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Identifying a stable bulk dmLT adjuvant formulation at a clinically relevant concentration.
Estrada, Marcus R; Bzami, Anan; Norton, Elizabeth B; White, Jessica A.
Afiliação
  • Estrada MR; PATH, 2201 Westlake Ave, Seattle, WA 98122, United States.
  • Bzami A; PATH, 2201 Westlake Ave, Seattle, WA 98122, United States.
  • Norton EB; Department of Microbiology and Immunology, Tulane University School of Medicine, 1430 Tulane Avenue, New Orleans, LA 70112, United States.
  • White JA; PATH, 2201 Westlake Ave, Seattle, WA 98122, United States. Electronic address: jawhite@path.org.
Vaccine ; 41(7): 1362-1367, 2023 02 10.
Article em En | MEDLINE | ID: mdl-36658044
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Toxinas Bacterianas / Proteínas de Escherichia coli Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Toxinas Bacterianas / Proteínas de Escherichia coli Idioma: En Ano de publicação: 2023 Tipo de documento: Article