How to evade the confrontation with the uncertainty relations

It is demonstrated that one can in principle register an arbitrarily small force acting on a free particle by employing only measurements of its coordinates.     

Rapid method for determining desmosine, isodesmosine, 5-hydroxylysine, tryptophan, lysinoalanine and the amino sugars in proteins and tissues

A rapid and sensitive chromatographic method is described for determining desmosine, isodesmosine, 5-hydroxylysine, tryptophan, lysinoalanine, glucosamine and galactosamine at picomole levels in protein and tissue hydrolysates. This method uses either an automated amino acid analyser with a 17.5 X 0.28 cm microcolumn packed with 6.0 +/- 0.5 micron spherical resin, thermostated at 52 degrees C, one buffer system (0.21 M sodium citrate, pH 5.125) and 3-nitrotyrosine as the internal standard, or conventional instruments using the same system but with larger diameter columns and resins (11.0 +/- 1.0 micron). This method should be especially valuable for determining collagen and elastin in tissue hydrolysates from the amounts of 5-hydroxylysine, and desmosine or isodesmosine present, respectively, and for studying protein hydroxylation, glycosylation, cross-linking formation, and the turnover rates of collagen and elastin in normal and diseased tissues.     

Photophysical studies of uranyl complexes: VIII. Luminescence spectra of UO2SO4 · 312H2O and two polymorphs of bis(urea) uranyl sulfate

The photoluminescence spectra of hydrated and anhydrous uranyl sulfates have been studied under conditions of high resolution at cryogenic temperatures. All uranyl sulfate systems were found to yield nonequivalent spectra: the energies for the electronic and vibronic origins were found to vary with the system, and certain uranyl vibrational frequencies exhibited a dependence on environment. These differences must reflect the various ways in which the uranyl centers are linked by the bridging sulfate groups, as this linking is the main difference between the various structures.     

Novel separation and preconcentration of trace amounts of copper(II) in water samples based on neocuproine modified magnetic microparticles

A novel, simple method based on magnetically assisted chemical separation (MACS) has been developed for analytical purposes. In this method, neocuproine modified magnetic microparticles was used for selective extraction and preconcentration of copper(II) ions from aqueous solutions. The advantages of this method include consumption of organic solvents almost eliminated and applications on unclear (containing suspended particles) samples without any preliminary filtration step. This method combines simplicity and selectivity of solvent extraction with easy separation of magnetic microparticles from solution with magnet. In addition, it can be considered as a simple method for determination of partition coefficient. The influence of different parameters, such as presence of extractant, amount of extractant loaded on the microparticles, reducing agent, pH, equilibrium time, ionic strength, type and least amount of stripping solution and limit of detection, were evaluated. Also, the effects of various cationic and anionic interferences on the percent recovery of copper were studied. Copper ions were extracted from solution at pH 6 and were stripped from microparticles with 0.5 M HNO₃. Extraction efficiencies for solutions with volumes up to 100 ml were >99%. Limit of detection was 1.5 μg/l. The method was applied to the recovery and determination of copper in different water samples.     

Fourier transform cyclic voltammetric technique for monitoring ultratrace amounts of salbutamol at gold ultra microelectrode in flowing solutions

This work introduce an easy and fast continuous cyclic voltammetric technique for the propose monitoring of ultra trace amounts of salbutamol in a flow–injection system. The potential waveform, which consisted of the potential steps for cleaning, stripping and potential ramp, was continuously applied on an Au disk microelectrode (with a radius of 12.5 μm). The detection method we propose has some advantages, the greatest of which are: (1) removing oxygen from the analyte solution is no longer necessary, and (2) it is a very fast and appropriate technique for the determination of the drug compound in a wide variety of chromatographic analysis methods. The detection limit for salbutamol was 2.0 × 10⁻⁹ M. The relative standard deviation (R.S.D.) of the proposed technique at 10 ng/mL was 3.5% for 10 runs. The effects of pH of eluent, accumulation potential, sweep rate, and accumulation time on the sensitivity of the method for the determination of the salbutamol were investigated. The proposed method was applied to the determination of salbutamol in pharmaceutical preparation and biological samples.     

Development a New Method for the Determination of Chloropromazine in Trace Amounts by Fast Fourier Continuous Cyclic Voltammetry at an Au Microelectrode in a Flowing System

In this study a new technique has been developed for the determination of chloropromazine in flow‐injection systems. The technique, named fast Fourier transformation continuous cyclic voltammetry (FFTCV), basically illustrates the benefits of sensitivity, selectivity, simplicity and low detection limit. It is also important to refer to the positive points, presented only by the use of this technique. Firstly, it is no longer necessary to remove the oxygen from the test solution. Furthermore, the quick determination of any such compound in many chromatographic methods is possible. Thirdly, the corresponding detection limit is of sub‐nanomolar level. Additionally, a special computer based numerical method is also introduced for the calculation of the analyte signal and noise reduction. The electrode response was calculated in accordance with the partial and total charge exchanges on the electrode surface, after the background current subtraction from that of noise. The integration range of currents was set for all the potential scan ranges, including oxidation and reduction of Au surface electrode, to obtain a sensitive determination. The performed experiments aimed at measuring the effects of different parameters on the method sensitivity. In the end of these measurements, it was concluded that the method was linear for the concentration range of 0.32–31900 pg/mL (r = 0.996) with a limit of detection and quantitation 0.1 and 0.32 pg/mL, respectively. For the achievement of these optimum results, the parameter values were set to 100 V/s for the scan rate, 0.4 s for accumulation time, 800 mV for accumulation potential and 2 for the pH.     

