Inverse colloidal crystal membranes for hydrophobic interaction membrane chromatography

A collaborative study on the robustness and portability of a capillary electrophoresis‐mass spectrometry method for peptide mapping was performed by an international team, consisting of 13 independent laboratories from academia and industry. All participants used the same batch of samples, reagents and coated capillaries to run their assays, whereas they utilized the capillary electrophoresis‐mass spectrometry equipment available in their laboratories. The equipment used varied in model, type and instrument manufacturer. Furthermore, different types of sheath‐flow capillary electrophoresis–mass spectrometry interfaces were used. Migration time, peak height and peak area of ten representative target peptides of trypsin‐digested bovine serum albumin were determined by every laboratory on two consecutive days. The data were critically evaluated to identify outliers and final values for means, repeatability (precision within a laboratory) and reproducibility (precision between laboratories) were established. For relative migration time the repeatability was between 0.05 and 0.18% RSD and the reproducibility between 0.14 and 1.3% RSD. For relative peak area repeatability and reproducibility values obtained were 3–12 and 9–29% RSD, respectively. These results demonstrate that capillary electrophoresis‐mass spectrometry is robust enough to allow a method transfer across multiple laboratories and should promote a more widespread use of peptide mapping and other capillary electrophoresis‐mass spectrometry applications in biopharmaceutical analysis and related fields.     

Thermal and environmental stability of poly(4-ethynyl-p-xylylene-co-p-xylylene) thin films

The aim of this paper was to test the thermal and environmental stability of poly(4-ethynyl-p-xylyleneco-p-xylylene) thin films prepared by chemical vapor deposition(CVD) and to optimize the reaction conditions of the polymer.Fourier transformed infrared spectroscopy(FTIR),thermogravimetric analysis(TGA) and fluorescence microscopy were employed to investigate the stability of the reactive polymer coatings in various environmental conditions.Chemical reactivity of the thin films were then tested by Huisgen 1,3-dipolar cycloaddition reaction(‘‘click' reaction).The alkyne functional groups on poly(4-ethynyl-p-xylylene-co-p-xylylene) thin films were found to be stable under ambient storage conditions and thermally stable up to 100 8C when annealed at 0.08 Torr in argon.We also optimized the click reaction conditions of azide-functionalized molecules with poly(4-ethynyl-p-xylylene-co-p-xylylene).The best reaction result was achieved,when copper concentration was 0.5 mmol/L,sodium ascorbate concentration to copper concentration was 5:1.In contrast,the azide concentration and temperature had no obvious effect on the surface reaction.     

Existence of solutions for the anti-plane stress for a new class of “strain-limiting” elastic bodies

The main purpose of this study is to establish the existence of a weak solution to the anti-plane stress problem on V-notch domains for a class of recently proposed new models that could describe elastic materials in which the stress can increase unboundedly while the strain yet remains small. We shall also investigate the qualitative properties of the solution that is established. Although the equations governing the deformation that are being considered share certain similarities with the minimal surface problem, the boundary conditions and the presence of an additional model parameter that appears in the equation and its specific range makes the problem, as well as the result, different from those associated with the minimal surface problem.     

Physicochemical characterization of nanotemplate engineered solid lipid nanoparticles

As the physicochemical characteristics of solid lipid nanoparticles (SLNs) play a critical role in their success, it is important to understand how the materials and process used in their preparation affect these properties. In this study, two stearyl alcohol-based formulations were prepared using nanotemplate engineering technology and characterized. Both formulations were of a small particle size (<100 nm), ellipsoidal shape, and low polydispersity. (1)H NMR spectroscopy confirmed that the SLNs have the expected solid core structure and PEGylated surface. Analysis of the bulk materials indicated that a number of complex interactions are present among the SLN components, including a eutectic between stearyl alcohol and Brij 78. The decreased crystallinity resulting from these interactions may allow for enhanced drug loading. Physiological stability was identified and confirmed as a potential problem due to the low melting point of the eutectic. However, it is expected that with appropriate formulation modifications nanotemplate engineered SLNs will possess the properties necessary for a successful drug delivery system.     

