ArticleProceedings of the National Academy of Sciences of the United States of America2025
Accessing robust vaccine coformulation stability by single adjuvant detection on a microelectrode.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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8 authors.
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Abstract
A significant question in next generation vaccine development is: How long are coformulated products stable on the shelf? The recent review by the US Food and Drug Administration of a single, prefilled syringe of the SHINGRIX™ vaccine has highlighted the importance of this question. While dynamic light scattering is well suited for measuring average particle sizes across populations, fundamental principles behind scattering limit the resolution to distinguish subtle differences at the tens of nanometer scale between similar samples. To address this, we introduce an alternative approach: stochastic electrochemistry, which allows for the investigation of specific properties of individual particles, one at a time. By introducing an electrochemically active species, hexacyanoferrate(II/III) into the vaccine solution, we observe discrete current drops when particles irreversibly collide with a microelectrode. Such events can be correlated directly with particle size. As a proof of concept, we use this technique to analyze the interactions of streptavidin-functionalized poly(lactic-co-glycolic acid) beads with biotinylated bovine serum albumin at vaccine-level concentrations and apply what we learned to the components of the SHINGRIX™ vaccine. We then present a time-trial comparison of data from current commercial SHINGRIX™ vaccines using dynamic light scattering and stochastic electrochemistry, analyzing the AS01
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