Supramolecular Study on the Interaction Between Ofloxacin and Methyl β-Cyclodextrin by Fluorescence Spectroscopy and its Analytical Application

The supramolecular interaction of ofloxacin (Oflo) and methyl β-cyclodextrin (Mβ-CD) has been examined by UV–vis, IR and fluorescence spectroscopy. The formation of inclusion complex has been confirmed based on the changes of the spectral properties. The results showed that Mβ-CD reacted with Oflo to form an inclusion complex. The Oflo and Mβ-CD complex formed a host-guest complex in 1:1 stoichiometry and inclusion constant (K?=?7.8?×?10^?3 L mol^?1) was ascertained by the typical double reciprocal plots. Furthermore, the thermodynamic parameters (?H°, ?S° and ?G°) associated with the inclusion process were also determined. In addition, solid inclusion complex was synthesized. Based on the significant enhancement of the fluorescence intensity of Oflo produced through complex formation, a simple, accurate, rapid and highly sensitive spectrofluorometric method for the determination of Oflo in pharmaceutical formulation was developed. The measurement of relative fluorescence intensity was carried out at 497 nm with excitation at 296 nm. The factors affecting the inclusion complex formation were studied and optimized. Under the optimum reaction conditions, linear relationships with good correlation coefficients (0.9995) were in the concentration range of 50–350 ng/mL for spectrofluorimetry. The limit of detection (LOD) was 11.5 ng/mL. The proposed method was successfully applied to the analysis of Oflo in pharmaceutical preparation.     

The Co-luminescence Effect of Eu–Gd–Ofloxacin–SDBS System and its Analytical Application

A fluorescence enhancement phenomenon in the europium (Eu)–Ofloxacin (OF)–Sodium Dodecyl Benzene Sulfonate (SDBS) fluorescence system was observed when Gd³⁺ was added. The fluorescence intensity of the systems was measured (λ _ex/λ _em = 280/612 nm) at pH 7.8. Under optimum conditions, a linear relationship between the enhanced fluorescence intensity and the Eu³⁺ concentration in the range of 5.0 × 10⁻¹⁰ ∼ 2.0 × 10⁻⁷ mol·L⁻¹ was observed. The detection limit of Eu³⁺ was 1.46 × 10⁻¹⁰ mol·L⁻¹ (S/N = 3). This method was used for the determination of trace amounts of europium in synthetic rare earth samples with satisfactory results. In addition, the interaction mechanism is also studied.     

Study on the New Fluorescence Enhancement System of Tb –N-(2 - Pyridinyl) Ketoacetamide-Et<Subscript>3</Subscript>N-Zn and its Application

A sensitive fluorescence enhancement system was developed for the determination of zinc (II). The fluorescence intensity of the Tb- N- (2 - Pyridinyl) ketoacetamide (PKA) system was greatly enhanced by the addition of triethylamine (Et₃N) and zinc nitrate in the methanol solution. The excitation and emission wavelengths were 329 nm and 546 nm, respectively. Under optimal conditions, the fluorescence intensities varied linearly with the concentration of Zn²⁺ in the range of 8.0×10⁻⁷−5.0×10⁻⁶ M with a detection limit of 9.9×10⁻⁸ M. The interferences of some substances were described. This method was applied to the determination of amounts of Zn²⁺ in soybean, rice, and wheat, respectively. The results showed that the proposed procedure is a high selective, simple, and rapid method to the determination of Zn²⁺ ion. The mechanism of fluorescence enhancement was also studied.     

Analytical Solution and Production of Coherent State of the Generalized Dissipative Two-Mode Optical System

We obtain the analytical solution to the master equation in the photon number representation by using algebraic dynamical method in the nonautonomous case. Based on the solution we find that a two-mode coherent sate can be produced within dissipative background, and the averaged photon number for each mode is related to the damping constant, external field amplitude and coupling constant between two modes.     

Determination of the Composition and Thickness of Co–Ni/Cr System Films by X-Ray Fluorescence

A procedure of determining the composition and thickness of Co–Ni/Cr two-layer films on Polycor by means of x-ray fluorescence is developed. The correction factors that take into account the effects of the mutual influence of the elements in the given system are calculated. The density of the materials entering into the composition of the films is determined experimentally. The metrological characteristics of the procedure are established.     

