Fabrication of a novel electrospun molecularly imprinted nanomembrane coupled with high‐performance liquid chromatography for the selective separation and determination of acesulfame

A novel in situ molecularly imprinted sol–gel nanomembrane using nylon 6 as backbone was prepared by the electrospinning technique and coupled on‐line with high‐performance liquid chromatography. The prepared electrospun membrane exhibited extensive selectivity toward acesulfame in the presence of some selected sweeteners in a beverage sample, while the porosity and mechanical stability remained. The prepared electrospun membrane could be applied for 35 consequence extractions without a significant change in extraction recovery, swelling, and flooding. To achieve the best condition and efficiency for on‐line extraction, the effect of influential parameters was investigated. The limit of detection (signal/noise = 3:1) and limit of quantification (signal/noise = 10:1) were 0.6 and 2.0 ng/mL for acesulfame in the beverage samples, respectively. The linearity for the acesulfame was in the range of 2.0–250 ng/mL in beverage samples. The coefficients of determination values were ≥0.997 for all runs. The extraction recoveries of acesulfame in the beverage samples were between 80 and 85%.     

Preparation of 99mTc-MIBI complex under ultrasound irradiation

The (37MBq) 99mTc-MIBI complex samples were prepared due to ultrasound irradiation technique or boiled water bath method as a standard method. The qualitative and quantitative studies have been performed. The accumulation of 99mTc-MIBI complexes prepared by two above mentioned modalities were approximately 3 ± 0.1 % in the rats’ heart. The ultrasound irradiation technique is recommended to prepared 99mTc-MIBI complex in efficiently amount. Our approach can potentially reduce medical risk to the patient by avoiding any delay in acute therapy particularly for myocardial infarction patients.     

A wide neighborhood interior-point algorithm for linear optimization based on a specific kernel function

This paper presents an interior point algorithm for solving linear optimization problems in a wide neighborhood of the central path introduced by Ai and Zhang (SIAM J Optim 16:400–417, 2005). In each iteration, the algorithm computes the new search directions by using a specific kernel function. The convergence of the algorithm is shown and it is proved that the algorithm has the same iteration bound as the best short-step algorithms. We demonstrate the computational efficiency of the proposed algorithm by testing some Netlib problems in standard form. To best our knowledge, this is the first wide neighborhood path-following interior-point method with the same complexity as the best small neighborhood path-following interior-point methods that uses the kernel function.

     

On Hochschild–Serre spectral sequence of Lie algebras

Using non-abelian exterior product and free presentation of a Lie algebra the Hochschild–Serre spectral sequence for cohomology of Lie algebras will be extended a step further. Also, some results about this sequence are obtained.     

Anion‐binding properties of two calix[4]arene derivatives containing two ferrocene imine or ferrocene amine units at the upper rim

Calix[4]arene derivatives containing ferrocene units at the upper rim have been synthesized and their anion‐binding and sensing investigated towards anions such as chloride, bromide and hydrogen sulfate by cyclic voltammetry. Electrochemical studies show that these redox‐active ligands electrochemically recognize chloride and bromide anions. These compounds have excellent selectivity for chloride and bromide ions, in the comparison with hydrogen sulfate anion. With ferrocenyl Schiff base calix[4]arene 1 an anodic shift as large as 302 mV is observed on addition of four equivalents of Cl⁻ anion. Also electrochemical and UV–vis spectroscopic titrations ferrocenyl calix[4]arene derivatives 1 with chloride and bromide ions and 2 (only with Cl⁻) indicate a 1:1 binding‐stiochiometry. Copyright © 2011 John Wiley & Sons, Ltd.     

Design and Synthesis of Some Novel Oxiconazole‐Like Carboacyclic Nucleoside Analogues,as Potential Chemotherapeutic Agents

The syntheses of some novel carboacyclic nucleosides, 17a – 17o , containing oxiconazole‐like scaffolds, are described (Schemes 1–3). In this series of carboacyclic nucleosides, pyrimidine as well as purine and other imidazole derivatives were employed as an imidazole successor in oxiconazole. These compounds could be prepared in good yields by using two different strategies (Schemes 1 and 2). Due to Scheme 1, the N‐coupling of nucleobases with 2‐bromoacetophenones was attained for 18a – 18e , and their subsequent oximation affording 19a – 19e and finally O‐alkylation with diverse alkylating sources resulted in the products 17a – 17g, 17n , and 17o . In Scheme 2, use of 2‐bromoacetophenone oximes 20 , followed by N‐coupling of nucleobases, provided 19f – 19j whose final O‐alkylation produced 17h – 17m (Scheme 2). For the rational interpretation of the dominant formation of (E)‐oxime ethers rather than (Z)‐oxime isomers, PM3 semiempirical quantum‐mechanic calculations were discussed and the calculations indicated a lower heat of formation for (E)‐isomers.     

Anion-directed self-assembly in coordination networks: architectural control via cooperative noncovalent interactions

The self-assembly of a new flexible tritopic pyrazine-pyridine ligand (pz-3-py) with HgX(2) (X = Cl, Br) was investigated. The results show that coordinated chloride and bromide anions play different roles, and two architecturally different coordination polymers were obtained with the anions used. Where X = Cl, in [Hg(μ(3)-pz-3-py)Cl(2)](n) (1), the 2D network is isolated, while for X = Br, in [Hg(μ-pz-3-py)Br(2)](n) (2), a 1D zigzag chain is constructed. Our results show that noncovalent interactions such as hydrogen bond, halogen···halogen, and halogen···π interactions, when acting cooperatively, are driving forces for the selection of different structures.     

RP-HPLC prefractionation and its application in expressional proteomics analysis of an in vitro viral infection model

Prefractionation of complex protein mixtures is an efficient method for increasing the separation power of 2-DE. RP-HPLC has been successfully utilized as a prefractionation method prior to 2-DE. Here we describe the optimization of an efficient RP-HPLC method for prefractionation of baby hamster kidney cell solubilized proteins. A step gradient elution of acetonitrile was optimized and collected fractions were further examined by SDS-PAGE and 2-DE. By utilizing this method an effective increase in separation power of 2-DE is accomplished. Moreover, we describe the application of this method to expressional proteome analysis of a virally infected cell model.     

Solvent extraction of no-carrier-added 103Pd from irradiated rhodium target with a-furyldioxime

Summary Solvent extraction of no-carrier-added ¹⁰³Pd was investigated from irradiated rhodium target with a-furyldioxime in chloroform from diluted hydrochloric acid. Extraction yield was 85.3% for a single extraction from 0.37M HCl and ¹⁰³Pd purity was better than 99%.     

Isocyanide-based multicomponent reactions: synthesis of 2-(1-(alkylcarbamoyl)-2,2-dicyanoethyl)-N-alkylbenzamide and 1,7-diazaspiro[4,4]nonane-2,4-dione derivatives

A four-component reaction between 2-formylbenzoic acid, malononitrile, isocyanides, and primary alkyl amines has been developed for an efficient preparation of 2-(1-(alkylcarbamoyl)-2,2-dicyanoethyl)-N-alkylbenzamide and 1,7-diazaspiro[4,4]nonane-2,6-dione derivatives under two different conditions. It is shown that simply by changing the reaction solvent from ethanol to dichloromethane and controlling the order of the addition of reagents, two completely different products can be obtained. These multicomponent reactions showed high atom economy.