Spectrofluorimetric Assessment of Doxycycline Hydrochloride in Pharmaceutical Tablets and Serum Sample Based on the Enhancement of the Luminescence Intensity of the Optical Sensor Sm<Superscript>3+</Superscript> Ion

A simple and sensitive spectrofluorimetric method for determination of trace amount of doxycycline hydrochloride (DC) in pharmaceutical tablets and serum samples was developed. In ammonia buffer solution of pH 8.9 the doxycycline hydrochloride can remarkably enhance the luminescence intensity of the Sm³⁺ ion in Sm³⁺- DC complex at λ_ex = 400 nm. The produced luminescence intensity of Sm³⁺- DC complex in DMSO is in proportion to the concentration of DC and used as optical sensor for its determination. The dynamic range for the determination of DC is 1 × 10⁻⁸ – 5 × 10⁻⁶ mol L⁻¹ and in case of quantum yield calculations is 7 × 10⁻⁹ – 5 × 10⁻⁶ mol L⁻¹ with detection limit of 6.5 × 10⁻¹⁰ mol L⁻¹. The enhancement mechanism of the luminescence intensity in the Sm³⁺- DC system has been also discussed. A comparison with other spectrofluorimetric methods for tetracycline derivatives in which Eu³⁺ ion is used instead of Sm³⁺ ion is also studied.     

Monitoring of all hydrogen isotopologues at tritium laboratory Karlsruhe using Raman spectroscopy

We have recorded Raman spectra for all hydrogen isotopologues, using a CW Nd:YVO₄ laser (5 W output power at 532 nm) and a high-throughput (f/1.8) spectrograph coupled to a Peltier-cooled (200 K) CCD-array detector (512 × 2048 pixels). A (static) gas cell was used in all measurements. We investigated (i) “pure” fillings of the homonuclear isotopologues H₂, D₂, and T₂; (ii) equilibrated binary fillings of H₂ + D₂, H₂ + T₂, and D₂ + T₂, thus providing the heteronuclear isotopologues HD, HT, and DT in a controlled manner; and (iii) general mixtures containing all isotopologues at varying concentration levels. Cell fillings within the total pressure range 13–985 mbar were studied, in order to determine the dynamic range of the Raman system and the detection limits for all isotopologues. Spectra were recorded for an accumulation period of 1000 s. The preliminary data evaluation was based on simple peak-height analysis of the ro-vibrational Q₁-branches, yielding 3σ measurement sensitivities of 5 × 10⁻³, 7 × 10⁻³, and 25 × 10⁻³ mbar for the tritium-containing isotopologues T₂, DT, and HT, respectively. These three isotopologues are the relevant ones for the KATRIN experiment and in the ITER fusion fuel cycle. While the measurement reported here were carried out with static-gas fillings, the cells are also ready for use with flowing-gas samples.     

The Sensitive Determination of Nucleic Acids Using Fluorescence Enhancement of Eu<Superscript>3+</Superscript>-BenzoylacetoneCetyltrimethylammonium Bromide-Nucleic Acid System

A new quantitative method for micro amounts of nucleic acids in aqueous solution is proposed using Eu³⁺-benzoylacetone (BA) complex as fluorescent probe in the presence of cetyltrimethyl-ammonium bromide (CTMAB). Under the optimum condition, the ratio of the fluorescence intensities with and without nucleic acids is proportional to the concentration of nucleic acid in the range of 1.0 × 10⁻⁹ to 5.0 × 10⁻⁶ g/mL for herring sperm DNA (hsDNA), 3.0 × 10⁻⁹ to 1.0 × 10⁻⁶ g/mL for calf thymus DNA(ctDNA) and 8.0 × 10⁻⁹ to 1.0 × 10⁻⁶ g/mL for yeast RNA (yRNA), and their detection limits are 0.33, 0.21 and 0.99 ng/mL, respectively. Actual sample (DNA of Arabidopsis thaliana) was determined satisfactorily. In addition, the interaction mechanism is also investigated.     

