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Vol 22, No 8 (2019)

Articles

RESEARCH OF THE ASSORTMENT OF DRUGS IN THE FORM OF OINTMENT

Gammel I.V., Zhukova O.V., Kononova S.V., Konnova M.A.

Abstract

Ointments traditionally occupy the largest share among other types of soft dosage forms presented in the domestic pharmaceutical market. The purpose of this work: marketing research range of drugs in the form of ointment (life cycle analysis and study of applications). Methods. Content analysis of official sources of information, their systematization and subsequent logical, structural and comparative analysis. Results. The number of medicines in the form of ointment allowed for medical use in Russia is established. Medicines in the form of ointments are represented by 116 international non-proprietary names, 308 trade names, 519 medicinal products. By type and method of application are distinguished ointment for local and external use, eye ointment, rectal ointment, and nasal ointment. The range of medicines in the form of ointment is structured according to the country-producer, enterprise-producer, pharmacotherapeutic group. A significant part of the domestic pharmaceutical market is represented by ointments of Russian production, the leading position in the number of proposals is taken by LTD "Synthesis". Drugs in the form of ointment are presented in 25 pharmacotherapeutic groups with a predominance of glucocorticoids, homeopathic remedies, locally irritating agents, tissue regeneration stimulants, antimicrobial agents. Conclusion. The stage of the life cycle of the nomenclature of drugs in the dosage form of ointment corresponds to «maturity». Positive dynamics of import substitution and reduction of import dependence of the domestic pharmaceutical market of ointments is noted.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):3-9
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QUANTITATIVE DETERMINATION OF GLYCEROL AND POTASSIUM ACETATE IN AQUEOUS SOLUTION BY THE METHOD OF 1H NUCLEAR MAGNETIC RESONANCE

Sheychenko V.I., Abramov Y.V., Blinova G.I.

Abstract

Methodical approaches to the application of 1H NMR spectroscopy for the simultaneous quantitative determination of potassium acetate and glycerol in highly concentrated aqueous solutions. The results obtained can be used in the manufacture and analysis of chemical composition of preservative solution used in preservation of biological substances in research institutions and museums biological focus. The 1H NMR spectrum was obtained with the following parameters: response time - 5 seconds; RF pulse length - 3.3 gs (10 degrees); relaxation delay - 10 seconds; the number of accumulations is 16. Then, the integral intensity of the signals is determined in the 1H NMR spectrum, after which the obtained values of the integrals in the ranges of chemical shifts 1.8 - 2.0; 3.4 - 3.8 and 4.6 - 4.9 ppm calculate the molar and mass percentage of each component. The high accuracy of the quantitative determination of the components of the preservative solution and the high economic efficiency compared with the method of potentiometric titration were determined.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):10-14
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STANDARDIZATION OF DENTAL PHARMACEUTICAL FILM BASED ON SUCCINIC ACID AND CHLORIDE CETYLPYRIDINIUM USING THE METHOD HIGHLY EFFICIENT LIQUID CHROMATOGRAPHY

Nozhkina N.N., Simonyan E.V., Sinitsky A.I.

Abstract

A method has been developed for the quantitative determination of succinic acid and cetylpyridinium chloride with the joint presence in dental medicinal films by high performance liquid chromatography. The evaluation of the suitability of the chromatographic system. The technique is validated by parameters: specificity, linearity, analytical domain, accuracy and precision. It was established that the technique is linear in the concentration range for succinic acid 0,05 to 0,15 mg/ml, forcetylpyridinium chloride - from 0,02 to 0,06 mg/ml, the correlation coefficient approaches 1; relative standard deviation of determination does not exceed 2%. The presented technique is characterized by a rather high sensitivity, rapidity, reproducibility and can be included in the draft pharmacopoeial article on dental medicinal film.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):15-20
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STANDARDIZATION OF HEPATOPROTECTIVE HERB TEA

Lubsandorzhieva P.B., Dargaeva T.D., Ferubko E.V.

