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使用新型99mTc-放射性叶酸对小鼠体内叶酸受体阳性恶性和正常组织进行单光子发射计算机断层扫描(SPECT)研究。

SPECT study of folate receptor-positive malignant and normal tissues in mice using a novel 99mTc-radiofolate.

作者信息

Müller Cristina, Forrer Flavio, Schibli Roger, Krenning Eric P, de Jong Marion

机构信息

Department of Nuclear Medicine, Erasmus Medical Center, Rotterdam, The Netherlands.

出版信息

J Nucl Med. 2008 Feb;49(2):310-7. doi: 10.2967/jnumed.107.045856. Epub 2008 Jan 16.

Abstract

UNLABELLED

The folate receptor (FR) is overexpressed on epithelial cancers (FR-alpha) and on activated, but not resting, macrophages (FR-beta) involved in a variety of inflammatory and autoimmune diseases. Therefore, folate-based radiopharmaceuticals have the potential to be used as imaging agents of FR-positive tumor and inflammatory cells. In this study SPECT/CT of FR-positive malignant and normal tissues and organs in mice was performed using an improved organometallic (99m)Tc-radiofolate.

METHODS

The (99m)Tc radiolabeling of the histidine-folate was performed using the tricarbonyl technique described earlier for preparation of other organometallic radiofolates. Nude male mice with FR-positive KB tumor xenografts were used. Biodistribution studies were performed 1, 4, and 24 h after injection of the (99m)Tc-His-folate (1.5 MBq/mouse). Images were acquired with a dedicated small-animal SPECT/CT camera 24 h after injection of the radiofolate (500 MBq/mouse). Ex vivo autoradiography was performed on tumors and FR-positive normal tissues. Adjacent sections were used for in vitro autoradiography of FRs after decay of the injected radioactivity.

RESULTS

The SPECT/CT studies revealed accumulation of the radiotracer in FR-positive KB tumor xenografts and kidneys as reported previously. At the same time, specific uptake of the radiofolate in normal tissues-that is, salivary glands and choroid plexus-could be visualized with SPECT. FR-specific accumulation in these tissues and organs was confirmed by coinjection of excess folic acid, which resulted in a complete blockade of radiofolate uptake. In addition, ex vivo and in vitro autoradiography of these organs and tissues confirmed FR expression and displayed radioactivity distribution patterns almost identical to those found on SPECT images. In biodistribution studies we found a high tumor uptake (4.29 +/- 0.67 %ID/g [percentage of the injected dose per gram of tissue], 4 h after injection) that was almost completely retained over time (3.51 +/- 0.37 %ID/g, 24 h after injection).

CONCLUSION

The novel (99m)Tc-histidine-folate showed improved in vivo characteristics compared with other organometallic radiofolates that allowed imaging of FR-positive malignant (KB tumor xenografts) and kidneys. For the first time, to our knowledge, specific tracer uptake in salivary glands and the choroid plexus could be visualized using a high-resolution animal SPECT/CT camera.

摘要

未标记

叶酸受体(FR)在上皮癌(FR-α)以及参与多种炎症和自身免疫性疾病的活化巨噬细胞(而非静息巨噬细胞,FR-β)上过度表达。因此,基于叶酸的放射性药物有潜力用作FR阳性肿瘤和炎症细胞的成像剂。在本研究中,使用改进的有机金属(99m)Tc-放射性叶酸对小鼠的FR阳性恶性和正常组织及器官进行了SPECT/CT检查。

方法

使用先前描述的用于制备其他有机金属放射性叶酸的三羰基技术对组氨酸-叶酸进行(99m)Tc放射性标记。使用携带FR阳性KB肿瘤异种移植的雄性裸鼠。在注射(99m)Tc-组氨酸-叶酸(1.5 MBq/小鼠)后1、4和24小时进行生物分布研究。在注射放射性叶酸(500 MBq/小鼠)后24小时,用专用的小动物SPECT/CT相机采集图像。对肿瘤和FR阳性正常组织进行离体放射自显影。在注射的放射性物质衰变后,相邻切片用于FR的体外放射自显影。

结果

SPECT/CT研究显示,放射性示踪剂在FR阳性KB肿瘤异种移植和肾脏中积聚,如先前报道。同时,用SPECT可以观察到放射性叶酸在正常组织(即唾液腺和脉络丛)中的特异性摄取。通过注射过量叶酸证实了这些组织和器官中FR特异性积聚,这导致放射性叶酸摄取完全被阻断。此外,这些器官和组织的离体和体外放射自显影证实了FR表达,并显示出与SPECT图像上几乎相同的放射性分布模式。在生物分布研究中,我们发现肿瘤摄取率很高(注射后4小时为4.29±0.67 %ID/g[每克组织注射剂量的百分比]),且随时间几乎完全保留(注射后24小时为3.51±0.37 %ID/g)。

结论

与其他有机金属放射性叶酸相比,新型(99m)Tc-组氨酸-叶酸显示出改善的体内特性,能够对FR阳性恶性肿瘤(KB肿瘤异种移植)和肾脏进行成像。据我们所知,首次使用高分辨率动物SPECT/CT相机可视化了唾液腺和脉络丛中的特异性示踪剂摄取。

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