Identity-creators and image-makers: Using citation analysis and thick description to put authors in their place

We describe the steps involved in constructing authors" citation identities (whom they cite) and citation images (who cites them). Familiarity with the intellectual, social, and institutional connections of these authors over time helps inform the analysis and augment the specificity of citation counts. Our study shows that authors" writing and referencing styles constitute a form of watermark for their scholarly output.     

Enabling the interactive display of large medical volume datasets by multiresolution bricking

In this paper, we present an approach to interactive out-of-core volume data exploration that has been developed to augment the existing capabilities of the LhpBuilder software, a core component of the European project LHDL (). The requirements relate to importing, accessing, visualizing and extracting a part of a very large volume dataset by interactive visual exploration. Such datasets contain billions of voxels and, therefore, several gigabytes are required just to store them, which quickly surpass the virtual address limit of current 32-bit PC platforms. We have implemented a hierarchical, bricked, partition-based, out-of-core strategy to balance the usage of main and external memories. A new indexing scheme is introduced, which permits the use of a multiresolution bricked volume layout with minimum overhead and also supports fast data compression. Using the hierarchy constructed in a pre-processing step, we generate a coarse approximation that provides a preview using direct volume visualization for large-scale datasets. A user can interactively explore the dataset by specifying a region of interest (ROI), which further generates a much more accurate data representation inside the ROI. If even more precise accuracy is needed inside the ROI, nested ROIs are used. The software has been constructed using the Multimod Application Framework, a VTK-based system; however, the approach can be adopted for the other systems in a straightforward way. Experimental results show that the user can interactively explore large volume datasets such as the Visible Human Male/Female (with file sizes of 3.15/12.03 GB, respectively) on a commodity graphics platform, with ease.     

The Juxtaposed approximate PageRank method for robust PageRank approximation in a peer-to-peer web search network

We present Juxtaposed approximate PageRank (JXP), a distributed algorithm for computing PageRank-style authority scores of Web pages on a peer-to-peer (P2P) network. Unlike previous algorithms, JXP allows peers to have overlapping content and requires no a priori knowledge of other peers’ content. Our algorithm combines locally computed authority scores with information obtained from other peers by means of random meetings among the peers in the network. This computation is based on a Markov-chain state-lumping technique, and iteratively approximates global authority scores. The algorithm scales with the number of peers in the network and we show that the JXP scores converge to the true PageRank scores that one would obtain with a centralized algorithm. Finally, we show how to deal with misbehaving peers by extending JXP with a reputation model. Partially supported by the EU within the 6th Framework Programme under contract 001907 “Dynamically Evolving, Large Scale Information Systems” (DELIS).     

Multiple Structure Reconstruction by Dual Dynamic Crosslinking Strategy Inducing Self-Reinforcing and Toughening the Polyurethane/Nanocellulose Elastomers

High-performance elastomers are expected to possess excellent healing and recycling ability, damage resistance in conjunction with high strength and toughness. Herein, a dual dynamic crosslinking strategy is implemented by multiple hydrogen and disulfide bonds to obtain a novel amorphous and transparent polyurethane/nanocellulose elastomer with excellent self-healing, self-reinforcing and toughening performance. First, hydrogen bonds are introduced in TEMPO-oxidized cellulose nanofibers (TCNF) by modification with 2-ureido-4[1H]-pyrimidone (UTCNF), while disulfide bonds (SS) are introduced in the polyurethane (PU) main chain, leading to the formation of dual dynamic cross-linking networks. The PU-SS-UTCNF elastomer can fully self-heal within 4.0 h at 50 °C. Surprisingly, for the first time, the PU-SS-UTCNF elastomer also self-strengthens and self-toughens after multiple hot-pressing, with tensile strength and toughness that increase by up to 401% and 257% compared to original elastomer samples, up to 50.0 MPa and 132.5 MJ m^-3. The self-strength and self-toughening effects are attributed to 1) reconstruction of dual dynamic networks that increase the cross-linking degree during the multiple hot-pressing processes; 2) multiple hydrogen bonds in the system are beneficial to the orientation of highly crystallized UTCNF, as a replacement of stress-induced process in deformation under external tensile force.     

