An environmentally benign method of sample preparation based on dispersive liquid–liquid microextraction and solidification of floating organic droplets (DLLME-SFO) coupled with high-performance liquid chromatography with ultraviolet detection has been developed for analysis of non-steroidal anti-inflammatory drugs (NSAIDs) in biological fluids. A low-toxicity solvent was used to replace the chlorinated solvents commonly used in conventional DLLME. Seven
conditions were investigated and optimized: type and volume of extraction solvent and dispersive solvent, extraction time, effect of addition of salt, and sample pH. Under the optimum conditions, good linearity was obtained in the range 0.01–10 µg mL−1, with coefficients of determination (r2) >0.9949. Detection limits were in the range 0.0034–0.0052 µg mL−1 with good reproducibility (RSD) and satisfactory inter-day and intra-day recovery (95.7–115.6 %). The method was successfully used for analysis of diclofenac, mefenamic acid, and ketoprofen in human urine. Analysis of urine samples from a patient 2 and 4 h after administration of diclofenac revealed concentrations of 1.20 and 0.34 µg mL−1, respectively.
Molecular imprinting is an approach to synthesize receptors with specific molecular recognition properties. A computational method was carried out to study interaction between template and monomer in prepolymerization mixture. The functional monomer and template complexes were optimized, at the minimum energy confirmation using Austin Model 1 semi empirical method within Restricted Hartree Fock formalism. The theoretical results showed that allylthiourea (functional monomer) has the largest interaction energy towards template (sodium nitrate) with the mole ratio of 4 : 1; functional monomer : template. The resulting polymers were characterized using Fourier Transform infrared spectroscopy, thermogravimetry analysis and field emission scanning electron microscopy. Rebinding experiments were carried out to evaluate binding capacity of the polymer. The adsorption data of ion imprinted polymer (IIP) were fitted with Langmuir-Freundlich isotherm model. Pseudo-second order kinetic model was used to describe the kinetic adsorption behavior of IIP. The experimental binding result showed good agreement with theoretical computation and the IIP was further used for nitrate ion detection. The results of membrane optimization indicated that the sensor, which composed of 30% polyvinylchloride, 60% nitrophenyl octyl ether as a plasticizer, 2% sodium tetraphenyl borate, and 10% IIP as ionophore exhibited an almost Nernstian slope with the limit of detection 3.9 × 10-6 M. The fabricated sensor had shown good potential in nitrate detection with wide linear range, low limit of detection and found to have good selectivity towards nitrate ion over other anion. 相似文献
This article deals with a forced Burgers equation (FBE) subject to the initial function, which is continuous and summable on . Large time asymptotic behavior of solutions to the FBE is determined with precise error estimates. To achieve this, we construct solutions for the FBE with a different initial class of functions using the method of separation of variables and Cole–Hopf like transformation. These solutions are constructed in terms of Hermite polynomials with the help of similarity variables. The constructed solutions would help us to pick up an asymptotic approximation and to show that the magnitude of the difference function of the true and approximate solutions decays algebraically to 0 for large time. 相似文献
The study of hydrolysis on biodegradable poly(butylene succinate) (PBS) is essential to predict the materials properties in a humid environment. In this study, PBS nanocomposites were exposed to different conditions of relative humidity (RH) and temperature. The moisture uptake increased with organo-montmorillonite (OMMT) loading and the RH of the testing environment. The exposure of PBS and the nanocomposites to a humid environment caused changes in the mechanical properties. The hydrolytic degradation becomes more pronounced upon hygrothermal aging at high temperature, whereby premature failure occurred. PBS nanocomposites were found to exhibit a better hydrolytic stability than neat PBS. The degradation was evaluated through Fourier transform infrared (FTIR) spectroscopy and gel permeation chromatography (GPC). A drastic reduction in the molecular weight of PBS has revealed the occurrence of degradation after exposure to moisture and heat. This has led to an alteration of the thermal behavior as investigated using differential scanning calorimetry (DSC). 相似文献
A thermostable lipase from Geobacillus zalihae strain T1 was chemically modified using propionaldehyde via reductive alkylation. The targeted alkylation sites were lysines,
in which T1 lipase possessed 11 residues. Far-UV circular dichroism (CD) spectra of both native and alkylated enzyme showed
a similar broad minimum between 208 and 222 nm, thus suggesting a substantial amount of secondary structures in modified enzyme,
as compared with the corresponding native enzyme. The hydrolytic activity of the modified enzymes dropped drastically by nearly
15-fold upon chemical modification, despite both the native and modified form showed distinctive α-helical bands at 208 and
222 nm in CD spectra, leading us to the hypothesis of formation of a molten globule (MG)-like structure. As cooperative unfolding
transitions were observed, the modified lipase was distinguished from the native state, in which the former possessed a denaturation
temperature (Tm) in lower temperature range at 61 °C while the latter at 68 °C. This was further supported by 8-anilino-1-naphthalenesulfonic
acid (ANS) probed fluorescence which indicated higher exposure of hydrophobic residues, consequential of chemical modification.