Direct interaction between an allosteric agonist pepducin and the chemokine receptor CXCR4

Cell surface heptahelical G protein-coupled receptors (GPCRs) mediate critical cellular signaling pathways and are important pharmaceutical drug targets. (1) In addition to traditional small-molecule approaches, lipopeptide-based GPCR-derived pepducins have emerged as a new class of pharmaceutical agents. (2, 3) To better understand how pepducins interact with targeted receptors, we developed a cell-based photo-cross-linking approach to study the interaction between the pepducin agonist ATI-2341 and its target receptor, chemokine C-X-C-type receptor 4 (CXCR4). A pepducin analogue, ATI-2766, formed a specific UV-light-dependent cross-link to CXCR4 and to mutants with truncations of the N-terminus, the known chemokine docking site. These results demonstrate that CXCR4 is the direct binding target of ATI-2341 and suggest a new mechanism for allosteric modulation of GPCR activity. Adaptation and application of our findings should prove useful in further understanding pepducin modulation of GPCRs as well as enable new experimental approaches to better understand GPCR signal transduction.     

Toric ideals of lattice path matroids and polymatroids

White has conjectured that the toric ideal of a matroid is generated by quadric binomials corresponding to symmetric basis exchanges. We prove a stronger version of this conjecture for lattice path polymatroids by constructing a monomial order under which these sets of quadrics form Gröbner bases. We then introduce a larger class of polymatroids for which an analogous theorem holds. Finally, we obtain the same result for lattice path matroids as a corollary.     

Minimizing weighted mean absolute deviation of job completion times from their weighted mean

We address a single-machine scheduling problem where the objective is to minimize the weighted mean absolute deviation of job completion times from their weighted mean. This problem and its precursors aim to achieve the maximum admissible level of service equity. It has been shown earlier that the unweighted version of this problem is NP-hard in the ordinary sense. For that version, a pseudo-polynomial time dynamic program and a 2-approximate algorithm are available. However, not much (except for an important solution property) exists for the weighted version. In this paper, we establish the relationship between the optimal solution to the weighted problem and a related one in which the deviations are measured from the weighted median (rather than the mean) of the job completion times; this generalizes the 2-approximation result mentioned above. We proceed to give a pseudo-polynomial time dynamic program, establishing the ordinary NP-hardness of the problem in general. We then present a fully-polynomial time approximation scheme as well. Finally, we report the findings from a limited computational study on the heuristic solution of the general problem. Our results specialize easily to the unweighted case; they also lead to an approximation of the set of schedules that are efficient with respect to both the weighted mean absolute deviation and the weighted mean completion time.     

Effect of pH on H2O2 production in the radiolysis of water

The yields of hydrogen peroxide have been measured in the radiolysis of aqueous solutions of acrylamide, bromide, nitrate, and air in the pH range of 1-13. Hydrogen peroxide is the main stable oxidizing species formed in the radiolysis of water, and its long-term yield is found to be very sensitive to the system used in the measurements. Experiments with γ-irradiation combined with model calculations show that the primary yields of hydrogen peroxide are nearly independent of pH in the range of 2-12. Slightly higher primary yields are suggested at very low pH in particular when O(2) is present, while the yields seem to decrease at very high pH. Irradiations were performed with 5 MeV H ions, 5 MeV He ions, and 10 MeV C ions to evaluate the intratrack and homogeneous kinetic contributions to H(2)O(2) formation with different ions. Many of the trends in hydrogen peroxide yields with pH observed with γ-irradiations are observed with irradiation by the heavy ions. The lower yields of radicals in the homogeneous phase with the heavier ions tend to minimize the effects of radicals on the hydrogen peroxide yields at long times.     

Reduction of CO2 on a tricarbonyl rhenium(I) complex: modeling a catalytic cycle

Tricarbonyl rhenium(I) complexes, such as Re(bpy)(CO)(3)Cl where bpy = 2,2'-bipyridyl, have demonstrated superior activity in catalyzing CO(2) reduction in the presence of sacrificial electron donors. We have utilized density functional theory (DFT) to investigate a potential pathway for formate production via a rhenium-hydride insertion mechanism in the presence of triethylamine (TEA). On the basis of prior studies, we re-examined the role of TEA and studied a catalytic cycle for CO(2) reduction in which TEA functions as both the hydrogen atom and the electron donor for reducing CO(2) into formate. The catalytic cycle is found to be exothermic with inclusion of solvation and may be viewed as a two-electron reduction of CO(2) because the net result is a transfer of hydride from TEA to CO(2). In addition, we have identified structures of key intermediates in the CO(2)-reduction process and found that the insertion step has a very modest barrier in acetonitrile. These findings provide a molecular-level understanding to formate production via CO(2) reduction mediated by transition-metal complexes. A theoretical investigation is underway to elucidate the formation of carbon monoxide, another common product in Re-catalyzed CO(2) reduction.     

On Cramér's theorem for general Euler products with functional equation

Actually the MSC does not, but should, include an item for regularized products. J.J. and S.L.