440 research outputs found
Non-linear spectroscopy of rubidium: An undergraduate experiment
In this paper, we describe two complementary non-linear spectroscopy methods
which both allow to achieve Doppler-free spectra of atomic gases. First,
saturated absorption spectroscopy is used to investigate the structure of the
transition in rubidium. Using a slightly
modified experimental setup, Doppler-free two-photon absorption spectroscopy is
then performed on the transition in
rubidium, leading to accurate measurements of the hyperfine structure of the
energy level. In addition, electric dipole selection rules of
the two-photon transition are investigated, first by modifying the polarization
of the excitation laser, and then by measuring two-photon absorption spectra
when a magnetic field is applied close to the rubidium vapor. All experiments
are performed with the same grating-feedback laser diode, providing an
opportunity to compare different high resolution spectroscopy methods using a
single experimental setup. Such experiments may acquaint students with quantum
mechanics selection rules, atomic spectra and Zeeman effect.Comment: 16 pages, 8 figure
Group analysis and exact solutions of a class of variable coefficient nonlinear telegraph equations
A complete group classification of a class of variable coefficient
(1+1)-dimensional telegraph equations , is
given, by using a compatibility method and additional equivalence
transformations. A number of new interesting nonlinear invariant models which
have non-trivial invariance algebras are obtained. Furthermore, the possible
additional equivalence transformations between equations from the class under
consideration are investigated. Exact solutions of special forms of these
equations are also constructed via classical Lie method and generalized
conditional transformations. Local conservation laws with characteristics of
order 0 of the class under consideration are classified with respect to the
group of equivalence transformations.Comment: 23 page
Comparative study of perindopril and perindopril metabolite pharmacokinetics using the HPLC/MS method
Perindopril is a prodrug which is converted to an active metabolite perindoprilat in the human organism. The present study led to the development of a fast and easily reproducible procedure for simultaneous detection of perinoprilat and its metabolite in plasma using HPLC with mass-spectrometric detector (LC-MS). Detection of the target substance was performed using atmospheric pressure electrospray ionization (API-ES) techniques in negative polarity in two modes: SIM1, ion, m/z=368,10 for perindopril and SIM2, ion, m/z=339,30 for perindoprilat. Retention time of perindopril was about 2,4 min, for perindoprilat - about 1,4 min. Sample processing was performed using solid-phase extraction. The methodâs limit of quantification was equal to 1 ng/ml for perindopril and 1 ng/ml for perindoprilat. The developed procedure was used to analyse pharmacokinetics and bioequivalence of medicines containing 8 mg of perindopril. Values of all calculated pharmacokinetic parameters had no statistically meaningful differences. Confidence intervals obtained fall within bioequivalence criterion (80-125% for AUC and 75-133% for ĐĄmax Đž Cmax/AUC). The medicines under analysis were found to be bioequivalent
Approaches to Pharmaceutical Analysis of Modern Peptide and Oligonucleotide Products as Illustrated by a Small Interfering RNA-Based Novel Therapeutic for the Treatment of Bronchial Asthma
Methods used to control the quality of peptide products depend on the level of development of analytical and bioorganic chemistry, and the level of instrumentation. Peptide identification is a difficult task and largely depends on the complexity of its structure. There does not exist a comprehensive and simple test, except for NMR, which, however, is rather expensive and time-consuming and involves complex data interpretations. Moreover, it does not allow for unambiguous determination of the peptide purity and formula (amino acid composition, sequence, chirality of amino acid residues). For this reason, a combination of methods is often used, including amino acid analysis, TLC/HPLC and mass spectrometry, and, less frequently, sequencing. Current international practice of peptide analysis is to use HPLC in combination with mass spectrometric, mainly tandem (HPLC-MS/MS), detection. According to literature sources the amino acid sequence of linear peptides can be analysed using various enzymes and subsequent identification of proteolysis products by mass spectrometry. This article presents approaches to the development of test methods for analysis of purity and identification testing of a small interfering RNA-based novel medicinal product, which will help standardise and control the quality of the production process
New results on group classification of nonlinear diffusion-convection equations
Using a new method and additional (conditional and partial) equivalence
transformations, we performed group classification in a class of variable
coefficient -dimensional nonlinear diffusion-convection equations of the
general form We obtain new interesting cases of
such equations with the density localized in space, which have large
invariance algebra. Exact solutions of these equations are constructed. We also
consider the problem of investigation of the possible local trasformations for
an arbitrary pair of equations from the class under consideration, i.e. of
describing all the possible partial equivalence transformations in this class.Comment: LaTeX2e, 19 page
Digital receivers for low-frequency radio telescopes UTR-2, URAN, GURT
This paper describes digital radio astronomical receivers used for decameter
and meter wavelength observations. This paper describes digital radio
astronomical receivers used for decameter and meter wavelength observations.
