Assessment of carcinogenic risk due to inhalation of polycyclic aromatic hydrocarbons in PM10 from an industrial city: a Korean case-study

This study investigated the effects of meteorological conditions and spatial variations on the toxicity of polycyclic aromatic hydrocarbons (PAHs) in airborne PM(10) in Ulsan, the largest industrial city in Korea. Daily PM(10) samples were collected on quartz microfiber filters using high volume samplers located in a downtown area, a residential area and an industrial area of Ulsan during spring and summer sampling periods. Sixteen individual PAHs were extracted into a mixture solution of dichloromethane and n-hexane (1:1, v/v) in an ultrasonic bath and were analyzed using a high performance liquid chromatography system with an ultra-violet detector (HPLC-UVD). The average total PAH concentrations from the three representative sampling sites of Ulsan ranged from 16.15 to 57.12 ng/m(3) in spring and from 11.11 to 34.56 ng/m(3) in summer. The toxicity equivalent concentrations (TEQs) of the PAHs in PM(10) of Ulsan ranged from 1.82 to 13.1 ng/m(3), with an average level of 4.17 ng/m(3). The highest TEQs were found in the downtown area, which had an average value of 6.30 ng/m(3) in spring and 5.52 ng/m(3) in summer. BaP and DahA were identified as the major carcinogenic PAHs that contributed to 34.8 and 59.4% of the total carcinogenic potency of PAHs in PM(10) in Ulsan. The identified TEQs were highly correlated (r(2) = 0.73-0.90, p<0.01) with the total PAH concentrations for each area. The TEQs showed a significant correlation (p < 0.01) with the concentration of air pollutants, including PM(10), PM(2.5) and NO(2).     

Water: a responsive small molecule

Unique among small molecules, water forms a nearly tetrahedral yet flexible hydrogen-bond network. In addition to its flexibility, this network is dynamic: bonds are formed or broken on a picosecond time scale. These unique features make probing the local structure of water challenging. Despite the challenges, there is intense interest in developing a picture of the local water structure due to water's fundamental importance in many fields of chemistry. Understanding changes in the local network structure of water near solutes likely holds the key to unlock problems from analyzing parameters that determine the three dimensional structure of proteins to modeling the fate of volatile materials released into the atmosphere. Pictures of the local structure of water are heavily influenced by what is known about the structure of ice. In hexagonal I(h) ice, the most stable form of solid water under ordinary conditions, water has an equal number of donor and acceptor bonds; a kind of symmetry. This symmetric tetrahedral coordination is only approximately preserved in the liquid. The most obvious manifestation of this altered tetrahedral bonding is the greater density in the liquid compared with the solid. Formation of an interface or addition of solutes further modifies the local bonding in water. Because the O-H stretching frequency is sensitive to the environment, vibrational spectroscopy provides an excellent probe for the hydrogen-bond structure in water. In this Account, we examine both local interactions between water and small solutes and longer range interactions at the aqueous surface. Locally, the results suggest that water is not a symmetric donor or acceptor, but rather has a propensity to act as an acceptor. In interactions with hydrocarbons, action is centered at the water oxygen. For soluble inorganic salts, interaction is greater with the cation than the anion. The vibrational spectrum of the surface of salt solutions is altered compared with that of neat water. Studies of local salt-water interactions suggest that the picture of the local water structure and the ion distribution at the surface deduced from the surface vibrational spectrum should encompass both ions of the salt.     

Gold nanoparticle effects in polymerase chain reaction: favoring of smaller products by polymerase adsorption

Gold nanoparticles were recently reported to reduce the formation of nonspecific products in polymerase chain reaction (PCR) at remarkably low temperatures, with hypothesized mechanisms including adsorption of DNA and heat-transfer enhancement. In contrast to these reports, we report that gold nanoparticles do not enhance the specificity of PCR but rather suppress the amplification of longer products while favoring amplification of shorter products, independent of specificity. Gold nanoparticles bearing a self-assembled monolayer of hexadecanethiol did not affect PCR, suggesting that surface interactions play an essential role. This role was further confirmed by experiments in which a similar effect on PCR was observed for the same total surface area of particles over a 100-fold range of per-particle surface area. The effect was seen with Taq and Tfl polymerases but not with Vent polymerase, and the effects of nanoparticles can be reversed by increasing the polymerase concentration or by adding bovine serum albumin (BSA). Transient high-temperature nanoparticle pre-exposure of PCR mix containing polymerase but not template or primers, followed by nanoparticle removal, modified subsequent nanoparticle-free PCR. Interaction between polymerase and gold nanoparticles was confirmed by changes in nanoparticle absorption spectrum and electrophoretic mobility in the presence of polymerase. Taken together, these results suggest that the nanoparticles nonspecifically adsorb polymerase, thus effectively reducing polymerase concentration.     

