371-Liao-RamanSpectra

Project

Title
Raman spectra data of cell spheroids on a multi-well plate treated with various concentrations of reagents
Description
Cell spheroids offer alternative in vitro cell models to monolayer cultured cells because they express complexities similar to thoseof 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 interspheroid heterogeneity, current Raman applications used in spheroidsanalysis allow the observation of only a few spheroids owing to the lowthroughput of Raman spectroscopy. In this study, the authors 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, their 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, they rapidly observed chemical changes in spheroids, and thus, this system can facilitate the application of Raman spectroscopy in analyzing the cellular responses of spheroids.
License
CC BY
Released at
Oct. 20, 2025, midnight
Updated at
Funding
This research was supported by Osaka University Innovation Bridge Grant and JST COI-NEXT under grant number JPMJPF2009.
# of image datasets
2

Papers

Papers
Paper information: 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.,
Pubmed ID: 37725051,
DOI: https://doi.org/10.1021/acs.analchem.3c02129,
URL: https://pubmed.ncbi.nlm.nih.gov/37725051/

Contacts

Contacts
Katsumasa Fujita (Contact) , Department of Applied Physics , Osaka University
Hao-Xiang Liao (data contributor) , Department of Applied Physics , Osaka University
Kazuki Bando (data contributor) , Department of Applied Physics , Osaka University
Menglu Li (data contributor) , Department of Applied Physics , Osaka University

Biosamples

Organisms
Homo sapiens (NCBI:txid9606)
Strains

Cells

Cell lines
Hep G2 cell
HeLa Cell

Ontologies

UBERON
Anatomical entities
GO: Biological processes
GO: Cellular components
GO: Molecular functions

Genetics

Gene names
Protein names
Genetic methods
Protein tags
Probes
Oligo Primer
Genotype

Treatments

Reagent or Compound
Concentration
Fold Dilution
actinomycin D (CHEBI:27666)
0, 0.1, 0.3, 1.0, 3.0, 10 micromolar (UO_0000064)
free fatty acid
0.01, 0.1, 0.25, 0.5, 1.0, 2.0 millimolar (UO_0000063)

Imaging Methods

Dimensions
NA,
X scales
NA,
Y scales
NA,
Z scales
NA,
T scales
NA,
Channels
NA,
Microscopy types
inelastic scattering of photons (Raman scattering) (FBbi:00000589)
Detection methods
Visualization methods
Illumination methods
Sources of contrast
Contrast enhancing methods
Resolution enhancing methods
Imaged parameters
Sample preparation methods

Instruments

Body
home-built device
Model
home-built device
Light source
CW laser
Detector
2D cooled CCD camera (PIXIS 400B eXcelon, Teledyne Princeton Instruments)
Objective
spherical lens
Filter set
Custom-made filter
Dichroic
Custom-made filter

Datasets

Dataset name
Organism
Gene / Protein
Dimensions
File size
SSBD:OMERO
Download
Homo sapiens (NCBI:txid9606)
NA
241KB
zip
Homo sapiens (NCBI:txid9606)
NA
1.1MB
zip