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Microcavity impedance sensor for real-time monitoring of activity and proliferation ability of 3D cells and preparation method

A technology for proliferative ability and cell activity, applied in biochemical equipment and methods, specific-purpose bioreactors/fermenters, material impedance, etc., can solve problems such as low efficiency, cumbersome operation, and high cost, and achieve monitoring activity and The effect of proliferative capacity

Active Publication Date: 2019-04-16
ZHEJIANG UNIV
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  • Abstract
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  • Application Information

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Problems solved by technology

At present, the activity of three-dimensional cells is mainly verified by live / dead fluorescent staining, which requires materials and equipment such as fluorescent dyes and confocal microscopes, which has problems such as low efficiency, high cost, and cumbersome operation.

Method used

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  • Microcavity impedance sensor for real-time monitoring of activity and proliferation ability of 3D cells and preparation method
  • Microcavity impedance sensor for real-time monitoring of activity and proliferation ability of 3D cells and preparation method
  • Microcavity impedance sensor for real-time monitoring of activity and proliferation ability of 3D cells and preparation method

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Embodiment Construction

[0032] The present invention will be described in detail below in conjunction with the accompanying drawings and specific embodiments, but the present invention is not limited.

[0033] The invention provides a microcavity impedance sensor for real-time monitoring of 3D cell activity and proliferation ability. The sensor uses a silicon wafer as a substrate and covers the substrate with SiO 2 layer, on SiO 2 Several trapezoidal microgroove structures are etched on the layer, and two counter electrodes are set on the side walls of the trapezoidal microgroove structures. 2 The edge of the layer is provided with a metal contact plate, and the counter electrode is connected to the metal contact plate through a lead wire, and an insulating layer is covered above the lead wire. The PMMA material cavity with a square ring in cross section is fixed on the substrate; 3D cells are seeded in the trapezoidal microgroove structure. Contact with the counter electrode to detect the impedance...

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Abstract

The invention discloses a 3D microcavity impedance sensor for real-time monitoring of activity and proliferation ability of cells and preparation method. The 3D microcavity impedance sensor is firstlymanufactured by adopting a micro-nano processing technology; 3D spherical cell culture is conducted on tumor cells; 3D spherical cells are inoculated into a trapezoidal microgroove structure in the microcavity impedance sensor, are attached to counter electrodes on the side wall of the microgroove and cause the reduction of the transfer efficiency of electrons on the electrode surfaces, so that the impedance values of the electrodes rise and are increased with diameter increase of proliferation spheres of the 3D spherical cell, and after an anti-tumor drug acts on the 3D spherical cells to cause apoptosis, the impedance values of the electrodes are decreased, and the activity and proliferation ability of the 3D spherical cells are monitored by calculating the change rate of the impedancevalues of the 3D spherical cells. The constructed microcavity impedance sensor can monitor the activity and proliferation ability of 3D spherical cells with high throughput in real time for a long time.

Description

technical field [0001] The invention relates to cell activity detection technology, in particular to a microcavity impedance sensor and a preparation method for real-time monitoring of 3D cell activity and proliferation ability. Background technique [0002] The preclinical efficacy and toxicity evaluation of candidate drugs is of great significance to drug discovery and development. Drug screening techniques often use in vitro cultured cells for primary screening of sensitive compounds. Traditional in vitro cultured cells are two-dimensional, and have problems such as contact inhibition and loss of heterogeneity. They are too different from three-dimensional cells grown in vivo, and cannot accurately reflect the situation of cells in vivo. Some drug screening results based on 2D cell experiments often show excellent curative effects, but there is no corresponding curative effect in subsequent animal experiments and clinical trials. These 2D cell-based drug screening techn...

Claims

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Application Information

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IPC IPC(8): C12M1/34C12Q1/02G01N27/02
CPCG01N27/021G01N33/5011
Inventor 王平潘宇祥顾陈磊邱勇孔留兵魏鑫伟
Owner ZHEJIANG UNIV
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