Solid-Phase Extraction of Metoprolol onto(Methacrylic acid-ethylene glycol dimethacrylate)-based Molecularly Imprinted Polymer and Its Spectrophotometric Determination

A new adsorbent for molecularly imprinted solid phase extraction (MISPE) of metoprolol was synthesized using methacrylic acid (MAA) as functional monomer and ethylene glycol dimethacrylate (EGDMA) as cross‐linking agent causing a non‐covalent, bulk, thermal radical‐polymerization. Control polymer (non‐imprinted polymer) was prepared under well defined conditions without the use of metoprolol. The synthesized polymers were characterized by IR spectroscopy, X‐ray diffraction and thermal analysis techniques. This polymer was used for the rapid extraction and preconcentration of metoprolol from real samples prior to spectrophotometric determination. Extraction efficiency and the influence of flow rates of sample and stripping solutions, pH, type of eluent for elution of metoprolol from polymer, break through volume and limit of detection were studied. The detection limit of the proposed method is 0.4 ng·mL^?1. The method was applied successfully to the recovery and determination of metoprolol in tablets, human urine and plasma samples.     

Synthesis and Pharmacological Evaluation of Some Novel Imidazo[2,1-b][1,3,4]thiadiazole Derivatives

Synthesis of bis‐1,3‐{6′‐arylimidazo[2,1‐b][1,3,4]thiadiazol‐2‐yl}‐1,2,2‐trimethylcyclopentane ( 3 ), bis‐1,3‐{thiadiazolo[2′,3′:2,1]imidazo[4,5‐b]quinoxalinyl}‐1,2,2‐trimethylcyclopentane ( 5 ) has been achieved by the reaction of bis‐(5′‐amino‐1′,3′,4′‐thiadiazolyl)‐1,2,2‐trimethylcyclopentane with α‐haloketones, 2,3‐dichloroquinoxaline respectively. Bromination of compound 3 furnished bis‐1,3‐{5′‐bromo‐6′‐arylimidazo[2,1‐b][1,3,4]thiadiazol‐2‐yl}‐1,2,2‐trimethylcyclopentane ( 4 ). The structural assignment of these compounds was supported by IR, ¹H NMR and elemental analysis data. The antimicrobial, anti‐inflammatory and antifungal activities of some of the compounds have also been evaluated.     

Reduction kinetics of mechanically activated hematite concentrate with hydrogen gas using nonisothermal methods

The reduction kinetics of both non-activated and mechanically activated hematite concentrate in a vibratory mill for different grinding periods have been studied using themogravimetry (TG). Changes in the structure of hematite were studied using X-ray diffraction analysis. The isoconversional method of Kissinger-Akahira-Sunose (KAS) was used to determine the activation energy of the different reactions. The Vyazovkin model-free kinetic method was also used for prediction of kinetic behavior of the samples for a given temperature.Fe₂O₃ was found to reduce to Fe in a two-step via Fe₃O₄. Intensive grinding resulted in improved resolution of overlapping reduction events. It was also established that the mechanical activation had a positive effect on the first step of reduction. With increasing the grinding time, the activation energy at lower extent of conversion (α ≤ 0.11) decreased from 166 to 106 kJ mol⁻¹ range in the initial sample to about 102-70 kJ mol⁻¹ in the sample ground for 9 h. The complexity of the reduction of hematite to magnetite and magnetite to iron was illustrated by the dependence of E on the extent of conversion, α(0.02 ≤ α ≤ 0.95). The values of E decreased sharply with α for 0.02 ≤ α ≤ 0.11 range in the initial sample and mechanically activated samples, followed by a slight decrease in the values of E during further reduction by α ≤ 0.85 in the ground samples up to 3 h. A slight increasing dependence of E on α for mechanically activated sample within 9 h in the second step of reduction was observed due to the finely agglomerated particles during intensive milling and subsequently the formation of a dense layer during the reduction processes. In addition, the dependence of ln A_α on α was detected and it was found that the ln A_α shows the same dependence on α as the apparent activation energies.     

Evaluation of physico-chemical properties of electron beam-irradiated polycarbonate film

In this work, polycarbonate (PC) film samples were irradiated with 10 MeV electrons at different doses ranging from 25 to 250 kGy. Characterization techniques viz. thermogravimetric analysis (TGA), Fourier transform infra-red spectroscopy (FTIR), X-ray diffraction analysis (XRD) and electron paramagnetic resonance (EPR) were exploited to understand the induced changes in the physico-chemical properties of the polymer. An increase in the decomposition temperature with increasing dose was observed, while the crystallinity remained unchanged as a result of the formation of cross-link bond. EPR technique characterized the stability of the free radicals in the irradiated PC. The result showed that cross-linking process occurs at low absorbed doses, whereas polymer degradation happens at higher doses.     

