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Mohamed Ibrahim A.,Fathy Mohamed,Farghal Ahmed I.A.,Temerak Sobhy A.H.,Sayed Alaa El-Din H. 한국응용곤충학회 2021 Journal of Asia-Pacific Entomology Vol.24 No.1
The mosquito Culex pipiens is the most widely distributed dipteran species in all regions of Egypt and the principal vector of Wuchereria bancrofti and certain arboviruses in human beings. For controlling C. pipiens vector, biological tools (e.g., larvivorous fish and bioinsecticides) are more potent and safer options to the environment, human beings, and beneficial organisms than chemical pesticides. The efficiency of O. niloticus juveniles as predatory fish species and two bioinsecticides, spinosad 24% and spinetoram 12%, was investigated against the C. pipiens developmental stages in the laboratory. The first trial evaluated the predatory efficacy of small-sized O. niloticus (2.1–2.6 cm; 250–315 mg) and large-sized O. niloticus (2.5–3.2 cm; 250–315 mg) against the 3rd larvae and pupae of C. pipiens. This is the first report in Egypt confirming the predation potential of O. niloticus as efficient predatory fish against the immature C. pipiens. Large-sized O. niloticus predated a greater number of 3rd of C. pipiens larvae and pupae than the small-sized ones. Furthermore, the daily consumption of C. pipiens larvae by small- and large-sized O. niloticus was significantly higher than the pupae. The second trial assessed the toxicity efficacy of spinosad 24% and spinetoram 12% against C. pipiens larvae and pupae. The results confirmed that the tested bioinsecticides showed higher potency toward C. pipiens larvae than pupae after exposure for 24 h and 48 h. Spinosad was more toxic toward 3rd C. pipiens larvae (LC 50 = 0.013 and 0.003 mg/L) and pupae (LC 50 = 320.69 and 44.28 mg/L) than spinetoram after 24 and 48 h. Herein, O. niloticus juveniles (as promising native predatory fish) and spinosyns bioinsecticides were more effective against C. pipiens in the larval stage than in the pupal stage. In conclusion, Nile tilapia juveniles and biorational compounds, spinosad 24% and spinetoram 12%, might be considered as promising and favorable environmental biological agents for controlling C. pipiens in Egypt. However, further trials are needed to investigate the potential of these agents in the control of this mosquito vector under field conditions.
Hozoi, L.,Gretarsson, H.,Clancy, J. P.,Jeon, B.-G.,Lee, B.,Kim, K. H.,Yushankhai, V.,Fulde, Peter,Casa, D.,Gog, T.,Kim, Jungho,Said, A. H.,Upton, M. H.,Kim, Young-June,van den Brink, Jeroen American Physical Society 2014 Physical review. B, Condensed matter and materials Vol.89 No.11
In the search for topological phases in correlated electron systems, materials with 5d transition-metal ions, in particular the iridium-based pyrochlores A2Ir2O7, provide fertile grounds. Several topological states have been predicted but the actual realization of such states is believed to critically depend on the strength of local potentials arising from distortions of the IrO6 cages. We test this hypothesis by measuring with resonant inelastic x-ray scattering the electronic level splittings in the A = Y, Eu systems, which we show to agree very well with ab initio quantum chemistry electronic-structure calculations for the series of materials with A = Sm, Eu, Lu, and Y. We find, however, that the primary source for quenching the spin-orbit interaction is not a distortion of the IrO6 octahedra but longer-range lattice anisotropies which inevitably break the local cubic symmetry.
M. M. Rashad,M. Rasly,I. A. Ibrahim,H. M. El-Sayed,A. A. Sattar 한국물리학회 2013 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.63 No.3
Co2Z-type hexagonal ferrite powders doped with La3+ ions (Ba3−XLaxCo2Fe24O41 where x =0.0, 0.05, 0.10 and 0.15) were prepared using a co-precipitation method. The results revealed thatsingle-phase Co2Z-type ferrite was formed from the precipitated precursor in the presence of sodiumdodecyl sulfate (SDS) as an anionic surfactant. The obtained precursor was preheated at 600 ℃ for4 h then post annealed at 1300 ℃ for 6 h. The crystallite size increased with increasing of La3+-ion molar ratio. The microstructure of the formed powders appeared to be a hexagonal-plateletlikestructure. The DC resistivity of the obtained Co2Z decreased with increasing La3+ content. The saturation magnetization (Ms = 53.7 - 55.5 emu/g) was slightly increased with increasingsubstitution of La3+ ion. Moreover, two resonance frequency peaks were observed through theimaginary part of complex magnetic permeability; meanwhile, a decrease in the real part of thecomplex magnetic permeability was observed through the X-band frequencies.
