AI Article Synopsis

  • The study compares the monoclonal antibody adalimumab and the Fc-fusion protein etanercept with their biosimilars under stress conditions of agitation and high temperature.
  • Various analytical methods, including capillary gel electrophoresis (CGE), reversed-phase liquid chromatography (RPLC), and size-exclusion chromatography (SEC), were utilized to discern differences in product stability and integrity.
  • Results showed that the biosimilar adalimumab had more fragments and aggregates than the reference, while the etanercept reference had more related species; all techniques proved to be complementary in the analysis.

Article Abstract

In this work, a monoclonal antibody, adalimumab, and an Fc-fusion protein, etanercept, were studied and compared to one of their biosimilars. Samples submitted to stress conditions (agitation and high temperature) were used for method development. The developed methods were also applied to samples reduced by beta-mercaptoethanol to evaluate their capability to distinguish the expected species. Capillary gel electrophoresis (CGE), reversed-phase liquid chromatography (RPLC), and size-exclusion chromatography (SEC) methods coupled with UV detection were used to analyze the biopharmaceuticals. Their complementarity was investigated. For further molecular weight determination, SEC-multi angle light scattering and RPLC-quadrupole time-of-flight were occasionally used. For adalimumab, a larger amount of fragments and aggregates was observed in the biosimilar compared with the reference product. For etanercept, more related species were found in the reference product. Those three separation techniques showed good complementarity. Indeed, RPLC enabled the separation of hydrophilic and hydrophobic degradation products. CGE provided good selectivity for several adalimumab fragments, and SEC was useful for the analysis of aggregates and certain fragments that cannot be separated by the other approaches. Moreover, those formulations were submitted to mild stress conditions (30°C, 300 rpm for 4 h) that mimic shipping conditions. No additional peak was found under these conditions for the two studied biopharmaceuticals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686473PMC
http://dx.doi.org/10.3389/fchem.2021.782099DOI Listing

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