This article presents the review of the research papers concerning nanobubble generation. In main section of this article, numerous methods of nanobubble generation have been discussed pinpointing the differences in results obtained in similar experimental setups. Different generation methods have been tabularized to present the composition of phases, the diameter of generated bubbles as well as the commentary concerning discrepancies within one method. The number of nanobubble applications in environmental processes is increasing in the last year; however, the thorough investigation of their generation methods is not covered in literature. This review article is gathering knowledge about nanobubble generation methods and is comparing results obtained by different research teams. It should lay foundation for future research concerning nanobubbles, what will lead to increasing the efficiency of various environmental processes, including wastewater flotation, metal recovery, and soil and groundwater remediation. Gas nanobubble dispersions as the important agent in environmental processes K. Ulatowski and P. Sobieszuk
Nanobubbles can enhance
both the proliferation and metabolic activity
of microorganisms (mainly bacteria) and the growth of the whole higher
organisms such as mice, fish, or plants. The critical fact is that
nanobubbles of different gases can affect given cells differently.
As animal cell cultures are used in industry and research studies,
investigations of their interactions with nanobubbles should be carried
out. This study aims to uncover whether the presence of nanobubbles
improves the proliferation rate and metabolic activity of L929 fibroblasts
and HL60 leukemia cells as exemplary animal cell lines of adherent
and non-adherent cells, respectively. The long-term (8-day) cultures
of both L929 and HL-60 cells with nanobubble addition to the appropriate
medium were carried out. The medium was not exchanged for the whole
duration of the culture. Nanobubbles of two gases – oxygen
and nitrogen – were dispersed in the appropriate media and
then used to culture cells. The density and viability of cells were
assessed microscopically while their metabolic activity was determined
using PrestoBlue or XTT assays. Additionally, we have performed the
analysis of substrate consumption rate during the growth and activity
of lactate dehydrogenase. We have shown that nanodispersion of both
gases enhances the proliferation rate and metabolic activity of L929.
For HL-60 cultures, reference cultures exhibited better viability,
cell density, and metabolic activity than those with either oxygen
or nitrogen nanobubbles. Obtained results clearly show that nanobubble
dispersions of both oxygen and nitrogen positively affect the cultures
of L929 while inhibiting the growth of HL-60 cells. We suspect that
a similar positive effect would be visible for other adherent cells,
similar to L929. Such results are promising for intensifying the growth
of animal or human cells in routine cell cultures.
Inhalation is a non-invasive method of local drug delivery to the respiratory system. This study analyzed the potential use of aqueous dispersion of oxygen nanobubbles (ADON) as a drug carrier with the additional function of oxygen supplementation to diseased lungs. The suitability of the membrane-based method of ADON preparation and, next, the stability of ADON properties during storage and after aerosolization in nebulizers of various designs (jet, ultrasonic, and two vibrating mesh devices) was investigated. The increased oxygen content in the aerosol generated in two mesh nebulizers suggests that the proposed concept may be helpful in the oxygen supplementation during drug delivery by aerosol inhalation without using an additional oxygen source. This application can increase the overall effectiveness of lung disease treatment and pulmonary rehabilitation.
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