Fluorescence Enhancement of a Polymer Planar Waveguide Doped with Rhodamine B and Ag Nanoparticles

Planar polymer multi-model waveguides doped with Ag nano-particles and rhodamine B are fabricated and investigated by the spectroscopy analysis method as well as the M-line method. Experimental results shown that fluorescence enhancement occurs when excited by a wide band wavelength with Ag nano-particle concentration at a certain level. The maximum enhancement factor in our experiment is obtained to be about 3.8 when excited by 350 nm. Our study may have potential applications in polymers optical elements, such as polymer waveguide lasers and amplifiers.     

Analytical Interaction of the Acoustic Wave and Turbulent Flame

A modified resonance model of a weakly turbulent flame in a high-frequency acoustic wave is derived analytically. Under the mechanism of Darrieus-Landau instability, the amplitude of flame wrinkles, which is as functions of the expansion coefficient and the perturbation wave number, increases greatly independent of the stationary＇ turbulence. The high perturbation wave number makes the resonance easier to be triggered but weakened with respect to the extra acoustic wave. In a closed burning chamber with the acoustic wave induced by the flame itself, the high perturbation wave number is to restrain the resonance for a realistic flame.     

Application of Gas Chromatography–Atomic Fluorescence Spectrometry Hyphenated System for Speciation of Butyltin Compounds in Water Samples

ABSTRACT

A laboratory-established capillary gas chromatography (GC)–atomic fluorescence spectrometry (AFS) hyphenated system was applied to butyltin speciation in water samples. Monobutyltin (MBT), dibutyltin (DBT), and tributyltin (TBT) were extracted and preconcentrated with headspace solid-phase microextraction (SPME) technique after derivatization using KBH₄, and then determined by GC-AFS directly. The experimental conditions—including the flow rates of carrier gas, argon and hydrogen–and the lamp current—were optimized in detail. Under the optimum conditions, the detection limits for MBT, DBT, and TBT, calculated as three times the baseline noise, were 10, 0.2, and 0.1 ng mL^?1 Sn, respectively. Good linear relationships were obtained when the concentrations of MBT, DBT, and TBT increased to 3000, 100, and 200 ng mL^?1 Sn. The relative standard deviations (RSDs) of five replicates were 5.2%, 7.4%, and 7.1% for MBT, DBT, and TBT, respectively. The recoveries of MBT, DBT, and TBT in three different types of water samples (seawater, tap water, and wastewater) were between 72.1% and 97.9%, indicating that the proposed method was accurate and feasible for speciation analysis of butyltin compounds in water samples.     

Output Intensity Variations of the Laser Used in a Prism Coupling System and Its Application

The output intensity variations of the laser used in a prism coupling system are observed and found to be induced by the external optical feedback, which comes from the reflection on the prism. The intensity variations are explained with laser theory. The trough in the intensity variation corresponds to the position of the prism when the output light beam propagates perpendicularly to the prism. Based on the trough a new method for rotating the prism and reading out the step numbers is proposed, by which the angle 0° in the system need not to be calibrated. It is proven by experiment that the new method would improve the accuracy of the refractive index up to ±0.00001 and thickness to ±1 nm.     

A Generalization of the Arzelà–Ascoli Theorem and its Application to Dyson Perturbation Theory

An approximate sequence U_n(t, t₀) for the time-development operator U(t,t₀) has been constructed, when n it approaches the Dyson series. A generalization of the Arzelà–Ascoli theorem for a set of continuous functions to a set of operators is given. We show that if the norm of H(t) in Equation (1.1) is a Lebesgue integrable function with respect to time t, then the Dyson series is uniformly weak convegent and Equation (1.1) has a unique solution. The preliminary application of the above results to quantum mechanics is studied.     