El-Said I. El-Shafey,Haider A. J. Al-Lawati,Wafa S. H. Al-Saidi 한국탄소학회 2016 Carbon Letters Vol.19 No.-
Date palm leaflets were used as a precursor to prepare dehydrated carbon (DC) via phosphoric acid treatment at 150°C. DC, acidified with H3PO4, was converted to activated carbon (AC) at 500°C under a nitrogen atmosphere. DC shows very low surface area (6.1 m2/g) while AC possesses very high surface area (829 m2/g). The removal of lisinopril (LIS) and chlorpheniramine (CP) from an aqueous solution was tested at different pH, contact time, concentration, and temperature on both carbons. The optimal initial pH for LIS removal was 4.0 and 5.0 for DC and AC, respectively. However, for CP, initial pH 9.0 showed maximum adsorption on both carbons. Adsorption kinetics showed faster removal on AC than DC with adsorption data closely following the pseudo second order kinetic model. Adsorption increases with temperature (25°C–45°C) and activation energy (Ea) is in a range of 19–25 kJ mol/L. Equilibrium studies show higher adsorption on AC than DC. Thermodynamic parameters show that drug removal is endothermic and spontaneous with physical adsorption dominating the adsorption process. Column adsorption data show good fitting to the Thomas model. Despite its very low surface area, DC shows ~70% of AC drug adsorption capacity in addition of being inexpensive and easily prepared.
Salwa Elmeligie,Azza T. Taher,Nadia A. Khalil,Ahmed H. El-said 대한약학회 2017 Archives of Pharmacal Research Vol.40 No.1
Novel series of 1,3,4-trisubstituted azetidin-2-one derivatives 8a–p were synthesized and proposed ascytotoxic agents acting via inhibition of tubulin at thecolchicine binding site. The design of the target compoundswas based upon modification in the structure of the vasculartargeting agent combretastatin A-4 (CA-4). The cisdouble bond linker in CA-4 was replaced with the azetidin-2-one ring aiming to prevent the cis/trans isomerizationthat suppresses the activity of CA-4, thereby enhancing itsantiproliferative activity. All new compounds were investigatedin vitro against MCF-7 and HCT-116 cell lines. Theinhibition of tubulin polymerization by four most potentcompounds 8g, 8j, 8n and 8o was also evaluated. Thesynthesis of the final targets was achieved adopting Staudingerreaction. Molecular modeling studies were performedto rationalize the biological results.
Kurls E. Anwer,Ahmed A. Farag,Eslam A. Mohamed,Eman M. Azmy,Galal H. Sayed 한국공업화학회 2021 Journal of Industrial and Engineering Chemistry Vol.97 No.-
The present investigation aims to synthesize and explore the influence of pyridine and pyran derivativeson the API X-65 steel corrosion in a 6 M H2SO4 solution. The compound was examined at differentconcentrations to optimized the best concentration for the corrosion inhibition effect, weight lossmeasurements, potentiodynamic polarization measurement (PDP), electrochemical impedance spectroscopy(EIS), scanning electron microscopy (SEM) and theoretical methods were used to evaluating theinhibition efficiency. The obtained adsorption data achieved the model of Langmuir isotherm. Thepyridine derivatives showed higher inhibition than pyran derivatives. The PDP tests proposed thatpyridine and pyran derivatives are mixed-type inhibitors. The EIS parameters demonstrate that thedouble-layer capacitance (Cdl) decreases with the increase of inhibitor concentration, which implies areduces dielectric constant. It was observed from experimental data that the inhibition efficiency reached92.7%, 89.1, 94.7, and 85.2% for concentration 2.66 10 3M of I, II, III and IV, respectively indicating theinhibition order is III > I > II > IV. The parameters derived from the theoretical quantum chemicalcalculations were found adequately correlated with the obtained experimental results.
