PATH, 2201 Westlake Ave, Seattle, WA 98122, United States.
Department of Microbiology and Immunology, Tulane University School of Medicine, 1430 Tulane Avenue, New Orleans, LA 70112, United States.
Vaccine. 2023 Feb 10;41(7):1362-1367. doi: 10.1016/j.vaccine.2023.01.005. Epub 2023 Jan 17.
Double mutant heat-labile toxin (dmLT) is a novel vaccine adjuvant under development with several different vaccine candidates. Studies using existing dmLT adjuvant stocks require significant dilution to achieve a clinically relevant dose. This dilution leads to wastage of the adjuvant. This manuscript describes a limited formulation study to improve the stability of bulk dmLT at a more clinically relevant concentration (20 µg/mL) with minimal changes to the existing bulk dmLT formulation. In vitro methods were used to evaluate dmLT stability after lyophilization and short-term accelerated stability studies. The addition of the excipient polysorbate 80 (PS80) at 0.05 % to the existing dmLT formulation was identified as the lead modification that provided improved stability of the lyophilized dmLT at 20 µg/mL through 4 weeks at 40 °C.
双突变不耐热肠毒素(dmLT)是一种新型疫苗佐剂,正在开发中,有几种不同的候选疫苗。使用现有 dmLT 佐剂库存进行的研究需要进行大量稀释才能达到临床相关剂量。这种稀释导致佐剂浪费。本文描述了一项有限的配方研究,以提高在更具临床相关性浓度(20μg/ml)下散装 dmLT 的稳定性,同时对现有散装 dmLT 配方进行最小的改动。采用体外方法评估了冷冻干燥后 dmLT 的稳定性以及短期加速稳定性研究。在现有的 dmLT 配方中添加 0.05%的赋形剂聚山梨醇酯 80(PS80)被确定为主要改进方法,通过在 40°C 下 4 周的时间,可提高 20μg/ml 冷冻干燥 dmLT 的稳定性。