Fabrication of a Novel Polymeric Scaffold for Amperometric Laccase Biosensor

Present work displays the preparation of an electrochemical biosensor using a conjugated polymer and laccase enzyme for catechol quantification in samples. The biosensing system is based on an enzyme immobilization on polymer modified graphite transducer surface. For that purpose, a random conjugated polymer, thienothiophene‐benzoxadiazole‐alt‐benzodithiophene (BOTT), was coated onto a graphite electrode surface via drop casting method followed by immobilization of a biomolecule (laccase) for sensing experiments. Herein, for the first time, we proposed a BOTT polymer as an inexpensive and effective way to fabricate highly sensitive and fast response biosensors. The proposed sensing system possessed superior properties with 0.38 μM limit of detection and 110.81 μA mM^?1 sensitivity. Furthermore, cyclic voltammetry and scanning electron microscopy techniques were used to examine the surface modifications. The proposed system could be useful for many future studies for catechol quantification in environmental samples.© 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 2333–2339     

Syntheses,structural characterizations and microbial activities of Ni(II) and Zn(II) 5-aminoisophthalate coordination polymers

Two coordination polymers with 5-aminoisophthalic acid (H₂aip), [Ni(μ-aip)(H₂O)₂(tmeda)]_n (1) and {H₂dap[Zn₂(μ-aip)(μ₃-aip)₂]?9H₂O}_n (2) (H₂aip = 5-aminoisophthalic acid, tmeda = N,N,N′-N′-tetramethylethylenediamine, dap = 1,3-diaminopropane) have been synthesized. Elemental and thermal analyses, magnetic susceptibilities, IR, AAS, mass and UV–vis spectroscopic studies have been performed to characterize the compounds. Nickel(II) has octahedral geometry by two oxygens of different carboxylates, bidentate, tmeda as bidentate chelating and two water ligands. Zn(II) has tetrahedral geometry by three oxygens of different carboxylate groups and one nitrogen by amine of aip. 1 crystallizes in the orthorhombic crystal system with space group Pccn and 2 in monoclinic crystal system with space group P2₁/c. Complex 2 exhibits photoluminescence properties in the solid state at room temperature. This study determined the susceptibility patterns of 1 and 2 against bacterial, yeast and mold micro-organisms. Antimicrobial activities were done on 12 different micro-organisms using the micro-dilution method. Tested microbial species were inhibited by 1 with a Minimum inhibitory concentrations (MIC) of 375–3000 μg mL^?1. Compound 2 showed antimicrobial activities against tested micro-organisms with a MIC of 188–1500 μg mL^?1. Compound 2 showed antibacterial activity against Legionella pneumophila sg1 375 μg mL^?1 (MIC value).     

An Electrochemical Acetylcholinesterase Biosensor Based on Fluorene(bisthiophene) Comprising Polymer for Paraoxon Detection

In this study, a novel conductive polymer comprising biosensor based on poly-2,2′-(9,9-dioctyl-9 h-fluorene-2,7-diyl)bistiophene (Poly(BT)) and acetylcholinesterase (AChE) was reported for the determination of paraoxon. This practical biosensor allowed to catalyze electrochemical oxidation of acetylthiocholine (+0.6 V vs. Ag reference). The detection range for acetylcholine chloride (AThCl) with Poly(BT)/AChE was found to be 0.025–4 mM. In pesticide analysis, wide linear ranges from 0.5 to 1 μg/L and 1 to 14 μg/L, and a low detection limit of 0.033 μg/L were estimated. Under optimum operating conditions, the developed biosensor was used for pesticide detection in milk and tap water samples, effectively.     

