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Estimation of chemical and physical effects of cavitation by analysis of cavitating single bubble dynamics.

ABSTRACT: Cavitation events create extreme conditions in a localized 'bubble collapse' region, leading to the formation of hydroxyl radicals, shockwaves and microscopic high-speed jets, which are useful for many chemical and physical transformation processes. Single bubble dynamics equations have been used previously to investigate the chemical and physical effects of cavitation. In the present study, the state of the art of the single bubble dynamics equations was reviewed and certain noteworthy modifications were implemented. Simulations reaffirmed previously reported collapse temperatures of the order ~5,000 K and collapse pressures well over ~1,000 bar under varying operating conditions. The chemical effects were assessed in terms of the hydroxyl radical generation rate (OHG), calculated by applying the minimization of the Gibb's Free Energy method using simulated collapse conditions. OHG values as high as 1x10¹²OH molecules per collapse event were found under certain operating conditions. A new equation was proposed to assess the physical effects, in terms of the impact pressure of the water jet - termed as the jet hammer pressure (JHP), formed due to the asymmetrical collapse of a bubble near a wall. The predicted JHP were found to be within a range of ~100 to 1000 bar under varying operating conditions. Important issues such as the onset of cavitation and chaotic solutions, for a cavitating single bubble dynamics were discussed. The Blake threshold pressure was found to be a sufficient criterion to capture the onset of cavitation. The impact of key operating parameters on the chemical and physical effects of cavitation were investigated exhaustively through simulations, over the parameter ranges relevant to acoustic and hydrodynamic cavitation processes. Presented methodology and results will be useful for optimisation and further investigations of a broad range of acoustic and hydrodynamic cavitation-based applications.

SUBMITTER: Pandit AV

PROVIDER: S-EPMC8339230 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Sonoporation is the membrane disruption generated by ultrasound and has been exploited as a non-viral strategy for drug and gene delivery. Acoustic cavitation of microbubbles has been recognized to play an important role in sonoporation. However, due to the lack of adequate techniques for precise control of cavitation activities and real-time assessment of the resulting sub-micron process of sonoporation, limited knowledge has been available regarding the detail processes and correlation of cavitation with membrane disruption at the single cell level. In the current study, we developed a combined approach including optical, acoustical, and electrophysiological techniques to enable synchronized manipulation, imaging, and measurement of cavitation of single bubbles and the resulting cell membrane disruption in real-time. Using a self-focused femtosecond laser and high frequency ultrasound (7.44MHz) pulses, a single microbubble was generated and positioned at a desired distance from the membrane of a Xenopus oocyte. Cavitation of the bubble was achieved by applying a low frequency (1.5MHz) ultrasound pulse (duration 13.3 or 40?s) to induce bubble collapse. Disruption of the cell membrane was assessed by the increase in the transmembrane current (TMC) of the cell under voltage clamp. Simultaneous high-speed bright field imaging of cavitation and measurements of the TMC were obtained to correlate the ultrasound-generated bubble activities with the cell membrane poration. The change in membrane permeability was directly associated with the formation of a sub-micrometer pore from a local membrane rupture generated by bubble collapse or bubble compression depending on ultrasound amplitude and duration. The impact of the bubble collapse on membrane permeation decreased rapidly with increasing distance (D) between the bubble (diameter d) and the cell membrane. The effective range of cavitation impact on membrane poration was determined to be D/d=0.75. The maximum mean radius of the pores was estimated from the measured TMC to be 0.106±0.032?m (n=70) for acoustic pressure of 1.5MPa (duration 13.3?s), and increased to 0.171±0.030?m (n=125) for acoustic pressure of 1.7MPa and to 0.182±0.052?m (n=112) for a pulse duration of 40?s (1.5MPa). These results from controlled cell membrane permeation by cavitation of single bubbles revealed insights and key factors affecting sonoporation at the single cell level.

Project description:Precise and high-speed sorting of individual target cells from heterogeneous populations plays an imperative role in cell research. Although the conventional fluorescence-activated cell sorter (FACS) is capable of rapid and accurate cell sorting, it occupies a large volume of the instrument and inherently brings in aerosol generation as well as cross-contamination among samples. The sorting completed in a fully enclosed and disposable microfluidic chip has the potential to eliminate the above concerns. However, current microfluidic cell sorters are hindered by the high complexities of the fabrication procedure and the off-chip setup. In this paper, a spark-cavitation-bubble-based fluorescence-activated cell sorter is developed to perform fast and accurate sorting in a microfluidic chip. It features a simple structure and an easy operation. This microfluidic sorter comprises a positive electrode of platinum and a negative electrode of tungsten, which are placed on the side of the main channel. By applying a high-voltage discharge on the pair of electrodes, a single spark cavitation bubble is created to deflect the target particle into the downstream collection channel. The sorter has a short switching time of 150 μs and a long lifespan of more than 100 million workable actions. In addition, a novel control strategy is proposed to dynamically adjust the discharge time to stabilize the size of the cavitation bubble for continuous sorting. The dynamic control of continuously triggering the sorter, the optimal delay time between fluorescence detection and cell sorting, and a theoretical model to predict the ideal sorting recovery and purity are studied to improve and evaluate the sorter performance. The experiments demonstrate that the sorting rate of target particles achieves 1200 eps, the total analysis throughput is up to 10,000 eps, the particles sorted at 4000 eps exhibit a purity greater than 80% and a recovery rate greater than 90%, and the sorting effect on the viability of HeLa cells is negligible.

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Estimation of chemical and physical effects of cavitation by analysis of cavitating single bubble dynamics.

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