Identifying author–inventors from Spain: methods and a first insight into results

The purpose of this paper is twofold: methodological and empirical. Methodologically, we describe a matching and disambiguation procedure for the identification of author–inventors (researchers who publish and patent) located in the same country. Our methodology aims to maximize precision and recall rates by taking into account national name writing customs and country-specific dictionaries for person and institution names (academic and non-academic) in the name matching stage and by including a recursive validation step in the person disambiguation stage. An application of this methodology to the identification of Spanish author–inventors is described in detail. Empirically, we present the first results of applying the described methodology to the matching of all SCOPUS 2003–2008 publications of Spanish authors to all 1978–2009 EPO applications with Spanish inventors. Using this data, we identify 4,194 Spanish author–inventors. A first look at their patenting and publication patterns reveals that they make quite a significant contribution to the country’s overall scientific and technological production in the time period considered: 27 % of all EPO patent applications invented in Spain and 15 % of all SCOPUS publications authored in Spain, excluding non-technological disciplines. To our knowledge, this is the first time that a large scale identification of author–inventors from Spain has been done, with no limitation in terms of fields, regions or types of institutions. We also make available online for scientific use an anonymized subset of the database (patent applications invented by authors affiliated to Spanish public universities).     

Power consumption reduction through elastic data rate adaptation in survivable multi-layer optical networks

Network survivability requires the provisioning of backup resources in order to protect active traffic against any failure scenario. Backup resources, however, can remain unused most of the time while the network is not in failure condition, inducing high power consumption wastage, if fully powered on. In this paper, we highlight the power consumption wastage of the additional resources for survivability in IP/multi-protocol label switching (MPLS) over dense wavelength division multiplexing multi-layer optical networks. We assume MPLS protection switching as the failure recovery mechanism in the network, a solution interesting for current network operators to ensure fast recovery as well as fine-grained recovery treatment per label switched path. Next, we quantitatively show how elastic optical technologies can effectively reduce such a power consumption by dynamically adjusting the data rate of the transponders to the carried amount of traffic.     

Does place of publication influence citation behavior?

Two separate studies have looked at the question of whether or not the sources cited by scientists when they publish in their own national journals differ somewhat from the sources they cite when they publish outside their own country. Data derived from studies of Philippine scientists and Korean mathematicians do suggest that place of publication may exert some influence on citation behavior. In particular, a scientist is more likely to cite national sources when publishing in a national journal than when publishing internationally.     

Concentrations of polychlorinated biphenyls in indoor air and polybrominated diphenyl ethers in indoor air and dust in Birmingham, United Kingdom: implications for human exposure

Polybrominated diphenyl ethers (PBDEs) and polychlorinated biphenyls (PCBs) were measured in air (using PUF disk passive samplers) in 31 homes, 33 offices, 25 cars, and 3 public microenvironments. Average concentrations of sigmaBDE (273 pg m(-3)) and sigmaPCB (8920 pg m(-3)) were an order of magnitude higher than those previously reported for outdoor air. Cars were the most contaminated microenvironment for sigmaBDE (average = 709 pg m(-3)), but the least for sigmaPCB (average = 1391 pg m(-3)). Comparison with data from a previous spatially consistent study, revealed no significant decline in concentrations of sigmaPCB in indoor air since 1997-98. Concentrations in indoor dust from 8 homes were on average 215.2 ng sigmaBDE g(-1), slightly higher than other European dust samples, but twenty times lower than Canadian samples. Inhalation makes an important contribution (between 4.2 and 63% for adults) to overall UK exposure to sigmaPCB. For sigmaBDE, dust ingestion makes a significant but--in contrast to Canada-a not overwhelming contribution (up to 37% for adults, and 69% for toddlers). Comparison of UK and Canadian estimates of absolute exposure to sigmaBDE suggest that differences in dust contamination are the likely cause of higher PBDE body burdens in North Americans compared to Europeans.     

Measurement of T1 and T2 relaxation times of the pancreas at 7 T using a multi-transmit system

Objective

To determine T₁ and T₂ relaxation times of healthy pancreas parenchyma at 7 T using a multi-transmit system.

Materials and methods

Twenty-six healthy subjects were scanned with a 7 T MR system using eight parallel transceiver antennas, each with two additional receive loops. A Look-Locker sequence was used to obtain images for T₁ determination, while T₂ was obtained from spin-echo images and magnetic resonance spectroscopy measurements with different echo times. T₁ and T₂ times were calculated using a mono-exponential fit of the average magnitude signal from a region of interest in the pancreas and were tested for correlation with age.

