Concentrations of VOCs and ozone in indoor environments: A case study in two Mediterranean cities during winter period

Building materials represent the largest surfaces indoors and are the major contributors of volatile organic compounds (VOCs) in the indoor environment. This study which is conducted in the frame of BUMA project (Prioritization of Building Materials Emissions), aims at assessing the human exposure to air hazards emitted by building materials. In this study, indoor and outdoor VOCs and ozone measurements from field campaigns in two Mediterranean cities (Nicosia and Athens in winter period) are presented and discussed. The field campaigns concern weekly measurements. The campaigns were conducted in four buildings in each city (1 Public building, 1 school and 2 houses) and concern weekly measurements. Passive samplers were used for collecting VOCs and ozone. Eight (8) hydrocarbons (benzene, toluene, ethylbenzene, m,p-xylene, a-pinene, o-xylene and d-limonene), five (5) carbonyl compounds (formaldehyde, acetaldehyde, proprionaldehyde, acetone and hexanaldehyde) and ozone have been measured. Additional air exchange measurements have been conducted using tracer gas techniques. Hazardous substances such as benzene, formaldehyde and acetaldehyde present indoor concentrations that range between 1.5-10.2, 5.8-43.2 and 4.5-15 μg/m3, respectively. VOC concentration data show a considerable variability due to the different indoor emission sources, ventilation rates and outdoor environment's influence. A significant contribution to indoor measured concentrations seems to come from the building materials. Ozone outdoor concentrations are reduced substantially inside, indicating relatively strong indoor ozone sinks

Calculating the energy spectra of magnetic molecules: application of real- and spin-space symmetries

The determination of the energy spectra of small spin systems as for instance given by magnetic molecules is a demanding numerical problem. In this work we review numerical approaches to diagonalize the Heisenberg Hamiltonian that employ symmetries; in particular we focus on the spin-rotational symmetry SU(2) in combination with point-group symmetries. With these methods one is able to block-diagonalize the Hamiltonian and thus to treat spin systems of unprecedented size. In addition it provides a spectroscopic labeling by irreducible representations that is helpful when interpreting transitions induced by Electron Paramagnetic Resonance (EPR), Nuclear Magnetic Resonance (NMR) or Inelastic Neutron Scattering (INS). It is our aim to provide the reader with detailed knowledge on how to set up such a diagonalization scheme.Comment: 29 pages, many figure

A preclinical evaluation of pemetrexed and irinotecan combination as second-line chemotherapy in pancreatic cancer

Gemcitabine (GEM)-based chemotherapy is regarded as the standard treatment of pancreatic adenocarcinoma, but yields a very limited disease control. Very few studies have investigated salvage chemotherapy after failure of GEM or GEM-containing chemotherapy and preclinical studies attempting to widen the therapeutic armamentarium, not including GEM, are warranted. MIA PaCa2, CFPAC-1 and Capan-1 pancreatic cancer cell lines were treated with GEM, fluouracil (5-FU), docetaxel (DCT), oxaliplatin (OXP), irinotecan (CPT-11), pemetrexed (PMX) and raltitrexed (RTX) as single agent. Pemetrexed, inducing apoptosis with IC50s under the Cmax in the three lines tested, appeared the most effective drug as single agent. Based on these results, schedule- and concentration-dependent drug interactions (assessed using the combination index) of PMX/GEM, PMX/DCT and PMX–CPT-11 were evaluated. The combinatory study clearly indicated the PMX and CPT-11 combination as the most active against pancreatic cancer. To confirm the efficacy of PMX–CPT-11 combination, we extended the study to a panel of 10 pancreatic cancer cell lines using clinically relevant concentrations (PMX 10 μM; CPT-11 1 μm). In eight of 10 lines, the PMX–CPT-11 treatment significantly reduced cell recovery and increased both the subG1 and caspase 3/7 fraction. After a 5-day wash out period, an increased fraction of subG1 and caspase3/7 persisted in PMX–CPT-11-pretreated cell lines and a significant reduction in the clonogenicity capacity was evident. Finally, in vivo, the PMX/CPT-11 combination showed the ability to inhibit xenograft tumours growth as second-line therapy after GEM treatment. The PMX and CPT-11 combination displays a strong schedule-independent synergistic cytotoxic activity against pancreatic cancer, providing experimental basis for its clinical testing as salvage chemotherapy in pancreatic cancer patients