Nanomechanics and morphology of simulated respiratory particles

02 June 2022, Version 2
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The impact of respiratory particle composition on the equilibrium morphology and phase are not well understood. Furthermore, the effects of these different phases and morphologies on the viability of viruses embedded within these particles are equally unknown. Physiologically relevant respiratory fluid analogues were constructed, and their hygroscopic behavior were measured using an ensemble technique. A relationship between hygroscopicity and protein concentration was determined, providing additional validation to the high protein content of respiratory aerosol measured in prior works (>90%). It was found that the salt component of the respiratory particles could crystallize as a single crystal, multiple crystals, or would not crystallize at all. It was found that dried protein particles at indoor-relevant climatic conditions could exist separately in a glassy (~77% of particles) or viscoelastic state (~23% of particles). The phase state and morphology of respiratory particles may influence the viability of embedded pathogens. We recommend that pathogen research aiming to mimic the native composition of respiratory fluid should use a protein concentration of at least 90% by solute volume to improve the representativity of the pathogen’s microenvironment.

Keywords

respiratory aerosol
droplet physicochemistry
virus viability
glassy aerosol
hygroscopic growth
atomic force microscopy
transmission electron microscopy

Supplementary materials

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Title
Electronic supplementary information regarding "Glassy aerosol may promote virus transmission"
Description
The electronic supplementary information contains additional information for the paper regarding data analysis and methods. Within, there are additional sections regarding: (1, 2) model fitting to hygroscopic growth data, (3) determining the efflorescence relative humidity of simulated respiratory fluid, (4) determining the phase diagram of simulated respiratory aerosol, and (5) atomic force microscopy data analysis.
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