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1.
Aviakosm Ekolog Med ; 45(3): 60-3, 2011.
Article in Russian | MEDLINE | ID: mdl-21916255

ABSTRACT

Functional testing of the bioreactor for stirring culture in microgravity was performed during the microgravity episodes aboard research airplane Il-76 following the Kepler parabolic flight path. The attempt to produce the gas vortex stirring effect in a given liquid volume was a failure. Nonetheless, the stirrer ventilator is capable to agitate liquid acting as a mechanical stirrer.


Subject(s)
Bioreactors , Microbiological Phenomena , Aircraft , Cell Culture Techniques , Gases/metabolism , Research Design , Space Flight , Weightlessness Simulation
2.
Atmos Environ (1994) ; 40(35): 6687-6695, 2006 Nov.
Article in English | MEDLINE | ID: mdl-32288551

ABSTRACT

A new personal bioaerosol sampler has recently been developed and verified to be very efficient for monitoring of viable airborne bacteria, fungi and viruses. The device is capable of providing high recovery rates even for microorganisms which are rather sensitive to physical and biological stresses. However, some mathematical procedure is required for realistic calculation of an actual concentration of viable bioaerosols in the air taking into account a rate of inactivation of targeted microorganisms, sampling parameters, and results of microbial analysis of collecting liquid from the sampler. In this paper, we develop such procedure along with the model of aerosol propagation for outdoor conditions. Combining these procedures allows one to determine the optimal sampling locations for the best possible coverage of the area to be monitored. A hypothetical episode concerned with terrorists' attack during music concert in the central square of Novosibirsk, Russia was considered to evaluate possible coverage of the area by sampling equipment to detect bioaerosols at various locations within the square. It was found that, for chosen bioaerosol generation parameters and weather conditions, the new personal sampler would be capable to reliably detect pathogens at all locations occupied by crowd, even at distances of up to 600 m from the source.

4.
Appl Environ Microbiol ; 70(12): 6963-7, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15574888

ABSTRACT

A new personal bioaerosol sampler has recently been developed and evaluated for sampling of viable airborne bacteria and fungi under controlled laboratory conditions and in the field. The operational principle of the device is based on the passage of air through porous medium immersed in liquid. This process leads to the formation of bubbles within the filter as the carrier gas passes through and thus provides effective mechanisms for aerosol removal. As demonstrated in previous studies, the culturability of sampled bacterium and fungi remained high for the entire 8-h sampling period. The present study is the first step of the evaluation of the new sampler for monitoring of viable airborne viruses. It focuses on the investigation of the inactivation rate of viruses in the bubbling process during 4 h of continuous operation. Four microbes were used in this study, influenza, measles, mumps, and vaccinia viruses. It was found that the use of distilled water as the collection fluid was associated with a relatively high decay rate. A significant improvement was achieved by utilizing virus maintenance fluid prepared by using Hank's solution with appropriate additives. The survival rates of the influenza, measles, and mumps viruses were increased by 1.4 log, 0.83 log, and 0.82 log, respectively, after the first hour of operation compared to bubbling through the sterile water. The same trend was observed throughout the entire 4-h experiment. There was no significant difference observed only for the robust vaccinia virus.


Subject(s)
Air Microbiology , Air Pollution, Indoor , Environmental Monitoring/methods , Viruses/growth & development , Culture Media , Environmental Monitoring/instrumentation , Measles virus/growth & development , Measles virus/isolation & purification , Mumps virus/growth & development , Mumps virus/isolation & purification , Orthomyxoviridae/growth & development , Orthomyxoviridae/isolation & purification , Particle Size , Vaccinia virus/growth & development , Vaccinia virus/isolation & purification , Viruses/isolation & purification
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