Results

The age range of the included subjects was 21–72 years. Average T₁ and T₂ relaxation times in healthy pancreas were 896 ± 149 ms, and 26.7 ± 5.3 ms, respectively. No correlation with age was found.

Conclusion

T₁ and T₂ relaxation times of the healthy pancreas were reported for 7 T, which can be used for image acquisition optimization. No significant correlations were found between age and T₁ or T₂ relaxation times of the pancreas. Considering their low standard deviation and no observable age dependence, these values may be used as a baseline to study potentially pancreatic tissue affected by disease.

     

Optimization of rhein-loaded polymeric nanoparticles using a factorial design and evaluation of the cytotoxic and anti-inflammatory effects

The aim of the work was to develop rhein loaded polymeric nanoparticles (R-PNPs). Nanoparticles were prepared by three methods, solvent emulsion-evaporation, double emulsion, and nanoprecipitation, by means of experimental design. Additionally, the effects of the best formulation on in vitro cytotoxicity and inflammation were evaluated. The solvent emulsion-evaporation method presented the highest encapsulation efficiency of the three techniques (38.41%), as well as had a mean diameter of 189.33?nm and a polydispersity index of less than 0.1. Despite efforts to optimize the encapsulation of rhein, the drug release from nanoparticles was close to 50% during the first 5?min, followed by a continuous release within 60?min. It was observed that macrophages exposed to the highest concentration of R-PNPs showed cell viability about 80% and at the lowest nanoparticle concentrations was closed to 100%. IL-1β in cell culture supernatants was decreased in the presence of R-PNPs and TNFα concentrations were lower than the sensitivity of the assay. ROS production was only inhibited with R-PNPs at concentrations of 2.5 and 5?μM. In conclusion, the solvent emulsion-evaporation was the best method evaluated to obtain nanoparticles with the desired specifications. It was possible to assess R-PNPs with low cytotoxicity and anti-inflammatory properties showed by the inhibition of IL-1β production and a low decrease in ROS production.     

Tuning Sulfur Oxidation States on Thioether‐Bridged Peptide Macrocycles for Modulation of Protein Interactions

Thioethers, sulfoxides, and sulfonium ions, despite diverse physicochemical properties, all engage in noncovalent interactions with proteins. Thioether‐containing macrocycles are also attracting attention as protein–protein interaction (PPI) inhibitors. Here, we used a model PPI between α‐helical mixed lineage leukemia (MLL) protein and kinase‐inducible domain interacting (KIX) domain to evaluate oxidation effects on sulfurcontaining macrocycle structure, stability, and protein affinity. Desolvation effects from various polarity states were evaluated computationally and experimentally at the side chain, amino acid, and peptide level. Sulfur‐containing side chains spanned polarity ranges between all‐hydrocarbon and lactam bridges for modulating solubility, cellular uptake, and affinity. Helical propensity studies showed that, although oxidized sulfur‐containing side chains could be tolerated, conformational effects were sequence‐dependent. In some cases, proteolytic stability, binding capacity with KIX, and increased helicity were obtained as first steps toward developing PPI inhibitors.     

Release of liposome-encapsulated calcein from liposome entrapping gelatin-carboxymethylcellulose films: a presentation of different possibilities

Liposome entrapment in films consisting of gelatin (GEL) or GEL/sodium carboxymethylcellulose (NaCMC) mixtures, as a method to alter drug release kinetics from polymeric films and/or incorporate sensitive bioactive molecules in solid films, was investigated. Bulk or thin complex (liposome trapping) films were formed by crosslinking (with glutaraldehyde) solutions of GEL or GEL/NaCMC in presence of calcein-encapsulating or rhodamine-labeled liposomes (Rho-Lip). Rho-Lip were observed by confocal microscopy to be homogenously distributed in the films. Calcein release from films was evaluated for periods up to 25 d, and it was found that several possibilities, concerning the release of the liposome-encapsulated molecule from the films, are offered; (i) Release can be sustained, if large liposomes are entrapped in the films. In this case the liposome-encapsulated molecules are released from the films only after they have been released from the vesicles, and the release can be controlled by modifying the film composition, the network density and/or the film geometry. (ii) Intact small unilamellar liposomes (SUV) can be released from the polymeric films depending on their swelling degree. The later can be controlled by modulating the film composition and amount of crosslinker. Film composition also affects the integrity of the film-entrapped liposomes during the crosslinking process, possibly due its effect on the density of the polymeric network of the film.