Microfluidics for the biological analysis of atmospheric ice-nucleating particles: Perspectives and challenges.

IF 2.6 4区 工程技术 Q2 BIOCHEMICAL RESEARCH METHODS
Biomicrofluidics Pub Date : 2025-02-27 eCollection Date: 2025-01-01 DOI:10.1063/5.0236911
Mark D Tarn, Kirsty J Shaw, Polly B Foster, Jon S West, Ian D Johnston, Daniel K McCluskey, Sally A Peyman, Benjamin J Murray
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引用次数: 0

Abstract

Atmospheric ice-nucleating particles (INPs) make up a vanishingly small proportion of atmospheric aerosol but are key to triggering the freezing of supercooled liquid water droplets, altering the lifetime and radiative properties of clouds and having a substantial impact on weather and climate. However, INPs are notoriously difficult to model due to a lack of information on their global sources, sinks, concentrations, and activity, necessitating the development of new instrumentation for quantifying and characterizing INPs in a rapid and automated manner. Microfluidic technology has been increasingly adopted by ice nucleation research groups in recent years as a means of performing droplet freezing analysis of INPs, enabling the measurement of hundreds or thousands of droplets per experiment at temperatures down to the homogeneous freezing of water. The potential for microfluidics extends far beyond this, with an entire toolbox of bioanalytical separation and detection techniques developed over 30 years for medical applications. Such methods could easily be adapted to biological and biogenic INP analysis to revolutionize the field, for example, in the identification and quantification of ice-nucleating bacteria and fungi. Combined with miniaturized sampling techniques, we can envisage the development and deployment of microfluidic sample-to-answer platforms for automated, user-friendly sampling and analysis of biological INPs in the field that would enable a greater understanding of their global and seasonal activity. Here, we review the various components that such a platform would incorporate to highlight the feasibility, and the challenges, of such an endeavor, from sampling and droplet freezing assays to separations and bioanalysis.

大气冰核粒子生物分析的微流体:展望与挑战。
大气冰核粒子(INPs)在大气气溶胶中所占的比例很小,但却是触发过冷液态水水滴冻结、改变云的寿命和辐射特性以及对天气和气候产生重大影响的关键。然而,由于缺乏关于其全球来源、汇、浓度和活动的信息,INPs非常难以建模,因此需要开发新的仪器以快速和自动化的方式量化和表征INPs。近年来,冰核研究小组越来越多地采用微流控技术作为对INPs进行液滴冻结分析的手段,使每次实验能够在低至水均匀冻结的温度下测量数百或数千个液滴。微流体的潜力远远不止于此,30多年来为医学应用开发了一整套生物分析分离和检测技术。这种方法可以很容易地适用于生物和生物源INP分析,以彻底改变该领域,例如,在冰核细菌和真菌的鉴定和定量方面。结合小型化采样技术,我们可以设想开发和部署微流体样品到答案平台,用于自动化,用户友好的采样和分析生物INPs,这将使我们能够更好地了解它们的全球和季节性活动。在这里,我们回顾了这样一个平台将包含的各种组成部分,以突出这样一个努力的可行性和挑战,从采样和液滴冷冻分析到分离和生物分析。
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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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