A Novel Size Exclusion Chromatography Method for the Analysis of Monoclonal Antibodies and Antibody-drug Conjugates by Using Sodium Iodide in the Mobile Phase.

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pharmaceutical Research Pub Date : 2024-09-04 DOI:10.1007/s11095-024-03763-6
Jian-Zhong Liu, Lei Li, Wei-Jie Fang
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Abstract

Purposes: Size exclusion chromatography (SEC) is widely used to characterize molecular size variants of antibody drugs. However, SEC analysis is hindered by secondary interactions (or nonspecific interactions) between proteins and stationary phase packing, which result in poor column efficiency. Previous studies have reported that chaotropic salt can inhibit these interactions, but the corresponding applications of this aspect are relatively rare. Therefore, this study introduces a novel approach using sodium iodide (NaI) as a mobile-phase component in SEC and investigates the influence of the mobile-phase composition on secondary interactions.

Methods: SEC analysis was performed on one antibody-drug conjugate and four monoclonal antibodies (mAbs) using three different mobile-phase systems (i.e., sodium chloride/L-arginine hydrochloride/NaI mobile phases system) to compare the column efficiency. Subsequently, mAb-1 was used as a model to investigate the effects of these factors on secondary interactions by adjusting the ionic strength (salt concentration) and pH of the NaI mobile-phase system.

Results: NaI exhibits superior column efficiency performance in the SEC analysis of most products. The ionic strength will affect nonideal electrostatic and hydrophobic interaction. An appropriate ionic strength can inhibit electrostatic interactions, while an excessive ionic strength increases hydrophobic interactions. pH primarily influences electrostatic interactions. Determining the appropriate pH necessitates consideration of the isoelectric point of the protein and the pH tolerance of the column.

Conclusions: In SEC analysis, using NaI as the salt component in the mobile phase reduces secondary interactions and improves column efficiency. This approach is advantageous for samples with intense secondary interactions and is a suitable alternative.

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在流动相中使用碘化钠分析单克隆抗体和抗体药物共轭物的新型尺寸排阻色谱法。
目的:尺寸排阻色谱法(SEC)被广泛用于鉴定抗体药物的分子尺寸变体。然而,蛋白质与固定相填料之间的二次相互作用(或非特异性相互作用)会阻碍 SEC 分析,导致色谱柱效率低下。以前的研究曾报道过混沌盐可以抑制这些相互作用,但这方面的相应应用相对较少。因此,本研究介绍了一种在 SEC 中使用碘化钠(NaI)作为流动相成分的新方法,并研究了流动相成分对二级相互作用的影响:采用三种不同的流动相体系(即氯化钠/L-精氨酸盐酸盐/NaI流动相体系)对一种抗体-药物共轭物和四种单克隆抗体(mAbs)进行了SEC分析,以比较柱效。随后,以mAb-1为模型,通过调整NaI流动相体系的离子强度(盐浓度)和pH值,研究这些因素对二次相互作用的影响:结果:在对大多数产品进行 SEC 分析时,NaI 的柱效表现优异。离子强度会影响非理想的静电和疏水相互作用。适当的离子强度可抑制静电作用,而过高的离子强度则会增加疏水作用。确定适当的 pH 值需要考虑蛋白质的等电点和色谱柱的 pH 耐受性:结论:在 SEC 分析中,使用 NaI 作为流动相中的盐成分可减少次级相互作用并提高色谱柱效率。这种方法适用于二次相互作用强烈的样品,是一种合适的替代方法。
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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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