Fluorescence Enhancement Effect for the Determination of Polychlorinated Biphenyls with Bovine Serum Albumin

A sensitive and selective method for the trace determination of 3, 3’, 4, 4’-tetrachlorobiphenyl (PCB77) by using bovine serum albumin (BSA) as a fluorescence probe was introduced. Under optimum conditions, the enhanced fluorescence intensity was proportional to the concentration of polychlorinated biphenyls in the range of 8.9 × 10⁻⁸–5.0 × 10⁻⁶ mol L⁻¹ for PCB77, and 5.0 × 10⁻⁷–5.0 × 10⁻⁶ mol L⁻¹ for 2, 2’, 5, 5’-tetrachlorbiphenyl (PCB52). The detection limits (S/N = 3) of PCB77 and PCB52 were 2.6 × 10⁻⁸ mol L⁻¹ and 2.9 × 10⁻⁷ mol L⁻¹, respectively. Furthermore, the fluorescence enhancement mechanism was discussed in detail. Results indicated that fluorescence enhancement of the system originated from the formation of BSA-PCBs complexes. In addition, PCBs were mainly bound to the tyrosine residues in BSA molecules.     

Integral energy spectrum of primary cosmic rays at high energies

The integral energy spectrum of primary cosmic rays has been obtained. In the energy range (2.4×10³−1.1×10⁵ GeV), the spectrum of all nuclei is consistent with a power law of indexγ=1.55±0.06 and the flux of all nuclei is:N(⩾E ₀)⋍(5.1±1.8)×10⁻¹×E ₀ ^−1.55 particles/cm² sterad. sec., whereE ₀ is in GeV. The spectrum of primaryα-particles in the energy range (4.4×10³−4.8×10⁴) GeV is also consistent with a power law of indexγ=1.71±0.12 and the flux is:N(⩾E ₀)=(4.2±1.4)×10⁻¹×E ₀ ^−1.71 , particles per cm² sterad. sec, whereE ₀ is in GeV.     

Differential capacitance of hybrid organic/inorganic CdSe/ZnS quantum dots light-emitting device

We have studied the differential capacitance of self-assembly hybrid organic/inorganic quantum dot (QD) light-emitting devices (QD-OLEDs) at room temperature in the frequency range of 1×10³ to 1×10⁶ Hz. Self-assembly CdSe/ZnS QDs monolayer was used to fabricate trilayer hybrid QD-OLEDs on indium tin oxide coated glass substrates. We observed negative differential capacitance (NDC) in both OLED and QD-OLEDs for the first time in the intermediate frequency range of 5×10³ to 5×10⁵ Hz. The onset and frequency range of NDC are strongly depended on the applied bias voltage. This behavior is described by a mathematical model. The simulated results showed that the NDC was due to the time-dependent transient current from the QDs and organic/metal interfacial states in the device. The probable mechanisms of NDC in organic devices are discussed.     

Target plasma formation by UHF power

The properties of plasma injected into an open magnetic trap of uniform field from an independent UHF source have been investigated. Plasma is created in the UHF source at the frequency of 2400 MHz (power input 150 W) in the electron cyclotron resonance (ECR) regime at the pressure of neutral argon (10⁻⁵−10⁻²) torr. It is established that a rather quiescent target plasma with controlled density within the range of (2 × 10⁸−2 × 10¹²) cm⁻³ and temperature 2–3eV is accumulated in the trap. It turned out that plasma lifetime in the trap is determined by a classical mechanism of particle escape at the expense of collisions, at fixed value of magnetic field in the trap it practically is not changed with the variation of neutral gas pressure and reaches the value ≈ 4×10⁻³ s at the magnetic field strength in the trap equal 1600 Oe.     

