开发单链免疫毒素 BMS-191352 的免疫测定及其在毒物动力学研究中的应用。

B Damle, D Hollenbaugh, J Timoszyk, L Tay, S Kaul
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引用次数: 3

摘要

BMS-191352 是一种单链融合蛋白,由嵌合 BR96 单克隆抗体的可变区和结合缺陷型假单胞菌外毒素 A(PE40)组成。该免疫毒素对表达 Lewis 抗原的肿瘤细胞具有强大的细胞毒性。为测定大鼠和狗 EDTA 血浆中 BMS-191352 的含量,开发并验证了一种灵敏、特异的双抗体夹心 ELISA 法。使用单克隆抗PE40抗体(EXA2-1H8)捕获血浆样品中的 BMS-191352。然后用生物素化的单克隆 BR96 抗生物素抗体(757-4-1)检测捕获的 BMS-191352,再加入链霉亲和素-辣根过氧化物酶结合物和显色剂 3,3',5,5'-四甲基联苯胺。在 450 纳米波长处测量光密度。大鼠和狗血浆中的标准曲线范围为 2-32 纳克/毫升。测定间和测定内精密度的 RSD 均在 9.2% 以内,准确度大于 89.0%。ELISA 方法被用于分析大鼠和狗毒物动力学研究中血浆样本中的 BMS-191352。这些研究表明,BMS-191352 的全身暴露量与剂量成正比,在狗体内 1.8-7.2 mg/m2 的剂量范围内,BMS-191352 的动力学呈线性关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an immunoassay for BMS-191352, a single-chain immunotoxin, and its application to toxicokinetic studies.

BMS-191352 is a single-chain fusion protein composed of the variable regions of chimeric BR96 monoclonal antibody and the binding defective form of Pseudomonas Exotoxin A (PE40). The immunotoxin exhibits potent cytotoxicity against tumor cells expressing the Lewis antigen. A sensitive and specific double antibody sandwich ELISA has been developed and validated for the determination of BMS-191352 in rat and dog EDTA plasma. A monoclonal anti-PE40 antibody (EXA2-1H8) was used to capture BMS-191352 in plasma samples. The captured BMS-191352 was then detected using a biotinylated monoclonal BR96 antiidiotypic antibody (757-4-1) followed by the addition of streptavidin-horseradish peroxidase conjugate and chromogen 3,3',5,5'-tetramethylbenzidine. The optical density was measured at 450 nm. The standard curve range in rat and dog plasma was 2-32 ng/mL. The RSD for the inter- and intra-assay precision was within 9.2% and the accuracy was greater than 89.0%. The ELISA method was applied to the analysis of BMS-191352 in plasma samples from toxicokinetic studies conducted in rats and dogs. These studies revealed that the systemic exposure of BMS-191352 was dose proportional and the kinetics of BMS-191352 were linear between the dose range of 1.8-7.2 mg/m2 in the dog.

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