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放射性标记单克隆抗体在异种移植裸鼠体内的生物动力学:校正特异性组织摄取的评估。

Biokinetics of radiolabeled monoclonal antibodies in heterotransplanted nude rats: evaluation of corrected specific tissue uptake.

作者信息

Ingvar C, Norrgren K, Strand S E, Brodin T, Jönsson P E, Sjögren H O

机构信息

Department of Surgery, Lund University, Sweden.

出版信息

J Nucl Med. 1989 Jul;30(7):1224-34.

PMID:2738703
Abstract

A tumor model is presented to study the biokinetics and localization of radiolabeled monoclonal antibodies (MAb) in the nude rat (Rowett RNu/RNu) heterotransplanted with human melanoma metastases. The nude rat is larger, less sensitive, and lives longer than the nude mouse. It is, therefore, well suited for in vivo studies of tumor localization with radiolabeled monoclonal antibodies. The tumor-to-host weight ratio was closer to the human situation for the nude rat than for the mouse, and quantitative imaging could be performed with a parallel hole collimator. We followed the antibody biokinetics for as long as 8 days, with repeated blood sampling and imaging. Specific uptake of MAb was higher in tumor tissue than in all other tissues except blood. Initial high uptake was also recorded in the bone marrow. The lymph glands showed a slow uptake of specific and control antibody. A simple in vitro correction procedure is described to calculate the corrected specific tissue uptake (STUcorr) that takes the blood activity into account. Thus it was shown that 80% of the tissue uptake in the dissected liver at 30 hr was due to labeled antibodies circulating in the blood. The specific tissue uptake ratio of antibodies 96.5 and OKT3 (nonspecific control) was unity for all other organs except for tumor tissue, where the ratio was greater than two and even higher when correction for blood content of labeled antibody was made.

摘要

本文提出了一种肿瘤模型,用于研究放射性标记单克隆抗体(MAb)在移植了人黑色素瘤转移灶的裸大鼠(Rowett RNu/RNu)中的生物动力学和定位。裸大鼠比裸小鼠体型更大、敏感性更低且寿命更长。因此,它非常适合用于放射性标记单克隆抗体的肿瘤定位体内研究。与小鼠相比,裸大鼠的肿瘤与宿主重量比更接近人类情况,并且可以使用平行孔准直器进行定量成像。我们通过重复采血和成像,对抗体生物动力学进行了长达8天的跟踪。除血液外,MAb在肿瘤组织中的特异性摄取高于所有其他组织。骨髓中也记录到了最初的高摄取。淋巴结对特异性抗体和对照抗体的摄取缓慢。描述了一种简单的体外校正程序,以计算考虑血液活性的校正特异性组织摄取(STUcorr)。结果表明,在30小时时,解剖肝脏中80%的组织摄取是由于血液中循环的标记抗体。除肿瘤组织外,抗体96.5和OKT3(非特异性对照)在所有其他器官中的特异性组织摄取率均为1,而在肿瘤组织中该比率大于2,在对标记抗体的血液含量进行校正后甚至更高。

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