Determination of Catechin in Aqueous Solution by Chemiluminescence Method

A method to determine catechin in aqueous solution by measuring chemiluminescence intensities using a stopped flow system has been studied. The lucigenin-hydrogen peroxide chemiluminescence reaction was chosen for the determination of catechin. Fe(II) ion was added to the chemiluminescence system to increase the sensitivity. The chemiluminescence intensity from the lucigenin system was increased by the addition of catechin. Effects of flow rates of reagent and sample and concentrations of lucigenin, hydrogen peroxide, Fe(II) ion and KOH were investigated. The calibration curve for catechin was linear over the range from 1.0×10⁻⁶ to 1.0×10⁻³ M and the detection limit was 3.0×10⁻⁷ M under the optimal experimental conditions.     

Study of Enhanced Chemiluminescence of Diperiodatocuprate (III) on 1,10-Phenanthroline/Hydrogen Peroxide/Cetyltrimethylammonium Bromide System

In the paper, a chemiluminescence (CL) system was developed based on the catalytical effect of diperiodatocuprate (III) (DPC) on the 1,10-phenanthroline (phen)/hydrogen peroxide (H₂O₂) in the presence of cetyltrimethylammonium bromide (CTAB). The effects of experimental conditions were investigated. Meanwhile the increase of CL intensity of the DPC/phen/H₂O₂/CTAB system is proportional to the concentration of phen in the range of low concentration. The linear range of the calibration curve is 5.0 × 10⁻⁹–1.0 × 10⁻⁶ mol L⁻¹, and the corresponding detection limit is 1.9 × 10⁻⁹ mol L⁻¹. The effects of phenolic compounds (PCs) on the system were investigated. Hydroquinone was used as an example to investigate the application of the CL system to the determination of PCs. The quenched CL intensity is linearly related to the logarithm of concentration of hydroquinone. The linear range of the calibration curve is 2.5 × 10⁻⁹–1.0 × 10⁻⁵ g mL⁻¹, and the corresponding detection limit is 1.8 × 10⁻⁹ g mL⁻¹. This phen and hydroquinone can be synchronously determined. The method was applied to the determination of hydroquinone in water samples and the recoveries were from 92% to 106%.     

Methods of reference signal and phase shifts in the multipass laser schemes for the detection of trace gas impurities

The application of the methods using the phase shift of modulated radiation and ICOS for the measurement of relatively low concentrations of gas impurities is considered. The measurement sensitivities of 0.01 ppbv and 6 × 10⁻¹¹ cm⁻¹ with respect to concentration and absorption coefficient, respectively, are obtained for the NO₂ molecules.     

Influence of the axial magnetic field on the current instability and on the collective acceleration of ions in plasma diodes

It is shown that, while suppressing transverse electron motion, the axial magnetic field with an induction of up to 6.8 × 10⁻² T in the gap of a plasma diode has no significant effect on the current instability and on the acceleration of ions at electron beam currents of ≤40 A. The increase in both the critical current and the period of current oscillations is related to an increase in the plasma density after applying the magnetic field. The maximum energy of the accelerated magnesium ions decreases by ≈25% at an induction of 1.7 × 10⁻² T and does not depend on the magnetic field in the range (1.7–6.8) × 10⁻² T.     

On magnetic field penetration into a granulated superconductor

The frequency dependence of the magnetic response of YBa₂Cu₃O_7−x high-temperature supercon-ducting ceramics is studied. The experimental results are obtained for different values of the constant ((0–99)×10⁻⁴ T) and variable ((0.18–7.24)×10⁻⁴ T) components of the external magnetic field in the frequency range from 60 Hz to 1 MHz. A simple qualitative model of the distributed Josephson medium is offered to account for the results obtained.     

