Vascular endothelial and smooth muscle cell culture on NaOH-treated poly(epsilon-caprolactone) films: a preliminary study for vascular graft development

Tissue engineering offers the potential of providing vessels that can be used to replace diseased and damaged native blood vessels. The endothelization of a synthetic vascular graft minimizes the failures associated with blood clotting and platelet activation. The aim of this study was to culture vascular-derived endothelial and smooth muscle cells on both untreated and NaOH-treated poly(epsilon-caprolactone) (PCL) films, a biocompatible and bio-resorbable polymer, and to evaluate the behavior of both cell types as a preliminary study for vascular graft development. PCL films were prepared by hot pressing; characterized by DSC, IR, SEM, and scanning force microscopy; and treated with NaOH to increase the surface hydrophilicity before cell culture. Endothelial and smooth muscle cells, isolated from pig cava vein, were characterized by immunofluorescence and confocal microscopy studies of endothelial nitric oxide synthase and alpha-smooth muscle actin. Good adhesion, growth, viability and morphology of both the endothelial and smooth muscle cells on PCL films were obtained, but a light stimulation of mitochondrial activity was observed during short culture times. NaOH treatment improved the adhesion and enhanced the proliferation in both cell types. This verified the possible use of this modified polymer as a support in the preparation of a synthetic vascular graft. [Diagram: see text] SEM micrograph of smooth muscle cells cultured on NaOH-treated PCL film. (Original magnification: 1000x).     

The electrophilic reactions of pentacyanonitrosylferrate(II) with hydrazine and substituted derivatives. Catalytic reduction of nitrite and theoretical prediction of eta(1)-, eta(2)-N(2)O bound intermediates

The electrophilic reactivity of the pentacyanonitrosylferrate(II) ion, [Fe(CN)(5)NO](2)(-), toward hydrazine (Hz) and substituted hydrazines (MeHz, 1,1-Me(2)Hz, and 1,2-Me(2)Hz) has been studied by means of stoichiometric and kinetic experiments (pH 6-10). The reaction of Hz led to N(2)O and NH(3), with similar paths for MeHz and 1,1-Me(2)Hz, which form the corresponding amines. A parallel path has been found for MeHz, leading to N(2)O, N(2), and MeOH. The reaction of 1,2-Me(2)Hz follows a different route, characterized by azomethane formation (MeNNMe), full reduction of nitrosyl to NH(3), and intermediate detection of [Fe(CN)(5)NO](3)(-). In the above reactions, [Fe(CN)(5)H(2)O](3)(-) was always a product, allowing the system to proceed catalytically for nitrite reduction, an issue relevant in relation to the behavior of the nitrite and nitric oxide reductase enzymes. The mechanism comprises initial reversible adduct formation through the binding of the nucleophile to the N-atom of nitrosyl. The adducts decompose through OH(-) attack giving the final products, without intermediate detection. Rate constants for the adduct-formation steps (k = 0.43 M(-)(1) s(-)(1), 25 degrees C for Hz) decrease with methylation by about an order of magnitude. Among the different systems studied, one-, two-, and multielectron reductions of bound NO(+) are analyzed comparatively, with consideration of the role of NO, HNO (nitroxyl), and hydroxylamine as bound intermediates. A DFT study (B3LYP) of the reaction profile allows one to characterize intermediates in the potential hypersurface. These are the initial adducts, as well as their decomposition products, the eta(1)- and eta(2)-linkage isomers of N(2)O.     

Neumann-like integrable models

A countable class of integrable dynamical systems, with four-dimensional phase space and conserved quantities in involution (Hn,In)$(H_n,I_n)$ are exhibited. For n=1$n=1$ we recover Neumann system on T^∗S²$T^{\ast }{S}^2$. All these systems are also integrable at the quantum level.     

Rapid Discrimination of Crystal Handedness by X-ray Natural Circular Dichroism (XNCD) Mapping

An original method for determining the handedness of individual non-centrosymmetric crystals in a mixture using a tightly-focused, circularly polarized X-ray beam is presented. The X-ray natural circular dichroism (XNCD) spectra recorded at the metal K-edge on selected crystals of [Δ-M(en)₃](NO₃)₂ and [Λ-M(en)₃](NO₃)₂ (M=Co^II, Ni^II) show extrema at the metal pre-edge (7712 eV for Co, 8335 eV for Ni). A mapping of a collection of some 220 crystals was performed at the respective energies by using left and right circular polarizations. The difference in absorption for the two polarizations, being either negative or positive, directly yielded the handedness of the crystal volume probed by the beam. By using this technique, it was found that the addition of l -ascorbic acid during the synthesis of [Co(en)₃](NO₃)₂ resulted in an enantiomeric enrichment of the Λ-isomer of 67±13 %, whereas the Ni analogue was similarly, but conversely, enriched in the Δ-isomer (65±22 %).     