Thulium(III) Ions Monitoring by a Novel Thulium(III) Microelectrode Based on a S‐N Schiff Base

This study presents for the first time development of a highly selective and sensitive thulium(III) micro‐sensor. Theoretical calculations were conducted on a S‐N Schiff base [thiophene‐2‐carbaldehyde‐(7‐methyl‐1,3‐benzothiazol‐2‐yl) hydrazone] (TCMH) in order to obtain a clue about the tendency of TCMH to Tm(III) and some other metal ions. Then, TCMH was used as a membrane‐active component to prepare a Tm(III)‐selective polymeric membrane microelectrode. In line with the resulting data, the electrode exhibits a Nernstian response toward Tm(III) ions for a very wide concentration range (1.0×10^?11–4.0×10^?6 M) with a detection limit of 1.0×10^?11 (ca. 1.5 ppt) and a very fast response time in the whole concentration range (<5 s). In addition, the results showed that the certain microelectrode could be applied in the pH range of 4.0–11.0 with a usage of more than one month without any considerable potential divergence.     

Novel Nitrite Membrane Sensor Based on Cobalt(II) Salophen for Selective Monitoring of Nitrite Ions in Biological Samples

A novel PVC-based membrane sensor based on the Co(II)-salophen complex (CSC) is described. The electrode revealed a Nernstian response over a wide nitrite ion concentration range (1.0×10^–6–1.0×10^–1M). The detection limit of the sensor is 8.0×10^–7M. The best performance was obtained with a membrane composition of 33% PVC, 61% ortho-nitrophenyloctyl ether, 3% cobalt(II)-salophen, and 3% hexadecyltrimethylammonium bromide. The potentiometric response of the sensor is independent of the pH of solution in the pH range 4.5–11.9. The electrode exhibits a very fast response time and good selectivity over a variety of common inorganic and organic anions, including fluoride, bromide, iodide, sulfite, nitrate, thiocyanate, thriiodide and perchlorate. The selectivity behavior of the proposed sensor shows substantial improvements compared to the previously reported electrodes for nitrite ion. The membrane sensor can be used for at least 2 months without any divergence in potential. The electrode was successfully applied to the monitoring of nitrite ion in water, sausage, flour, wheat, cheese and milk.     

Sub-Second Accumulation and Stripping for Pico-Level Monitoring of Amikacin Sulphate by Fast Fourier Transform Cyclic Voltammetry at a Gold Microelectrode in Flow-Injection Systems

A novel chemiluminogenic reagent, refered to as spiro form fluorescein hydrazide, was synthesized, and its application to chemiluminescence (CL) determination of Co²⁺ is described. The method is based on the catalytic effect of Co²⁺ on the autoxidation of sulfite in basic solution to generate a series of powerful oxidative intermediates, which then oxidize colorless, nonfluoresent fluorescein hydrazide to generate strong CL emission. The CL signal is linearly related to the concentration of Co²⁺ in the range of 0.1–200nM with a detection limit of 0.04nM. The optimal conditions for the detection of Co²⁺ were evaluated, and the possible CL mechanism is discussed. The proposed method has been applied to the determination of Co²⁺ in pharmaceutical preparations and in soil samples.     

Novel PVC-based copper(II) membrane sensor based on 2-(1'-(4'-(1'-hydroxy-2'-naphthyl)methyleneamino)butyl iminomethyl)-1-naphthol.

A copper(II) ion-selective PVC membrane sensor based on 2-(1'-(4'-(1'-hydroxy-2'-naphthyl)methyleneamino)butyl iminomethyl)-1-naphthol (BHNB) as a novel Schiff base containing a sensing material has been successfully developed. The sensor exhibits a good linear response of 29 mV per decade within the concentration range of 10(-1)-10(-6) M of Cu2+. The sensor shows good selectivity for copper(II) ion in comparison with alkali, alkaline earth, transition and heavy metal ions. The BHNB-based sensor is suitable for use with aqueous solutions of pH 3.5-7.0 and displays minimal interference by Sr(II), Cd(II), Hg(II), Zn(II) and Pb(II), which are known to interfere with other previously suggested electrodes. The proposed membrane electrode was used as a sensor for determining the Cu(II) content in black tea samples. It was also applied as an indicator electrode in the potentiometric titration of Cu2+ ions with EDTA.