Based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, a small number
of lysine residues were confirmed to be alkylated. 相似文献
(1S,2S)-N1,N2-Bis(3-chlorobenzyl)cyclohexane-1,2-diamine 1a′ and (1S,2S)-N1,N2-bis(4-chlorobenzyl)cyclohexane-1,2-diamine 1b′ were used to prepare chiral Cu(II) complexes Cu-Y-1a, Cu-Y-1b, Cu-mZSM5-1a, and Cu-mZSM5-1b by a flexible ligand method using copper exchanged zeolite Y and mesoporous ZSM-5. The characterization of zeolite supported complexes was performed by microanalysis, IR-, diffuse reflectance spectroscopy (DRS), EPR spectroscopy, specific rotation and thermogravimetric analysis (TGA). The catalytic activity of these supported complexes was explored for the asymmetric nitroaldol reaction of various aldehydes with nitromethane at 0 °C. Excellent yields (up to 99%) of β-hydroxy nitroalkane with an ee of up to 94% were achieved in the case of benzaldehyde as substrate. Significantly, the performance of the supported catalyst was better in terms of enantioselectivity than the complex under homogenous conditions. The supported catalysts were recycled four times with no observable loss in performance and no leaching of the catalytically active complex during the nitroaldol reaction. 相似文献
New Schiff base ligand L derived from the condensation reaction of 2-amino-3-formylchromone with (R)-2-amino-2-phenylethanol was synthesized and characterized which involves combination element of ammine functionality and naturally occurring heterocyclic chromone, 4H-benzopyran-4-one. Subsequently, their complexes 1 and 2 with Cu(NO?)? and Zn(NO?)?, respectively were prepared. The DNA binding studies of the ligand L and complexes 1 and 2 with CT-DNA as compared to classical anticancer drug cisplatin were carried out by employing different optical methods viz, UV-vis, fluorescence, circular dichroism and viscosity measurements. Furthermore, the absorption studies, 1H and 31P with mononucleotides were also monitored to examine the base specific interactions of the transition metal complexes which revealed a higher propensity of copper(II) complex 1 for 5'-GMP while for zinc(II) complex 2 towards 5'-TMP involving groove binding mechanism of the complexes towards DNA. The complex 1 exhibits a remarkable DNA cleavage activity with pBR322 DNA in presence of different activators and cleavage reaction involves various oxygen species suggesting the involvement of active oxygen species for the DNA scission. 相似文献
Extraction and chromatographic separation of the extracts of dried stem barks of Glycosmis macrantha lead to isolation of two new acridone alkaloids, macranthanine and 7-hydroxynoracronycine, and a known acridone, atalaphyllidine. The structures of these alkaloids were determined by detailed spectral analysis and also by comparison with reported data. 相似文献
The reaction of glycerol with urea to form glycerol carbonate is mostly reported in the patent literature and to date there have been very few fundamental studies of the reaction mechanism. Furthermore, most previous studies have involved homogeneous catalysts whereas the identification of heterogeneous catalysts for this reaction would be highly beneficial. This is a very attractive reaction that utilises two inexpensive and readily available raw materials in a chemical cycle that overall, results in the chemical fixation of CO(2). This reaction also provides a route to up-grade waste glycerol produced in large quantities during the production of biodiesel. Previous reports are largely based on the utilisation of high concentrations of metal sulfates or oxides, which suffer from low intrinsic activity and selectivity. We have identified heterogeneous catalysts based on gallium, zinc, and gold supported on a range of oxides and the zeolite ZSM-5, which facilitate this reaction. The addition of each component to ZSM-5 leads to an increase in the reaction yield towards glycerol carbonate, but supported gold catalysts display the highest activity. For gold-based catalysts, MgO is the support of choice. Catalysts have been characterised by XRD, TEM, STEM and XPS, and the reaction has been studied with time-on-line analysis of products via a combination of FT-IR spectroscopy, HPLC, (13)C NMR and GC-MS analysis to evaluate the reaction pathway. Our proposed mechanism suggests that glycerol carbonate forms via the cyclization of a 2,3-dihydroxypropyl carbamate and that a subsequent reaction of glycerol carbonate with urea yields the carbamate of glycerol carbonate. Stability and reactivity studies indicate that consecutive reactions of glycerol carbonate can limit the selectivity achieved and reaction conditions can be selected to avoid this. The effect of the catalyst in the proposed mechanism is discussed. 相似文献
Lactic acid produced by fermentation process mostly contains a number of aliphatic carboxylic acids as impurities. In this work, carboxylic acid impurities in lactic acid samples from a number of sources were determined at ppm levels. A simple HPLC method was developed that utilized a new generation polar embedded reverse phase, 20mM phosphate buffer at pH 2.20 (±0.05) and UV detection at 210 nm. The method enabled quantitative analysis of the above acids in lactic acid matrix. The experimental conditions for column temperature, mobile phase pH and flow rate were optimized. A detailed validation of the method was performed for linearity, precision, accuracy, selectivity, limit of detection (LOD), limit of quantitation (LOQ), ruggedness and repeatability and reproducibility (R&R). 相似文献