143 research outputs found
Highly Efficient Photocatalytic Hydrogen Evolution Using a Self-Assembled Octupolar Molecular System
Reversible and Irreversible Interactions of Poly(3-hexylthiophene) with Oxygen Studied by Spin-Sensitive Methods
Understanding of degradation mechanisms in polymer:fullerene
bulk-heterojunctions on the microscopic level aimed at improving their
intrinsic stability is crucial for the breakthrough of organic photovoltaics.
These materials are vulnerable to exposure to light and/or oxygen, hence they
involve electronic excitations. To unambiguously probe the excited states of
various multiplicities and their reactions with oxygen, we applied combined
magneto-optical methods based on multifrequency (9 and 275 GHz) electron
paramagnetic resonance (EPR), photoluminescence (PL), and PL-detected magnetic
resonance (PLDMR) to the conjugated polymer poly(3-hexylthiophene) (P3HT) and
polymer:fullerene bulk heterojunctions (P3HT:PCBM; PCBM =
[6,6]-phenyl-C61-butyric acid methyl ester). We identified two distinct
photochemical reaction routes, one being fully reversible and related to the
formation of polymer:oxygen charge transfer complexes, the other one,
irreversible, being related to the formation of singlet oxygen under
participation of bound triplet excitons on the polymer chain. With respect to
the blends, we discuss the protective effect of the methanofullerenes on the
conjugated polymer bypassing the triplet exciton generation
Tracing of backward energy transfer from LH1 to LH2 in photosynthetic membranes grown under high and low irradiation.
By introducing derivative transient absorption spectroscopy, we obtain rate constants for backward and forward energy transfer between LH1 and LH2 complexes in purple bacterial membranes. We find that backward energy transfer is strongly reduced in membranes grown under low irradiation conditions, compared to high light grown ones. We conclude that backward energy transfer is managed actively by the bacteria to avoid LH1 exciton deactivation under high irradiation conditions. The analytical method is generally applicable to excitonically coupled systems
Epithelial Proinflammatory Response and Curcumin-Mediated Protection from Staphylococcal Toxic Shock Syndrome Toxin-1
Staphylococcus aureus initiates infections and produces virulence factors, including superantigens (SAgs), at mucosal surfaces. The SAg, Toxic Shock Syndrome Toxin-1 (TSST-1) induces cytokine secretion from epithelial cells, antigen presenting cells (APCs) and T lymphocytes, and causes toxic shock syndrome (TSS). This study investigated the mechanism of TSST-1-induced secretion of proinflammatory cytokines from human vaginal epithelial cells (HVECs) and determined if curcumin, an anti-inflammatory agent, could reduce TSST-1-mediated pathology in a rabbit vaginal model of TSS. TSST-1 caused a significant increase in NF-κB-dependent transcription in HVECs that was associated with increased expression of TNF- α, MIP-3α, IL-6 and IL-8. Curcumin, an antagonist of NF-κB-dependent transcription, inhibited IL-8 production from ex vivo porcine vaginal explants at nontoxic doses. In a rabbit model of TSS, co-administration of curcumin with TSST-1 intravaginally reduced lethality by 60% relative to 100% lethality in rabbits receiving TSST-1 alone. In addition, TNF-α was undetectable from serum or vaginal tissue of curcumin treated rabbits that survived. These data suggest that the inflammatory response induced at the mucosal surface by TSST-1 is NF-κB dependent. In addition, the ability of curcumin to prevent TSS in vivo by co-administration with TSST-1 intravaginally suggests that the vaginal mucosal proinflammatory response to TSST-1 is important in the progression of mTSS
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