Evaluation of intermolecular interactions required for thermostability of a recombinant adenovirus within a film matrix

J Control Release. 2022 Jan:341:118-131. doi: 10.1016/j.jconrel.2021.11.012. Epub 2021 Nov 12.

Abstract

Thermostability of vaccines and biologic drugs are key to increasing global access to a variety of life-saving agents. In this report, we characterize interactions between a novel zwitterionic surfactant and adenovirus serotype 5 which allow the virus to remain stable at room temperature in a thin film matrix. Complexity of the adenovirus capsid and the polydispersity of the surfactant required use of a variety of techniques to achieve this goal. The CMC of the surfactant in Tris buffer (pH 6.5) was estimated to be 0.7-1.17 × 10-4 M by the pyrene 1:3 ratio method. TEM images depict micelle formation around virus capsids. An estimated Kd of the virus-surfactant interaction of 2.25 × 10-9 M was determined by isothermal titration calorimetry. Associated data suggest that this interaction may be thermodynamically favorable and entropically driven. A competitive saturation study and TEM images indicate that the surfactant also binds to hexon proteins on the virus capsid. Taken together, these data support the working hypothesis that the surfactant is capable of forming micelles in the solid and liquid state and that it forms a protective coating around the virus by binding to hexon proteins on the virus capsid during the film forming process.

Keywords: Amphipols; Film; Micelle; Vaccine; Virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae* / genetics
  • Capsid
  • Capsid Proteins / genetics
  • Micelles
  • Surface-Active Agents* / chemistry

Substances

  • Capsid Proteins
  • Micelles
  • Surface-Active Agents