Abstract

Previously, the chemical composition of volatile compounds has been studied in the 6-component herb tea intending for the treatment and prevention of pathological craving for alcohol, consisting of flowers of Tanacetum vulgare L., leaves of Urtica dioica L., herb of Artemisia absinthium L., Achillea millefolium L. and Thymus serpyllum L. and rhizomes of Acorus calamus L. The herb tea inhibited lipid peroxidation of biological membranes of hepatocytes, reduced the phenomenon of cytolysis and cholestasis in alcoholic hepatitis in experiments on rats. The aim of this article is herb tea standartization by content of phenolic compounds responsible for the pharmacological activity of herb tea. Herb tea samples of production of the MIP "Arura" (Ulan-Ude), HPLC and HPLC/MS methods, pharmacopoeial methods for determining the amount of substances were used in study. Phenolic compounds have been idendified in herb tea by HPLC: cinaroside, quercetin, o-coumaric, gallic, caffeic, cinnamic acid. It was found that the herb tea contains (in qg / g): luteolin (44.85), cinaroside (3.36), rutin (0.18), quercetin (0.10) using HPLC / MS. The content of the sum of substances in herb tea were determined (%): flavonoids in terms of luteolin (1.25), phenolic acids in terms of caffeic acid (0.17), triterpene saponins (6.99), essential oil (0.73) , ascorbic acid (0.16), organic acids (2.71), polysaccharides (3.40) using pharmacopoeial methods. The optimal parameters for the extraction of flavonoids from herb tea were determined: double extraction of herb tea with 70 % ethyl alcohol, with a phase ratio of 1:50 for 2 hours (1 hour each extraction) for standartization of herb tea. Spectrophotometric method was validated, the relative error of an individual result does not exceed 3,21%. Standards for the content of biologically active substances were established: the amount of flavonoids in terms of luteolin - not less than 0.8%; tannins - not less than 4.0%; essential oil - not less than 0.5% based on the results obtained from the analysis of the five series of herb tea.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):21-26
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MIDAZOLAM MICROENCAPSULATION AS A METHOD OF MODIFYING ITS PHARMACOKINETICS

Judin M.A., Chepur S.V., Aleshina O.I., Bykova A.F., Ivanov I.M.

Abstract

Purpose of the study. The selection of the most optimal method for obtaining the microencapsulated form of midazolam, which improves the kinetics of its release from microparticles. Materials and methods. Methods of emulsification, double emulsification, nanoprecipitation and spray drying were used to create a microencapsulated form of midazolam. The efficiency of incorporation and distribution of midazolam between the matrix and the surface of the particles was evaluated using the HPLC methods. Results. It's shown that the application of the spray drying method provides the maximum inclusion of midazolam in polymer matrices for samples based on alginate (more than 44 %) and polylactide-co-glicolide (more than 60 %). The in vitro release kinetics of midazolam is characterized by a gentle curve for sodium alginate-based samples compared to polylactide-co-glicolide samples. Findings. The most optimal midazolam incorporation and release parameters are achieved using PLGA- and alginate-based polymeric matrices. This allows us to consider samples based on them as promising means to increase the anticonvulsant effect in the treatment of toxic convulsive syndrome.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):27-32
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PHARMACOLOGICAL EFFICACY FERULOPSIS HYSTRIX (BUNGE) PIMENOV OF DRY EXTRACT IN EXPERIMENTAL OF INDOMETHACIN-INDUCED GASTROPATHY

Salchak S.M., Razuvaeva Y.G., Arakchaa K.D., Toropova A.A., Olennikov D.N.

Abstract

The purpose of the study was to evaluate the gastroprotective effect of dry extract from the roots and rhizomes of Ferulopsis hystrix (Bunge) Pimenov in indomethacin-induced gastropathy. Materials and methods. The studies were carried out on white Wistar rats. The indomethacin-induced gastropathy was simulated by a single intragastric administration of indomethacin in dose of 60 mg/kg. The F. hystrix dry extract in the doses 100 and 200 mg/kg was administered to animals I and II experimental groups for 7 days before the modeling of gastropathy. Animals of the III experimental groups were received the preparation of comparison - plantaglucid in the 300 mg/kg. The gastroprotective effect of F. hystrix was estimated taking into account the Pauls' index which was calculated for erosions and strip-like ulcers as well as taking into account the morphometric indices (the depth of erosions) of the stomach mucosa. Results. The F. hystrix dry extract in the dose of 200 mg/kg was decreased the average number of erosions and stripe-like ulcers by 2 (p≤ 0.05) and 5 (p≤ 0.05) times and the Pauls' index - by 2 and 20 times respectively as compared to the control. The F. hystrix extract in the doses of 100 and 200 mg/kg was reduced the depth of erosions by 35% and 74% respectively as compared to the control. Conclusion. Thus, F. hystrix has the gastroprotective effect in indomethacin-induced gastropathy. The F. hystrix dry extract in the dose of 200 mg/kg manifests the gastroprotective effect surpassing the effect of the preparation of comparison - plantaglucide.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):33-38
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A NEW METHOD OF TINCTURE PREPARATION ON THE BASE OF ARTEMISIAE JACUTICAE HERBA

Dylenova E.P., Randalova T.E., Zhigzhitzhapova S.V., Radnaeva L.D.

