123 research outputs found

    Synergy of piracetam and aminalon in the cerebroprotective effect of olatropyl.

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    Optimization of pharmacotherapy of neurological and psychosomatic diseases led to the creation of comΒ­bined medicines containing two or more components with different mechanisms of action, differently affecting the pathogenesis and clinical manifestations of specific forms of pathology. Combined drugs that help normalize the central regulatory mechanisms of the development of somatic pathology, improve brain metabolism and hemodynamics, stabilize the cortical-subcortical relationships, the disorders of which lie at the base of many forms of neurological and psychosomatic pathology have been particularly popular in recent years. In this article we propose options for optiΒ­mizing nootropic therapy with olatropyl, which is a combination of two "true" nootropics - gamma-aminobutyric acid (aminalone) and piracetam in one drug form. Such a combination allows one-stage implementation of a complex of multifaceted and diverse effects on the central nervous system characteristic of both piracetam and aminalone, but achieved through fundamentally different mechanisms of action of these agents. The mechanism of action of olatropil demonstrates the pronounced synergism of the monocomponents of the preparation. This combination allows to reduce the therapeutic dosages of each of the active substances by 2 times, which, in turn, leads to a decrease in the incidence and severity of possible side effects; leveling the exciting effect of piracetam and providing higher safety and efficacy. The drug is an effective tool for the therapy of various forms of cerebrovascular pathology, improving cognitive functions, mental activity, psychoemotional status, autonomic functions, favorably affecting the quality of life of patients. The uniqueness of the mechanism of action of olatropil, consisting in the occurrence of the fact of pharmacodynamic synergy in the combined use of piracetam and aminalone in a single dosage form, contributes to the enhancement of positive pharmacological effects and the leveling of a number of negative elements of pharmacodynamics of preparation constituents

    Synergy of piracetam and aminalon in the cerebroprotective effect of olatropyl.

    Get PDF
    Optimization of pharmacotherapy of neurological and psychosomatic diseases led to the creation of comΒ­bined medicines containing two or more components with different mechanisms of action, differently affecting the pathogenesis and clinical manifestations of specific forms of pathology. Combined drugs that help normalize the central regulatory mechanisms of the development of somatic pathology, improve brain metabolism and hemodynamics, stabilize the cortical-subcortical relationships, the disorders of which lie at the base of many forms of neurological and psychosomatic pathology have been particularly popular in recent years. In this article we propose options for optiΒ­mizing nootropic therapy with olatropyl, which is a combination of two "true" nootropics - gamma-aminobutyric acid (aminalone) and piracetam in one drug form. Such a combination allows one-stage implementation of a complex of multifaceted and diverse effects on the central nervous system characteristic of both piracetam and aminalone, but achieved through fundamentally different mechanisms of action of these agents. The mechanism of action of olatropil demonstrates the pronounced synergism of the monocomponents of the preparation. This combination allows to reduce the therapeutic dosages of each of the active substances by 2 times, which, in turn, leads to a decrease in the incidence and severity of possible side effects; leveling the exciting effect of piracetam and providing higher safety and efficacy. The drug is an effective tool for the therapy of various forms of cerebrovascular pathology, improving cognitive functions, mental activity, psychoemotional status, autonomic functions, favorably affecting the quality of life of patients. The uniqueness of the mechanism of action of olatropil, consisting in the occurrence of the fact of pharmacodynamic synergy in the combined use of piracetam and aminalone in a single dosage form, contributes to the enhancement of positive pharmacological effects and the leveling of a number of negative elements of pharmacodynamics of preparation constituents

    Role of the Nuclear and Electromagnetic Interactions in the Coherent Dissociation of the Relativistic 7^7Li Nucleus into the 3^3H + 4^4He Channel

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    The differential cross section in the transverse momentum QQ and a total cross section of (31Β±4)(31\pm4) mb for the coherent dissociation of a 3-A-GeV/cc 7^7Li nucleus through the 3^3H+4+^4He channel have been measured on emulsion nuclei. The observed QQ dependence of the cross section is explained by the predominant supposition of the nuclear diffraction patterns on light (C, N, O) and heavy (Br, Ag) emulsion nuclei. The contributions to the cross section from nuclear diffraction (Q≀400Q\le400 MeV/cc) and Coulomb (Q≀50(Q\le50 MeV/cc) dissociations are calculated to be 40.7 and 4 mb, respectively.Comment: ISSN 0021-3640, Pleiades Publishing, Ltd., 200

    Fragmentation channels of relativistic 7^7Be nuclei in peripheral interactions

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    Nuclei of 7^7Li were accelerated at the JINR Nuclotron. After the charge-exchange reaction involving these nuclei at an external target a second 7^7Be beam of energy 1.23A GeV was formed. This beam was used to expose photo-emulsion chambers. The mean free path for inelastic 7^7Be interactions in emulsion Ξ»\lambda=14.0Β±\pm0.8 cm coincides within the errors with those for 6^6Li and 7^7Li nuclei. More than 10% of the 7^7Be events are associated with the peripheral interactions in which the total charge of the relativistic fragments is equal to the charge of the 7^7Be and in which charged mesons are not produced. An unusual ratio of the isotopes is revealed in the composition of the doubly charged 7^7Be fragments: the number of 3^3He fragments is twice as large as that of 4^4He fragments. In 50% of peripheral interactions, a 7^7Be nucleus decays to two doubly charged fragments. The present paper gives the channels of the 7^7Be fragmentation to charged fragments. In 50% of events, the 7^7Be fragmentation proceeds only to charged fragments involving no emission of neutrons. Of them, the 3^3He+4^4He channel dominates, the 4^4He+d+p and 6^6Li+pchannels constitute 10% each. Two events involving no emission of neutrons are registered in the 3-body 3^3He+t+p and 3^3He+d+d channels. The mean free path for the coherent dissociation of relativistic 7^7Be nuclei to 3^3He+4^4He is 7Β±\pm1 m. The particular features of the relativistic 7^7Be fragmentation in such peripheral interactions are explained by the 3^3He+4^4He 2-cluster structure of the 7^7Be nucleus.Comment: 10 pages, 3 figures, 3 tables, conference: Conference on Physics of Fundamental Interactions, Moscow, Russia, 5-9 Dec 200

