Fe3O4 magnetic nanoparticles(MNPs) were synthesised, characterised, and used as a peroxidase mimetic to accelerate levofloxacin sono-degradation in an ultrasound(US)/H2O2 system. The Fe3O4 MNPs were in nanometre scale...Fe3O4 magnetic nanoparticles(MNPs) were synthesised, characterised, and used as a peroxidase mimetic to accelerate levofloxacin sono-degradation in an ultrasound(US)/H2O2 system. The Fe3O4 MNPs were in nanometre scale with an average diameter of approximately 12 to 18 nm. The introduction of Fe3O4 MNPs increased levofloxacin sono-degradation in the US/H2O2 system. Experimental parameters, such as Fe3O4 MNP dose, initial solution p H, and H2O2 concentration, were investigated by a one-factor-at-a-time approach. The results showed that Fe3O4 MNPs enhanced levofloxacin removal in the p H range from 4.0 to 9.0. Levofloxacin removal ratio increased with Fe3O4 MNP dose up to 1.0 g·L-1and with H2O2 concentration until reaching the maximum. Moreover, three main intermediate compounds were identified by HPLC with electrospray ionisation tandem mass spectrometry, and a possible degradation pathway was proposed. This study suggests that combination of H2O2, Fe3O4 MNPs and US is a good way to improve the degradation efficiency of antibiotics.展开更多
Platinum nanoparticles （NPs） are reported to mimic various anfioxidant enzymes and thus may produce a positive biological effect by reducing reactive oxygen species （ROS） levels. In this manuscript, we report Pt N...Platinum nanoparticles （NPs） are reported to mimic various anfioxidant enzymes and thus may produce a positive biological effect by reducing reactive oxygen species （ROS） levels. In this manuscript, we report Pt NPs as an enzyme mimic of ferroxidase by depositing platinum nanodots on gold nanorods （Au@Pt NDRs）. Au@Pt NDRs show pH-dependent ferroxidase-like activity and have higher activity at neutral pH values. Cytotoxicity results with human cell lines （lung adenocarcinoma A549 and normal bronchial epithelial cell line HBE） show that Au@Pt NDRs are taken up into cells via endocytosis and translocate into the endosome/lysosome. Au@Pt NDRs have good biocompatibility at NDR particle concentrations lower than 0.15 nM. However, in the presence of H202, lysosome- located NDRs exhibit peroxidase-like activity and therefore increase cytotoxicity. In the presence of FeE＋, the ferroxidase-like activity of the NDRs protects cells from oxidative stress by consuming H202. Thorough consideration should be given to this behavior when employinK Au@Pt NDRs in biological svstems.展开更多
基金Supported by the National Natural Science Foundation of China(51009115)Shaanxi Provincial Department of Education Key Laboratory Project(13JS067)+2 种基金the Hall of Shaanxi Province Science and Technology(2013JK0881)the Research Plan Project of Water Resources Department of Shaanxi Province(2013slkj-07)the Innovation of Science and Technology Fund of Xi'an University of Technology(211302)
文摘Fe3O4 magnetic nanoparticles(MNPs) were synthesised, characterised, and used as a peroxidase mimetic to accelerate levofloxacin sono-degradation in an ultrasound(US)/H2O2 system. The Fe3O4 MNPs were in nanometre scale with an average diameter of approximately 12 to 18 nm. The introduction of Fe3O4 MNPs increased levofloxacin sono-degradation in the US/H2O2 system. Experimental parameters, such as Fe3O4 MNP dose, initial solution p H, and H2O2 concentration, were investigated by a one-factor-at-a-time approach. The results showed that Fe3O4 MNPs enhanced levofloxacin removal in the p H range from 4.0 to 9.0. Levofloxacin removal ratio increased with Fe3O4 MNP dose up to 1.0 g·L-1and with H2O2 concentration until reaching the maximum. Moreover, three main intermediate compounds were identified by HPLC with electrospray ionisation tandem mass spectrometry, and a possible degradation pathway was proposed. This study suggests that combination of H2O2, Fe3O4 MNPs and US is a good way to improve the degradation efficiency of antibiotics.
文摘Platinum nanoparticles （NPs） are reported to mimic various anfioxidant enzymes and thus may produce a positive biological effect by reducing reactive oxygen species （ROS） levels. In this manuscript, we report Pt NPs as an enzyme mimic of ferroxidase by depositing platinum nanodots on gold nanorods （Au@Pt NDRs）. Au@Pt NDRs show pH-dependent ferroxidase-like activity and have higher activity at neutral pH values. Cytotoxicity results with human cell lines （lung adenocarcinoma A549 and normal bronchial epithelial cell line HBE） show that Au@Pt NDRs are taken up into cells via endocytosis and translocate into the endosome/lysosome. Au@Pt NDRs have good biocompatibility at NDR particle concentrations lower than 0.15 nM. However, in the presence of H202, lysosome- located NDRs exhibit peroxidase-like activity and therefore increase cytotoxicity. In the presence of FeE＋, the ferroxidase-like activity of the NDRs protects cells from oxidative stress by consuming H202. Thorough consideration should be given to this behavior when employinK Au@Pt NDRs in biological svstems.
