Detail of Fig4_HepG2FFA

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Project
Title
Raman spectrua data of HepG2 spheroids treated with various concentrations of FFA
Description
Raman spectra data of HepG2 spheroids treated with various concentrations of FFA (free fatty acid: 0 mM, 0.01 mM, 0.1 mM, 0.25 mM, 0.5 mM, 1.0 mM, 2.0 mM). Multiple spectra data is deposited for each concentration of FFA.
Release, Updated
2025-01-31
License
CC BY
Kind
Image data
File Formats
.xlsx
Data size
1.1 MB

Organism
Homo sapiens ( NCBI:txid9606 )
Strain(s)
-
Cell Line
Hep G2 cell

Datatype
-
Molecular Function (MF)
Biological Process (BP)
Cellular Component (CC)
Biological Imaging Method
inelastic scattering of photons ( Fbbi:00000589 )
X scale
-
Y scale
-
Z scale
-
T scale
-

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
Liao HX, Bando K, Li M, Fujita K. Multifocal Raman Spectrophotometer for Examining Drug-Induced and Chemical-Induced Cellular Changes in 3D Cell Spheroids. Anal Chem. 2023 Oct 3;95(39):14616-14623.
Related paper(s)

Hao-Xiang Liao, Kazuki Bando, Menglu Li, Katsumasa Fujita (2023) Multifocal Raman Spectrophotometer for Examining Drug-Induced and Chemical-Induced Cellular Changes in 3D Cell Spheroids., Analytical chemistry

Published in 2023 Sep 19 (Electronic publication in Sept. 19, 2023, midnight )

(Abstract) Cell spheroids offer alternative in vitro cell models to monolayer cultured cells because they express complexities similar to those of in vivo tissues, such as cellular responses to drugs and chemicals. Raman spectroscopy emerged as a powerful analytical tool for detecting chemical changes in living cells because it nondestructively provides vibrational information regarding a target. Although multiple iterations are required in drug screening to determine drugs to treat cell spheroids and assess the inter-spheroid heterogeneity, current Raman applications used in spheroids analysis allow the observation of only a few spheroids owing to the low throughput of Raman spectroscopy. In this study, we developed a multifocal Raman spectrophotometer that enables simultaneous analysis of multiple spheroids in separate wells of a regular 96-well plate. By utilizing 96 focal spots excitation and parallel signal collection, our system can improve the throughput by approximately 2 orders of magnitude compared to a conventional single-focus Raman microscope. The Raman spectra of HeLa cell spheroids treated with anticancer drugs and HepG2 cell spheroids treated with free fatty acids were measured simultaneously, and concentration-dependent cellular responses were observed in both studies. Using the multifocal Raman spectrophotometer, we rapidly observed chemical changes in spheroids, and thus, this system can facilitate the application of Raman spectroscopy in analyzing the cellular responses of spheroids.

Contact
Katsumasa Fujita , Osaka University , Department of Applied Physics , Department of Applied Physics
Contributors

OMERO Dataset
OMERO Project
Source