UPLC-based assay to assess the hydrophobicity of Antibody-Drug Conjugate (ADC) payloads

J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Jun 1:1146:122075. doi: 10.1016/j.jchromb.2020.122075. Epub 2020 Mar 31.

Abstract

Antibody-Drug Conjugates (ADCs) consist of antibodies attached to cytotoxic small molecules or biological agents (i.e., payloads) through chemical linkers which may be cleavable or non-cleavable. The development of new ADCs is challenging, particularly the process of attaching the linker-payload construct to the antibody (i.e., the conjugation process). One of the major problems associated with conjugation is high hydrophobicity of the payload which can lead to low yields of the ADC through aggregation and/or lower than desired Drug-Antibody Ratios (DARs). We report here a UPLC-based assay that can be used to study the physicochemical properties of ADC payloads at an early stage of development, and to provide information on whether the hydrophilic-hydrophobic balance is suitable for conjugation or further physicochemical optimization is required. The assay is relatively simple to establish and should be of use to those working in the ADC area.

Keywords: ADC payload; Aggregation; Analytical method development; Antibody Drug Conjugate (ADC); Conjugation; High-Performance Liquid Chromatography (HPLC); Hydrophobicity; Ultra-Performance Liquid Chromatography (UPLC).

MeSH terms

  • Biological Assay / methods*
  • Calicheamicins / chemistry
  • Chromatography, High Pressure Liquid
  • Doxorubicin / chemistry
  • Flurbiprofen / chemistry
  • Hydrophobic and Hydrophilic Interactions
  • Ibuprofen / chemistry
  • Immunoconjugates / chemistry*
  • Irinotecan / chemistry
  • Ketoprofen / chemistry
  • Maytansine / chemistry
  • Molecular Conformation
  • Norfloxacin / chemistry
  • Pentachlorophenol / chemistry
  • Protein Multimerization
  • Structure-Activity Relationship
  • Tandem Mass Spectrometry / methods*
  • Tolnaftate / chemistry

Substances

  • Calicheamicins
  • Immunoconjugates
  • Tolnaftate
  • Maytansine
  • Flurbiprofen
  • Irinotecan
  • Doxorubicin
  • Ketoprofen
  • Pentachlorophenol
  • Norfloxacin
  • Ibuprofen