Since 1998, digital receivers performing on-the-fly dynamic spectrum
calculations or waveform data recording without data loss have been used at the
UTR-2 radio telescope, the URAN VLBI system, and the GURT new generation radio
telescope. Here we detail these receivers developed for operation in the strong
interference environment that prevails in the decameter wavelength range. Data
collected with these receivers allowed us to discover numerous radio
astronomical objects and phenomena at low frequencies, a summary of which is
also presented.Comment: 24 pages, 15 figure
Analysis of Pharmacokinetic Parameters of Acetylsalicylic Acid for Prediction of Potential Nephrotoxic Effects
Nonsteroidal anti-inflammatory drugs, including acetylsalicylic acid, can have a dose-dependent nephrotoxic effect. The study of the pharmacokinetics of acetylsalicylic acid products will contribute to timely detection and correction of side effects caused by this medicinal product.The aim of the study was to evaluate potential nephrotoxic effects following a single oral administration of 75 mg of acetylsalicylic acid, based on the analysis of the pharmacokinetic parameters.Materials and methods: the study involved 24 healthy volunteers who received 75 mg of acetylsalicylic acid (tablets) once orally. The measurement of the active metabolite of acetylsalicylic acidâsalicylic acidâin blood plasma was performed by HPLC/MS using an Agilent 1200 liquid chromatography system coupled to an Agilent 6140 tandem mass spectrometer. Agilent Eclipse XDB-C18 column (4.6 mmĂ150 mm; 5.0 ÎŒm) was used for chromatographic separation. The test procedure used in the study was validated. The results obtained were used to calculate the pharmacokinetic parameters: Cmax (maximum concentration), Tmax (time to maximum concentration), T1/2 (half-life of the drug), AUC0-t (area under the pharmacokinetic curve from 0 to the last time point of the curve), AUC0-â (total area under the pharmacokinetic curve from 0 to â), MRT (mean residence time of the drug in the blood), Kel (elimination rate constant), Cl/F (total clearance), Vd/F (apparent volume of distribution). The Statistics (22.0.0.0) software was used for statistical processing of the results.Results: T1/2 of salicylic acid in blood plasma was determined to be 1.6 ± 0.5 h, Cmax was 4523.0 ± 725.0 ng/mL, and Tmax was 0.98 ± 0.4 h. AUC0ât was equal to 16183.0 ± 3823.0 ngĂh/m, Vd/F was 12.0 ± 3.1 L/kg, and MRT was 2.9 ± 0.6 h.Conclusions: the analysis of the pharmacokinetic parameters demonstrated a high absorption rate, intensive distribution, and moderate elimination rate of salicylic acid (the main metabolite of acetylsalicylic acid), indicating a low risk of nephrotoxic effects associated with the studied dose of the drug
Comparative Dissolution Kinetics of Several Multisource Thioctic Acid Products
The relationship between dissolution and bioavailability is an example of the interdependency between the quality of a medicinal product and its safety and efficacy. The uniqueness of thioctic acid is that it can exist in an oxidised and a reduced form, showing lipophilic (lipoic acid) and hydrophilic (dihydrolipoic acid) properties. Bioavailability studies of thioctic acid are necessary to evaluate the expected therapeutic effect and mitigate side effects of the medicinal product.The aim of the study was to carry out equivalence dissolution testing to compare the release of thioctic acid from medicinal products produced by several manufacturers.Materials and methods: the study used a reference medicinal product and three multisource medicinal products by different manufacturers; more specifically, film-coated tablets containing 600 mg of thioctic acid. The experiment was carried out in dissolution media at pH of 6.8±0.05 and 1.2±0.05. Statistical analysis was performed by calculating the average amounts of the substance dissolved, the standard deviation (SD), and the relative standard deviation (RSD, %) using Microsoft Office Excel 2007.Results: The authors chose the testing conditions (dissolution media pH values of 6.8±0.05 and 1.2±0.05) taking into account the nature and characteristics of thioctic acid. The comparison of thioctic acid release profiles based on the calculation of the similarity factor (f2) showed that the dissolution profiles of multisource medicinal products 2 and 3 at pH 6.8 were equivalent to that of the reference medicinal product (more than 85% of the active pharmaceutical ingredient released within 15 minutes) and the dissolution profile of multisource medicinal product 1 was not equivalent to it (with f2 of 28).Conclusions: the established differences in the rate and degree of active ingredient release from the studied medicinal products may indicate possible differences in their pharmacological effectiveness in vivo
Reduction Operators of Linear Second-Order Parabolic Equations
The reduction operators, i.e., the operators of nonclassical (conditional)
symmetry, of (1+1)-dimensional second order linear parabolic partial
differential equations and all the possible reductions of these equations to
ordinary differential ones are exhaustively described. This problem proves to
be equivalent, in some sense, to solving the initial equations. The ``no-go''
result is extended to the investigation of point transformations (admissible
transformations, equivalence transformations, Lie symmetries) and Lie
reductions of the determining equations for the nonclassical symmetries.
Transformations linearizing the determining equations are obtained in the
general case and under different additional constraints. A nontrivial example
illustrating applications of reduction operators to finding exact solutions of
equations from the class under consideration is presented. An observed
connection between reduction operators and Darboux transformations is
discussed.Comment: 31 pages, minor misprints are correcte
Group Analysis of Variable Coefficient Diffusion-Convection Equations. I. Enhanced Group Classification
We discuss the classical statement of group classification problem and some
its extensions in the general case. After that, we carry out the complete
extended group classification for a class of (1+1)-dimensional nonlinear
diffusion--convection equations with coefficients depending on the space
variable. At first, we construct the usual equivalence group and the extended
one including transformations which are nonlocal with respect to arbitrary
elements. The extended equivalence group has interesting structure since it
contains a non-trivial subgroup of non-local gauge equivalence transformations.
The complete group classification of the class under consideration is carried
out with respect to the extended equivalence group and with respect to the set
of all point transformations. Usage of extended equivalence and correct choice
of gauges of arbitrary elements play the major role for simple and clear
formulation of the final results. The set of admissible transformations of this
class is preliminary investigated.Comment: 25 page
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