风速波动时基于UKF-DFNN的变桨距控制

针对风速大于额定风速时风速波动引起风电机组的功率波动及变桨距系统频繁启停的问题,提出基于无迹卡尔曼滤波(unscented Kalman filter,简称UKF)与动态模糊神经网络(dynamic fuzzy neural network,简称DFNN)相结合的变桨距控制策略.为了消除传统变桨距控制中风速作为输入信号时产生的时延,将风电机组转速及输出功率作为反馈输入量.利用UKF对反馈输入量进行实时滤波处理,且将滤波后的数据用DFNN动态调整其权重,得到精确的桨距角指令值.采用Matlab/Simulink构建仿真模型,将UKF-DFNN控制与模糊PID、径向基函数(radial basis function,简称RBF)神经网络控制进行对比分析.仿真结果表明:所提策略能提高风速波动时系统的鲁棒性、抑制桨距角的波动范围、输出稳定的功率.     

基于启发算法的含大规模新能源电力系统静态安全域分析

大规模新能源并网使电力系统不确定性增加,传统稳定性分析方法存在局限性,因此考虑从三维静态安全域(static security region, SSR)的角度进行系统静态稳定性分析。针对常规算法耗时长、精度低的不足,提出IPSO-RLS混合算法,该算法基于连续潮流数据,追踪系统稳定运行的电压、有功和无功功率安全域临界点,并形成SSR临界曲面。利用DIgSILENT/Power Factory软件对哈密电网三个风电场区域进行案例仿真并分析。最后,用灵敏度分析法验证SSR曲面的稳定性及可行性。结果表明,IPSO-RLS混合算法分析含高比例新能源电力系统SSR具有较好的鲁棒性和实用性。     

Determination of ivacaftor by liquid chromatography techniques in pharmaceutical formulation with interlaboratory comparison and characterization of five novel degradation products by high-performance liquid chromatography ion trap time-of-flight mass spectrometry

Cystic fibrosis is a life-threatening genetic disease that causes damage to the lungs. Ivacaftor, the first drug to target the underlying defect of the disease caused by specific mutations, improves outcomes and reduces hospitalizations. In this study, quantitative determination of ivacaftor was performed by liquid chromatography, while high-resolution mass spectrometric analyses were performed for qualitative determination. The validation studies of the developed methods were performed according to International Conference on Harmonisation Q2(R1) guideline. Ivacaftor was separated from its degradation product by using Phenomenex Kinetex C₁₈ (150 × 3 mm, 2.6 µm) column. The isocratic mobile phase for binary pump configuration was 0.1% (v/v) formic acid in water and 0.1% (v/v) formic acid in acetonitrile (27:63) (v/v), pH = 2.5; the flow rate of 0.25 mL/min was used in all methods. In the degradation studies, five degradation products were identified using high-performance liquid chromatography ion trap time-of-flight mass spectrometric analyses: three of them have never been reported up to date; whereas the other two were existing in the literature and they were having Chemical Abstracts Services registry numbers since they were synthesized before for various other purposes. Also, analysis of an in-lab prepared chemical equivalent of Kalydeco^® and interlaboratory comparison were performed.     

Liquid chromatographic determination of lumacaftor in the presence of ivacaftor and identification of five novel degradation products using high-performance liquid chromatography ion trap time-of-flight mass spectrometry

Lumacaftor is a transmembrane conductance regulator potentiator drug, prescribed for the treatment of cystic fibrosis in patients who are homozygous for the F508del mutation. Quantitation of lumacaftor besides its degradation products and ivacaftor was achieved on a fused-core silica particle column packed with pentafluorophenylpropyl stationary phase (Ascentis Express F5, 2.7 μm particle size 100 mm × 4.6 mm; Supelco) using gradient elution (A: 0.1% [v/v] formic acid in water, B: 0.1% [v/v] formic acid in acetonitrile [the mobile phase pH 2.5]). A constant flow rate at 1 mL/min was applied, and the detection was realized using a photodiode array detector set at 216 nm. The pseudo tablet formulation of the lumacaftor/ivacaftor fixed-dose combination preparation, namely, Orkambi®, was prepared in vitro and used for the analytical performance validation and method application studies. In addition, five novel degradation products, four of which even have no Chemical Abstracts Services registry number, were identified using high-resolution mass spectrometry instrument, and their possible mechanisms of formation were proposed. According to current literature, this paper can be regarded as the most comprehensive liquid chromatographic study on lumacaftor determination, among its counterparts.