Bundgaardpersson2805

Antibiotics are widespread in the environment with notable ecological risk, for which efficient and green removal technologies are demanded. As a kind of g-C3N4-based material with remarkable photocatalytic property, OCN is an oxygen- and nitrogen-linked carbon nitride organic polymer which can be synthesized through a single-step thermal polymerization method. In this study, OCN was applied for the visible-light-driven photocatalytic degradation of a typical fluoroquinolone (FQ) antibiotics enrofloxacin (ENR). The photocatalysis process achieved over 97% ENR removal within 60 min with 0.4 mg/L OCN and 4 mg/L ENR at pH 8.2. LGK-974 nmr The photocatalytic mechanism of OCN at different pH was studied for the first time. It was shown that O2⋅-, 1O2 and h+ made contributions at neutral or basic pH and 1O2 contributes the most (57.6% at pH 8.2), while ⋅OH played a role only under acidic condition with a contribution rate of 23.8% at pH 3.2. The cleavage of the piperazine ring and the quinolone ring were two main degradation pathways. The common water constituents humic acid and NO3- showed a dual effect, but HCO3- and Cl- inhibited the degradation. The effect of different water matrices was tested under natural sunlight and it was only a tiny disturbance to the degradation rates. The biotoxicity test conducted using Vibrio fischeri indicated that the toxicity of degradation products became negligible after 3 h. This study demonstrated that OCN is a promising candidate for the advanced treatment and in-situ remediation.Phytoremediation is a technique that reduces the impact and environmental toxicity of toxic agents. Plectranthus neochilus, a species of aromatic plant, has already promoted phytoremediation of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). In addition, it was unclear whether the degradation of 2,4-D alone allows for a non-toxic environment (decontamination efficiency). Therefore, the aim of the present study was to verify the changes of the volatile compounds and concentrated essential oil of P. neochilus after phytoremediation of 2,4-D and the subsequent antibacterial activity of this essential oil concentrate. In addition, the toxicity of the plant's tea and the aqueous medium (waste) after the decontamination of 2,4-D was analyzed. The exposure to 2,4-D did not cause many changes in the volatile compounds, nor in the essential oil concentrate from the plant. Therefore, this essential oil concentrate can be used as an antimicrobial after phytoremediation. Regarding the use of this plant in tea form, it was found to be unsafe, even after phytoremediation, as this tea was toxic to the Drosophila melanogaster model (death of up to 100% of flies). The aqueous medium after 2,4-D phytoremediation became less toxic than the initial one (bioassays with Artemia salina and Allium cepa in the waste groups). However, the efficiency of phytoremediation with this plant must be improved. Therefore, we are performing new studies with P. necohilus and 2,4-D in aqueous medium.Fenton-like reactions at near neutral pHs are limited by the slow reduction of ferric species. Enhancing generation of from solid peroxides is a promising strategy to accelerate the rate-limiting step. Herein, the H2O2 release and Fenton-like reactions of four solid peroxides, MgO2, CaO2, ZnO2 and urea hydrogen peroxide (UHP), were investigated. Results indicated that UHP can release H2O2 instantly and show a similar behavior as H2O2 in the Fenton-like reactions. MgO2 released H2O2 quickly in phosphate buffered solutions, which was comparable to CaO2 but faster than ZnO2. Metal peroxides induced higher initial phenol degradation rates than UHP and H2O2 when the same theoretic H2O2 dosages and Fe(III)-EDTA were used. MgO2 displayed a superior performance for phenol degradation at pH 5, resulting in more than 93% phenol reduction at 1.5 h. According to kinetic analyses, the generation rate of in the MgO2 system was 18 and 3.4 times higher than those in ZnO2 and CaO2 systems, respectively. The addition of MgO2 significantly promoted H2O2 based Fenton-like reactions by increasing production of , and the mixture of MgO2 and H2O2 had an improved utilization efficiency of active oxygen than the MgO2 system. The findings suggested the critical roles of metal peroxides in favoring Fenton-like reactions and inspired strategies to simultaneously accelerate Fenton-like reactions and improve utilization efficiency of active oxygen.Styrene increases serum prolactin (PRL) concentration. Hyperprolactinemia is associated with poor prognosis in lung cancer patients, but the mechanism of PRL action is unclear. The aims of this study were to (i) investigate the mechanism of PRL-action receptor in NSCLC cells (ii) measure whether PRL was secreted by NSCLC cells and its stimulatory mechanism in vitro and in vivo. We found that cell proliferation was increased after treatment of a pharmacological dose of PRL in A549 cells, which through up regulation of growth hormone receptor (GHR) and downstream of JAK2/STAT3/VEGF pathway. All NSCLC cells in the present study secreted PRL and expressed GHR, but not PRLR. Inhibition of GHR protein level led to decrease the PRL-induced cell proliferation. PRL was detected in NSCLC cells culture medium. Knockdown of intracellular PRL downregulated JAK2/STAT3 protein activities and GHR and VEGF protein levels. Furthermore, knockdown of intracellular PRL reduced the cell proliferation and the ability of colony-forming. In lung cancer tissues, PRL, GHR and VEGF levels were higher in the tumor tissues than in normal tissues and the protein expressions of these three proteins are positively correlated, respectively. High expression levels of both PRL and GHR cause a poor survival rate in lung cancer patients. Taken together, our results suggested that extracellular and intracellular PRL were involved in cell proliferation through GHR. Combination of in vitro and in vivo results, GHR and PRL are important targets for suppressing NSCLC cell proliferation, which might improve the survival rate in NSCLC patients.Over the past several years, it has become increasingly acknowledged that Organically Bound Tritium (OBT) is the most pertinent tritium form for understanding its behavior and distribution within the biosphere. The fate of tritium actually depends on the accessibility and exchangeability of hydrogen atoms for isotopic exchanges in natural organic matter, especially in widespread biomass biomolecules like carbohydrates or proteins. The present work is therefore aimed at providing a means for improving the knowledge of tritium speciation and distribution on environmental matrices by evaluating the impact of molecular structure of various carbohydrate molecules on OBT behavior. We are thus proposing to assess the exchange capacities of hydrogen from a gas-solid isotopic exchange methodology in wheat grains, water-milfoil and apple environmental matrices using starch, cellulose/proteins and simple carbohydrates as their respective main constituents. For wheat grains, a good agreement was obtained between experimental and theoretical values as a result of the predominantly simple molecular structure of starch.