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1.
Molecules ; 25(11)2020 Jun 02.
Article in English | MEDLINE | ID: mdl-32498444

ABSTRACT

Recent developments in the area of nanotechnology have focused on the development of nanomaterials with catalytic activities. The enzyme mimics, nanozymes, work efficiently in extreme pH and temperature conditions, and exhibit resistance to protease digestion, in contrast to enzymes. We developed an environment-friendly, cost-effective, and facile biological method for the synthesis of ZnO-Pd nanosheets. This is the first biosynthesis of ZnO-Pd nanosheets. The synthesized nanosheets were characterized by UV-visible spectroscopy, X-ray diffraction (XRD), scanning electron microscopy, transmission electron microscopy, and energy-dispersive X-ray. The d-spacing (inter-atomic spacing) of the palladium nanoparticles in the ZnO sheets was found to be 0.22 nm, which corresponds to the (111) plane. The XRD pattern revealed that the 2θ values of 21.8°, 33.3°, 47.7°, and 56.2° corresponded with the crystal planes of (100), (002), (112), and (201), respectively. The nanosheets were validated to possess peroxidase mimetic activity, which oxidized the 3,3',5,5'-tetramethylbenzidine (TMB) substrate in the presence of H2O2. After 20 min of incubation time, the colorless TMB substrate oxidized into a dark-blue-colored one and a strong peak was observed at 650 nm. The initial velocities of Pd-ZnO-catalyzed TMB oxidation by H2O2 were analyzed by Michaelis-Menten and Lineweaver-Burk plots, resulting in 64 × 10-6 M, 8.72 × 10-9 Msec-1, and 8.72 × 10-4 sec-1 of KM, Vmax, and kcat, respectively.


Subject(s)
Biomimetic Materials/chemical synthesis , Palladium/chemistry , Zinc Oxide/chemistry , Biomimetic Materials/chemistry , Green Chemistry Technology , Metal Nanoparticles/chemistry , Microscopy, Electron, Transmission , Particle Size , Peroxidase/metabolism , X-Ray Diffraction
2.
J Med Food ; 9(2): 138-44, 2006.
Article in English | MEDLINE | ID: mdl-16822197

ABSTRACT

Cell apoptosis is now known to play an important role in the maintenance of cellular homeostasis and anticarcinogenesis. Selaginella tamariscina (ST) is a traditional medicinal plant for treatment of advanced cancer in the Orient. In the present study, the anticancer effect of ST was investigated by analyzing its potential to induce apoptosis in human leukemia HL-60 cells. ST-induced cytotoxicity of HL-60 cells was monitored by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The apoptosis was determined by microscopic examination of apoptotic morphology, determination of DNA fragmentation by electrophoresis, activation of caspase-3, and protein expression of procaspase-3, poly(ADP-ribose) polymerase (PARP) cleavage, Bcl-2, and Bax. ST was cytotoxic to HL-60 cells in a dose-dependent manner. However, ST-induced cytotoxicity was suppressed by reactive oxygen species scavengers, including superoxide dismutase (SOD) and catalase. ST caused DNA fragmentation and nuclear condensation, all characteristics of apoptosis. ST-induced apoptosis is accompanied by the activation of caspase-3 and the specific proteolytic cleavage of PARP. Concomitantly, ST treatments led to an increase in the proapoptotic Bax levels, while Bcl-2 expression was decreased. Moreover, this effect was attenuated by SOD and catalase. These results suggest that oxidative stress may be involved in the cytotoxicity of ST, and that ST-induced apoptosis of HL-60 cells is primarily mediated by the caspase activation pathway.


Subject(s)
Apoptosis/drug effects , Caspases/metabolism , Plant Extracts/pharmacology , Selaginellaceae/chemistry , Antineoplastic Agents/pharmacology , Caspase 3 , Enzyme Activation/drug effects , HL-60 Cells , Humans , Phytotherapy , Proto-Oncogene Proteins c-bcl-2/analysis , bcl-2-Associated X Protein/analysis
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