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甲氨蝶呤-单克隆抗体791T/36偶联物在人肿瘤异种移植裸鼠体内的生物分布及肿瘤定位

Biodistribution and tumour localization of a methotrexate-monoclonal-antibody 791T/36 conjugate in nude mice with human tumour xenografts.

作者信息

Pimm M V, Clegg J A, Garnett M C, Baldwin R W

机构信息

Cancer Research Campaign Laboratories, University of Nottingham, UK.

出版信息

Int J Cancer. 1988 Jun 15;41(6):886-91. doi: 10.1002/ijc.2910410620.

Abstract

The blood kinetics and tumour localization of a conjugate of methotrexate (MTX) and MAb 791T/36 were examined in nude mice with human tumour xenografts. The antibody moiety of the conjugate was detected by labelling with 125I and the drug moiety was assayed using a radioimmunoassay for methotrexate. After radioiodination, the drug moiety was co-precipitable with the radiolabel when TCA or rabbit anti-mouse IgG antiserum was used. Following i.v. injection, serum kinetics of both the antibody and the drug moieties of the conjugate were essentially similar, and the integrity of serum-borne conjugate was confirmed by the co-precipitation of radiolabel and drug. The radiolabelled antibody moiety of the conjugate localized in tumour xenografts, with 5-7% of the injected dose being present per gram of tissue within 6 hr of injection, and the levels were maintained for up to 4 days. Analysis of tumour levels of the MTX moiety showed a progressive uptake over the 4-day observation period with up to 4% of the injected dose being present per gram of tumour when the experiment was terminated. Parallel studies with free MTX showed rapid clearance from the blood and a maximum of 0.35% of the dose/g of tumour 30 min after injection. Control immunoglobulin conjugated to MTX did not show tumour localization of either the antibody or the drug moieties. These studies confirm that in vivo MTX remains bound to antibody in this type of drug antibody conjugate and demonstrate site-specific targeting of this therapeutic agent.

摘要

在患有人类肿瘤异种移植的裸鼠中,检测了甲氨蝶呤(MTX)与单克隆抗体791T/36偶联物的血液动力学和肿瘤定位。通过用125I标记来检测偶联物的抗体部分,并用甲氨蝶呤放射免疫分析法测定药物部分。放射性碘化后,当使用三氯乙酸(TCA)或兔抗小鼠IgG抗血清时,药物部分可与放射性标记物共沉淀。静脉注射后,偶联物的抗体和药物部分的血清动力学基本相似,并且通过放射性标记物和药物的共沉淀证实了血清中偶联物的完整性。偶联物的放射性标记抗体部分定位于肿瘤异种移植中,注射后6小时内每克组织中存在5 - 7%的注射剂量,并且该水平维持长达4天。MTX部分的肿瘤水平分析显示,在4天的观察期内摄取逐渐增加,实验终止时每克肿瘤中存在高达4%的注射剂量。与游离MTX的平行研究表明,其从血液中快速清除,注射后30分钟时每克肿瘤中最多存在0.35%的剂量。与MTX偶联的对照免疫球蛋白未显示抗体或药物部分的肿瘤定位。这些研究证实,在体内MTX在这种类型的药物 - 抗体偶联物中仍与抗体结合,并证明了这种治疗剂的位点特异性靶向作用。

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