A novel amperometric glucose biosensor based on reconstitution of glucose oxidase on thiophene-3-boronic acid polymer layer

The biosensor was constructed for determination of glucose by using glucose oxidase enzyme immobilized on poly(thiophene-3-boronic acid) (PTBA). Boronic acid functionalized polythiophene layer was obtained by electrochemical polymerization of Thiophene (Th) and thiophene-3-boronic acid (TBA) with different monomer rations. The reconstitution of the apo-glucose oxidase (apo-GOx) on a complexed flavin adenine dinucleotide (FAD) linked to polythiophene boronic acid (PTBA) monolayer yields an electrically contacted enzyme monolayer. The GOx-reconstituted enzyme electrode exhibited excellent electrocatalytic activities toward the reduction and oxidation of hydrogen peroxide as well. The PTBA/FAD/GOx biosensor shows an excellent performance for glucose at +0.4 V with a high sensitivity (2.14 μA/mM) and lower response time (～5 s) in a wide concentration range of 0.5–18 mM (correlation coefficient of 0.9952). Furthermore, the effects of applied potential, pH, temperature, electroactive interference, stability and reusability of the biosensors were discussed.     

Semiperfect Modules with Respect to a Preradical

In an earlier paper [8] the authors introduced strongly and properly semiprime modules. Here properly semiprime modules M are investigated under the condition that every cyclic submodule is M-projective (self-pp-modules). We study the idempotent closure of M using the techniques of Pierce stalks related to the central idempotents of the self-injective hull of M. As an application of our theory we obtain several results on (not necessarily associative) biregular, properly semiprime, reduced and Firings. An example is given of an associative semiprime PSP ring with polynomial identity which coincides with its central closure and is not biregular (see 3.6). Another example shows that a semiprime left and right FP-injective Pl-ring need not be regular (see 4.8). Some of the results were already announced in [7].     

A One-Time Excess Inventory Disposal Decision Under a Stationary Base-Stock Policy

We consider a stochastic inventory system that has been operated under a policy different from the one that will be implemented in the future. Such a situation may arise as a result of changes in model assumptions leading to the implementation of a different policy. Before the new policy is implemented, there may be some units on hand which may exceed the optimal order-up-to level. Hence, one needs to evaluate a one-time inventory disposal decision immediately before the new policy replaces the policy in use. For this purpose, we develop three models under different assumptions that describe the demand during the disposal period and present analytical results characterizing their optimal solutions.     

A Vulnerability Parameter of Networks

Mathematical Notes - The vulnerability in a communication network is the measurement of the strength of the network against damage that occurs in nodes or communication links. It is important that...     

Palladium(II)‐N‐heterocyclic carbene complexes: synthesis,characterization and catalytic application

N‐Heterocyclic carbenes (NHCs) are of great importance and are powerful ligands for transition metals. A new series of sterically hindered benzimidazole‐based NHC ligands (LHX) ( 2a , 2b , 2c , 2d , 2e , 2f ), silver–NHC complexes ( 3a , 3b , 3c , 3d , 3e , 3f ) and palladium–NHC complexes ( 4a , 4b , 4c , 4d , 4e , 4f ) have been synthesized and characterized using appropriate spectroscopic techniques. Studies have focused on the development of a more efficient catalytic system for the Suzuki coupling reaction of aryl chlorides. Catalytic performance of Pd–NHC complexes and in situ prepared Pd(OAc)₂/LHX catalysts has been investigated for the Suzuki cross‐coupling reaction under mild reaction conditions in aqueous N,N‐dimethylformamide (DMF). These complexes smoothly catalyzed the Suzuki–Miyaura reactions of electron‐rich and electron‐poor aryl chlorides. Copyright © 2014 John Wiley & Sons, Ltd.     

Computational estimates of thermochemistry and pKa values of cyclopropenyl imine superbases

The thermochemical properties of superbase species derived from cyclopropeneimine are estimated by computations on systems of isodesmic reactions. Proton affinities, gas phase basicities, and pK_a values are well represented by computations incorporating G4 and CBS‐QB3 schemes augmented for large systems by DFT calculations with functionals M06‐2X and ωB97DX in the cc‐pVTZ Dunning basis. Our calculations show that relative base strengths in gas are enhanced by alkyl substitution, either by methyl groups or larger species. For acetonitrile solution, alkyl substitution seems to weaken the base. © 2013 Wiley Periodicals, Inc.     

Effervescence-assisted dispersive liquid-liquid microextraction based on deep eutectic solvent for preconcentration and FAAS determination of copper in aqueous samples

A new effervescence-assisted dispersive liquid-liquid microextraction, EA-DLLME, technique was developed for preconcentration and flame atomic absorption spectrometric determination of copper in aqueous samples. Effervescence assistance and DES combination for metal ion extraction was used for the first time. In the presented study, six different effervescence powders were examined to achieve maximum extraction efficiency. In addition, 1,5 diphenyl carbazide was used as complexing agent and DES prepared by mixing choline chloride and phenol was used as extraction solvent. The effect of several parameters such as pH, concentration of complexing agent, composition and volume of DES, amount of THF, composition and amount of effervescent agent were examined. Performed experiments showed that optimum pH was 6.0, the best effervesce powder composition was NaH₂PO₄:Na₂CO₃ with 2 × 10^?3:1 × 10^?3 molar ratio and the amount of effervesce powder was 0.4 g. Under optimum conditions enhancement factor, limit of detection and limit of quantification were calculated as 78, 2.9 and 9.7 μg L^?1, respectively. In addition, to prove precision of the method intra-day relative standard deviations were calculated for 10 and 50 μg L^?1 Cu²⁺ concentrations and found as 2.1% and 1.3%, respectively. The proposed method showed good linearity within the range of 10.0–100 μg L^?1. Finally, proposed method was successfully applied to determination of copper traces in aqueous samples.     

Determination of some trace metals with a new synthesized polymer resin by FAAS in various tea and herbal plants samples

In this work, a new polymer resin with a functional groups capable of holding trace metals has been synthesized. The structure of polymer resin has been examined by BET-N₂ method analyzer, IR spectrometer, scanning electron microscope (SEM) and elemental microanalyser. The synthesized polymer resin was used for the simultaneous separation and preconcentration of the trace metals from various tea and herbal plants samples. After extraction process, flame atomic absorption spectrometry (FAAS) was used to determine the trace metals. The analytical parameters and solid phase extraction (SPE) performance such as pH, sample volume, flow rates of sample, flow rates of eluent, concentration, volume and type of eluent and effect of interference ions, were investigated. The limits of detection (DL) of the SPE procedure for trace metals, were calculated to be (3s) in the range of 0.9?4.0 μg L^?1 (n = 21) and the factors of preconcentration (PF) were obtained at 200 for Cd, Co, Cu, Fe, Ni and Zn, and at 50 for Cr, Mn and Pb ions and the relative standard deviation (RSD) at ≤ 2% (n = 11).