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排序方式: 共有82条查询结果,搜索用时 46 毫秒
1.
2.
Bacillus thuringiensis and recombinant Escherichia coli proteinaceous protoxins were subject to proteolysis and analyzed by capillary electrokinetic chromatography. Three resulting toxins (65 kDa) were baseline-resolved within 22 min using a 10 mM borate, pH 11 separation buffer consisting of 25 mM sodium dodecyl sulfate (SDS) and 30 mM phytic acid. The toxins displayed differential interactions with the SDS and phytic acid phases to effect their separation. The ion-pairing interaction between the analyte and phytic acid was also useful in preventing adsorption to the capillary walls and thus enhanced separation resolution and efficiency. The use of electrokinetic chromatography allows achievement of the separation in a significantly shorter time than conventional high-performance liquid chromatography (HPLC) using a diethylaminoethyl (DEAE) weak-anion exchanger. 相似文献
3.
Maleš Željan Plazibat Miško Vundać Vjera Bilušić Žuntar Irena Pilepić Kroata Hazier 《平面色谱法杂志一现代薄层色谱法》2004,17(4):280-285
JPC – Journal of Planar Chromatography – Modern TLC - The flowering tops of Hypericum hirsutum, H. montanum, H. perforatum subsp. angustifolium, H. perforatum subsp. perforatum, and H.... 相似文献
4.
An array of eight interdigitated microband gold electrodes (IDEs) has been developed together with electrophoretic separation for analysis of chlorinated hydroquinones (ClHQs) and benzoquinones (ClBQs). The IDE chip positioned very close to the separation capillary outlet served as an amplification/detection system without the requirement for frequent "capillary-electrode" alignment. ClHQs, electrophoretically migrating to the IDE surface, were oxidized at +1.1 V by seven electrodes of the array and then detected by the remaining electrode, poised at -0.1 V. Conversely, ClBQs were detected at +1.1 V by the detecting electrode after having been reduced at the 7 adjacent electrodes poised at -0.1 V. There was an amplification effect on both the detecting electrode as well as the adjacent electrodes because of the recycle between ClHQs and ClBQs. The detecting "amplification" current response was dependent on the potentials applied, the position of the detecting electrode on the array, the number of adjacent electrodes being used for recycling and the distance between the oxidative and reductive electrodes. Micellar electrokinetic chromatography (MEKC) separation of the analytes was achieved using 30 mM sodium dodecyl sulfate (SDS) with a detection limit in the range of 2-20 micro M. In addition to a facile "capillary-electrode" alignment, the important aspect described here was the capability of detecting through recycling a reduced compound (in the case of ClHQs) at a negative potential to circumvent fouling and electroactive interferences. An appealing feature was also the concurrent oxidation/reduction detection for each compound to ascertain peak assignment, as interfering compounds are less likely to exhibit the same oxidative/reductive characteristics and electrophoretic mobilities as the target analytes. 相似文献
5.
Milena Jelikić-Stankov Dejan Stankov Dušan Malešev Zorica Radović 《Mikrochimica acta》1991,103(1-2):65-70
By means of spectroscopic methods it has been found that demeclocycline reacts with molybdate ions forming a complex compound [MoO3HDMTC]2–. The relative stability constant of this compound has been determined by applying spectrophotometric methods. Under optimum conditions for complex formation a very sensitive spectrophotometric method for the estimation of demeclocycline in the concentration range 5.0–35.1 g/ml is proposed. The detection limit of the method is 2.5 g/ml of demeclocycline. The relative standard deviation (n=10) varies between 0.76% and 1.46%. The method proved to be accurate and sensitive for the analysis of the demeclocycline content in tablets. 相似文献
6.
Lourdes Infantes MaryF. Mahon Louise Male PaulR. Raithby SimonJ. Teat Jürgen Sauer Nadine Jagerovic Jos Elguero Sam Motherwell 《Helvetica chimica acta》2003,86(4):1205-1221
The structures of six new tetrazines have been determined and their molecular packing has been compared to the supermolecular architecture observed in related carboxylic acid dimers. In the tetrazines, covalent N? N bonds are considered to replace the intermolecular O? H???O hydrogen bonds of the carboxylic acids. In the systems investigated, it is apparent that, in the majority of cases, the covalent six‐membered ring of the tetrazine is an appropriate replacement for the carboxylic acid synthon. This apparent interplay between molecular and supramolecular units may have applications in the crystal engineering of new materials. 相似文献
7.
Marianayagam NJ Khan F Male L Jackson SE 《Journal of the American Chemical Society》2002,124(33):9744-9750
The FK506-FKBP12 binding-domain of the kinase FRAP (FRB) forms a classic up-down four-helical bundle. The folding pathway of this protein has been investigated using a combination of equilibrium and kinetic studies. The native state of the protein is stable with respect to the unfolded state by some 7 kcal mol(-1) at pH 6.0, 10 degrees C. A kinetic analysis of unfolding and refolding rate constants as a function of chemical denaturant concentration suggests that an intermediate state may be populated during folding at low concentrations of denaturant. The presence of this intermediate state is confirmed by refolding experiments performed in the presence of the hydrophobic dye 8-anilinonaphthalene-1 sulfonate (ANS). ANS binds to the partially folded intermediate state populated during the folding of FRB and undergoes a large change in fluorescence that can be detected using stopped-flow techniques. Analysis of the kinetic data suggests that the intermediate state is compact and it may even be a misfolded species that has to partially unfold before it can reach the transition state. Folding and unfolding rate constants in water are approximately 150-200 s(-1) and 0.005-0.06 s(-1), respectively, at neutral pH and 10 degrees C. The folding of FRB is somewhat slower than for other all-helical proteins, probably as a consequence of the formation of a metastable intermediate state. The folding rate constant in the absence of any populated intermediate can be estimated to be 8800 s(-1). Despite the presence of an intermediate state, which effectively slows folding, the protein still folds rapidly with a half-life of 5 ms at 10 degrees C. The dependence of the rate constants on denaturant concentration indicates that the transition state for folding is compact with some 80% of the surface area exposed in the unfolded state buried in the transition state. Data presented for FRB is compared with kinetic data obtained for other all-helical proteins. 相似文献
8.
