TY - JOUR
T1 - Miniaturized Cell Fluorescence Imaging Device Equipped with Multielectrode Array
AU - Sais, Barbara Teixeira
AU - Haruta, Makito
AU - Tso, Kuang Chih
AU - Hagita, Mizuki
AU - Hagiwara, Takanori
AU - Sugie, Kenji
AU - Kimura, Ayaka
AU - Takehara, Hironari
AU - Tashiro, Hiroyuki
AU - Sasagawa, Kiyotaka
AU - Ohta, Jun
N1 - Funding Information:
This study was supported by the Japan Society for the Promotion of Science (JSPS) (19K16883, 18H03780).
Publisher Copyright:
© 2022 M Y U Scientific Publishing Division. All rights reserved.
PY - 2022
Y1 - 2022
N2 - In this study, a fabrication method for a system composed of a fluorescence imaging module and a multielectrode array (MEA) chamber is described. It is important to measure both fluorescence intensity and electrical activity to obtain a better understanding of a physiological activity, such as spikes or action potentials, of cells. However, observing these physiological traits long-term with cultured cells is difficult using a conventional microscope. In this study, we developed a small fluorescence imaging device with an MEA that can be used in a conventional CO2 incubator. The fluorescence imaging module was composed of a CMOS image sensor, a fiber-optic plate (FOP), a blue LED, and optical filters. The FOP enabled the device to be miniaturized through lensless fluorescence imaging. The MEA chamber was fabricated with micro gold electrodes deposited on the FOP. By using the FOP for the bottom of the chamber, we measured both the fluorescence signal and electrophysiology signal in the same experiment. The performance of the device was evaluated with neuronal blastoma cells. Our device enabled us to observe fluorescence images and MEA signals.
AB - In this study, a fabrication method for a system composed of a fluorescence imaging module and a multielectrode array (MEA) chamber is described. It is important to measure both fluorescence intensity and electrical activity to obtain a better understanding of a physiological activity, such as spikes or action potentials, of cells. However, observing these physiological traits long-term with cultured cells is difficult using a conventional microscope. In this study, we developed a small fluorescence imaging device with an MEA that can be used in a conventional CO2 incubator. The fluorescence imaging module was composed of a CMOS image sensor, a fiber-optic plate (FOP), a blue LED, and optical filters. The FOP enabled the device to be miniaturized through lensless fluorescence imaging. The MEA chamber was fabricated with micro gold electrodes deposited on the FOP. By using the FOP for the bottom of the chamber, we measured both the fluorescence signal and electrophysiology signal in the same experiment. The performance of the device was evaluated with neuronal blastoma cells. Our device enabled us to observe fluorescence images and MEA signals.
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U2 - 10.18494/SAM3758
DO - 10.18494/SAM3758
M3 - Article
AN - SCOPUS:85130635212
SN - 0914-4935
VL - 34
SP - 1587
EP - 1599
JO - Sensors and Materials
JF - Sensors and Materials
IS - 4
ER -