RESUMO
Novel BaTiO3 hierarchical porous microspheres were achieved by using H2Ti2O5·H2O (HTO) hierarchical microspheres as a precursor template via a facile solvothermal method. Interestingly, the BaTiO3 microspheres were constructed with two-dimensional (2D) nanosheets, which were composed of many order nanocrystals with crystal-axis-orientation. The special hierarchical structure, which is both macroporous and mesoporous, exhibits a large specific surface area and a high total pore volume. The photocatalytic performance of BaTiO3 hierarchical microspheres for degradation of methyl orange (MO) under UV-light irradiation was tested, its apparent rate being up to 0.10183 min-1, almost 23 times higher than that for nanoscale BaTiO3 particles. The attractive photocatalytic properties are considered to benefit from the effective features of hierarchical BaTiO3 microspheres, such as the ultrathin thickness of nanosheets and their ordered interconnected macro-mesoporous structure and intrinsic photocatalytic activity. This study offers an in situ topochemical conversion route to synthesis of other titanium-based perovskite hierarchical nanostructures, and thus opening the door for the synthesis of other titanium-based functional materials and expanding their potential application.
RESUMO
OBJECTIVE: The oxidation of benzo (a) pyrene mediated by 5-lipoxygenase (5-LOX) were investigated in HBE cells in order to provide further proof that lipoxygenase is the alternative pathway for the oxidation of xenobiotics. METHODS: Enzymic experiment: Soybean lipoxygenase (SLO), substrate (benzo[a] pyrene) and other component react in the enzymic system and the reaction product are detected by spectrophotometry. At the same time, in vitro detect of benzo (a) pyrene-DNA adducts with a UV spectrophotometer and HPLC. Cellular experiment: After HBE cells exposure to different poison (B[a]P 4, 8, 16, 32, 64, 128µmol/L, AA-861, naproxen or α- naphthoflavone 0.1, 1, 10 µmol/L) for 24 hours, the effect of benzo (a) -pyrene on cell survival rate were assessed by reductions of tetrazolium dye (MTT) and flow cytometry in cultured HBE cells, and the protein expressions of 5-lipoxygenase in the cells are tested by western-blot, and the DNA damages by the single cell gel electrophoresis. And then, the effect of the specific inhibitor of 5-lipoxygenase (AA-861) on 5-lipoxygenase protein expression and DNA damage in the cells are detected. RESULTS: SLO can catalyze the co-oxidation of benzo (a) pyrene to generate benzo (a) pyrene-7,8-epoxide in the presence of hydrogen peroxide. GTP can inhibit the reaction , the IC50 value is 0.46 mg/L, the model equation is Probit (P) = 0.8985+2.6824 Log (dose). SLO can catalyze the co-oxidation of benzo (a) pyrene to generate a new product, but fail to form DNA adducts in vitro. HBE cell viability decreased with the benzo (a) pyrene concentration increased , but AA-861 and naproxen can inhibit it. Flow cytometry and single cell gel electrophoresis experiments show, Benzo (a) pyrene can induce 5-lipoxygenase protein expression, but AA-861 cannot in HBE. Benzo (a) pyrene causes toxic action and DNA damage in HBE, which can significantly inhibit by AA-861, the difference is statistically significant (P < 0.05). CONCLUSIONS: The co-oxidate of benzo (a) pyrene by 5-LOX turns into electrophiles that covalently bind to DNA and induce DNA damage, which can be significantly inhibited by AA-861.