Alaa Youssef,Dalia A. Al-Mahdy,Rabab H. Sayed,Mouchira A. Choucry,Hesham El-Askary 한국식품영양과학회 2022 Journal of medicinal food Vol.25 No.9
Alopecia or hair loss is a widespread issue that has significant effects on personal well-being for both genders nationally and internationally. In addition, alopecia causes extreme emotional stress and negatively impacts the psychological health and self-esteem of cancer patients suffering from chemotherapy-induced alopecia. Unfortunately, available synthetic medications are costly, invasive, or have extreme adverse effects. On the contrary, natural and herbal hair loss products are widely available in the local and international markets in variable pharmaceutical forms with different mechanisms of action, namely, androgen antagonists, nutritional supplements, vasodilators, and 5α-reductase inhibitors or dihydrotestosterone blockers. Thus, it is of great importance to encourage researchers to investigate these natural alternatives that can act as potent therapeutic agents having diverse mechanisms of action as well as limited side effects. Currently, natural remedies are considered a fast-rising pharmaceutical segment with demand from a wide range of consumers. In this study, we present a review of reported herbal remedies and herb combinations recommended for hair loss and their mode of action, along with an overview of available market products and formulations, their composition, and declared effects. In addition, a general outline of the different forms of alopecia, its causes, and recommended treatments are mentioned as well. This was all done with the aim of assisting further studies with developing standardized natural formulations for alopecia as many were found to lack standardization of their bioactive ingredients and efficiency confirmation.
Amplitude analysis ofe+e−→ϒ(nS)π+π−ats=10.866 GeV
Garmash, A.,Bondar, A.,Kuzmin, A.,Abdesselam, A.,Adachi, I.,Aihara, H.,Al Said, S.,Asner, D. M.,Aulchenko, V.,Aushev, T.,Ayad, R.,Bakich, A. M.,Bala, A.,Bhardwaj, V.,Bobrov, A.,Bonvicini, G.,Bozek, A. American Physical Society 2015 PHYSICAL REVIEW D - Vol.91 No.7
Measurement of time-dependent CP asymmetries in B0→KS0ηγ decays
Nakano, H.,Ishikawa, A.,Sumisawa, K.,Yamamoto, H.,Adachi, I.,Aihara, H.,Al Said, S.,Asner, D. M.,Aulchenko, V.,Aushev, T.,Ayad, R.,Babu, V.,Badhrees, I.,Bansal, V.,Behera, P.,Beleñ,o, C.,Bhuyan, American Physical Society 2018 Physical Review D Vol.97 No.9
<P>We report a measurement of time-dependent CP violation parameters in B-0 -> K-S(0)eta gamma decays. The study is based on a data sample, containing 772 x 10(6)B(B)over-bar pairs, that was collected at the Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric-energy e(+)e(-) collider. We obtain the CP violation parameters of S = -1.32 +/- 0.77(stat) +/- 0.36(syst) and A = -0.48 +/- 0.41(stat) f 0.07(syst) for the invariant mass of the K-S(0)eta system up to 2.1 GeV/c(2).</P>
Mahmood A. Hamed,Seiichi Nakata,Kazuya Shiogama,Kenji Suzuki,Ramadan H. Sayed,Yoichi Nishimura,Noboru Iwata,Kouhei Sakurai,Badawy S. Badawy,Ken-ichi Inada,Hayato Tsuge,Yutaka Tsutsumi 대한이비인후과학회 2017 Clinical and Experimental Otorhinolaryngology Vol.10 No.3
Objectives. Cholesteatoma is a nonneoplastic destructive lesion of the temporal bone with debated pathogenesis and bone resorptive mechanism. Both molecular and cellular events chiefly master its activity. Continued research is necessary to clarify factors related to its aggressiveness. We aimed to investigate the expression of Ki-67, cytokeratin 13 (CK13) and cytokeratin 17 (CK17) in acquired nonrecurrent human cholesteatoma and correlate them with its bone destructive capacity. Methods. A prospective quantitative immunohistochemical study was carried out using fresh acquired cholesteatoma tissues (n=19), collected during cholesteatoma surgery. Deep meatal skin tissues from the same patients were used as control (n=8). Cholesteatoma patients were divided into 2 groups and compared (invasive and noninvasive) according to a grading score for bone resorption based upon clinical, radiologic and intraoperative findings. To our knowledge, the role of CK17 in cholesteatoma aggressiveness was first investigated in this paper. Results. Both Ki-67 and CK17 were significantly overexpressed in cholesteatoma than control tissues (P<0.001 for both Ki-67 and CK17). In addition, Ki-67 and CK17 were significantly higher in the invasive group than noninvasive group of cholesteatoma (P=0.029, P=0.033, respectively). Furthermore, Ki-67 and CK17 showed a moderate positive correlation with bone erosion scores (r=0.547, P=0.015 and r=0.588, P=0.008, respectively). In terms of CK13, no significant difference was found between cholesteatoma and skin (P=0.766). Conclusion. Both Ki-67 and CK17 were overexpressed in cholesteatoma tissue and positively correlated with bone resorption activity. The concept that Ki-67 can be a predictor for aggressiveness of cholesteatoma was supported. In addition, this is the first study demonstrating CK17 as a favoring marker in the aggressiveness of acquired cholesteatoma.