A new algorithm is proposed for the determination of aerosol particle size distribution from a set of screen diffusion battery penetrations. The idea is to determine the size spectra of the fractions of particles separated by the sections of diffusion battery, so the total size distribution is the sum of the spectra of fractions. The spectrum of each fraction is approximated by the lognormal function, which is defined by two parameters: the standard geometric deviation (SGD) and geometric mean diameter. The SGD value is chosen to be 1.35 for each fraction. The geometric mean diameters of fractions are calculated from the diffusion battery penetrations. For this purpose, analytical formulas are derived to link the mean single-fiber collection efficiency for each fraction with the experimentally measured penetrations. Then the mean diameters of fractions are calculated from the collection efficiencies using the fan model filtration theory. To achieve a better size resolution, numerical approach is proposed to calculate the particle size spectrum using the analytical solution as an initial approximation. The validity of the analytical and numerical solutions is investigated by comparing them with the spectra determined by means of transmission electron microscopy and gravity settling. For this purpose, the aerosol is generated using the evaporation-nucleation technique, Collison-type nebulizer, and hot-wire bulb generator. It is found that the analytical solution demonstrates a good sizing accuracy but relatively poor size resolution, while the numerical approach results in both good sizing accuracy and good size resolution for the two-mode aerosol.
Under pandemic-caused emergency, evaluation of the potential of existing antiviral drugs for the treatment of COVID-19 is relevant. Triazavirin, an antiviral drug developed in Russia for per-oral administration, is involved in clinical trials against SARS-CoV-2 coronavirus. This virus has affinity to epithelial cells in respiratory tract, so drug delivery directly in lungs may enhance therapeutic effect and reduce side effects for stomach, liver, kidneys. We elaborated ultrasonic method of triazavirin aerosol generation and investigated the inhalation delivery of this drug in mice. Mean particle size and number concentration of aerosol used in inhalation experiments are 560 nm and 4 × 10
5
cm
−3
, respectively. Aerosol mass concentration is 1.6 × 10
−4
mg/cm
3
. Inhalation for 20 min in a nose-only chamber resulted in 2 mg/kg body delivered dose and 2.6 μg/mL triazavirin concentration in blood plasma. Elimination rate constant determined in aerosol administration experiments was
k
e
= 0.077 min
−1
, which agrees with the value measured after intravenous delivery, but per-oral administration resulted in considerably lower apparent elimination rate constant of pseudo-first order, probably due to non-linear dependence of absorption rate on triazavirin concentration in gastrointestinal tract. The bioavailability of triazavirin aerosol is found to be 85%, which is about four times higher than for per-oral administration.
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