Khetarpal V K, Storbeck L S
Rhône-Poulenc Rorer, Collegeville, PA 19426.
Cancer Chemother Pharmacol. 1995;35(4):313-7. doi: 10.1007/BF00689450.
RG 83852 is a murine monoclonal antibody that preferentially inhibits the high-affinity binding of epidermal growth factor (EGF) to its receptor. Since overexpression of EGF receptor has been implicated in some human malignancies, the antibody is under investigation as a potential anticancer agent. The present work characterized the tissue distribution and elimination of 131I-labeled antibody in rats following i.v. administration. 131I-RG 83852 was given in a 2.22 mg/kg dose to rats, and 4, 24, 48, and 72 h afterwards 131I activity excreted in the urine and feces and that present in various tissues was determined. The plasma contained the highest concentration of radioactivity at all times. At 4 h the plasma contained about 12% of the injected dose (ID)/ml, and radioactivity in this compartment accounted for almost 70% ID. The plasma elimination of 131I-derived activity occurred linearily at a rate of about 0.48% ID/h. Except in the thyroid, the concentration of 131I activity in all tissues was much lower than in the plasma (tissue-to-plasma ratio < or = 0.1). In the thyroid, accumulation of radioactivity (4% ID at 24 h) was presumably due to trapping of 131I released from the antibody as a result of biodegradation. The urinary excretion occurred at a rate of about 0.5% ID/h; the fecal excretion was minimal. The biodistribution results are consistent with the protein structure of the antibody. Based on the available disposition data, it is proposed that elimination of the antibody involves degradation, a process that follows zero-order kinetics, followed by excretion of the labeled product(s) in the urine.
RG 83852是一种鼠单克隆抗体,它优先抑制表皮生长因子(EGF)与其受体的高亲和力结合。由于EGF受体的过表达与某些人类恶性肿瘤有关,该抗体正作为一种潜在的抗癌药物进行研究。目前的工作对静脉注射后大鼠体内131I标记抗体的组织分布和消除情况进行了表征。以2.22 mg/kg的剂量给大鼠注射131I-RG 83852,在给药后4、24、48和72小时,测定尿液和粪便中排泄的131I活性以及各组织中的131I活性。血浆在所有时间点都含有最高浓度的放射性。在4小时时,血浆中含有约12%的注射剂量(ID)/毫升,该隔室中的放射性几乎占ID的70%。131I衍生活性的血浆消除以约0.48% ID/小时的速率呈线性发生。除甲状腺外,所有组织中131I活性的浓度均远低于血浆(组织与血浆的比率≤0.1)。在甲状腺中,放射性的积累(24小时时为4% ID)可能是由于生物降解导致抗体释放的131I被捕获。尿液排泄速率约为0.5% ID/小时;粪便排泄量极少。生物分布结果与抗体的蛋白质结构一致。根据现有的处置数据,提出抗体的消除涉及降解,这是一个遵循零级动力学的过程,随后标记产物在尿液中排泄。