Removal of lindane using electrokinetic soil flushing coupled with air stripping

Journal of Applied Electrochemistry - This paper evaluates the remediation of soil spiked with lindane using a combined treatment consisting of electrokinetic soil flushing (EKSF) with air...     

Size of web domains and interlinking behavior of higher education institutions in Europe

The aim of this paper is to empirically test whether interlinking patterns between higher education institutions (HEIs) conform to a document model, where links are motivated by webpage content, or a social relationship model, where they are markers of underlying social relationships between HEIs. To this aim, we analyzed a sample of approximately 400 European HEIs, using the number of pages on their web domains and the total number of links sent and received; in addition we test whether these two characteristics are associated with organizational size, reputation, and the volume of teaching and research activities. Our main findings are as follows: first, the number of webpages of HEI websites is strongly associated with their size, and to a lesser extent, with the volume of their educational activities, research orientation, and reputation; differences between European countries are rather limited, supporting the insight that the academic Web has reached a mature stage. Second, the distribution of connectivity (as measured by the total degree of HEI’s) follows a lognormal distribution typical of social networks between organizations, while counts of weblinks can be predicted with good precision from organizational characteristics. HEIs with larger websites tend to send and receive more links, but the effect is rather limited and does not fundamentally modify the resulting network structure. We conclude that aggregated counts of weblinks between pairs of HEIs are not significantly affected by the web policies of HEIs and thus can be considered as reasonably robust measures. Furthermore, interlinking should be considered as proxies of social relationships between HEIs rather than as reputational measures of the content published on their websites.     

Structural Determinants of the Selectivity of 3‐Benzyluracil‐1‐acetic Acids toward Human Enzymes Aldose Reductase and AKR1B10

The human enzymes aldose reductase (AR) and AKR1B10 have been thoroughly explored in terms of their roles in diabetes, inflammatory disorders, and cancer. In this study we identified two new lead compounds, 2‐(3‐(4‐chloro‐3‐nitrobenzyl)‐2,4‐dioxo‐3,4‐dihydropyrimidin‐1(2H)‐yl)acetic acid (JF0048, 3 ) and 2‐(2,4‐dioxo‐3‐(2,3,4,5‐tetrabromo‐6‐methoxybenzyl)‐3,4‐dihydropyrimidin‐1(2H)‐yl)acetic acid (JF0049, 4 ), which selectively target these enzymes. Although 3 and 4 share the 3‐benzyluracil‐1‐acetic acid scaffold, they have different substituents in their aryl moieties. Inhibition studies along with thermodynamic and structural characterizations of both enzymes revealed that the chloronitrobenzyl moiety of compound 3 can open the AR specificity pocket but not that of the AKR1B10 cognate. In contrast, the larger atoms at the ortho and/or meta positions of compound 4 prevent the AR specificity pocket from opening due to steric hindrance and provide a tighter fit to the AKR1B10 inhibitor binding pocket, probably enhanced by the displacement of a disordered water molecule trapped in a hydrophobic subpocket, creating an enthalpic signature. Furthermore, this selectivity also occurs in the cell, which enables the development of a more efficient drug design strategy: compound 3 prevents sorbitol accumulation in human retinal ARPE‐19 cells, whereas 4 stops proliferation in human lung cancer NCI‐H460 cells.     

Survey on the content of vitisin A and hydroxyphenyl-pyranoanthocyanins in Tempranillo wines

Little is known about the content and development of pyranoanthocyanins, pigments mainly formed during red wine ageing, in commercial wines. Some of the major pyranoanthocyanins in a wide selection of 1–10 years-old Spanish Tempranillo wines and also in a 29 years wide-vertical series of Tempranillo wines from an individual cellar have been determined. Great variability in pyranoanthocyanin concentrations was found (range, mg/l): vitisin A, 0–10.76; pinotin A, 0–4.26; and malvidin 3-glucoside-4-vinylphenol, 0.03–1.37. Vitisin A and malvidin 3-glucoside-4-vinylphenol were already present in 1–2 years-old wines, whereas pinotin A was only detectable in a few of the 1 and 2 years-old wines. Vitisin A tended to decrease with wine age, while hydroxyphenyl-pyranoanthocyanins showed the reverse trend. However, the aforementioned trends were interrupted by various temporary maxima, most likely due to some “refreshment” of the oldest wines (i.e., addition of young wine), as suggested by unexpected high concentrations of malvidin 3-glucoside, in contrast to the results found in the wine vertical series. The effects of addition of young wine on aged wine pyranoanthocyanin concentrations were confirmed by wine refreshment experiments.     

