利用Fab-Selective Limited Proteolysis nSMOL联合校准曲线对Brentuximab Vedotin、Rituximab和Cetuximab的多重LCMS生物分析在治疗药物监测中的应用

N. Iwamoto, M. Takanashi, A. Hamada, T. Shimada
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引用次数: 7

摘要

背景:近年来,使用质谱法进行单克隆抗体(mAb)生物分析已开始被认为是除ELISA之外的一种有效的单克隆抗体测定技术。我们最近开发了一种使用质谱法进行单克隆抗体(mAb)生物分析的高精度方法。该方法是纳米表面和分子取向限制(nSMOL)蛋白水解,可用于多种抗体药物的LCMS生物分析。方法:nSMOL是由蛋白酶纳米颗粒直径(200 nm)和抗体树脂孔径(100 nm)的差异组成的fab选择性有限蛋白水解。为了限制抗体的蛋白水解,将含有单克隆抗体的蛋白A树脂(孔径:100 nm)浆液加入血浆中,抗体Fc区在25°C下用温和的涡流固定在树脂上10 min。用PBS洗涤抗体固定化树脂,用胰蛋白酶偶联FG球(直径:200 nm)进行有限的蛋白水解。这两种直径的差异使得抗体上Fab区的蛋白被有限地水解。nSMOL蛋白水解后,生成的肽仅通过简单的过滤收集。结果:在这项研究中,我们已经证明了使用nSMOL对抗体-药物偶联物(ADC) Brentuximab vedotin进行生物分析的第一个完整验证数据集,使用nSMOL进行蛋白水解。利用nSMOL蛋白水解法进行的完全验证符合小分子药物化合物开发中生物分析方法验证指南的标准。结论:nSMOL也是精确定量血浆ADC(如Brentuximab vedotin)的重要方法。此外,我们报道了nSMOL蛋白水解不仅可以用于血浆中每种单抗的单分析物,也可以用于多分析物的生物分析,因此,nSMOL蛋白水解是多种临床药代动力学研究和治疗药物监测的可行的多重生物分析方法。
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Multiplex LCMS Bioanalysis of Brentuximab Vedotin, Rituximab and Cetuximab towards Therapeutic Drug Monitoring Application by Combined Calibration Curve Using Fab-Selective Limited Proteolysis nSMOL
Background: Recently, monoclonal antibody (mAb) bioanalysis using mass spectrometry has begun to be recognized as useful technology for mAbs measurement other than ELISA. We have recently exploited a high-precision method for bioanalysis of monoclonal antibody (mAb) using mass spectrometry. The method is nano-surface and molecular-orientation limited (nSMOL) proteolysis, which is useful for LCMS bioanalysis of many kinds of antibody drugs. Methods: nSMOL is Fab-selective limited proteolysis which consists of the difference of protease nanoparticle diameter (200 nm) and antibody resin pore diameter (100 nm). For limited proteolysis of antibody, Protein A resin (pore: 100 nm) slurry was added to plasma including monoclonal antibody, and the antibody Fc region was immobilized to the resin at 25°C for 10 min with gentle vortexing. Antibody-immobilized resin was washed with PBS, and limited proteolysis was performed with trypsin-conjugated FG beads (diameter: 200 nm). Limited proteolysis of Fab region on antibody was achieved by these two diameter difference. After nSMOL proteolysis, the generated peptides were collected by only simple filtration. Results: In this study, we have demonstrated that the first full validation dataset for bioanalysis using nSMOL of antibody-drug conjugate (ADC), Brentuximab vedotin, in human plasma using nSMOL proteolysis. Full validation using nSMOL proteolysis fulfilled criteria of guideline on bioanalytical method validation in pharmaceutical development for small molecule drug compounds. Conclusions: These results indicate that nSMOL is also significant method for precise quantification of ADC in plasma, such as Brentuximab vedotin. Furthermore, we report that nSMOL proteolysis is able to apply for not only single-analyte but also multi-analyte bioanalysis of each mAbs in plasma, so that, nSMOL proteolysis is feasible multiplex bioanalysis for many clinical pharmacokinetic study and therapeutic drug monitoring.
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