On the dynamics and optimization of a non-smooth bistable oscillator – Application to energy harvesting

Bistable nonlinear oscillators can transform slow sinusoidal excitations into higher frequency periodic or quasi-periodic oscillations. This behaviour can be exploited to efficiently convert mechanical oscillations into electrical power, but being nonlinear, their dynamical behaviour is relatively complicated. In order to better understand the dynamics of bistable oscillators, an approximate bilinear analytical model, which is valid for narrow potential barriers, is developed. This model is expanded to the case of wider potential with experimental verification. Indeed, the model is verified by numerical simulations and a suitable Poincaré section that the analytical model captures most of bifurcations for large amplitude vibrations and can be used to optimize the harvested power of such devices. The method of Shaw and Holmes [1] is enhanced by exploiting symmetry to obtain closed form expressions of the Poincaré section and mapping.     

Study on the Cofluorescence Effect of Europium (III)–Yttrium (III)–Balofloxacin–Sodium Dodecyl Sulfate System and Its Analytical Application

A new fluorescence enhancement phenomenon in the europium(III)–balofloxacin–sodium dodecyl sulfate system was observed when yttrium(III) was added. Based on this, a sensitive cofluorescence assay for the estimation of balofloxacin was established. Under the optimized conditions, the enhanced fluorescence signal was linear over the concentration of balofloxacin ranging from 3.0 × 10^?9 to 7.0 × 10^?6 mol L^?1 with a correlation coefficient of 0.9993. The detection limit (3 σ) was determined as 8.3 × 10^?10 mol L^?1. The presented method was successfully applied to determination of balofloxacin in pharmaceutical preparations, human serum, and urine. The possible fluorescence enhancement mechanism was also discussed.     

Simultaneous Extension and Enhancement of the HHG Plateau by Using Combined Lasers Irradiating on a United Two-Atom System

We present the high-order harmonic generation spectrum from a united two-atom system simultaneously exposed to a fundamental Ti:sapphire and its 33rd harmonic (H33) lasers by numerically solving a one-dimensional timedependent Schroedinger equation. At a suitable inter-nuclear separation, the harmonic plateau is widened from Ip 3.2Up in the single-atom case up to Ip 5.6Up in the united-atom case. Furthermore, the plateau is heightened in excess of six orders of magnitude by using the combined lasers compared with the case of the fundamental laser alone. Such a scheme can step by step accomplish the following processes: through a single H33 photon resonance transition an appropriate amount of electrons are first populated to an excited state, in which the electrons are easily ionized and subsequently accelerated by the fundamental laser; then they can recombine with the neighbouring atom, so that high-efficiency emissions of the harmonics beyond Ip 3.2Up are successfully realized.     

Effects of Room Temperature Ionic Liquids on Fluorescence Characteristics of 17β-estradiol and its Derivative

Previous reports have seldom concerned about the RTILs (Room temperature ionic liquids), and their effects on derivatization reaction or derivatives. In this study, we reported that the effects of four different RTILs, i.e., [EMIM]PF₆, [BMIM]PF₆, [HMIM]PF₆ and [OMIM]PF₆, on fluorescence spectra of 17 β-estradiol (E2), and its derivatization solvent dansyl chloride (DNSCl) and the derivative. [BMIM]PF₆ had a significant quenching effect on the fluorescence intensity of E2, suggesting the formation of [BMIM]PF₆/E2 complexes and possible buried E2 molecular in a more hydrophobic microenvironment. The estimated Stern-Volmer quenching constant (Ksv = 0.3519) proved that E2 quenching caused by [BMIM]PF₆ was a dynamic quenching process. Four RTILs, with different alkyl chain-length in imidazolium cation, resulted in different quenching intensities to E2 as follows: [EMIM]PF₆ > [BMIM]PF₆ > [HMIM]PF₆ > [OMIM]PF₆. At 5 mg L⁻¹ of DNSCl, [BMIM]PF₆, [HMIM]PF₆ and [OMIM]PF₆ increased the fluorescence intensities of E2 in water by 8.5, 7.6 and 6.1 times, respectively, and a 37-nm hypsochromic shift occurred. The fluorescence intensity for [BMIM]PF₆-extracted derivative of E2 increased more than two times compared with that for the control. In conclusion, this study demonstrated that above four hexafluorophosphate salt ionic liquids could be used in derivatization reaction to enhance fluorescent sensitivity in E2 trace residual analysis.     