How old is the Web? Characterizing the age and the currency of the European scientific Web

The aim of this paper is to model and study the age of the Web using a sample of about four million of web pages from the 16 European Research Area countries obtained during 2004 and 2005. Web page time-stamp (date when the web pages were created or last changed for last time), format and size in bytes data have been analysed. Several indicators are introduced to measure longitudinal aspects of the Web. Half-age is proposed as a measure of the age distribution because this is found to be exponential. “Web Update Index” and “Lifespan Index” are introduced to measure the changing rate of a small sample over time. Results show that the British Web space has the youngest Web pages while the Greek and Belgian ones have the oldest. The study also compared Web pages topics and found that Biology pages are more stable than Physics pages.     

Visibility of collaboration on the Web

The emerging influence of new information and communication technologies (ICT) on collaboration in science and technology has to be considered. In particular, the question of the extent to which collaboration in science and in technology is visible on the Web needs examining. Thus the purpose of this study is to examine whether broadly similar results would occur if solely Web data was used rather than all available bibliometric co-authorship data. For this purpose a new approach of Web visibility indicators of collaboration is examined. The ensemble of COLLNET members is used to compare co-authorship patterns in traditional bibliometric databases and the network visible on the Web. One of the general empirical results is a high percentage (78%) of all bibliographic multi- authored publications become visible through search of engines in the Web. One of the special studies has shown Web visibility of collaboration is dependent on the type of bibliographic multi-authored papers. The social network analysis (SNA) is applied to comparisons between bibliographic and Web collaboration networks. Structure formation processes in bibliographic and Web networks are studied. The research question posed is to which extent collaboration structures visible in the Web change their shape in the same way as bibliographic collaboration networks over time. A number of special types of changes in bibliographic and Web structures are explained. This revised version was published online in June 2006 with corrections to the Cover Date.     

Simulation of transport and extravasation of nanoparticles in tumors which exhibit enhanced permeability and retention effect

Determining the factors that influence the delivery of sub-micron particles to tumors and understanding the relative importance of each of these factors is fundamental to the optimization of the particle delivery process. In this paper, a model that combines random walk with the pressure driven movement of nanoparticles in a tumor vasculature is presented. Nanoparticle movement in a cylindrical tube with dimensions similar to the tumor's blood capillary with a single pore is simulated. Nanoparticle velocities are calculated as a pressure driven flow over imposed to Brownian motion. The number and percentage of nanoparticles leaving the blood vessel through a single pore is obtained as a function of pore size, nanoparticle size and concentration, interstitial pressure, and blood pressure. The model presented here is able to determine the importance of these controllable parameters and thus it can be used to understand the process and predict the best conditions for nanoparticle-based treatment. The results indicate that the nanoparticle delivery gradually increases with pore size and decreases with nanoparticle size for tumors with high interstitial fluid pressure (in this work we found this behavior for head and neck carcinoma and for metastatic melanoma with interstitial pressures of 18 mmHg and 19 mmHg, respectively). For tumors with lower interstitial fluid pressure (rectal carcinoma with 15.3 mmHg) however, delivery is observed to have little sensitivity to particle size for almost the entire nanoparticle size range. Though an increase in nanoparticle concentration increases the number of nanoparticles being delivered, the efficiency of the delivery (percentage of nanoparticles delivered) is found to remain closely unaffected.     

Tau Exon 10 Inclusion by PrPC through Downregulating GSK3β Activity

Tau protein is largely responsible for tauopathies, including Alzheimer’s disease (AD), where it accumulates in the brain as insoluble aggregates. Tau mRNA is regulated by alternative splicing, and inclusion or exclusion of exon 10 gives rise to the 3R and 4R isoforms respectively, whose balance is physiologically regulated. In this sense, one of the several factors that regulate alternative splicing of tau is GSK3β, whose activity is inhibited by the cellular prion protein (PrP^C), which has different physiological functions in neuroprotection and neuronal differentiation. Moreover, a relationship between PrP^C and tau expression levels has been reported during AD evolution. For this reason, in this study we aimed to analyze the role of PrP^C and the implication of GSK3β in the regulation of tau exon 10 alternative splicing. We used AD human samples and mouse models of PrP^C ablation and tau overexpression. In addition, we used primary neuronal cultures to develop functional studies. Our results revealed a paralleled association between PrP^C expression and tau 4R isoforms in all models analyzed. In this sense, reduction or ablation of PrP^C levels induces an increase in tau 3R/4R balance. More relevantly, our data points to GSK3β activity downstream from PrP^C in this phenomenon. Our results indicate that PrP^C plays a role in tau exon 10 inclusion through the inhibitory capacity of GSK3β.