TY - JOUR
T1 - Non-invasive methods of monitoring Fe3O4 magnetic nanoparticle toxicity in human liver HepaRG cells using impedance biosensing and Coherent anti-Stokes Raman spectroscopic (CARS) microscopy
AU - Kuhn, Joel
AU - McDonald, Alison
AU - Mongoin, Cyril
AU - Anderson, Graham
AU - Lafeuillade, Guillemette
AU - Mitchell, Stephen
AU - Elfick, Alistair P. D.
AU - Bagnaninchi, Pierre O.
AU - Yiu, Humphrey H. P.
AU - Nelson, Leonard j.
PY - 2024/4
Y1 - 2024/4
N2 - Functionalized nanoparticles have been developed for use in nanomedicines for treating life threatening diseases including various cancers. To ensure safe use of these new nanoscale reagents, various assays for biocompatibility or cytotoxicity in vitro using cell lines often serve as preliminary assessments prior to in vivo animal testing. However, many of these assays were designed for soluble, colourless materials and may not be suitable for coloured, non-transparent nanoparticles. Moreover, cell lines are not always representative of mammalian organs in vivo. In this work, we use non-invasive impedance sensing methods with organotypic human liver HepaRG cells as a model to test the toxicity of PEG-Fe3O4 magnetic nanoparticles. We also use Coherent anti-Stokes Raman Spectroscopic (CARS) microscopy to monitor the formation of lipid droplets as a parameter to the adverse effect on the HepaRG cell model. The results were also compared with two commercial testing kits (PrestoBlue and ATP) for cytotoxicity. The results suggested that the HepaRG cell model can be a more realistic model than commercial cell lines while use of impedance monitoring of Fe3O4 nanoparticles circumventing the uncertainties due to colour assays. These methods can play important roles for scientists driving towards the 3Rs principle – Replacement, Reduction and Refinement.
AB - Functionalized nanoparticles have been developed for use in nanomedicines for treating life threatening diseases including various cancers. To ensure safe use of these new nanoscale reagents, various assays for biocompatibility or cytotoxicity in vitro using cell lines often serve as preliminary assessments prior to in vivo animal testing. However, many of these assays were designed for soluble, colourless materials and may not be suitable for coloured, non-transparent nanoparticles. Moreover, cell lines are not always representative of mammalian organs in vivo. In this work, we use non-invasive impedance sensing methods with organotypic human liver HepaRG cells as a model to test the toxicity of PEG-Fe3O4 magnetic nanoparticles. We also use Coherent anti-Stokes Raman Spectroscopic (CARS) microscopy to monitor the formation of lipid droplets as a parameter to the adverse effect on the HepaRG cell model. The results were also compared with two commercial testing kits (PrestoBlue and ATP) for cytotoxicity. The results suggested that the HepaRG cell model can be a more realistic model than commercial cell lines while use of impedance monitoring of Fe3O4 nanoparticles circumventing the uncertainties due to colour assays. These methods can play important roles for scientists driving towards the 3Rs principle – Replacement, Reduction and Refinement.
KW - Coherent anti-Stokes Raman spectroscopic (CARS) microscopy
KW - HepaRG cells
KW - Impedance biosensing
KW - Lipid dynamics
KW - Magnetite
KW - Nanotoxicity
KW - PEGylated MNPs
UR - http://www.scopus.com/inward/record.url?scp=85187559528&partnerID=8YFLogxK
U2 - 10.1016/j.toxlet.2024.02.010
DO - 10.1016/j.toxlet.2024.02.010
M3 - Article
C2 - 38428546
SN - 0378-4274
VL - 394
SP - 92
EP - 101
JO - Toxicology Letters
JF - Toxicology Letters
ER -