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一种用于细胞活力分析的具有垂直平行电极的简易微铣微流控阻抗细胞仪。

A Simple Micromilled Microfluidic Impedance Cytometer with Vertical Parallel Electrodes for Cell Viability Analysis.

作者信息

Eades Jason, Audiffred Julianne F, Fincher Micah, Choi Jin-Woo, Soper Steven A, Monroe William Todd

机构信息

Department of Biological and Agricultural Engineering, Louisiana State University and Agricultural Center, Baton Rouge, LA 70803, USA.

Department of Electrical and Computer Engineering, Michigan Technological University, Houghton, MI 49931, USA.

出版信息

Micromachines (Basel). 2023 Jan 22;14(2):283. doi: 10.3390/mi14020283.

Abstract

Microfluidic impedance cytometry has been demonstrated as an effective platform for single cell analysis, taking advantage of microfabricated features and dielectric cell sensing methods. In this study, we present a simple microfluidic device to improve the sensitivity, accuracy, and throughput of single suspension cell viability analysis using vertical sidewall electrodes fabricated by a widely accessible negative manufacturing method. A microchannel milled through a 75 µm platinum wire, which was embedded into poly-methyl-methacrylate (PMMA), created a pair of parallel vertical sidewall platinum electrodes. Jurkat cells were interrogated in a custom low-conductivity buffer (1.2 ± 0.04 mS/cm) to reduce current leakage and increase device sensitivity. Confirmed by live/dead staining and electron microscopy, a single optimum excitation frequency of 2 MHz was identified at which live and dead cells were discriminated based on the disruption in the cell membrane associated with cell death. At this frequency, live cells were found to exhibit changes in the impedance phase with no appreciable change in magnitude, while dead cells displayed the opposite behavior. Correlated with video microscopy, a computational algorithm was created that could identify cell detection events and determine cell viability status by application of a mathematical correlation method.

摘要

微流控阻抗细胞术已被证明是一种用于单细胞分析的有效平台,它利用了微纳加工特性和介电细胞传感方法。在本研究中,我们展示了一种简单的微流控装置,该装置利用一种广泛可用的负性制造方法制造的垂直侧壁电极,提高了单个悬浮细胞活力分析的灵敏度、准确性和通量。通过在75 µm铂丝上铣削微通道,并将其嵌入聚甲基丙烯酸甲酯(PMMA)中,形成了一对平行的垂直侧壁铂电极。在定制的低电导率缓冲液(1.2±0.04 mS/cm)中对Jurkat细胞进行检测,以减少电流泄漏并提高装置灵敏度。通过活/死染色和电子显微镜确认,确定了一个单一的最佳激发频率2 MHz,在该频率下,基于与细胞死亡相关的细胞膜破坏来区分活细胞和死细胞。在这个频率下,发现活细胞的阻抗相位发生变化,幅度没有明显变化,而死细胞则表现出相反的行为。与视频显微镜相关联,创建了一种计算算法,该算法可以通过应用数学相关方法识别细胞检测事件并确定细胞活力状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c305/9959585/6765b6ed6295/micromachines-14-00283-g0A1.jpg

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