Membrane integrity Cell membrane integrity of MDA-MB-231 cells was evaluated by determining the activity of lactate dehydrogenase (LDH) leaking

out of the cell, according to the manufacturer’s instructions (in vitro toxicology assay kit, TOX7, Sigma, USA). The LDH assay is based on the release of the cytosolic enzyme LDH from cells with damaged cellular membranes. Thus, in cell culture, AuNPs induced cytotoxicity and were quantitatively analyzed by measuring the activity of LDH in the supernatant. Briefly, cells were exposed to various concentrations of AuNPs for 24 h, and then 100 μL per well of each cell-free supernatant was transferred in triplicates into wells in a 96-well plate, and 100 μL of LDH-assay reaction mixture was added to each selleck chemicals llc www.selleckchem.com/products/ulixertinib-bvd-523-vrt752271.html well. After 3-h incubation under standard conditions,

the optical density of the generated color was determined at a wavelength of 490 nm using a Microplate Reader. Determination of ROS Intracellular reactive oxygen species (ROS) were measured based on the intracellular peroxide-dependent oxidation of 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA, Molecular Probes, Eugene, OR, USA) to form the fluorescent compound 2′,7′-dichlorofluorescein (DCF), as previously CYT387 datasheet described. Cells were seeded onto 24-well plates at a density of 5 × 104 cells per well and cultured for 24 h. After washing twice with PBS, fresh medium containing 100 μM of AuNPs, 1 mM H2O2, or AgNPs (5 μg/mL) was added, and the cells were incubated for 24 h. For the control, cells were added to 20 μM of DCFH-DA and incubation continued for 30 min at 37°C. The cells were rinsed with PBS, 2 mL of PBS was added to each well, and fluorescence intensity was determined with a spectrofluorometer (Gemini EM) with excitation at 485 nm and emission at 530 nm. For the control, had antioxidant N-acetyl-l-cystein (NAC, 5 mM) was added to the cells grown in 24-well plates (for 24 h) for 1 h prior

to exposure to AuNPs, 1 mM H2O2, or AgNPs (5 μg/mL) for 24 h. We then added 20 μM of DCFH-DA, and the cells were incubated for 30 min at 37°C before measuring DCF fluorescence changes as described. Results and discussion Extracellular synthesis of AuNPs Primary characterization of the ability of Ganoderma spp. mushroom extract for AuNP synthesis was analyzed. The ifenprodil Figure  1 inset shows tubes with the Ganoderma spp. mycelia extract [1], HAuCl4[2], and extract after reaction with HAuCl4 ions for 24 h [3]. As expected, the color changed from pale yellow to deep purple in the presence of the extract, which indicates AuNP formation and is evidence of synthesis. Figure 1 Synthesis and characterization of AuNPs. The figure inset shows tubes containing samples of the Ganoderma spp. extract (1); 1 mM aqueous HAuCl4 (2); extract after incubation with HAuCl4 (3). The absorption spectrum of AuNPs exhibited a strong broad peak at 520 nm, and this band was assigned to surface plasmon resonance of the particles.