Comparing Different Light Models for Virtual Electrodes in Optoelectronic Tweezers.

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
ELECTROPHORESIS Pub Date : 2025-03-18 DOI:10.1002/elps.8131
Ernesto Guzman-Saleh, Victor H Perez-Gonzalez, Rodrigo Martinez-Duarte
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引用次数: 0

Abstract

Optoelectronic tweezers (OET) allow for the physical manipulation of particles of interest via dielectrophoresis (DEP) in microfluidic devices. To produce the nonuniform electric field required to enable DEP, light is used to expose a photoconductive film and create a so-called virtual electrode (VE). Several attempts have been made to model the light profile used to excite the photoconductive layer and produce the VE. However, no comparison of the models has been presented in the literature. Here, we present a comparative study among the rectangular, Gaussian, and saturated-Gaussian models in mapping to light profiles obtained experimentally. These models were then used to predict the activation of a VE and the distribution of the electric field in an OET system. From this comparison, it is possible to conclude that the saturated-Gaussian model should be the preferred choice to study these systems. Moreover, VEs were also compared numerically to conventional gold electrodes used regularly in DEP applications, concluding that very relevant differences exist between the electric fields produced by these two types of electrodes.

光电镊子中虚拟电极不同光模型的比较。
光电镊子(OET)允许通过微流控装置中的介电电泳(DEP)对感兴趣的粒子进行物理操作。为了产生DEP所需的非均匀电场,使用光来暴露光导膜并创建所谓的虚拟电极(VE)。已经进行了几次尝试来模拟用于激发光导层和产生VE的光剖面。然而,文献中没有对这些模型进行比较。在这里,我们提出了矩形、高斯和饱和高斯模型在映射到实验获得的光剖面中的比较研究。这些模型随后被用于预测VE的激活和OET系统中的电场分布。从这个比较中可以得出结论,饱和高斯模型应该是研究这些系统的首选。此外,我们还将ve与DEP应用中经常使用的传统金电极进行了数值比较,得出结论,这两种电极产生的电场之间存在非常相关的差异。
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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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