ANTIBODY CO-FORMULATION TOOLBOX AND CAPABILITIES ESTABLISHED IN WUXI BIOLOGICS

Q2 Medicine Antibody Therapeutics Pub Date : 2023-07-01 DOI:10.1093/abt/tbad014.018
Anyuan Liu, J. Weng, Fangyuan Zhou, Kewei Wang, Hongbing Wu, S. Wang, Jeremy Guo
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Abstract

Abstract Introduction Co-formulation containing two or more antibodies (mAbs) is deemed to hold distinct merits such as better treatment efficacy, higher efficiency and extended intellectual property right, attracting the demands from both patients and pharmaceutical companies. However, there are only limited numbers of approved drug products, partially due to the technical challenges in formulation development and analytical methods. Herein, we present WuXi Biologics efforts to accelerate the development of co-formulation drug products. Methodology We have established an antibody co-formulation specific toolbox with a dedicated team for co-formulation product development addressing the formulation and analytical challenges. Our co-formulation analytical expertise includes size exclusion-high performance liquid chromatography (SE-HPLC), caliper-sodium dodecyl sulfate reduced and non-reduced (Caliper-SDS-R & NR), imaged capillary isoelectric focusing (iCIEF), ion-exchange chromatography (IEC), reverse phase-liquid chromatography (RP-LC), hydrophobic interaction chromatography (HIC), Composition-Gradient Multi-Angle Light Scattering (CG-MALS), differential scanning calorimetry (DSC), enzyme-linked immunosorbent assay (ELISA) based and/or cell based potency, and peptide mapping with mass spectrometry etc. Results Remarkably, couple of antibodies co-formulation cases have completed successfully. Take one co-formulation case for instance, specifically, no substantial molecular interactions were observed between the two antibodies according to the results of differential light scattering (DLS) and CG-MALS. Besides, the main peaks of two mAbs were co-eluted in SE-HPLC and Caliper-SDS-NR, respectively. SE-HPLC and Caliper-SDS-NR methods were optimized to evaluate the purity of this co-formulation. As a result, the purity of these two mAbs in this co-formulation was comparable with its individual antibody respectively. Given the isoelectric point of two mAbs in this co-formulation differs by 1.0, iCIEF has been developed to separate the peaks of two mAbs completely. In another case, the isoelectric point of two mAbs differed by just 0.4, CEX has been developed. iCIEF and CEX method were optimized to evaluate the charge variants and determine the concentration ratio of these two mAbs in co-formulation product.
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抗体联合制剂工具箱和无锡生物制剂公司建立的能力
包含两种或两种以上抗体的联合制剂(mab)被认为具有更好的治疗效果、更高的效率和更长的知识产权等独特的优点,吸引了患者和制药公司的需求。然而,批准的药品数量有限,部分原因是由于配方开发和分析方法方面的技术挑战。在此,我们介绍了药明康德生物制品加快联合制剂药物产品开发的努力。我们已经建立了一个抗体联合制剂专用工具箱,并配备了一个专门的团队,用于联合制剂产品开发,解决制剂和分析方面的挑战。我们的合作配方分析专业技术包括粒径排除-高效液相色谱(SE-HPLC),卡尺-十二烷基硫酸钠还原和非还原(卡尺- sds -r & NR),成像毛细管等电聚焦(iCIEF),离子交换色谱(IEC),反相液相色谱(RP-LC),疏水相互作用色谱(HIC),成分梯度多角度光散射(CG-MALS),差示扫描量热法(DSC),基于酶联免疫吸附测定(ELISA)和/或基于细胞的效价,以及用质谱法绘制肽图等。结果2例抗体联合制剂均成功完成。以一个共制剂案例为例,根据差分光散射(DLS)和CG-MALS的结果,两种抗体之间没有观察到实质性的分子相互作用。此外,两个单抗的主峰分别在SE-HPLC和Caliper-SDS-NR中共洗脱。优化了SE-HPLC法和Caliper-SDS-NR法对该制剂的纯度进行评价。因此,该共制剂中这两种单克隆抗体的纯度分别与其单个抗体相当。考虑到该共制剂中两个单抗的等电点相差1.0,我们开发了iCIEF来完全分离两个单抗的峰。在另一种情况下,两个单抗的等电点仅相差0.4,则CEX已经形成。优化了iCIEF和CEX两种方法,用于评价两种单抗的电荷变化,确定两种单抗在共制剂中的浓度比。
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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
期刊最新文献
AI-based antibody discovery platform identifies novel, diverse, and pharmacologically active therapeutic antibodies against multiple SARS-CoV-2 strains. FcRider: a recombinant Fc nanoparticle with endogenous adjuvant activities for hybrid immunization. A pan-allelic human SIRPα-blocking antibody, ES004-B5, promotes tumor killing by enhancing macrophage phagocytosis and subsequently inducing an effective T-cell response. Correction to: A case study of a bispecific antibody manufacturability assessment and optimization during discovery stage and its implications. The process using a synthetic library that generates multiple diverse human single domain antibodies.
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