D-(+)-iso-methanocarbathymidine: a high-affinity substrate for herpes simplex virus 1 thymidine kinase

The stereoselective syntheses of the (+)-D and (-)-L enantiomers of iso-methanocarbathymidine (iso-MCT) was achieved through two independent linear approaches that converged on two antipodal enantiomers, common to a key precursor used in the synthesis of racemic iso-MCT. In the study reported herein we identified (+)-3 [D-(+)-iso-MCT] as the active enantiomer that was exclusively recognized by the herpes simplex virus 1 thymidine kinase (HSV1-tk), as was predicted by molecular modeling. For this purpose, a human osteosarcoma (HOS) cell line modified to contain and express HSV1-tk from herpes simplex virus 1 (HSV1) was used to determine the cytotoxicity of the compounds by an assay that measures the level of ATP in the cells. The work demonstrates that changes in the substitution pattern of rigid bicyclo[3.1.0]hexane nucleosides, which, relative to normal nucleosides, appear unconventional, can lead to the spatial optimization of pharmacophores and vastly improved substrate recognition.     

The Effect of Brine Ingredients on Carrot Texture during Thermal Processing in Relation to Pectin Depolymerization due to the β-Elimination Reaction

ABSTRACT:  Thermal texture degradation of carrots was studied at a temperature of 100 °C in aqueous solutions containing sodium chloride, citric acid, ascorbic acid, and ethylenediaminetetraacetic acid (EDTA) at different concentrations. To enhance the texture of the final product, the carrot samples were pretreated at 65 °C for 30 min in an aqueous calcium chloride solution (5 g/L). For all case studies considered, the pH of the solutions was adjusted to pH = 6.0. In parallel, both the changes in degree of esterification (DE) and the progress of the β-elimination reaction of carrot pectin under the same conditions were investigated. The kinetic parameters for texture degradation (rate constant k_t and final texture value [TP_∞/TP₀]) were estimated using a fractional conversion model. The results indicate that both the rate constant for texture degradation ( k_t ) and the rate constant for the β-elimination reaction ( k_b ) increased with increasing additive concentration, while the final texture values (TP_∞/TP₀) and DE decreased with increasing additive concentration in all systems studied. A high correlation was observed between the relative rate constant for texture degradation and the relative rate constant for the β-elimination reaction on the one hand, and the relative final texture value and the relative rate constant for the β-elimination reaction on the other hand, suggesting that the influence of the solutes on texture degradation can be explained by their influence on the β-elimination reaction.     

X‐ray diffraction,Raman, and differential thermal analyses of the thermal aging of a Kevlar®‐PBI blend fabric

A previous study of the effects of thermal aging on the tensile properties of a fabric made of a 60–40 wt % blend of Kevlar and PBI fibers has shown that exposure to elevated temperatures between 190 and 320°C results in a rapid decrease in tensile breaking force retention. In this article, X‐ray diffraction and Raman spectroscopy analyses were carried out to evaluate the consequences of thermal aging on the material's crystallinity. Differential thermal analyses were also undertaken to examine the evolution of the glass transition temperature of PBI following thermal exposure. X‐ray diffraction profiles show a gradual increase in the crystallinity with temperature and aging time, whereas a complete disappearance of spectral lines for aged samples in Raman analysis suggests instead a decrease in crystallinity as a consequence of exposure to elevated temperatures. The seemingly contradictory outcome obtained when using the two techniques led to the proposal of a new, alternative hypothesis to explain the observed results. This hypothesis involves two simultaneous events that occur during thermal aging: the increase of crystallite size in the direction parallel to coplanar sheets, and the disruption of the crystalline lattice in the direction perpendicular to those sheets. The glass transition temperature of PBI was found to shift towards the lower temperatures after thermal aging, a phenomenon that can be associated with random polymer chain scission caused by thermal aging. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Optimising water and phosphorus management in the urban environmental sanitation system of Hanoi, Vietnam

Many areas in the world face clean water scarcity problems and phosphorus reserves are likely to be depleted in the near future. Still, a large amount of clean water is used to transport excreta through sewer systems. Most of the wastewater generated worldwide is discharged untreated into aquatic systems and leads to water pollution and loss of valuable nutrients. In Hanoi, Vietnam's capital city, high population and economic growth as well as industrialisation have led to a decrease in groundwater level and to serious river and lake pollution. A probabilistic model, simulating the impact of measures on groundwater abstraction and nutrient recovery, was used to determine the impact of policy changes in Hanoi. The results obtained reveal that harmonising environmental sanitation and agricultural systems with one another will considerably increase nutrient recovery for food production, lower expenditure for artificial fertilisers and reduce the nutrient load into the environment. The model can be applied in urban areas of developing countries to assist in the design of environmental sanitation concepts.     

Comparisons of fish meat extract desalination by electrodialysis using different configurations of membrane stack

The desalination of fish meat extract was performed via electrodialysis based on different membrane stack configurations (i.e., conventional electrodialysis or packed-bed electrodialysis) at a constant current. The salt removal and brix change showed that the diluted fish meat extract could be effectively desalted using electrodialysis, while the mostly nutritional ingredients remained in the dilution. Compared with the conventional electrodialysis (ED), a lower membrane stack potential meant lower energy consumption and higher current efficiency for the same salt removal in the packed-bed electrodialysis (PBED). The results indicated that the PBED might be more suitable for use in the fish meat extract desalination due to the effects of ion exchange resins in enhancing ion electromigration and mitigating membrane fouling.     

Inverted mesa-type quartz crystal resonators fabricated by deep-reactive ion etching

In this letter, we present experimental data showing Q change versus thickness for a quartz-crystal resonator fabricated with deep-reactive ion etching. Measurements show that Q increases as etch depth increases, and further that Q can be optimized as a function of etch depth and diameter of the resonator.