Insights into the fluid dynamics of bioaerosol formation in a model respiratory tract

IF 2.6 4区 工程技术 Q2 BIOCHEMICAL RESEARCH METHODS
Biomicrofluidics Pub Date : 2024-09-17 DOI:10.1063/5.0219332
Sudipta Saha, Manish Kumar Manna, Aranyak Chakravarty, Sourav Sarkar, Achintya Mukhopadhyay, Swarnendu Sen
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引用次数: 0

Abstract

Bioaerosols produced within the respiratory system play an important role in respiratory disease transmission. These include infectious diseases such as common cold, influenza, tuberculosis, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) among several others. It is, therefore, of immense interest to understand how bioaerosols are produced within the respiratory system. This has not been extensively investigated. The present study computationally investigates how bioaerosols are produced in a model respiratory tract due to hydrodynamic interactions between breathed air and a thin mucus layer, which lines the inner surface of the tract. It is observed that Kelvin–Helmholtz instability is established in the thin mucus layer due to associated fluid dynamics. This induces interfacial surface waves which fragment forming bioaerosols under certain conditions. A regime map is created—based on pertinent dimensionless parameters—to enable identification of such conditions. Analysis indicates that bioaerosols may be produced even under normal breathing conditions, contrary to expectations, depending on mucus rheology and thickness of the mucus layer. This is possible during medical conditions as well as during some treatment protocols. However, such bioaerosols are observed to be larger (∼O(100)μm) and are produced in less numbers (∼100), as compared to those produced under coughing conditions. Treatment protocols and therapeutic strategies may be suitably devised based on these findings.
对模型呼吸道中生物气溶胶形成的流体动力学的见解
呼吸系统内产生的生物气溶胶在呼吸道疾病传播中起着重要作用。这些疾病包括普通感冒、流感、肺结核、严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)等传染病。因此,了解生物气溶胶是如何在呼吸系统中产生的具有极大的意义。但目前尚未对此进行广泛研究。本研究通过计算研究了生物气溶胶是如何在模型呼吸道中产生的,原因是呼吸空气与呼吸道内表面的薄粘液层之间的流体动力相互作用。研究发现,由于相关的流体动力学,粘液薄层中出现了开尔文-赫尔姆霍兹不稳定性。这诱发了界面表面波,在特定条件下碎片形成生物气溶胶。根据相关的无量纲参数绘制了一个状态图,以便识别这些条件。分析表明,根据粘液流变学和粘液层厚度的不同,即使在正常呼吸条件下,也可能产生与预期相反的生物气溶胶。在医疗条件和某些治疗方案中都有可能出现这种情况。不过,与咳嗽条件下产生的生物气溶胶相比,这种生物气溶胶的体积更大(∼O(100)μm),产生的数量更少(∼100)。根据这些发现,可以适当制定治疗方案和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biomicrofluidics
Biomicrofluidics 生物-纳米科技
CiteScore
5.80
自引率
3.10%
发文量
68
审稿时长
1.3 months
期刊介绍: Biomicrofluidics (BMF) is an online-only journal published by AIP Publishing to rapidly disseminate research in fundamental physicochemical mechanisms associated with microfluidic and nanofluidic phenomena. BMF also publishes research in unique microfluidic and nanofluidic techniques for diagnostic, medical, biological, pharmaceutical, environmental, and chemical applications. BMF offers quick publication, multimedia capability, and worldwide circulation among academic, national, and industrial laboratories. With a primary focus on high-quality original research articles, BMF also organizes special sections that help explain and define specific challenges unique to the interdisciplinary field of biomicrofluidics. Microfluidic and nanofluidic actuation (electrokinetics, acoustofluidics, optofluidics, capillary) Liquid Biopsy (microRNA profiling, circulating tumor cell isolation, exosome isolation, circulating tumor DNA quantification) Cell sorting, manipulation, and transfection (di/electrophoresis, magnetic beads, optical traps, electroporation) Molecular Separation and Concentration (isotachophoresis, concentration polarization, di/electrophoresis, magnetic beads, nanoparticles) Cell culture and analysis(single cell assays, stimuli response, stem cell transfection) Genomic and proteomic analysis (rapid gene sequencing, DNA/protein/carbohydrate arrays) Biosensors (immuno-assay, nucleic acid fluorescent assay, colorimetric assay, enzyme amplification, plasmonic and Raman nano-reporter, molecular beacon, FRET, aptamer, nanopore, optical fibers) Biophysical transport and characterization (DNA, single protein, ion channel and membrane dynamics, cell motility and communication mechanisms, electrophysiology, patch clamping). Etc...
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