A soluble single-point mutant of full-length Mos1 mariner transposase (MW = 40.7 kDa) has been overexpressed in Escherichia coli, puri®ed to 95% homogeneity and crystallized. This provides the ®rst example of the crystallization of a eukaryotic transposase. The native crystals diffract to 2.5 A Ê resolution and show tetragonal symmetry, with unit-cell parameters a = b = 44.5, c = 205.6 A Ê . Multiplewavelength anomalous data from a selenomethionyl form of the protein and data from a heavy-atom derivative have been collected.
In order to precisely control the wind power generation systems under nonlinear variable wind velocity, this paper proposes a novel maximum power tracking (MPPT) strategy for wind turbine systems based on a hybrid wind velocity forecasting algorithm. The proposed algorithm adapts the bat algorithm and improved extreme learning machine (BA-ELM) for forecasting wind speed to alleviate the slow response of anemometers and sensors, considering that the change of wind speed requires a very short response time. In the controlling strategy, to optimize the output power, a state feedback control technique is proposed to achieve the rotor flux and rotor speed tracking purpose based on MPPT algorithm. This method could decouple the current and voltage of induction generator to track the reference of stator current and flux linkage. By adjusting the wind turbine mechanical speed, the wind energy system could operate at the optimal rotational speed and achieve the maximal power. Simulation results verified the effectiveness of the proposed technique.
Abstract. To investigate the possibility of liquid proliposomes being carriers for oral delivery, nimodipine liquid proliposomes-based soft capsules (NPSC) were prepared. Nimodipine proliposomes were characterized by transmission electron microscopy (TEM), conversion rate from proliposomes to liposomes, entrapment efficiency, particle size, and zeta potential. Accelerated stability testing of NPSC was carried out for 3 months at 40±2°C, 75±5% RH. The concentration of nimodipine in plasma of New Zealand rabbits of NPSC, nimodipine soft capsules, and hydrated liposomes was studied. Results showed that nimodipine proliposomes were automatically converted into liposomes when exposed to a water phase in 30 s. The average diameter was 378.6±26.5 nm in distilled water with entrapment efficiency (EE%) of 84.7±5.9%, while the average diameter was 316.9±34.6 nm in 0.1 M hydrochloric acid solution with EE% of 72.8±4.7%. Accelerated stability test showed that there was no change in drug content, particle size, and EE% except for a decrease in dissolution of nimodipine. In vivo experiments, areas under the plasma level-time curve of NPSC and nimodipine-hydrated liposomes increased 2.41 and 2.34 times more than that of nimodipine soft capsules, peak concentration increased 2.87 and 2.92 times, time of peak concentration from 0.75 to 2 and 1 h, respectively. Nimodipine-hydrated liposomes presented similar pharmacokinetic parameters compared with NPSC. Results suggested that NPSC offered a potential way to improve oral delivery of nimodipine.
Ionic-liquid-based dispersive liquid–liquid microextraction combined with high performance liquid chromatography was used to determine four fluoroquinolone drugs in meat.
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