Studies on use of differential thermal and thermogravimetric techniques for checking compositions of some drug formulations

The suitability of the differential thermal and thermogravimetric techniques for the determination of compositions of solid and soft drug formulations has been studied. A total of 117 pharmaceutical preparations have been examined, including powders, dusting powders, capsules, granulates, tablets, tablets for sucking, effervescent tablets, dragees, suppositories and ointments. Both techniques have been shown to be applicable for identification of pharmaceutical preparations. A specification has been made of thermal processes which can be employed for assaying the main components of the preparations. A rough estimate of the relative errors has been given.

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Zusammenfassung Die Eignung der differentialthermoanalytischen und thermogravimetrischen Methoden zur Bestimmung der Zusammensetzung fester und weicher ArzeneiprÄparate wurde studiert. Eine Gesamtzahl von 117 pharmazeutischen PrÄparaten, einschliesslich Pulver, Streupulver, Kapseln, Granulate, Tabletten, Saugtabletten, Brausetabletten, Dragees, Suppositorien und Salben wurde untersucht. Beide Methoden erwiesen sich als anwendbar zur Identifizierung pharmazeutischer PrÄparate. Eine Spezifizierung der zur Bestimmung der Hauptkomponenten der PrÄparate geeigneten thermischen Prozesse wurde durchgeführt. Eine grobe SchÄtzung der relativen Fehler wurde gegeben.

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Résumé On a étudié l'utilité des techniques ATD et TG pour déterminer la composition des préparations pharmaceutiques solides et molles. On a soumis à l'examen un total de 117 préparations pharmaceutiques comprenant des poudres, des talcs, des capsules, des granulats, des tablettes, des tablettes à sucer, des tablettes effervescentes, des dragées, des suppositoires et des onguents. Les deux techniques se sont montrées applicables à l'identification des préparations pharmaceutiques. On a effectué une spécification des processus thermiques qui se prÊtent au dosage des composants essentiels des préparations. On a donné une évaluation approximative des erreurs relatives.

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Oil-in-water emulsions stabilized by highly charged polyelectrolyte-grafted silica nanoparticles

Fully sulfonated poly(styrenesulfonate) brushes were grown from the surface of colloidal silica particles and used to prepare stable trichloroethylene-in-water and heptane-in-water Pickering emulsions. These particles were highly charged and colloidally stable in water but could not be dispersed in trichloroethylene or heptane. Both two-phase (emulsion plus neat water) and three-phase (emulsion separating neat oil and water phases) systems were observed, with water-continuous emulsion phases in all cases. Emulsion phases containing as much as 83% (v/v) oil were stable for over six months. Poly(styrenesulfonate)-grafted particles were very efficient emulsifiers; stable emulsion phases were prepared when using as little as 0.04 wt% particles. The emulsifying effectiveness of the poly(styrenesulfonate)-grafted silica particles can be attributed to the hydrophobicity of the vinylic polymer backbone that makes this highly charged polyelectrolyte unusually surface active at the oil/water interface.     

Electron impact mass spectrometry of some 6-substituted tetrazolo[1,5-c]pyrimidin-5(6H)-ones

The electron impact mass spectra of 6-methyltetrazolo[1,5-c]pyrimidin-5(6H)-one, its 7- and 8-methyl derivatives, three 8-halo derivatives and two related nucleosides are reported. On the basis of the high-resolution data and detected metastable ions, the fragmentation routes of their molecular ions are proposed. Coexistence of the tautomeric forms of the title compounds of cyclic (tetrazole) or linear (azide) structure can be suggested owing to the fragmentation pathways identified for the bases. Decomposition of the related nucleosides lies in the breaking of nucleoside bonds to produce the appropriate base and sugar fragments.     

Protective properties of redox polymer film deposited on stainless steel

We propose a novel composite organic-inorganic coating in the form of a redox polymer film for protection of stainless steel against general corrosion in strong acid medium (2 M H₂SO₄). We utilize an anion exchange polymer, protonated poly(4-vinylpyridine), into which hexacyanoferrate anions have been introduced. Owing to the presence of Fe(CN)₆^3–/4– at the interface formed by the film and the steel, a sparingly soluble metal hexacyanoferrate (mostly Prussian blue, PB) is formed as an overcoating on the steels surface, presumably on the passive (metal oxide) layer. The redox polymer film on the steel seems to act as a composite three-dimensional bilayer-type coating in which hexacyanoferrate(III,II) anions (that are capable of effective charge storage) exist in the outer portions of the film, whereas the inner PB layer improves the systems overall adherence and stability. By analogy to a conducting polymer (e.g. polyaniline, polypyrrole), introduction of the redox polymer composite film leads to stabilization of the steel substrates potential within the passive range.Contribution to the 3rd Baltic Conference on Electrochemistry, Gdansk-Sobieszewo, Poland, 23–26 April 2003Dedicated to the memory of Harry B. Mark, Jr. (28 February 1934–3 March 2003)     

Stability investigations of laser with saturable absorber

Stability of steady solutions of semiclassical laser-absorber model is investigated. It is found that the solutions exhibit instabilities for all values of cavity losses and, for some values of parameters, additional instability, connected with phase, appears. It is also shown by a numerical calculation that in an unstable region periodic and erratic motion can exist above criticallity.Supported in part by the Polish Ministery of Science, Technology and Higher Education, Project M.R.I.7     

Geometrical meaning of the Poincaré group gauge theory

We find a condition (6) under which a gauge theory of the Poincaré group is equivalent to the Einstein-Cartan theory of gravitation.     