Dr. Chao Zhao Dr. Louise Male Dr. Tzu-Yu Chen Joseph A. Barker Dr. Ian J. Shannon Dr. Paul A. Anderson 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(61):13865-13868
(NH4)2[Zn2(O3PCH2CH2COO)2]⋅5 H2O (BIRM-1) is a new metal phosphonate material, synthesized through a simple hydrothermal reaction between zinc nitrate and 3-phosphonopropionic acid, using urea and tetraethylammonium bromide as the reaction medium. In common with other metal–organic framework materials, BIRM-1 has a large three-dimensional porous structure providing potential access to a high internal surface area. Unlike most others, it has the advantage of containing ammonium cations within the pores and has the ability to undergo cation exchange. Additionally, BIRM-1 also exhibits a reversible dehydration behavior involving an amorphization-recrystallization cycle. The ability to undergo ion exchange and dynamic structural behavior are of interest in their own right, but also increase the range of potential applications for this material. Here the crystal structure of this new metal phosphonate and its ion exchange behavior with K+ as an exemplar are studied in detail, and its unusual structure-reviving property reported. 相似文献
9.
Bal Sydulu Singu Umashankar Male Palaniappan Srinivasan Srinivas Pabba 《Journal of Solid State Electrochemistry》2014,18(7):1995-2003
Polyaniline sulphate salt titanium dioxide composite (PANI-H2SO4·TiO2) was synthesized by chemical in situ polymerization of aniline in the presence of TiO2. The effect of anionic surfactant (sodium lauryl sulphate) in this reaction was also assessed. During the polymerization reaction, sodium lauryl sulphate (SLS) is converted to dodecyl hydrogen sulphate (DHS) in the presence of acidic medium and gets doped onto polyaniline along with sulphuric acid dopant, i.e. formation of polyaniline-sulphate-dodecyl hydrogen sulphate-titanium dioxide composite (PANI-H2SO4-DHS·TiO2). In the PANI-H2SO4-DHS·TiO2 composite, the presence of DHS is confirmed by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and energy-dispersive X-ray analysis (EDAX) and TiO2 is confirmed by XRD and EDAX results. In PANI-H2SO4-DHS·TiO2 system, the nanoparticle of TiO2 (10–20 nm) is uniformly embedded on nanofibres (20–60 nm) of PANI-H2SO4-DHS, and some part of PANI-H2SO4-DHS·TiO2 forms core–shell morphology, wherein TiO2 is in core and PANI-H2SO4-DHS in shell forms. Stability of PANI-H2SO4-DHS increases due to the incorporation of stable TiO2. Utility of PANI-TiO2 composite was carried out in supercapacitor cell system by performing cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance spectroscopic techniques in 1 M H2SO4 solution. Very low values of solution resistance, charge transfer resistance and time constant are obtained between 0.2 and 0.6 V. Initial specific capacitance values for the cell carried out at low and high current densities are found to be 280 and 205 F g?1, respectively, and after 1,700 charge–discharge cycles, its retention in the specific capacitance values is found to be the same (65–66 %) with coulombic efficiency of 98–100 %. A capacitor can work even at a high discharge rate. The efficiency of oxidizing and doping power increases with the use of a surfactant. Moreover, the use of a long chain surfactant dopant containing polyaniline as an electrode material plays an important role to increase the performance of the supercapacitor by allowing the electrolyte to easily enter and come out from PANI electrodes. 相似文献
10.
l,l′-dimethylferricinium (DMFe+),a stable and pH-insensitive blue dye, was prepared via enzymatic oxidation of a 1,1′-dimethylferrocene (DMFe):2-hydroxypropyl-β-cyclodextrin
(HPCD) watersoluble inclusion complex, using bilirubin oxidase immobilized onto porous aminopropyl glass beads via glutaraldehyde
activation. In the presence of glucose, DMFe+ was reduced to DMFe by reacting with the reduced glucose oxidase (FADH2), and the absorbance decrease was followed at 650 nm. In acetate pH 5.2 buffer, the response to glucose in blood serum was
nonlinear, especially in the low concentration range, because of a competition for the reduced glucose oxidase between the
DMFe+ dye and oxygen. At this pH, endogenous ceruloplasmin was also observed to oxidize residual DMFe (16%) in the dye preparation,
causing an increase in absorbance at 650 nm. An assay protocol was then developed using maleate buffer, pH 6.5, to overcome
these interferences as well as mutarotation of α-D-glucose. The results obtained for glucose in the blood serum samples agreed
well with those of the reference hexokinase/glucose-6-phosphate dehydrogenase method. 相似文献