    Selective electrochemical deposition of indium in-between silicon nanowire arrays fabricated by metal-assisted chemical etching

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    Indium electrodeposition in-between silicon nanowire arrays fabricated by silver-assisted chemical etching of lightly-doped (100)-oriented silicon wafers is evaluated. It is concluded based on SEM and EDX analysis of indium's distribution that, by utilizing pulsed-mode electrodeposition and maintaining a sufficiently low duty cycle value, indium particles can be formed exclusively at the very bottom of each consecutive pore on the residual silver particles left over from metal-assisted etching. This result differs significantly from irregular pore filling along with surface and subsurface deposition observed in the cases of continuous galvanostatic deposition regimes at prolonged durations or in the absence of residual silver particles. Bottommost fusible metal deposit localization, which is unattainable on porous silicon fabricated by electrochemical anodization, is presumed to be optimal for the growth of germanium crystallites inside the pores via the electrochemical liquid-liquid-solid approach and subsequent silicon-germanium alloy formation through thermal annealing

    Germanium electrodeposition into porous silicon for silicon-germanium alloying

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    A method of germanium electrodeposition from a GeO2-based aqueous solution into the pore channels of anodic mesoporous silicon formed on n-type highly-doped (100) silicon wafers is described. The effect of deposition time, pore channel shape and preconditioning of porous silicon layers in hydrofluoric acid is evaluated. Recommendations are given in regards to the optimal parameter combinations to ensure uniform pore channel filling with germanium. The possibility of producing silicon-germanium alloys by subsequent rapid heat treatment of the germanium-filled porous silicon layers is established

    Topology of "white" stars in relativistic fragmentation of light nuclei

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    In the present paper, experimental observations of the multifragmentation processes of light relativistic nuclei carried out by means of emulsions are reviewed. Events of the type of "white" stars in which the dissociation of relativistic nuclei is not accompanied by the production of mesons and the target-nucleus fragments are considered. A distinctive feature of the charge topology in the dissociation of the Ne, Mg, Si, and S nuclei is an almost total suppression of the binary splitting of nuclei to fragments with charges higher than 2. The growth of the nuclear fragmentation degree is revealed in an increase in the multiplicity of singly and doubly charged fragments with decreasing charge of the non-excited part of the fragmenting nucleus. The processes of dissociation of stable Li, Be, B, C, N, and O isotopes to charged fragments were used to study special features of the formation of systems consisting of the lightest Ξ±\alpha, d, and t nuclei. Clustering in form of the 3^3He nucleus can be detected in "white" stars via the dissociation of neutron-deficient Be, B, C, and N isotopes.Comment: 20 pages, 3 figures, 9 tables, conference: Conference on Physics of Fundamental Interactions, Moscow, Russia, 1-5 Mar 2004.(Author's translation

    Π‘Π΅Ρ€ΠΎΠ½Π΅Π³Π°Ρ‚ΠΈΠ²Π½ΠΎΠ΅ Ρ‚Π΅Ρ‡Π΅Π½ΠΈΠ΅ Π²ΠΈΡΡ†Π΅Ρ€Π°Π»ΡŒΠ½ΠΎΠ³ΠΎ сифилиса Ρƒ хирургичСских Π±ΠΎΠ»ΡŒΠ½Ρ‹Ρ…

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    Π’ΠΈΡΡ†Π΅Ρ€Π°Π»ΡŒΠ½Ρ‹ΠΉ сифилис Π΄ΠΈΠ°Π³Π½ΠΎΡΡ‚ΠΈΡ€ΡƒΡŽΡ‚ ΠΏΡ€ΠΈ ΠΆΠΈΠ·Π½ΠΈ лишь Ρƒ 10 % ΠΏΠ°Ρ†ΠΈΠ΅Π½Ρ‚ΠΎΠ². ΠšΡ€ΠΈΡ‚Π΅Ρ€ΠΈΠΈ ΠΈΠ½Ρ‚Ρ€Π°ΠΎΠΏΠ΅Ρ€Π°Ρ†ΠΈΠΎΠ½Π½ΠΎΠΉ диагностики Π²ΠΈΡΡ†Π΅Ρ€Π°Π»ΡŒΠ½ΠΎΠ³ΠΎ сифилиса Ρ‚Ρ€Π΅Π±ΡƒΡŽΡ‚ дальнСйшСго изучСния, ΠΏΠΎΡΠΊΠΎΠ»ΡŒΠΊΡƒ Π½ΠΈ макроскопичСская ΠΎΡ†Π΅Π½ΠΊΠ° пораТСния, Π½ΠΈ морфологичСская диагностика Π½Π΅ ΠΏΠΎΠ·Π²ΠΎΠ»ΡΡŽΡ‚ достовСрно Π²Π΅Ρ€ΠΈΡ„ΠΈΡ†ΠΈΡ€ΠΎΠ²Π°Ρ‚ΡŒ Π΄ΠΈΠ°Π³Π½ΠΎΠ·
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