Pfizer Inc., 1 Burtt Rd, Andover, MA 01810, United States of America.
Pfizer Inc. (retired), 1 Burtt Rd, Andover, MA 01810, United States of America.
J Immunol Methods. 2024 Oct;533:113742. doi: 10.1016/j.jim.2024.113742. Epub 2024 Aug 15.
Stability of conjugated critical reagents supporting ligand binding assays to enable biotherapeutic drug development is a universal concern. Formulation buffer employed for long-term cold storage may be key to mitigate protein aggregation issues. We investigated biophysical and functional attributes of murine mAb and human multispecific drug labeled with biotin, ruthenium, and Alexa fluor 647 frozen at -80 °C in PBS or a protein storage buffer for 3-15 months. Aggregation was observed at 4 months in mAb A-Ru (11.2%) and -Alexa (10%) in PBS followed by precipitation and reduced biological binding at 15 months. Increased aggregation in drug Ru (11.7%, 6 months) and Alexa (6.9%, 15 months) were noted but without impact on performance. There were no observations with biotin labeled reagents.
共轭关键试剂的稳定性支持配体结合分析,以实现生物治疗药物的开发是普遍关注的问题。用于长期冷藏的制剂缓冲液可能是减轻蛋白质聚集问题的关键。我们研究了在 PBS 或蛋白质储存缓冲液中于-80°C 冷冻 3-15 个月的标记有生物素、钌和 Alexa fluor 647 的鼠源单抗和人源多特异性药物的生物物理和功能特性。在 PBS 中,单抗 A-Ru(11.2%)和-Alexa(10%)在 4 个月时观察到聚集,随后在 15 个月时沉淀且生物结合活性降低。在药物 Ru(11.7%,6 个月)和 Alexa(6.9%,15 个月)中观察到聚集增加,但对性能没有影响。标记有生物素的试剂没有观察到聚集。