Synthesis,Characterization and X‐ray Crystal Structure of a Chromium(III) Complex Obtained from a Proton‐Transfer Compound Containing 1,10‐Phenanthroline‐2,9‐dicarboxylic Acid and 2,6‐Pyridinediamine

The novel 1,10‐phenanthroline‐2,9‐dicarboxylate containing Chromium(III) complex, (pydaH)[Cr(phendc)₂] · 5H₂O, was synthesized using proton‐transfer compound LH₂, (pydaH₂)²⁺(phendc)^2?, (pyda: 2,6‐pyridinediamine; phendcH₂: 1,10‐phenanthroline‐2,9‐dicarboxylic acid) and thoroughly characterized by elemental analysis, IR spectroscopy, X‐ray crystallography and cyclic voltammetry. The complex crystallizes in the monoclinic space group P2₁/n with four formula units in the unit cell. The unit cell dimensions are: a = 13.962(3) Å, b = 14.529(3) Å, c = 16.381(3) Å and β = 106.691(4)°. In this complex, 1,10‐phenanthroline‐2,9‐dicarboxylate acts as a tridentate ligand and the lattice is composed of anionic hexacoordinated complex, [Cr(phendc)₂]^?, 2,6‐pyridiniumdiamine counter ion, (pydaH)⁺, and five lattice water molecules. Crystallographic characterization revealed that the resulting supramolecular structure is strongly stabilized by complicated network of hydrogen bonds between the crystallization water molecules, counter ion and both coordinated and uncoordinated carboxylate groups. There is no relevant π‐π interaction for this anionic complex between pyda or phendc moieties. The electrochemical studies indicated over potential for both the cathodic and anodic peaks of the complex with respect to the free Cr³⁺ ion, as a consequence of the energy requirement for rearrangement of the ligand at electrode surface.     

Monte Carlo simulation of photon densities inside the dermis in LLLT (low level laser therapy)

In this work, the photon distribution of He:Ne laser within dermis tissue is studied. The dermis as a highly scattering media was irradiated by a low power laser. The photon densities as well as the corresponding isothermal contours were obtained by two different numerical methods, i.e., Lambert-Beer and Welch. The results were compared to that of Monte Carlo subsequently.     

Quantum experiments with macroscopic mechanical objects

Recent achievements in the isolation of macroscopic mechanical objects from a heat bath make it possible to implement quantum measurements with such systems. In this case, either a free mass or an oscillator can be used as a test object. The advantage of the first variant is in significantly longer relaxation times achieved for free masses. The advantage of the second variant is in the absence of restrictions on the limiting measurement accuracy associated with internal losses in the meter. This restriction can be bypassed, retaining a long relaxation time typical of free masses, if a test oscillator with a ponderomotive electromagnetic rigidity is used. Estimates show that the potential sensitivity of this test body for the modern level of technology may be considerably higher than the standard quantum limit.     

A dysprosium nanowire modified carbon paste electrode for determination of levodopa using fast Fourier transformation square-wave voltammetry method

A new detection technique called the fast Fourier transform square-wave voltammetry (FFT-SWV) is based on the measurements of electrode admittance as a function of potential. The response of the detector (microelectrode) is fast, which makes the method suitable for most applications involving flowing electrolytes. The carbon paste electrode was modified by nanostructures to improve better sensitivity. The response is generated by a redox processes. The redox property of L-dopa was used for determination of it in human serum and urine samples. The support electrolyte that provided a more defined and intense peak current for L-dopa determination was at 0.05 mol l^?1 acetate buffer pH 7.0. Synthesized dysprosium nanowires make more effective surface like nanotubes [1], [2], [3], [4] so they are good candidates for using as a modifier for electrochemical reactions. The drug presented one irreversible oxidation peaks at 360 mV versus Ag/AgCl by modified nanowire carbon paste electrode which produced high current and reduced the oxidation potential about 80 mV.Furthermore, signal-to-noise ratio has significantly increased by application of discrete fast Fourier transform (FFT) method, background subtraction and two-dimensional integration of the electrode response over a selected potential range and time window. To obtain the much sensitivity the effective parameters such as frequency, amplitude and pH was optimized. As a result, C_DL of 4.0 × 10^?9 M and an LOQ of 7.0 × 10^?9 M were found for determination for L-dopa. A good recovery was obtained for assay spiked urine samples and a good quantification of L-dopa was achieved in a commercial formulation.