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Anti-CEA monoclonal antibody: technetium-99m labeling and the validation process of a scintigraphic animal model with a non-cellular antigenic implant.

机译:抗CEA单克隆抗体:-99m标记和具有非细胞抗原植入物的闪烁显像动物模型的验证过程。

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摘要

Animal models are currently used to verify the biodistribution of different radiopharmaceuticals before its clinical application in Nuclear Medicine; however, there may be some limitations. The utilization of labelled anti-tumor monoclonal antibodies (MoAb) in experimental models often requires implant of human antigens (usually a cellular implant), which cannot be achieved in immunocompetent animals. Our purpose was to label an anti-CEA MoAb with technetium-99m (99Tc) and to validate a simplified animal model using a noncellular antigenic implant. MoAb was directly labelled with 99mTc, after reduction with 2-mercaptoethanol. Labeling efficiency was checked by ascending chromatography and immunoreactive fraction was measured in plastic wells sensitized with the antigen. Radiopharmaceutical biodistribution was evaluated by dissection and scintigraphy in 5 mice groups; following the subcutaneous administration of Al(OH)3, CEA adsorbed Al(OH)2 and a control group evaluation. Labeling efficiency was 94+/-3%, which showed to be stable for 24 hr, with immunoreactive fraction above 50%. Invasive biodistribution evaluation showed prolonged blood retention, hepatic and renal uptake. A significant increase in uptake was observed in scintigraphic studies of animals with CEA-adsorbed Al(OH)3 implants compared with the other groups (p<0.05). The non-cellular antigenic implant model simplifies the pre-clinical evaluation of labelled MoAb.
机译:目前,动物模型被用于验证不同放射性药物在核医学中的临床应用之前的生物分布;但是,可能会有一些限制。在实验模型中利用标记的抗肿瘤单克隆抗体(MoAb)通常需要植入人类抗原(通常是细胞植入物),而这是在有免疫能力的动物中无法实现的。我们的目的是用99m((99Tc)标记抗CEA MoAb,并使用非细胞抗原植入物验证简化的动物模型。用2-巯基乙醇还原后,将MoAb直接用99mTc标记。通过上升色谱法检查标记效率,并在用抗原致敏的塑料孔中测量免疫反应分数。通过解剖和闪烁显像法对5个小鼠组的放射性药物生物分布进行了评估。皮下注射Al(OH)3后,CEA吸附Al(OH)2,并进行对照组评估。标记效率为94 +/- 3%,显示24小时稳定,免疫反应分数高于50%。侵袭性生物分布评估显示血液滞留时间延长,肝和肾脏摄取延长。与其他组相比,在采用CEA吸附的Al(OH)3植入物的动物的闪烁显像研究中,观察到摄取显着增加(p <0.05)。非细胞抗原植入物模型简化了标记MoAb的临床前评估。

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