Polypyrrole nanotube modified by gold nanoparticles for improving the neural microelectrodes

Journal of Solid State Electrochemistry - High selectivity and low impedance are preferred properties for neural microelectrodes. The localized and controlled release of drugs from the...     

Enhancement of Human γ-Interferon Production in Recombinant <Emphasis Type="Italic">E. coli</Emphasis> Using Batch Cultivation

Development of inexpensive and simple culture media and appropriate induction conditions are always favorable for industry. In this research, chemical composition and stoichiometric data for γ-interferon production and recombinant Escherichia coli growth were used in order to achieve a simple medium and favorable induction conditions. To achieve this goal, the effects of medium composition and induction conditions on the production of γ-interferon were investigated in batch culture of E. coli BL21 (DE3) [pET3a-ifnγ]. These conditions were considered as suitable conditions for the production of γ-interferon: 2.5× M9 medium, supplemented with a mixture of amino acids (milligram per liter), including glutamic acid 215, aspartic acid 250, lysine 160, and phenylalanine 90, and induction at late-log phase (OD₆₀₀ = 4.5). Under these conditions, dry cell weight of 6 ± 0.2 g/l and γ-interferon concentration of 2.15 ± 0.1 g/l were obtained. Later, without changing the concentration ratio of amino acids and glucose, the effect of increase in the primary glucose concentration on productivity of γ-interferon was investigated. It was found that 25 g/l glucose will result in maximum attainable biomass and recombinant human γ-interferon. At improved conditions, a dry cell weight of 14 ± 0.2 g/l, concentration and overall productivity of γ-interferon 4.2 ± 0.1 g/l and 420 ± 10 mg/l h, respectively, were obtained.     

Isolation of PHA–Producing Bacteria from Date Syrup Waste

Since the major problem associated with the industrial production of Polyhydroxyalkanoates (PHAs) is their high production cost, this study was carried out using date syrup as the major carbon source to decrease the production cost and also help to supply other nutrient requirements. To isolate PHA–producing bacteria for this purpose, microorganisms were isolated from the syrup waste of a local date factory. These purified colonies were screened for intracellular granules by staining with Sudan Black. The positive-staining strains were grown for production of PHAs in 5% date syrup as carbon source supplemented with mineral salt medium. The culture was incubated at 30 °C with shaking at 140 rpm for 60 h. Among positively stained bacteria, the best PHA producers were selected on the basis of cell growth, cell dry weight, PHA content and the monomer composition of PHA. One of them could utilize date syrup for growth and produce the homopolymer of Polyhydroxybutyrate (PHB) with a cell density of about 5.1 g/L and maximum concentration of PHB equal to 3.6 g/L which is 71% of cell dry weight. Another one produces copolymer of Poly (hydroxybutyrate-hydroxyvalerate) in date syrup media with a maximum concentration of 2.2 g/L containing 10 wt % valerate in shake flask cultivation.     

Preparation of antibacterial ZnO NP-containing schizophyllan/bacterial cellulose nanocomposite for wound dressing

Cellulose - Nanocomposite hydrogel is helpful to provide a moist and ideal environment for wound healing. In this research study, a nanocomposite hydrogel was prepared based on schizophyllan (SPG)...     

Evaluation of the effect of nanoporous nanorods Zn<Subscript>2</Subscript>(bdc)<Subscript>2</Subscript>(dabco) dimension on ibuprofen loading and release

This work presents an experimental investigation of drug loading in metal-organic frameworks (MOFs). Porous metal organic framework [Zn₂(bdc)₂(dabco)] was synthesized under solvothermal conditions. Characterization of samples was studied by IR spectroscopy, X-ray powder diffraction, thermogravimetric analysis, ultraviolet–visible spectroscopy, N₂ adsorption porosimetry and scanning electron microscopy. In vitro cytotoxicity assessment and IC₅₀ values for the human hepatoma cell (HuH7) was determined by MTT assay. Two different sizes of Zn₂(bdc)₂(dabco) were prepared by solvothermal method under the presence and absence of modulator. The prepared samples were used for ibuprofen loading. Ibuprofen loadings of 22 and 30 % (w/w) were obtained for samples with average diagonal sizes of 250 and 100 nm, respectively. The release of ibuprofen from these materials was prolonged for 2 and 3 weeks for 250 and 100 nm samples, respectively. The results obtained in this study revealed that two significant factors, surface area and pore size, affect ibuprofen drug loading and release.     

Performance evaluation of fast Fourier-transform continuous cyclic-voltammetry pesticide biosensor

In this work, a method for the fast monitoring of OPs in flow-injection systems was evaluated. The fast Fourier transform continuous cyclic-voltammetry (FFTCCV) at the carbon-paste electrode in a flowing solution system was used for determination of OPs. In this method the S/N ratio is enhanced by using of fast Fourier transform of the analyte and signal integration. FFTCCV can be considered as a new sensitive, accurate and fast method for determination of drugs and some pesticides. However, in order to obtain better sensitivity for a specific target, experimental parameters should be optimized. Response surface methodology (RSM) was applied to optimize three effective parameters (enzyme activity, multiwall carbon nanotube quantity and acidic sol–gel quantity). The optimum values for the tested parameters were enzyme amount H0.169 U cm⁻², multiwall carbon nanotube (MWCNT) 0.607 mL and acidic sol–gel 1.012 mL. The optimum feed pH, feed flow rate, ATChCl concentration and sweeping-rate were found to be 7.4, 0.34 mL min⁻¹, 0.750 mM and 10 V s⁻¹, respectively. The long-term stability of this flow-through system was 80% of its initial response after 120 days. Based on an incubation time of 12 min, it was found that the detection limit for paraoxon was equal to 1.7 × 10⁻⁷ mg L⁻¹ (6.2 × 10⁻¹³ M). The developed biosensor exhibited good repeatability and reproducibility. This study provides a new, modern, sensitive tool for the analysis of organophosphate pesticides.