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单链免疫毒素BMS-191352免疫分析方法的建立及其在毒代动力学研究中的应用。

Development of an immunoassay for BMS-191352, a single-chain immunotoxin, and its application to toxicokinetic studies.

作者信息

Damle B, Hollenbaugh D, Timoszyk J, Tay L, Kaul S

机构信息

Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, NJ 08543, USA.

出版信息

J Immunoassay. 1998 May-Aug;19(2-3):145-65. doi: 10.1080/01971529808005478.

Abstract

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.

摘要

BMS-191352是一种单链融合蛋白,由嵌合型BR96单克隆抗体的可变区和铜绿假单胞菌外毒素A(PE40)的结合缺陷型组成。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。已开发并验证了一种灵敏且特异的双抗体夹心ELISA法,用于测定大鼠和犬EDTA血浆中的BMS-191352。使用单克隆抗PE40抗体(EXA2-1H8)捕获血浆样本中的BMS-191352。然后使用生物素化的单克隆BR96抗独特型抗体(757-4-1)检测捕获的BMS-191352,随后加入链霉亲和素-辣根过氧化物酶结合物和发色剂3,3',5,5'-四甲基联苯胺。在450nm处测量光密度。大鼠和犬血浆中的标准曲线范围为2-32ng/mL。批间和批内精密度的相对标准偏差(RSD)在9.2%以内,准确度大于89.0%。ELISA法应用于分析大鼠和犬毒代动力学研究中的血浆样本中的BMS-191352。这些研究表明,BMS-191352的全身暴露呈剂量比例关系,在犬中剂量范围为1.8-7.2mg/m2时,BMS-191352的动力学呈线性。

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