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111铟标记的前列腺酸性磷酸酶特异性抗体及其通过双环二乙烯三胺五乙酸酐进行位点特异性衍生的F(ab')2片段在正常小鼠体内的生物分布。

Biodistribution in normal mice of an 111In-labelled prostatic acid phosphatase-specific antibody and its F(ab')2 fragments derivatized site-specifically or via bicyclic diethylenetriaminepentaacetic acid anhydride.

作者信息

Perälä M, Vihko P, Södervall M, Heikkilä J, Vihko R

机构信息

Biocenter, University of Oulu, Finland.

出版信息

Eur J Nucl Med. 1990;16(8-10):621-6. doi: 10.1007/BF00998159.

Abstract

In this study we examined optimization of derivatization of monoclonal antibodies and their fragments intended for use as radiopharmaceutical in radioimaging and/or radioimmunotherapy of prostatic cancer. Two different principles were used to conjugate diethylenetriaminepentaacetic acid (DTPA) to a monoclonal antibody (Mab, subclass IgG1) raised against human prostatic acid phosphatase (PAP). In addition, the F(ab')2 fragments of this Mab were also derivatized. We used the cyclic anhydride of DTPA (CA-DTPA) as a chelating agent for these two protein moieties. Furthermore, the Mab and the F(ab')2 fragments were modified site-specifically by attaching linkers, N-(p-aminobenzyl)diethylenetriaminetetraacetic acid (p-NH2-Bz-DTTA) and 1-(p-aminobenzyl)diethylenetriaminepentaacetic acid (p-NH2-Bz-DTPA), to the carbohydrate components of the parent molecules. In this study, biodistribution of the 111In-labelled derivatives was investigated in normal mice. All the derivatives of IgG1 demonstrated a slower blood clearance than the corresponding derivatives of the F(ab')2 fragments. This property was particularly pronounced in the site-specifically conjugated derivatives of IgG1. All the derivatives studied accumulated in the liver, kidney, and spleen. The CA-DTPA derivatives of F(ab')2 fragments showed the highest kidney-to-blood ratios of radioactivity compared with the other compounds studied. The derivatives of IgG1 showed a higher percentage of the injected dose in liver and spleen tissues than the derivatives of the F(ab')2 fragments. The F(ab')2 fragments studied also gave rise to site-specific derivatives, which demonstrated that carbohydrates were also present in this part of the molecule. They behaved similarly to the CA-DTPA F(ab')2 derivative in other respects, but the kidney accumulation was lower at 72 and 120 h.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在本研究中,我们考察了用于前列腺癌放射性成像和/或放射免疫治疗的放射性药物的单克隆抗体及其片段衍生化的优化方法。采用两种不同的原理将二乙烯三胺五乙酸(DTPA)与针对人前列腺酸性磷酸酶(PAP)的单克隆抗体(Mab,IgG1亚类)偶联。此外,该Mab的F(ab')2片段也进行了衍生化。我们使用DTPA的环状酸酐(CA-DTPA)作为这两种蛋白质部分的螯合剂。此外,通过将连接体N-(对氨基苄基)二乙烯三胺四乙酸(p-NH2-Bz-DTTA)和1-(对氨基苄基)二乙烯三胺五乙酸(p-NH2-Bz-DTPA)连接到亲本分子的碳水化合物成分上,对Mab和F(ab')2片段进行位点特异性修饰。在本研究中,对111In标记的衍生物在正常小鼠体内的生物分布进行了研究。所有IgG1衍生物的血液清除速度均比相应的F(ab')2片段衍生物慢。这一特性在IgG1的位点特异性偶联衍生物中尤为明显。所有研究的衍生物都在肝脏、肾脏和脾脏中蓄积。与其他研究的化合物相比,F(ab')2片段的CA-DTPA衍生物显示出最高的肾脏与血液放射性比值。IgG1衍生物在肝脏和脾脏组织中的注射剂量百分比高于F(ab')2片段衍生物。所研究的F(ab')2片段也产生了位点特异性衍生物,这表明该分子的这一部分也存在碳水化合物。它们在其他方面的行为与CA-DTPA F(ab')2衍生物相似,但在72小时和120小时时肾脏蓄积较低。(摘要截短于250字)

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