纺织细胞培养的电流体控制:确定将细胞培养与电流体技术相结合所需的适当条件。

IF 3 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS ELECTROPHORESIS Pub Date : 2024-06-04 DOI:10.1002/elps.202400021
Sujani B. Y. Abeywardena, Zhilian Yue, Gordon G. Wallace, Peter C. Innis
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引用次数: 0

摘要

电场驱动的微流控技术(又称电流体技术)与低成本纺织品基底相结合,是一种极具吸引力的新型分析工具。基于纺织品的电流体技术主要在纱线基底上进行探索,目前还处于早期阶段,对三维结构的研究很少。此外,纺织品结构作为一种低成本的替代品,很少用于细胞分析。在此,我们研究了新型三维纺织品结构,并开发了有利于直接集成三维细胞培养的最佳电泳设计和条件,开发了基于纺织品的集成细胞培养电流体平台,并对其进行了优化,以平衡电动性能和细胞存活率要求。值得注意的是,为满足细胞存活率和电泳流动性的要求,电解质的组成条件存在差异,这就需要开发一种电解质,以满足一个平台中这两种成分的最低要求。人类真皮成纤维细胞培养物与明胶甲基丙烯酰(GelMA)水凝胶涂层电流体平台成功整合,并在不同电场下使用 5 mM TRIS/HEPES/300 mM 葡萄糖进行了研究。在涂有 2.5% GelMA 的织物上观察到了更高的分析流动性,这也有利于细胞的良好附着、存活和增殖。细胞存活率也随着施加电场的大小和持续时间的减少而增加,在高达 20 V cm-1 的电场中细胞存活率良好。
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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Electrofluidic control for textile-based cell culture: Identification of appropriate conditions required to integrate cell culture with electrofluidics

Electric field–driven microfluidics, known as electrofluidics, is a novel attractive analytical tool when it is integrated with low-cost textile substrate. Textile-based electrofluidics, primarily explored on yarn substrates, is in its early stages, with few studies on 3D structures. Further, textile structures have rarely been used in cellular analysis as a low-cost alternative. Herein, we investigated novel 3D textile structures and develop optimal electrophoretic designs and conditions that are favourable for direct 3D cell culture integration, developing an integrated cell culture textile-based electrofluidic platform that was optimised to balance electrokinetic performance and cell viability requirements. Significantly, there were contrasting electrolyte compositional conditions that were required to satisfy cell viability and electrophoretic mobility requiring the development of and electrolyte that satisfied the minimum requirements of both these components within the one platform. Human dermal fibroblast cell cultures were successfully integrated with gelatine methacryloyl (GelMA) hydrogel-coated electrofluidic platform and studied under different electric fields using 5 mM TRIS/HEPES/300 mM glucose. Higher analyte mobility was observed on 2.5% GelMA-coated textile which also facilitated excellent cell attachment, viability and proliferation. Cell viability also increased by decreasing the magnitude and time duration of applied electric field with good cell viability at field of up to 20 V cm−1.

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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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