selective targeting system. The HBED-CC-EDBE-folate (HCEF) precursor was readily labeled with Ga in 5 minutes at room temperature (98% radiochemical yield; 99% radiochemical purity after isolation). In cellular uptake tests, higher uptakes of Ga-HCEF were observed for the CT26 and KB cell lines (which express folate receptors) than for the A549 cell line (which does not). Finally, in vivo micro-PET measurements over 2 hours of binding in BALB/c mice into which CT26 tumors had been transplanted showed the selective accumulation of Ga-HCEF in the folate receptor-expressing CT26 tumors. These results confirmed the potential of Ga-HCEF as a PET diagnostic agent for tumors that express folate receptors.

摘要

镓是一种发射正电子的放射性核素,可与双功能螯合剂和生物活性物质结合用作正电子发射断层扫描(PET)诊断剂。HBED-CC是一种无环螯合剂,在温和条件下能快速被镓标记。为了靶向癌细胞,生物活性物质可与HBED-CC的羧基末端偶联。由于叶酸能与多种癌细胞表面过度表达的叶酸受体强烈结合,因此通过一个基于聚乙二醇的小分子连接体(EDBE)将其与HBED-CC偶联,以生成一种活性的、受体选择性靶向系统。HBED-CC-EDBE-叶酸(HCEF)前体在室温下5分钟内即可轻松被镓标记(放射化学产率为98%;分离后放射化学纯度为99%)。在细胞摄取试验中,观察到CT26和KB细胞系(表达叶酸受体)对镓-HCEF的摄取高于A549细胞系(不表达叶酸受体)。最后,在移植了CT26肿瘤的BALB/c小鼠体内进行的2小时结合的体内微型PET测量显示,镓-HCEF在表达叶酸受体的CT26肿瘤中选择性积聚。这些结果证实了镓-HCEF作为表达叶酸受体肿瘤的PET诊断剂的潜力。

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