Impact of cattle slurry application methods on ammonia losses and grassland nitrogen use efficiency.

Optimal manure management is required to ensure efficient nutrient supply to farmland and to avoid adverse environmental impacts. Accordingly, ammonia (NH3) emissions associated with different slurry application techniques were investigated in grassland trials under different soil and weather conditions across Germany. Cattle slurry was applied in two dressings, early in spring and after the first silage cut, with a target amount of 170 kg N ha-1. The application treatments comprised: trailing shoe (TS), acidified slurry applied with trailing shoe (TS + A), open slot injection (SI), and slurry treated with a nitrification inhibitor (NI) applied by slot injection (SI + NI). In addition, slurry application techniques were compared with a non-N-fertilized control and a mineral fertilizer treatment (calcium ammonium nitrate, CAN). NH3 measurements followed each N application event. NH3 losses were equivalent to 1-39% of total ammoniacal nitrogen (TAN) applied. The average NH3 mitigation potential of the different slurry application techniques compared to TS was 45.7 ± 7, 21.2 ± 6.2 and 13.7 ± 8.2% for TS + A, SI and SI + NI, respectively. The use of nitrification inhibitor with slot injected slurry did not increase NH3 losses relative to TS (p > 0.05). Mean apparent N use efficiency was two times higher for CAN (49%) than the slurry treatments (24%) but was comparable between SI + NI and CAN in five out of the eight cases. Our results indicate that mean TAN related NH3 emissions of tested treatments (3.3, 22.6, 12.2, 17.8 and 19.3% for CAN, TS, TS + A, SI and SI + NI, respectively) were generally lower than described in previous studies. Moreover, the results suggested possible increases in NH3 mitigation and N use efficiency when cattle slurry is applied with acidification or injection techniques. We found no evidence that NI addition to slot injected slurry, a treatment discussed as a measure to reduce N2O emission and nitrate leaching, changed NH3 emission.

Spectral characteristics of the supramolecular complexes of polypyrrolic sensitizers and cyclodextrin carriers: usage in photodynamic therapy of tumors.

The objective of our work was to describe the photophysical properties (absorption and fluorescence) of the sensitizers TPPS4, ZnTPPS4 a PdTPPS4 and above all the complexes of these sensitizers with cyclodextrin carriers HP-alpha-CD, HP-beta-CD and HP-gamma-CD (2-hydroxypropyl-alpha, beta, gamma-cyclodextrin) in a suitable environment for the cultivation of cancerous cell lines, and to determine the optimal radioactive conditions for maximizing photodynamic effects in cancerous cells.

The cellular uptake of sensitizers bound to cyclodextrin carriers.

Photodynamic therapy of cancer uses the interaction of sensitizers and light to destroy cancer cells. In this study we tested the cellular uptake of meso-tetrakis(4-sulfonatophenyl)porphine (TPPS4) and its complex PdTPPS4 in the presence or absence of 2-hydroxypropyl-cyclodextrins (hpCDs) on G361 human melanoma cells. Self-fluorescence in G361 cells were measured by Perkin-Elmer LS50B luminometer equipped with well plate reader accessory. Morphological changes in cells have been evaluated using inversion fluorescent microscope Olympus IX 70 and image analysis. The uptake of the sensitizer PdTPPS4 at the given time interval from 1 to 48 hours is markedly higher than the uptake of TPPS4. The highest uptake was found for sensitizer PdTPPS4 in combination with hpbetaCD. TPPS4 and PdTPPS4 especially in the supramolecular complex with nontoxic cyclodextrin carriers represent efficient sensitizers for photodynamic therapy in vitro on G361 cells.

Assessment of cellular damage by comet assay after photodynamic therapy in vitro.

The aim of this study was analysis of DNA damage in the cell line of the human melanoma G361 after photodynamic therapy (PDT) by comet assay. Photodynamic therapy is based on cytotoxic action of sensitizers (10 microM ZnTPPS4 fixed into 1 mM cyclodextrin hpbetaCD) and light with a suitable wavelength. Single-cell gel electrophoresis (SCGE, comet assay) is a rapid and sensitive method for detecting DNA strand breaks at the level of single cells. Great amount of DNA damage was detected with the dose of irradiation of 0.1; 0.5 J and 2.5 J x cm(-2). Only radiation dose of visible light in the presence of sensitizers can induce DNA breaks of tumour cells. Cells with DNA damage appear as fluorescent comets with tails of DNA fragmentation. In contrast, cells with undamage DNA appear as round spots, because their intact DNA does not migrate out of the cell.