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用于(64)Cu 抗体成像的双功能螯合剂的比较。

Comparison of bifunctional chelates for (64)Cu antibody imaging.

机构信息

MDS Nordion, Vancouver, BC, V6T 2A3, Canada.

出版信息

Eur J Nucl Med Mol Imaging. 2010 Nov;37(11):2117-26. doi: 10.1007/s00259-010-1506-1. Epub 2010 Jun 16.

Abstract

PURPOSE

Improved bifunctional chelates (BFCs) are needed to facilitate efficient (64)Cu radiolabeling of monoclonal antibodies (mAbs) under mild conditions and to yield stable, target-specific agents. The utility of two novel BFCs, 1-Oxa-4,7,10-triazacyclododecane-5-S-(4-isothiocyanatobenzyl)-4,7,10-triacetic acid (p-SCN-Bn-Oxo-DO3A) and 3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-triene-4-S-(4-isothiocyanatobenzyl)-3,6,9-triacetic acid (p-SCN-Bn-PCTA), for mAb imaging with (64)Cu were compared to the commonly used S-2-(4-isothiocyanatobenzyl)-1,4,7,10-tetraazacyclododecane-tetraacetic acid (p-SCN-Bn-DOTA).

METHODS

The BFCs were conjugated to trastuzumab, which targets the HER2/neu receptor. (64)Cu radiolabeling of the conjugates was optimized. Receptor binding was analyzed using flow cytometry and radioassays. Finally, PET imaging and biodistribution studies were done in mice bearing either HER2/neu-positive or HER2/neu-negative tumors.

RESULTS

(64)Cu-Oxo-DO3A- and PCTA-trastuzumab were prepared at room temperature in >95% radiochemical yield (RCY) in <30 min, compared to only 88% RCY after 2 h for the preparation of (64)Cu-DOTA-trastuzumab under the same conditions. Cell studies confirmed that the immunoreactivity of the mAb was retained for each of the bioconjugates. In vivo studies showed that (64)Cu-Oxo-DO3A- and PCTA-trastuzumab had higher uptake than the (64)Cu-DOTA-trastuzumab at 24 h in HER2/neu-positive tumors, resulting in higher tumor to background ratios and better tumor images. By 40 h all three of the (64)Cu-BFC-trastuzumab conjugates allowed for clear visualization of the HER2/neu-positive tumors but not the negative control tumor.

CONCLUSION

The antibody conjugates of PCTA and Oxo-DO3A were shown to have superior (64)Cu radiolabeling efficiency and stability compared to the analogous DOTA conjugate. In addition, (64)Cu-PCTA and Oxo-DO3A antibody conjugates may facilitate earlier imaging with greater target to background ratios than the analogous (64)Cu-DOTA antibody conjugates.

摘要

目的

需要改进双功能螯合剂(BFCs),以促进单克隆抗体(mAbs)在温和条件下的有效(64)Cu 放射性标记,并生成稳定的、针对特定靶点的试剂。两种新型 BFCs,1-Oxa-4,7,10-三氮杂环十二烷-5-S-(4-异硫氰酸苯甲基)-4,7,10-三乙酸(p-SCN-Bn-Oxo-DO3A)和 3,6,9,15-四氮杂双环[9.3.1]十五烷-1(15),11,13-三烯-4-S-(4-异硫氰酸苯甲基)-3,6,9-三乙酸(p-SCN-Bn-PCTA),用于 mAb 与(64)Cu 的成像,与常用的 S-2-(4-异硫氰酸苯甲基)-1,4,7,10-四氮杂环十二烷-四乙酸(p-SCN-Bn-DOTA)进行了比较。

方法

将 BFC 与曲妥珠单抗缀合,该曲妥珠单抗靶向 HER2/neu 受体。优化了缀合物的(64)Cu 放射性标记。使用流式细胞术和放射分析分析受体结合。最后,在携带 HER2/neu 阳性或 HER2/neu 阴性肿瘤的小鼠中进行了 PET 成像和生物分布研究。

结果

(64)Cu-Oxo-DO3A 和 PCTA-曲妥珠单抗在室温下以>95%的放射化学产率(RCY)在<30 分钟内制备,而在相同条件下,(64)Cu-DOTA-曲妥珠单抗的制备需要 2 小时才能达到 88%的 RCY。细胞研究证实,每种生物缀合物的 mAb 免疫反应性都得到了保留。体内研究表明,与(64)Cu-DOTA-曲妥珠单抗相比,(64)Cu-Oxo-DO3A 和 PCTA-曲妥珠单抗在 24 小时时在 HER2/neu 阳性肿瘤中的摄取率更高,导致更高的肿瘤与背景比和更好的肿瘤图像。到 40 小时,三种(64)Cu-BFC-曲妥珠单抗缀合物都可以清晰地观察到 HER2/neu 阳性肿瘤,但不能观察到阴性对照肿瘤。

结论

与类似的 DOTA 缀合物相比,PCTA 和 Oxo-DO3A 的抗体缀合物显示出更高的(64)Cu 放射性标记效率和稳定性。此外,与类似的(64)Cu-DOTA 抗体缀合物相比,(64)Cu-PCTA 和 Oxo-DO3A 抗体缀合物可能更容易更早地进行成像,具有更高的靶与背景比。

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