Uniform saturation in linear inequality systems

Redundant constraints in linear inequality systems can be characterized as those inequalities that can be removed from an arbitrary linear optimization problem posed on its solution set without modifying its value and its optimal set. A constraint is saturated in a given linear optimization problem when it is binding at the optimal set. Saturation is a property related with the preservation of the value and the optimal set under the elimination of the given constraint, phenomena which can be seen as weaker forms of excess information in linear optimization problems. We say that an inequality of a given linear inequality system is uniformly saturated when it is saturated for any solvable linear optimization problem posed on its solution set. This paper characterizes the uniform saturated inequalities and other related classes of inequalities. This work was supported by the MCYT of Spain and FEDER of UE, Grant BFM2002-04114-C02-01.     

Few associative triples,isotopisms and groups

Let Q be a quasigroup. For \(\alpha ,\beta \in S_Q\) let \(Q_{\alpha ,\beta }\) be the principal isotope \(x*y = \alpha (x)\beta (y)\). Put \(\mathbf a(Q)= |\{(x,y,z)\in Q^3;\) \(x(yz)) = (xy)z\}|\) and assume that \(|Q|=n\). Then \(\sum _{\alpha ,\beta }\mathbf a(Q_{\alpha ,\beta })/(n!)^2 = n^2(1+(n-1)^{-1})\), and for every \(\alpha \in S_Q\) there is \(\sum _\beta \mathbf a(Q_{\alpha ,\beta })/n! = n(n-1)^{-1}\sum _x(f_x^2-2f_x+n)\ge n^2\), where \(f_x=|\{y\in Q;\) \( y = \alpha (y)x\}|\). If G is a group and \(\alpha \) is an orthomorphism, then \(\mathbf a(G_{\alpha ,\beta })=n^2\) for every \(\beta \in S_Q\). A detailed case study of \(\mathbf a(G_{\alpha ,\beta })\) is made for the situation when \(G = \mathbb Z_{2d}\), and both \(\alpha \) and \(\beta \) are “natural” near-orthomorphisms. Asymptotically, \(\mathbf a(G_{\alpha ,\beta })>3n\) if G is an abelian group of order n. Computational results: \(\mathbf a(7) = 17\) and \(\mathbf a(8) \le 21\), where \(\mathbf a(n) = \min \{\mathbf a(Q);\) \( |Q|=n\}\). There are also determined minimum values for \(\mathbf a(G_{\alpha ,\beta })\), G a group of order \(\le 8\).     

Removing dead transitions in timed-arc Petri nets

Timed-arc Petri nets (TAPNs) are a timed extension of Petri nets where tokens are assigned an age indicating the time elapsed from its creation, and PT-arcs (place to transition arcs) are labelled with time intervals that are used to restrict the age of the tokens that can be used to fire the adjacent transition. This is a rather pathological model, as reachability is undecidable, whereas some other known properties of Petri nets, like boundedness, coverability and even termination, are decidable. This article focuses on the problem of detecting dead transitions, i.e. transitions that can be removed from the model since they can never become enabled. We prove that this problem is decidable for TAPNs with natural times, and we present an algorithm that can be used to find dead transitions in the particular case of 1-safe TAPNs.     

Dimeric (isoquinoline)(N‐salicylidene‐d,l‐glutamato)copper(II) ethanol solvate

The title racemic complex, bis[μ‐N‐(2‐oxidobenzylidene)‐d ,l ‐glutamato(2−)]bis[(isoquinoline)copper(II)] ethanol disolvate, [Cu₂(C₁₂H₁₁NO₅)₂(C₉H₇N)₂]·2C₂H₆O, adopts a square‐pyramidal Cu^II coordination mode with a tridentate N‐salicylideneglutamato Schiff base dianion and an isoquinoline ligand bound in the basal plane. The apex of the pyramid is occupied by a phenolic O atom from the adjacent chelate molecule at an apical distance of 2.487 (3) Å, building a dimer located on the crystallographic inversion center. The Cu...Cu spacing within the dimers is 3.3264 (12) Å. The ethanol solvent molecules are hydrogen bonded to the dimeric complex molecules, forming infinite chains in the a direction. The biological activity of the title complex has been studied.     

Anodic and Cathodic Platinum Dissolution Processes Involve Different Oxide Species

The degradation of Pt-containing oxygen reduction catalysts for fuel cell applications is strongly linked to the electrochemical surface oxidation and reduction of Pt. Here, we study the surface restructuring and Pt dissolution mechanisms during oxidation/reduction for the case of Pt(100) in 0.1 M HClO₄ by combining operando high-energy surface X-ray diffraction, online mass spectrometry, and density functional theory. Our atomic-scale structural studies reveal that anodic dissolution, detected during oxidation, and cathodic dissolution, observed during the subsequent reduction, are linked to two different oxide phases. Anodic dissolution occurs predominantly during nucleation and growth of the first, stripe-like oxide. Cathodic dissolution is linked to a second, amorphous Pt oxide phase that resembles bulk PtO₂ and starts to grow when the coverage of the stripe-like oxide saturates. In addition, we find the amount of surface restructuring after an oxidation/reduction cycle to be potential-independent after the stripe-like oxide has reached its saturation coverage.