Crystal packing of two 5‐substituted 2‐methyl‐4‐nitro‐1H‐imidazoles

Infinite chains connected by N—H...N hydrogen bonding form the primary packing motif in two closely related 4‐nitroimidazole derivatives, viz. 5‐bromo‐2‐methyl‐4‐nitro‐1H‐imidazole, C₄H₄BrN₃O₂, (I), and 2‐methyl‐4‐nitro‐1H‐imidazole‐5‐carbonitrile, C₅H₄N₄O₂, (II). These chains are almost identical, even though in (II) there are two symmetry‐independent molecules in the asymmetric unit. The differences appear in the interactions between the chains; in (I), there are strong C—Br...O halogen bonds, which connect the chains into a two‐dimensional grid, while in (II), the cyano group does not participate in specific interactions and the chains are only loosely connected into a three‐dimensional structure.     

INVESTIGATION OF THE ATRP OF n-BUTYL METHACRYLATE USING THE Cu（I）／N,N,N＇ N＂ N＂-PENTAMETHYLDIETHYLENETRIAMINE CATALYST SYSTEM

The polymerization of n-butyl methacrylate was investigated using the Atom Transfer Radical Polymerization technique with CuBr and CuCl/N,N,N‘,N“,N“-pentamethyldiethylenetriamine catalytic systems. Various combinations of catalyst systems and initiators were utilized in order to optimize the polymerization conditions and to obtain well-defined polymers (i.e. controlled molecular weights and low polydispersities). It has been found that the optimal initiator for this system is a chlorine-based initiator, when the catalyst used is a Cu(I) salt in conjunction with the N,N,N‘,N“,N“-pentamethyldiethylenetriamine ligand. Bromine-based initiators tend to result in large amounts of initial termination, leading to polymers with less than ideal chain end functionality, even if CuCI is used as the Cu(I) species to invoke the halogen exchange. Additionally, the effects of the polymerization temperature, copper(I) species and the initiator structure were determined.     

Density functional theory of adsorption of mixtures of charged chain particles and spherical counterions

We propose a microscopic density functional theory to describe nonuniform ionic fluids composed of chain molecules with charged "heads" and spherical counterions. The chain molecules are modeled as freely jointed chains of hard spheres, the counterions are oppositely charged spheres of the same diameter as all segments of chain molecules. The theory is based on the approach of Yu and Wu [J. Chem. Phys. 117, 2368 (2002)] of adsorption of chain molecules and on theory of adsorption of electrolytes [O. Pizio, A. Patrykiejew, and S. Sokolowski, J. Chem. Phys. 121, 11957 (2004)]. As an application of the proposed formalism we investigate the structure and adsorption of fluids containing segments of different length in a slitlike pore.     

Determination of total carbon and total organic carbon from volatile air pollutants

Summary The method developed based on the determination of TC and TOC in the form of the total amount of CO₂ requires application of the proper techniques for the final determination of CO₂. The possibility of using a stream of carrier gas at a convenient flow-rate for desorbing quantitatively CO₂ concentrated on a molecular sieve permits use of a wide variety of known analytical techniques for the final determination of CO₂. Various methods were compared on the basis of both absolute and calibration measurements. The absolute methods chosen were gravimetric (classical or an automated version based on application of a gravimetric automat and automatic recording balance), thermogravimetric analysis and coulometry. The calibration methods included thermal conductivity, the flame-ionization detector (after conversion of CO₂ into methane) and infrared absorption. Usefulness of the methods was evaluated on the basis of comparative statistical analysis of experimental data with respect to precision (Snedecor'sF-test and Bartlett'sU ²-test) and accuracy (Student'st-test).

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Zusammenfassung Das entwickelte Verfahren zur Bestimmung des TC- und TOC-Gehaltes in Form der gesamten Menge CO₂ erfordert die Anwendung geeigneter Analysentechniken zur Endbestimmung dieser Verbindung. Die Möglichkeit einer Desorption des am Molekularsieb angereicherten CO₂ in einem Gasstrom mit geeignetem Durchfluß erlaubt zur Endbestimmung von CO₂ die Anwendung einer Reihe verschiedener Analysenverfahren. Die Anwendbarkeit verschiedener, auf Absolutverfahren und auch auf relativen Messungen beruhender Methoden wurde vergleichend untersucht. Die folgenden Methoden zur CO₂-Bestimmung wurden gewählt: die Gravimetrie (klassische oder automatisierte unter Einsatz eines Wägeautomaten und einer registrierenden Waage), die Thermogravimetrie und die Coulometrie. Von den relativen Methoden wurden die Thermokonduktometrie, der Flammenionisationsdetektor (nach Umsetzung von CO₂ zu Methan) und das IR-Absorptionsmeßverfahren geprüft. Die Anwendbarkeit der Methoden wurde mit Hilfe statistischer Prüfverfahren beurteilt, wobei die Präzision (SnedecorsF-Test und BartlettsU ²-Test) und die Genauigkeit (Studentst-Test) der erhaltenen Analysenwerte verglichen wurden.