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用于前哨淋巴结定位的(99m)Tc标记甘露糖基化葡聚糖的注射部位放射性

Injection site radioactivity of (99m)Tc-labeled mannosylated dextran for sentinel lymph node mapping.

作者信息

Yamaguchi Aiko, Hanaoka Hirofumi, Pirmettis Ioannis, Uehara Tomoya, Tsushima Yoshito, Papadopoulos Minas, Arano Yasushi

机构信息

Graduate School of Pharmaceutical Sciences, Chiba University , 1-8-1 Inohana, Chuo-ku, Chiba 260-8675, Japan.

出版信息

Mol Pharm. 2015 Feb 2;12(2):514-9. doi: 10.1021/mp500592e. Epub 2014 Dec 29.

Abstract

The high and persistent radioactivity at the injection site hinders the accuracy and expansion of sentinel lymph node (SLN) mapping. We investigated the mechanism underlying the undesirable radioactivity after subcutaneous injection of (99m)Tc-labeled mannosylated dextran ((99m)Tc(CO)3-DCM20), a SLN mapping agent targeting mannose receptors on macrophages and dendritic cells, in a mouse model. Biodistribution studies were performed 1 h after subcutaneous injection of (99m)Tc(CO)3-DCM20 from the rear footpad of mice in the presence of varying molar amounts of DCM20 or DC15, a modified dextran without mannose. Biodistribution studies were also conducted after subcutaneous injection of [(125)I]radioiodinated mannosyl-neoglycoalbumin ((125)I-NMA) from the rear footpad. The distribution of fluorescence-labeled DCM20 and DC15 at the injection site was also compared 1 h after subcutaneous injection by immunofluorescent histochemistry. The radioactivity levels of (99m)Tc(CO)3-DCM20 at the injection site and popliteal lymph node, a SLN in this model, decreased with an increase in the molar amounts of DCM20, whereas no significant changes in biodistribution were observed after injection of (99m)Tc(CO)3-DCM20 with varying molar amounts of DC15. (125)I-NMA exhibited rapid elimination of radioactivity from both the popliteal lymph node and the injection site. The fluorescence-labeled DCM20 colocalized well with CD68-positive cells such as macrophages and dendritic cells at the injection site. While partial colocalization was observed between DC15 and CD68-positive cells, the signal intensity was very weak. These findings suggest that specific binding of (99m)Tc(CO)3-DCM20 to the mannose receptor on macrophages and dendritic cells would be responsible for the sustained radioactivity levels at the injection site. These results also imply that discriminated blockage of (99m)Tc(CO)3-DCM20 binding to mannose receptors at the injection sites would reduce the radioactivity at the injection site.

摘要

注射部位的高放射性和持续性放射性阻碍了前哨淋巴结(SLN)定位的准确性和推广。我们在小鼠模型中研究了皮下注射(99m)Tc标记的甘露糖化葡聚糖((99m)Tc(CO)3-DCM20)后出现不良放射性的潜在机制,(99m)Tc(CO)3-DCM20是一种靶向巨噬细胞和树突状细胞上甘露糖受体的SLN定位剂。在存在不同摩尔量的DCM20或DC15(一种无甘露糖的修饰葡聚糖)的情况下,从小鼠后足垫皮下注射(99m)Tc(CO)3-DCM20 1小时后进行生物分布研究。从后足垫皮下注射[(125)I]放射性碘化甘露糖基新糖白蛋白((125)I-NMA)后也进行了生物分布研究。皮下注射1小时后,还通过免疫荧光组织化学比较了荧光标记的DCM20和DC15在注射部位的分布。(99m)Tc(CO)3-DCM20在注射部位和腘窝淋巴结(该模型中的一个SLN)的放射性水平随着DCM20摩尔量的增加而降低,而注射不同摩尔量的DC15的(99m)Tc(CO)3-DCM20后未观察到生物分布的显著变化。(125)I-NMA在腘窝淋巴结和注射部位均表现出放射性的快速消除。荧光标记的DCM20在注射部位与巨噬细胞和树突状细胞等CD68阳性细胞共定位良好。虽然在DC15和CD68阳性细胞之间观察到部分共定位,但信号强度非常弱。这些发现表明,(99m)Tc(CO)3-DCM20与巨噬细胞和树突状细胞上的甘露糖受体的特异性结合是注射部位放射性持续存在的原因。这些结果还意味着,在注射部位特异性阻断(99m)Tc(CO)3-DCM2

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