Broad-Spectrum Bactericidal Activity of a Synthetic Random Copolymer Based on 2-Methoxy-6-(4-Vinylbenzyloxy)-Benzylammonium Hydrochloride

Low-molecular-weight organic ammonium salts exert excellent antimicrobial effects by interacting lethally with bacterial membranes. Unfortunately, short-term functionality and high toxicity limit their clinical application. On the contrary, the equivalent macromolecular ammonium salts, derived from the polymerization of monomeric ammonium salts, have demonstrated improved antibacterial potency, a lower tendency to develop resistance, higher stability, long-term activity, and reduced toxicity. A water-soluble non-quaternary copolymeric ammonium salt (P7) was herein synthetized by copolymerizing 2-methoxy-6-(4-vinylbenzyloxy)-benzylammonium hydrochloride monomer with N, N-di-methyl-acrylamide. The antibacterial activity of P7 was assessed against several multidrug-resistant (MDR) clinical isolates of both Gram-positive and Gram-negative species. Except for colistin-resistant Pseudomonas aeruginosa, most isolates were susceptible to P7, also including some Gram-negative bacteria with a modified charge in the external membrane. P7 showed remarkable antibacterial activity against isolates of Enterococcus, Staphylococcus, Acinetobacter, and Pseudomonas, and on different strains of Escherichia coli and Stenotrophomonas maltophylia, regardless of their antibiotic resistance. The lowest minimal inhibitory concentrations (MICs) observed were 0.6–1.2 µM and the minimal bactericidal concentrations (MBC) were frequently overlapping with the MICs. In 24-h time–kill and turbidimetric studies, P7 displayed a rapid non-lytic bactericidal activity. P7 could therefore represent a novel and potent tool capable of counteracting infections sustained by several bacteria that are resistant to the presently available antibiotics.     

Mechanisms Underlying Dichotomous Procoagulant COAT Platelet Generation—A Conceptual Review Summarizing Current Knowledge

Procoagulant platelets are a subtype of activated platelets that sustains thrombin generation in order to consolidate the clot and stop bleeding. This aspect of platelet activation is gaining more and more recognition and interest. In fact, next to aggregating platelets, procoagulant platelets are key regulators of thrombus formation. Imbalance of both subpopulations can lead to undesired thrombotic or bleeding events. COAT platelets derive from a common pro-aggregatory phenotype in cells capable of accumulating enough cytosolic calcium to trigger specific pathways that mediate the loss of their aggregating properties and the development of new adhesive and procoagulant characteristics. Complex cascades of signaling events are involved and this may explain why an inter-individual variability exists in procoagulant potential. Nowadays, we know the key agonists and mediators underlying the generation of a procoagulant platelet response. However, we still lack insight into the actual mechanisms controlling this dichotomous pattern (i.e., procoagulant versus aggregating phenotype). In this review, we describe the phenotypic characteristics of procoagulant COAT platelets, we detail the current knowledge on the mechanisms of the procoagulant response, and discuss possible drivers of this dichotomous diversification, in particular addressing the impact of the platelet environment during in vivo thrombus formation.     

Toxicity of a polymer-graphene oxide composite against bacterial planktonic cells, biofilms, and mammalian cells

It is critical to develop highly effective antimicrobial agents that are not harmful to humans and do not present adverse effects on the environment. Although antimicrobial studies of graphene-based nanomaterials are still quite limited, some researchers have paid particular attention to such nanocomposites as promising candidates for the next generation of antimicrobial agents. The polyvinyl-N-carbazole (PVK)-graphene oxide (GO) nanocomposite (PVK-GO), which contains only 3 wt% of GO well-dispersed in a 97 wt% PVK matrix, presents excellent antibacterial properties without significant cytotoxicity to mammalian cells. The high polymer content in this nanocomposite makes future large-scale material manufacturing possible in a high-yield process of adiabatic bulk polymerization. In this study, the toxicity of PVK-GO was assessed with planktonic microbial cells, biofilms, and NIH 3T3 fibroblast cells. The antibacterial effects were evaluated against two Gram-negative bacteria: Escherichia coli and Cupriavidus metallidurans; and two Gram-positive bacteria: Bacillus subtilis and Rhodococcus opacus. The results show that the PVK-GO nanocomposite presents higher antimicrobial effects than the pristine GO. The effectiveness of the PVK-GO in solution was demonstrated as the nanocomposite "encapsulated" the bacterial cells, which led to reduced microbial metabolic activity and cell death. The fact that the PVK-GO did not present significant cytotoxicity to fibroblast cells offers a great opportunity for potential applications in important biomedical and industrial fields.     

Synthesis and characterization of thermoresponsive N-isopropylacrylamide/methacrylated pullulan hydrogels

Thermosensitive hydrogels were prepared by free radical polymerization starting from a methacrylated pullulan derivative (acting as the cross-linker) and using N-isopropylacrylamide (NIPAAM) as the monomer. Several hydrogels were obtained by changing the monomer to cross-linker ratio. A significant thermosensitivity was observed only when the molar amount of NIPAAM incorporated in the network was at least eight times higher that of methacrylate groups on pullulan. The hydrogel with high amount of NIPAAM deswells more than 80% after the T-jump. The lower critical solution temperature of thermosensitive hydrogels decreases with increasing amount of NIPAAM. The mechanical properties of the hydrogels are strongly affected by the percentage of incorporated NIPAAM and by the temperature.