Janet Wolfe, President of Wolfe Laboratories, said, “ADCs are a rapidly growing class of oncology therapeutics that are incredibly promising, yet complex. Given the complexity of ADCs, the ability to control and fully characterize the conjugation sites will enable streamlined and cost-effective ADC discovery and development and may positively affect a conjugate’s development potential and commercial value. Wolfe is expanding its research efforts in this important area to better predict and control the pharmaceutical properties of ADCs. This type of research exemplifies our commitment to providing translational drug development solutions and actionable, meaningful information to our customers.”
The physiochemical stability of ADCs during manufacturing, storage and administration is an important factor influencing their therapeutic efficacy; however, it has remained unclear how covalent modifications alter the stability of these conjugates. Wolfe Laboratories researchers utilized analytical methods such as size-exclusion chromatography, dynamic light scattering and ion exchange chromatography to characterize the size and charge of conjugates created through conjugating fluorophores to lysine residues in the constant (Fc) region of IgG1. This research offers new understanding related to the effects of chemical conjugation on the stability of ADCs, providing important information on the effects of drug-to-antibody ratio and fluorophore hydrophobicity on the stability of Fc-conjugates.
The abstract titled, “The influence of payload on the physiochemical stability of Fc-conjugates,” was presented on April 7, 2013 and authored by: Nicholas Boylan, Robert J. Proos, Janet Wolfe and Jennifer S. Laurence.
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