Optimization of non-linear gradient in hydrophobic interaction chromatography for the analytical characterization of antibody-drug conjugates

被引:29
作者
Bobaly, Balks [1 ]
Randazzo, Giuseppe Marco [1 ]
Rudaz, Serge [1 ]
Guillarme, Davy [1 ]
Fekete, Szabolcs [1 ]
机构
[1] Univ Geneva, Univ Lausanne, Sch Pharmaceut Sci, CMU Rue Michel Servet 1, CH-1211 Geneva 4, Switzerland
基金
瑞士国家科学基金会;
关键词
Hydrophobic interaction chromatography; Antibody-drug-conjugate; Method development; Retention modelling; Non-linear gradient; PHASE LIQUID-CHROMATOGRAPHY; PRACTICAL METHOD DEVELOPMENT; MONOCLONAL-ANTIBODIES; MASS-SPECTROMETRY; MOBILE-PHASE; STRUCTURAL-CHARACTERIZATION; ORGANIC MODIFIER; SEPARATION; VARIANTS; TEMPERATURE;
D O I
10.1016/j.chroma.2016.12.047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The goal of this work was to evaluate the potential of non-linear gradients in hydrophobic interaction chromatography (HIC), to improve the separation between the different homologous species (drug-to antibody, DAR) of commercial antibody-drug conjugates (ADC). The selectivities between Brentuximab Vedotin species were measured using three different gradient profiles, namely linear, power function based and logarithmic ones. The logarithmic gradient provides the most equidistant retention distribution for the DAR species and offers the best overall separation of cysteine linked ADC in HIC. Another important advantage of the logarithmic gradient, is its peak focusing effect for the DARO species, which is particularly useful to improve the quantitation limit of DARO. Finally, the logarithmic behavior of DAR species of ADC in HIC was modelled using two different approaches, based on i) the linear solvent strength theory (LSS) and two scouting linear gradients and ii) a new derived equation and two logarithmic scouting gradients. In both cases, the retention predictions were excellent and systematically below 3% compared to the experimental values. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:82 / 91
页数:10
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