Effect of Viscosity on the Spin Exchange of TCNE and TEMPO Radicals with Iron(III) Acetylacetonate

The spin exchange of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) and the radical anion of tetracyanoethene (TCNE), with iron acetylacetonate, Fe(acac)₃, was investigated as a function of solvent viscosity and temperature by X-band EPR spectroscopy. Acetone, methanol, ethanol, 1-propanol, 1-pentanol, 1-hexanol, 1-octanol, and chloroform were used as solvents because they provide a wide range of viscosity. The spin exchange rate constants measured in the different solvents ranged from 3 × 10⁸ to 8 × 10⁹ M⁻¹ s⁻¹, and from 7 × 10⁸ to 1 × 10¹⁰ M⁻¹ s⁻¹ for the TEMPO/Fe(acac)₃ and the TCNE/Fe(acac)₃ systems, respectively. The spin exchange rate constants, k _e, are compared with the corresponding diffusion rate constants. It was found that the k _e values correlate well with those of diffusion and hence the intermolecular spin exchange is strongly diffusion-controlled. The activation energies and pre-exponential factors are calculated from the Arrhenius plots.     

Radiation removal of lead and cadmium complexed with ethylenediamine tetraacetic ACID from aqueous solutions

The removal of lead (100 mg/L) and cadmium (27 mg/L) complexed with ethylenediamine tetraacetic acid (EDTA) in presence of different scavengers has been investigated. The experiments show that in acidic solutions, the EDTA complexed lead may be reduced at a dose of 40 kGy up to 97% without the addition of typical OH radical scavengers such as Na(K) formate. The addition of OH radical scavengers as 1×10⁻³ mol/L HCOOK, 2×10⁻³ mol/L carbonate or 2×10⁻³ mol/L bicarbonate (wide range of pH) results in no further improvement. The bubbling of the solution with nitrogen or oxygen also exhibits no positive effect. On the contrary, saturation with nitrous oxide in the presence of scavengers has a modest positive influence, whereas in the system which is scavenger-free, high negative effect (30 %) was observed. The presence of nitrate (e _aq ⁻ scavenger) appears to be important for an effective reduction of complexed lead. The efficient removal of cadmium complexed with EDTA proceeds up to 96 % at a dose of 40 kGy with an addition of 5×10⁻³ mol/L of carbonate as the OH radical scavenger and simultaneously pH buffer (pH 10.5). After irradiation, the cadmium is present in the final form of CdCO₃.     

Control of acceptor doping in MOCVD HgCdTe epilayers

The acceptor doping of mercury cadmium telluride (HgCdTe) layers grown by MOCVD are investigated. (111)HgCdTe layers were grown on (100)GaAs substrates at 350°C using horizontal reactor and interdiffused multilayer process (IMP). TDMAAs and AsH3 were alternatively used as effective p-type doping precursors. Incorporation and activation rates of arsenic have been studied. Over a wide range of Hg_1−xCd_xTe compositions (0.17 < x < 0.4), arsenic doping concentration in the range from 5×10¹⁵ cm⁻³ to 5×10¹⁷ cm⁻³ was obtained without postgrowth annealing. The electrical and chemical properties of epitaxial layers are specified by measurements of SIMS profiles, Hall effect and minority carrier lifetimes. It is confirmed that the Auger-7 mechanism has decisive influence on carrier lifetime in p-type HgCdTe epilayers.     

Diagnostics of height distribution of InAs/GaAs quantum dot arrays by means of carbon tetrachloride treatment in vapor phase epitaxy conditions

A technique for determination of InAs quantum dots bimodal distribution has been developed. This technique is based on vapor-chemical etching of quantum dot arrays coated with thin GaAs layers and on combined investigation of the morphology and photoluminescence spectra of etched quantum-size structures. It has been shown that, in some growth modes of quantum-size heterostructures by metal-organic vapor phase epitaxy, bimodal arrays of large and small quantum dots are formed. The surface concentration of large and small dots has been established to be about 2 × 10⁹ and 3 × 10¹⁰ cm⁻², respectively.     

