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U87 and U118 glioblastoma <t>cell</t> <t>viability.</t> Notes: Cell viability was determined using the <t>XTT</t> assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).
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Millipore xtt-based in vitro toxicology assay kit (tox2; xtt means 2,3-bis-[2-methoxy-4-nitro-5-sulfophenyl]-2h-tetrazolium-5-carboxanilide inner salt)
Proliferation of HCT116 cells treated with DCPIP and <t>DCPIP</t> <t>NPs</t> . Cell proliferation was determined by the <t>XTT</t> method. The concentrations of the free DCPIP and DCPIP NPs were calculated to be equal. Proliferation of untreated cells (0 μg) was taken as 100%. The measurements of the treated cells were normalized to the control measurement (100%). All measurements are reported as mean ± SD (n = 3). The asterisk (*) indicates p < 0.05.
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Average 90 stars, based on 1 article reviews
xtt-based in vitro toxicology assay kit (tox2; xtt means 2,3-bis-[2-methoxy-4-nitro-5-sulfophenyl]-2h-tetrazolium-5-carboxanilide inner salt) - by Bioz Stars, 2026-03
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U87 and U118 glioblastoma cell viability. Notes: Cell viability was determined using the XTT assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).

Journal: International Journal of Nanomedicine

Article Title: Diamond, graphite, and graphene oxide nanoparticles decrease migration and invasiveness in glioblastoma cell lines by impairing extracellular adhesion

doi: 10.2147/IJN.S146193

Figure Lengend Snippet: U87 and U118 glioblastoma cell viability. Notes: Cell viability was determined using the XTT assay. Cells were exposed to diamond nanoparticles (ND), graphite nanoparticles (NG), and graphene oxide (nGO) at concentrations of 10, 20, 50, 100, and 200 μg/mL for 24 h. Values are expressed as mean ± standard deviation (n=4, each experiment in duplicate). Statistical significance between control (C) and the treated cells is indicated by an asterisk (multifactor analysis of variance [ANOVA]; P <0.05). There was statistical significance between U87 and U118 viability ( P =0.0000) and the interaction between cell line and the type of nanoparticle ( P =0.0000).

Article Snippet: Cell viability was evaluated using an XTT-based cell proliferation assay kit (Sigma-Aldrich).

Techniques: XTT Assay, Standard Deviation

Proliferation of HCT116 cells treated with DCPIP and DCPIP NPs . Cell proliferation was determined by the XTT method. The concentrations of the free DCPIP and DCPIP NPs were calculated to be equal. Proliferation of untreated cells (0 μg) was taken as 100%. The measurements of the treated cells were normalized to the control measurement (100%). All measurements are reported as mean ± SD (n = 3). The asterisk (*) indicates p < 0.05.

Journal: Journal of Nanobiotechnology

Article Title: Inhibition of angiogenesis- and inflammation-inducing factors in human colon cancer cells in vitro and in ovo by free and nanoparticle-encapsulated redox dye, DCPIP

doi: 10.1186/1477-3155-8-17

Figure Lengend Snippet: Proliferation of HCT116 cells treated with DCPIP and DCPIP NPs . Cell proliferation was determined by the XTT method. The concentrations of the free DCPIP and DCPIP NPs were calculated to be equal. Proliferation of untreated cells (0 μg) was taken as 100%. The measurements of the treated cells were normalized to the control measurement (100%). All measurements are reported as mean ± SD (n = 3). The asterisk (*) indicates p < 0.05.

Article Snippet: The toxicity of DCPIP and DCPIP NPs on the proliferation of HCT116 cells was determined by using the XTT-based In Vitro Toxicology Assay kit (Sigma-Aldrich).

Techniques: