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61.
A simple, rapid and efficient sample preparation technique, dispersive liquid-liquid microextraction, coupled with gas chromatography-flame ionization detection has been developed to determine N-methylpyrrolidine in cefepime. The effect of various experimental factors on the preparation procedure, such as the nature and volume of extraction and disperser solvents, extraction time, the nature of buffer and its pH, and salt effect, was investigated, optimized and the following results were obtained: extraction solvent, chloroform; dispersive solvent and solvent for dissolving cefepime, a mixture of methanol/water (88:12, v/v); salting out agent, NaCl; and buffer, carbonate/bicarbonate (C=0.5?M, pH=12). The optimized conditions were applied to the real sample (cefepime) for the extraction and determination of N-methylpyrrolidine. The calibration graph is linear from 0.02 to 850?mg/L with the square of correlation coefficient 0.999. LOD and LOQ are 6.4 and 21.2?μg/L in solution, respectively, and 0.2 (2×10(-5) ) and 0.6 (6×10(-5) ) μg/g (%, w/w) in cefepime powder, respectively, using sample size 50?mg. Repeatability of the method is good and RSD% for six repeated experiments (C=170?mg/L) is 6.35%. 相似文献
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Parvin Farshchi Seyed Khatiboleslam Sadrnezhaad Naser Moharram Nejad Mahmood Mahmoodi Leila Ibrahimi Ghavam Abadi 《Journal of nanoparticle research》2011,13(8):3511-3519
Using survey data, public awareness of and attitudes toward nanotechnology are examined in Iran (N = 759). Iran is a developing country with a national nanotechnology action plan for a ten year period starting from 2003
and has been active in the field of research and development of nanotechnology meanwhile. First, the results show that majority
of people are still not familiar with nanotechnology and perceived risks posed by this technology are not considered to be
a lot and most people feel its benefits outweigh the risks. The emotions toward this technology are of a hopeful and positive
nature and this technology is looked upon favorably in Iran. In particular, our results reveals that although the level of
trust is high specially in scientists to communicate the risks with the public, there are a great number who just have some
trust not quite a lot of it. Knowing that it is a hard and time-consuming effort to manage a nation’s view on nanotechnology,
extensive research as well as collaboration with other countries is needed to effectively communicate the risks in time. 相似文献
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The synthesis and crystal structure of a novel hydrate of lithium cyclohexaphosphate are reported. Li6P6O18·10H2O crystallizes in the space group C2/c with a = 15.113(5), b = 12.006(2), c = 15.892(2) Å, = 122.85(2)°, and Z = 4. The structure consists of P6O18 ring layers stacked along the c direction in between which are located the lithiumions and water molecules. Two LiO4 tetrahedra share common edges with LiO5 pseudosquare pyramids to form two independant Li3O9 units. About 50% of the water molecules have fractional occupancy rates and form fragments of molecules. A linear relationship is established between the relative cell volume V/Z and the hydration degree, n, for all the known hydrates: Li6P6O18·nH2O. 相似文献
67.
Debbie van der Burg Leila Josefsson Saara Mikkonen Véronique Chotteau Åsa Emmer Hermann Wätzig Cari E. Sänger-van de Griend 《Electrophoresis》2022,43(9-10):922-929
The rapidly growing, competitive biopharmaceutical market requires tight bioprocess monitoring. An integrated, automated platform for the routine online/at-line monitoring of key factors in the cell culture medium could greatly improve process monitoring. Mono- and disaccharides, as the main energy and carbon source, are one of these key factors. A CE-LIF method was developed for the analysis of several mono- and disaccharides, considering requirements and restrictions for analysis in an integrated, automated monitoring platform, such as the possibility for miniaturization to microchip electrophoresis. Analysis was performed after fluorescent derivatization with 8-aminopyrene-1,3,6-trisulfonic acid. The derivatisation reaction and the separation BGE were optimized using design of experiments. The developed method is applicable to the complex matrix of cell culture medium and proved transferable to microchip electrophoresis. 相似文献
68.
Leila Hasniou Belkacem Nessark Naima Maouche 《Russian Journal of Applied Chemistry》2017,90(4):633-640
In the present work, a new composite material poly(3T + 6T + TiO2) was electrochemically synthesized. This composite material was synthesized in a solution of (CH2Cl2/TBAP) containing the monomers (terthiophene), (sexithiophene) and semiconductor (TiO2) particles. The preparedsamples were characterized electrochemically by cyclic voltamperometry (CV) and spectrometry analysis by scanning electron microscopy (SEM), ultraviolet-visible (UV-Vis) absorption spectroscopy, energy dispersive X-ray spectroscopy (EDX) and fourier transform infrared spectroscopy (FTIR), respectively. The effect of TiO2 concentration in the solution on dispersed microparticle entity and on the photocurrent response was investigated. The results showed that TiO2 particles were dispersed and codeposited into the copolymer poly(3T + 6T + TiO2) matrix, and titanium atom was confirmed by EDX spectra. From SEM images, the TiO2 has a spherical shape and micrometer size. The FTIR spectrum indicated that titanium dioxide do not show a significant modification in terms of band shape and no interaction between polymers and TiO2 particles. Furthermore, the results showed that the composite films with different amounts of TiO2 exhibit good photocurrent properties which imply that these composites films can be used in various fields, such as photoelectrochemical applications as photovoltaic cells. 相似文献
69.
A dispersive liquid‐liquid microextraction method based on the dispersion of 1,2‐dichlorobenzene as an extraction solvent into an aqueous phase in the presence of ethanol as a dispersive solvent for the preconcentration of Co2+ and Ni2+ ions is discussed. 1‐Nitroso 2‐naphtol was used as a chelating agent prior to the extraction and the preconcentrated analyte was determined by flame atomic absorption spectrometry. The effect of various experimental parameters including the extraction and dispersive solvent type and volume, pH, amount of the chelating agent, etc. on the microextraction and complex formation was investigated for finding the optimum conditions. The enhancement factors were about 61.9 and 51.8, the calibration graphs were linear in the range of 10‐150 μgL?1 and 10‐250 μgL?1 with detection limits of 2.42 μgL?1 and 1.59 μgL?1, and RSD (n = 5) of 3.08% and 2.17% for cobalt and nickel, respectively. The method was successfully applied to the determination of Co and Ni in water and vitamin B12. 相似文献
70.