Acoustofluidic manipulation for submicron to nanoparticles.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Wei Wei, Zhaoxun Wang, Bingnan Wang, Xinyuan He, Yaping Wang, Yang Bai, Qingrui Yang, Wei Pang, Xuexin Duan
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引用次数: 0

Abstract

Particles, ranging from submicron to nanometer scale, can be broadly categorized into biological and non-biological types. Submicron-to-nanoscale bioparticles include various bacteria, viruses, liposomes, and exosomes. Non-biological particles cover various inorganic, metallic, and carbon-based particles. The effective manipulation of these submicron to nanoparticles, including their separation, sorting, enrichment, assembly, trapping, and transport, is a fundamental requirement for different applications. Acoustofluidics, owing to their distinct advantages, have emerged as a potent tool for nanoparticle manipulation over the past decade. Although recent literature reviews have encapsulated the evolution of acoustofluidic technology, there is a paucity of reports specifically addressing the acoustical manipulation of submicron to nanoparticles. This article endeavors to provide a comprehensive study of this topic, delving into the principles, apparatus, and merits of acoustofluidic manipulation of submicron to nanoparticles, and discussing the state-of-the-art developments in this technology. The discourse commences with an introduction to the fundamental theory of acoustofluidic control and the forces involved in nanoparticle manipulation. Subsequently, the working mechanism of acoustofluidic manipulation of submicron to nanoparticles is dissected into two parts, dominated by the acoustic wave field and the acoustic streaming field. A critical analysis of the advantages and limitations of different acoustofluidic platforms in nanoparticles control is presented. The article concludes with a summary of the challenges acoustofluidics face in the realm of nanoparticle manipulation and analysis, and a forecast of future development prospects.

亚微米到纳米粒子的声流体操纵。
从亚微米到纳米级的粒子可大致分为生物和非生物类型。亚微米到纳米级的生物颗粒包括各种细菌、病毒、脂质体和外泌体。非生物粒子包括各种无机、金属和碳基粒子。有效操纵这些亚微米级到纳米级粒子,包括对它们进行分离、分类、富集、组装、捕获和运输,是不同应用的基本要求。声学流体技术因其独特的优势,在过去十年中已成为操纵纳米粒子的有力工具。虽然最近的文献综述概括了声流体技术的发展,但专门针对亚微米到纳米粒子的声学操纵的报道却很少。本文试图对这一主题进行全面研究,深入探讨亚微米到纳米粒子声流体操纵的原理、设备和优点,并讨论这一技术的最新发展。文章首先介绍了声流体控制的基本理论和纳米粒子操纵所涉及的力。随后,将亚微米到纳米粒子的声流体操纵工作机制分为两部分,分别由声波场和声流场主导。文章对不同声流体平台在纳米粒子控制方面的优势和局限性进行了批判性分析。文章最后总结了声流体技术在纳米粒子操纵和分析领域面临的挑战,并预测了未来的发展前景。
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
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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