Feasibility of Freeze-Drying Oil-in-Water Emulsion Adjuvants and Subunit Proteins to Enable Single-Vial Vaccine Drug Products

To generate potent vaccine responses, subunit protein antigens typically require coformulation with an adjuvant. Oil-in-water emulsions are among the most widely investigated adjuvants, based on their demonstrated ability to elicit robust antibody and cellular immune responses in the clinic. However...

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Veröffentlicht in:Journal of pharmaceutical sciences 2017-06, Vol.106 (6), p.1490-1498
Hauptverfasser: Iyer, Vidyashankara, Cayatte, Corinne, Marshall, Jason D., Sun, Jenny, Schneider-Ohrum, Kirsten, Maynard, Sean K., Rajani, Gaurav Manohar, Bennett, Angie Snell, Remmele, Richard L., Bishop, Steve M., McCarthy, Michael P., Muralidhara, Bilikallahalli K.
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Sprache:eng
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Zusammenfassung:To generate potent vaccine responses, subunit protein antigens typically require coformulation with an adjuvant. Oil-in-water emulsions are among the most widely investigated adjuvants, based on their demonstrated ability to elicit robust antibody and cellular immune responses in the clinic. However, most emulsions cannot be readily frozen or lyophilized, on account of the risk of phase separation, and may have a deleterious effect on protein antigen stability when stored long term as a liquid coformulation. To circumvent this, current emulsion-formulated vaccines generally require a complex multivial presentation with obvious drawbacks, making a single-vial presentation for such products highly desirable. We describe the development of a stable, lyophilized squalene emulsion adjuvant through innovative formulation and process development approaches. On reconstitution, freeze-dried emulsion preparations were found to have a minimal increase in particle size of ∼20 nm and conferred immunogenicity in BALB/c mice similar in potency to freshly prepared emulsion coformulations in liquid form.
ISSN:0022-3549
1520-6017
DOI:10.1016/j.xphs.2017.02.024