Enhanced Photocatalytic Properties of PET Filaments Coated with Ag-N Co-Doped TiO2 Nanoparticles Sensitized with Disperse Blue Dyes

In this study, the effects of disperse blue dye-sensitization on the photocatalytic properties of the Ag-N co-doped TiO2 nanoparticles loaded on polyethylene terephthalate (PET) filaments are investigated under visible light irradiation. The microstructure and photocatalytic properties of the as-synthesized TiO2 nanocomposites, as well as the as-prepared PET filaments, are systematically characterized. The photocatalytic performance of the PET filaments coated with the Ag-N co-doped TiO2 nanoparticles sensitized with disperse blue dyes is evaluated via its capacity of photo-degrading methyl orange (MO) dyes under visible light irradiation. It is found that the holes are the predominant reactive radical species and the hydroxyl and superoxide radicals play a subordinate role in the photocatalytic reaction process. The reaction rate constant of the photocatalytic composite filaments is nearly 4.0 times higher than that of the PET filaments loaded solely with TiO2 nanoparticles. The resultant photocatalytic composite filaments are evident to be capable of repeatedly photo-degrading MO dyes without losing its photocatalytic activity significantly

The protection of glycyrrhetinic acid (GA) towards acetaminophen (APAP)-induced toxicity partially through fatty acids metabolic pathway

Background: Acetaminophen (APAP)-induced liver toxicity remains the key factor limiting the clinical application of APAP, and herbs are the important sources for isolation of compounds preventing APAP-induced toxicity.Aims: To investigate the protection mechanism of glycyrrhetinic acid towards APAP-induced liver damage using metabolomics method.Methods: APAP-induced liver toxicity model was made through intraperitoneal injection (i.p.) of APAP (400 mg/kg). Glycyrrhetinic acid was dissolved in corn oil, and intraperitoneal injection (i.p.) of glycyrrhetinic acid (500 mg/kg body weight) was performed for 20 days before the injection of APAP. UPLC-ESI-QTOF MS was employed to analyze the metabolomic profile of serum samples.Results: The pre-treatment of glycyrrhetinic acid significantly protected APAP-induced toxicity, indicated by the histology of liver, the activity of ALT and AST. Metabolomics showed that the level of   palmtioylcarnitine and oleoylcarnitine significantly increased in serum of APAP-treated mice, and the pre-treatment with GA can prevent this elevation of these two fatty acid-carnitines.Conclusion: Reversing the metabolism pathway of fatty acid is an important mechanism for the protection of glycyrrhetinic acid towards acetaminophen-induced liver toxicity.Keywords: Glycyrrhetinic acid (GA), acetaminophen (APAP), metabolomics, fatty aci

A Dispersive Analysis on the f0(600)f_0(600) and f0(980)f_0(980) Resonances in γγ→π+π−,π0π0\gamma\gamma\to\pi^+\pi^-, \pi^0\pi^0 Processes

We estimate the di-photon coupling of $f_0(600)$, $f_0(980)$ and $f_2(1270)$ resonances in a coupled channel dispersive approach. The $f_0(600)$ di-photon coupling is also reinvestigated using a single channel $T$ matrix for $\pi\pi$ scattering with better analyticity property, and it is found to be significantly smaller than that of a $\bar qq$ state. Especially we also estimate the di-photon coupling of the third sheet pole located near $\bar KK$ threshold, denoted as $f_0^{III}(980)$. It is argued that this third sheet pole may be originated from a coupled channel Breit-Wigner description of the $f_0(980)$ resonance.Comment: 24 pages and 13 eps figures. A nuerical bug in previous version is fixed. Some results changed. References and new figures added. Version to appear in Phys. Rev.