Profiling Antibody Drug Conjugate Positional Isomers: A System-of-Equations Approach

Citations Over TimeTop 10% of 2012 papers

Abstract

Antibody drug conjugates enable the targeted delivery of potent chemotherapeutic agents directly to cancerous cells. They are made by the chemical conjugation of cytotoxins to monoclonal antibodies, which can be achieved by first reducing interchain disulfide bonds followed by conjugation of the resulting free thiols with drugs. This process yields a controlled, but heterogeneous, population of conjugated products that contains species with various numbers of drugs linked to different former interchain disulfide cysteine residues on the antibodies. We have developed a mathematical approach using inputs from capillary electrophoresis and hydrophobic interaction chromatography to determine the positional isomer distribution within a population of antibody drug conjugates. The results are confirmed by analyzing isolated samples of specific drug-to-antibody ratio species. The procedure is amenable to rapid determination of positional isomer distributions and features low material requirements. A survey of several antibody drug conjugates based on the same IgG framework and small molecule drug combination has shown a very similar distribution of isomers among all of the molecules using this technique, suggesting a robust conjugation process.

Related Papers

• → Studies of Reversible Conjugate Additions(2013)61 cited
• → Electrochemical detection for capillary electrophoresis(1991)54 cited
• → Differential inhibition of hepatic ferrochelatase by regioisomers of N-butyl-, N-pentyl-, N-hexyl-, and N-isobutylprotoporphyrin IX.(1988)15 cited
• → Mechanisms of Cysteine S ‐conjugate β‐Lyases(1998)39 cited
• Advance in Research of Electrochemiluminescence of Ru(bpy)_3~(2+) Subjected to Capillary Electrophoresis(2010)