Probing the Sol-Gel Transition in SiO2 Hydrogels—A New Application of Near-Infrared Fluorescence

Picosecond time-resolved fluorescence spectroscopy has enabled us to use a near-infrared fluorescent dye to probe the sol-gel transition in SiO₂ hydrogels, polymerized from sulfuric acid and sodium silicate solution, for the first time. We compare the microviscosity surrounding the probe during the sol-to-gel transition as predicted by two alternative models which both describe the decay of fluorescence anisotropy well. The results for one rotational time and a residual anisotropy imply that macrogelation of the sol leads to relatively small changes in the mobility of the fluorophore caused by small changes in microviscosity, but after much longer times, e.g., 1500 min, the mobility of the fluorophore decreases, reflecting a rapid increase in microviscosity of over several orders in magnitude. In sharp contrast, analysis of the anisotropy in terms of two rotational times predicts little change in microviscosity over the whole polymerization process.     

The Calibration Kit Spectral Fluorescence Standards—A Simple and Certified Tool for the Standardization of the Spectral Characteristics of Fluorescence Instruments

With the Calibration Kit Spectral Fluorescence Standards BAM-F001-BAM-F005, we developed a simple tool for the characterization of the relative spectral responsivity and the long-term stability of the emission channel of fluorescence instruments under routine measurement conditions thereby providing the basis for an improved comparability of fluorescence measurements and eventually standardization. This first set of traceable fluorescence standards, which links fluorescence measurements to the spectral radiance scale in the spectral range of 300-770 nm and has been optimized for spectrofluorometers, can be employed for different measurement geometries and can be adapted to different fluorescence techniques with proper consideration of the underlying measurement principles.     

Influence of cosmic radiation spectrum and its variation on the relative efficiency of LiF thermoluminescent detectors – Calculations and measurements

Lithium fluoride thermoluminescent detectors (TLD) were used for cosmic radiation dosimetry already in early 1960s. Since that time they have been constantly applied in numerous space missions for personal dosimetry, area monitoring, phantom measurements and dosimetry for biological experiments. The relative efficiency of TLDs, defined as the ratio of their response to a given radiation and to a reference radiation, is not constant, but depends on ionization density. This raises a question about the relative efficiency of TLDs exposed to the complex cosmic radiation spectrum encountered in Earth's orbit, which consists of a variety of particles, including heavy ions, the spectrum of which covers an extremely broad energy range. The present work is an attempt to find an answer to this question.The particle energy spectra were calculated for realistic flight conditions of the International Space Station (ISS). The calculation of the Galactic Cosmic Ray (GCR) component was based on the input spectra generated with the DLR model for solar minimum (2009) and solar maximum (2000) conditions. Contributions of trapped protons were estimated based on the AP8 model for solar minimum and maximum taking into account the altitude variations of the ISS. The interactions of the primary particles with the ISS were simulated with GEANT4 using a shielding geometry derived from the mass distribution of the Columbus Laboratory of the ISS and several constant aluminum shieldings. The calculated spectra were convoluted with the experimental data on the relative TL efficiency measured for ions ranging from H to Xe at various particle accelerators for two commonly applied TL-materials, namely LiF:Mg,Ti and LiF:Mg,Cu,P.The results showed the differences in the average TL-efficiency for these two TL-materials. For LiF:Mg,Ti the relative efficiency is within a few percent from unity for any of the analyzed values of shielding, altitude and solar cycle conditions. This means that one can assume cosmic radiation doses measured in Low Earth Orbit (LEO) with LiF:Mg,Ti detectors to be correct within such uncertainty. LiF:Mg,Cu,P underestimates the cosmic radiation doses by more than 15% in all cases. Altitude and solar cycle were found to have a very weak influence on the TL efficiency. In contrast, the influence of shielding thickness is quite significant. The reason for this is a change of contributions of radiation field components: trapped protons dominate at low shielding (97% of dose at 1 g/cm²), but are negligible above 60 g/cm², as well as changes within GCR spectrum (increase of dose due to lower LET secondaries for higher shielding). Shielding thickness affects both TLD types in different ways: the efficiency of LiF:Mg,Cu,P increases with increasing shielding thickness, while the efficiency of LiF:Mg,Ti shows some fluctuations, with a weak minimum for 60 g/cm². The response ratio of these TLDs decreases monotonically with the shielding thickness and could be used as an indicator for the average shielding conditions in which the TLDs were exposed.