Abstract

The aim of the research was to develop a new method of tincture preparation from the closely related species of Artemisia absinthium L. - Artemisia jacutica Drob. The object of the study was Artemisiae jacuticae herba collected in Eravninsky region (Buryatia) in 2018 in a flowering stage. The quality of tincture was evaluated by the sum of extractives and the sum of flavonoids referred to determined using UV-spectrophotometry. Extraction on an orbital shaker significantly increases the duration and efficiency of extraction. During the analysis we found that the optimal extractant is 50% ethanol that produces 32,14% of extractives and 0.53% of flavonoids. The best yield of extractives was found during extraction of 0.5 mm raw material, and was 30,29%, and the amount of flavonoids - 0.38%. According to the results, the optimal ration was 1:5 (33,25% of extractives and 0,59% - flavonoids). It was found that the optimal extraction time is 60 minutes, two times. More than that, we obtained tinctures using maceration method lasting from 1 to 7 days. It was revealed that the maximum yield of extractive substances was observed on the 7th day (29.19% - extractives, 0.32% - flavonoids). Thus, we have set the optimal terms of tincture preparation from A. jacuticae herba for the better extractives' efficiency, that included the type of extractant, raw materials' fineness, the ratio of raw material: extractant and duration of extraction.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):39-43
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AGE DEPENDENCY OF ESSENTIAL AND TOXIC ELEMENT LEVELS IN HAIR OF FREQUENTLY ILL CHILDREN

Isankina L.N., Lobanova Y.N., Volok V.P., Kulesh V.I., Skalny A.V.

Abstract

Both toxic and essential elements may play a significant role in the immune system disturbances in frequently ill children (FIC), but the age dependency of this influence is not well understood. Aim. The goal of this study was to measure the levels of clinically relevant essential and toxic elements in hair of FIC and to assess their correlation with the age of the subjects. Materias and Methods. Hair samples of 200 children were assayed for the levels of chemical elements using inductively coupled plasma mass spectrometry (ICP-MS) on a NexION 300D spectrometer after microwave decomposition. Results. In comparison with healthy children, the younger group of FIC (2 to 7 y/o) was characterized by a significant increase in the hair levels of arsenic (+ 24%), selenium (+ 11%) and potassium (2.5 times), while the zinc level was lower (- 27%). In the group of FIC over 7 years old the level of arsenic was similarly higher than in the control group (+ 30%). A significant increase of the levels of calcium (+ 27%), cobalt (+ 50%) and selenium (+ 18%) relative to the corresponding control values was found only for the older group. Correlation analysis demonstrated that high susceptibility to colds is associated with changes in the age dynamics of the elemental profile. Conclusions. Obtained results indicate the existence of pronounced age-dependent disturbances in the elemental status of children susceptible to frequent respiratory infections.
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):44-52
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NEW MEASUREMENT PROCEDURE OF THE ACETALDEHYDE CONCENTRATION IN WORK PLACE AIR

Kuzovkova A.A., Krymskaya T.P., Ivashkevich L.S.

Abstract

The purpose of the work is to develop measurement procedure of the acetaldehyde concentration in work place air on the basis of headspace chromatographic analysis. According to the measurement procedure, acetaldehyde from the work place air is concentrated into distilled water in a volume of 5 cm3 placed in three cooled successively connected absorption devices. Acetaldehyde extraction from the absorption solution is carried out by gas extraction by heating the sample in a closed volume in the presence of sodium sulfate at a concentration of 0,2 g/cm3 using an automatic equilibrium vapor dispenser (vapor volume - 2 cm3). The headspace chromatographic analysis is carried out by gas chromatography simultaneously with polar ZB-Wax and weakly polar DB-624 capillary columns. The acetaldehyde mass concentration in the work place air is established by the method of absolute calibration. In the process of the metrological certification of the measurement procedure, indicators of precision and accuracy were established in the range of measurements of acetaldehyde mass concentrations in the work place air from 1.0 to 10.0 mg/m3. The limit of repeatability of the developed measurement procedure is 17.6%, the limit of intermediate precision is 22.4%, the relative expanded uncertainty is 15% with a confidence probability of p = 0.95 and coverage factor k = 2, the accuracy indicator is not significantly different from unity. The measurement procedure MVI.MN 6023-2018 «Acetaldehyde mass concentration in the work place air. The measurement procedure by gas chromatography» was certified by the Belarusian State Institute of Metrology (metrology certificate No. 1115/2018 dated July 25, 2018).
Problems of Biological Medical and Pharmaceutical Chemistry. 2019;22(8):53-57
pages 53-57 views

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