A New Spectrofluorimetric Method for Determination of Trace Amounts 5-Hydroxytryptamine in Human Urine and Serum

A new spectrofluorimetric method was developed for the determination of trace amount of 5-hydroxytryptamine (5-HT) in human urine and serum samples. In the NaAc-HAc buffer solution of pH=5.80, 5-HT can react with formaldehyde-acetylacetone system to form a new compound which sends yellow green fluorescence at 533nm and the enhanced fluorescence intensity is in proportion to the concentration of 5-HT. Optimum conditions for the determination of 5-HT were also investigated. The dynamic range and detection limit for the determination of 5-HT are 5.35×10⁻⁷∼1.07×10⁻⁴ mol/L and 2.08×10⁻⁷ mol/L, respectively. The developed method is simple, practical and can be successfully applied to determination of 5-HT in human urine and serum samples. Moreover, the enhancement mechanisms of the fluorescence intensity in the 5-HT - formaldehyde-acetylacetone system have been also discussed.     

Pyrophosphate Selective Recognition in Aqueous Solution Based on Fluorescence Enhancement of a New Aluminium Complex

A novel and simple fluorescence enhancement method for selective pyrophosphate(PPi) sensing was proposed based on a 1:1 metal complex formation between bis(8-hydroxy quinoline-5-solphonat) chloride aluminum(III) (Al(QS)₂Cl), (L) and PPi in aqueous solution. The linear response range covers a concentration range of 1.6 × 10⁻⁷ to 1.0 × 10⁻⁵ mol/L of PPi and the detection limit of 2.3 × 10⁻⁸ mol/L. The association constant of L-PPi complex was calculated 2.6 × 10⁵ L/mol. L was found to show selectively and sensitively fluorescence enhancement toward PPi over than I₃^-, NO₃^-, CN⁻, CO₃²⁻, Br⁻, Cl⁻, F⁻, H₂PO4⁻ and SO₄²⁻, which was attributed to higher stability of inorganic complex between pyrophosphate and L.     

Formation of ordered helium pores in amorphous silicon subjected to low-energy helium ion irradiation

Thin transparent (for transmission electron microscopy, TEM) self-supported Si(001) films are irradiated on the (110) end face by low-energy (E=17 keV) He⁺ ions at doses ranging from 5×10¹⁶ to 4.5×10¹⁷ cm⁻² at room temperature. The TEM study of the irradiated Si films along the ion range shows that an a-Si layer forms in the most heavily damaged region and helium pores (bubbles) with a density of up to 3×10¹⁷ cm⁻³ and 2–5 nm in diameter nucleate and grow across the entire width of this layer. The growth of nanopores in the a-Si layer is accompanied by their linear ordering into chains oriented along the ion tracks. The absence of pores in the region that remains crystalline and has the maximal concentration of implanted helium is explained by the desorption of helium atoms from the thin film during the irradiation. After annealing at 600°C, the volume of immobile pores in the remaining a-Si layer increases owing to the capture of helium atoms from the amorphous matrix. Solid solution is shown to be the prevalent state of the helium implanted into the amorphous silicon. Linear features with a diameter close to 1 nm and density of about 10⁷ cm⁻¹ discovered in the helium-doped a-Si layer are identified as low-energy He⁺ ion tracks.     

Photoluminescence as a tool for the study of the electronic surface properties of gallium arsenide

Electronic surface parameters of GaAs have been determined from a qualitative and quantitative analysis of the relative photoluminescence intensity at 300 K. Characteristics of etched (100) surfaces ofn- andp-type liquid phase epitaxial GaAs have been found to be governed by negative surface charges. A density of charged surface states of about 10¹² cm⁻² and a band bending of 0.59 eV have been found forn-type material with an electron concentration of 1.1×10¹⁷ cm⁻³. Forp-type samples with hole densities ranging from 6×10¹⁵ to 4.3×10¹⁸ cm⁻³ the estimated density of negatively charged surface states was below 2×10¹¹ cm⁻², and the band bending was not more than a few kT.