TY - JOUR
T1 - Low Cytotoxicity and Genotoxicity of Two-Dimensional MoS2 and WS2
AU - Appel, Jennie H.
AU - Li, Duo O.
AU - Podlevsky, Joshua D.
AU - Debnath, Abhishek
AU - Green, Alexander
AU - Wang, Qing
AU - Chae, Junseok
N1 - Funding Information:
We thank Dr. Julien Chen for HEK293f cell culture protocols. Q.H.W. and A.A.G. acknowledge support from Arizona State University startup funds. This work is supported by the NSF Graduate Research Fellowship under Grant DGE-1311230.
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/3/14
Y1 - 2016/3/14
N2 - Atomically thin transition-metal dichalcogenides (TMDs) have attracted considerable interest because of their unique combination of properties, including photoluminescence, high lubricity, flexibility, and catalytic activity. These unique properties suggest future uses for TMDs in medical applications such as orthodontics, endoscopy, and optogenetics. However, few studies thus far have investigated the biocompatibility of mechanically exfoliated and chemical vapor deposition (CVD)-grown pristine two-dimensional TMDs. Here, we evaluate pristine molybdenum disulfide (MoS2) and tungsten disulfide (WS2) in a series of biocompatibility tests, including live-dead cell assays, reactive oxygen species (ROS) generation assays, and direct assessment of cellular morphology of TMD-exposed human epithelial kidney cells (HEK293f). Genotoxicity and genetic mutagenesis were also evaluated for these materials via the Ames Fluctuation test with the bacterial strain S. typhimurium TA100. Scanning electron microscopy of cultured HEK293f cells in direct contact with MoS2 and WS2 showed no impact on cell morphology. HEK293f cell viability, evaluated by both live-dead fluorescence labeling to detect acute toxicity and ROS to monitor for apoptosis, was unaffected by these materials. Exposure of bacterial cells to these TMDs failed to generate genetic mutation. Together, these findings demonstrate that neither mechanically exfoliated nor CVD-grown TMDs are deleterious to cellular viability or induce genetic defects. Thus, these TMDs appear biocompatible for future application in medical devices.
AB - Atomically thin transition-metal dichalcogenides (TMDs) have attracted considerable interest because of their unique combination of properties, including photoluminescence, high lubricity, flexibility, and catalytic activity. These unique properties suggest future uses for TMDs in medical applications such as orthodontics, endoscopy, and optogenetics. However, few studies thus far have investigated the biocompatibility of mechanically exfoliated and chemical vapor deposition (CVD)-grown pristine two-dimensional TMDs. Here, we evaluate pristine molybdenum disulfide (MoS2) and tungsten disulfide (WS2) in a series of biocompatibility tests, including live-dead cell assays, reactive oxygen species (ROS) generation assays, and direct assessment of cellular morphology of TMD-exposed human epithelial kidney cells (HEK293f). Genotoxicity and genetic mutagenesis were also evaluated for these materials via the Ames Fluctuation test with the bacterial strain S. typhimurium TA100. Scanning electron microscopy of cultured HEK293f cells in direct contact with MoS2 and WS2 showed no impact on cell morphology. HEK293f cell viability, evaluated by both live-dead fluorescence labeling to detect acute toxicity and ROS to monitor for apoptosis, was unaffected by these materials. Exposure of bacterial cells to these TMDs failed to generate genetic mutation. Together, these findings demonstrate that neither mechanically exfoliated nor CVD-grown TMDs are deleterious to cellular viability or induce genetic defects. Thus, these TMDs appear biocompatible for future application in medical devices.
KW - bacterial mutagenesis
KW - biocompatibility
KW - molybdenum disulfide
KW - oxidative stress
KW - transition-metal dichalcogenides
KW - tungsten disulfide
KW - two-dimensional materials
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U2 - 10.1021/acsbiomaterials.5b00467
DO - 10.1021/acsbiomaterials.5b00467
M3 - Article
AN - SCOPUS:84969256039
SN - 2373-9878
VL - 2
SP - 361
EP - 367
JO - ACS Biomaterials Science and Engineering
JF - ACS Biomaterials Science and Engineering
IS - 3
ER -