


Vol 74, No 5 (2025)
- Year: 2025
- Articles: 7
- URL: https://journals.eco-vector.com/0367-3014/issue/view/13840
- DOI: https://doi.org/10.29296/25419218-2025-05
Pharmaceutical chemistry and pharmacognosy
Phytochemical and microbiological study of acer tataricum leaves
Abstract
Introduction. The Tatar maple (Acer tataricum L.) is a deciduous tree or tall shrub up to 8 m tall, which is widespread in Central, Eastern and Southeastern Europe, Asia Minor and the Caucasus. The analysis of scientific literature suggests the prospects of Tatar maple as a source of biologically active compounds. Thus, the leaves of the Tatar maple contain phenolic compounds (methyl gallate, tannins), which may have antimicrobial activity. The extract of Acer tataricum subsp. is being actively studied abroad. ginnala is a remedy with anti-inflammatory and antioxidant effects. Of great interest are polyphenols of species of the genus Acer L. – derivatives of gallic acid (ginnalin A, etc.), which have anti-cancer activity.
The aim is study of the antibacterial activity of ginnalin A and water-alcohol extraction from the leaves of the Tatar maple (Acer tataricum L.)
Material and methods. The leaves of the Tatar maple (harvest date – June 2024) in the area of the Sokolikh Mountains of Samara (Dubki Forest Park) were used as the material. The drying of raw materials was carried out naturally under a canopy without direct sunlight. By the method of modified maceration from leaves based on an extractant – ethyl alcohol at a concentration of 70% in a ratio of “raw material – extractant” 1:5, a tincture was obtained, a 0.3% solution of ginnalin A was prepared in 70% ethyl alcohol, as well as a comparison preparation – eucalyptus tincture. Ginnalin A was isolated using column chromatography from evaporated water-alcohol extraction of Tatar maple leaves and identified based on physico-chemical constants, as well as UV and NMR spectra data. The determination of the minimum inhibitory concentration was carried out by double serial dilution in a Muller-Hinton nutrient broth (Bio-Rad, USA). Strains of Pseudomonas aeruginosa (ATCC 27853), Staphylococcus aureus subsp. aureus (ATCC 25923), Escherichia coli (ATCC 25922), Bacillus cereus (ATCC 29213), Candida albicans (ATCC 90028), Klebsiella pneumoniae (ATCC 13883), Enterococcus faecalis were used as test cultures. (ATCC 29212), Acinetobacter baumannii (ATCC 17978). Incubation was carried out at a temperature of 35°C for 24 hours. The results were evaluated visually by the presence/absence of microbial growth in the wells of the tablet with appropriate dilutions of the studied samples.
Results. As a result of a comparative microbiological study, it was found that tincture of Tatar maple leaves in 70% ethyl alcohol and ginnalin A have antibacterial activity against strains of P. aeruginosa, S. aureus, E. coli, B. cereus, C. albicans, K. pneumoniae, E. faecalis, A. baumannii. The tincture of Tatar maple leaves in 70% ethyl alcohol and ginnalin A have the most pronounced antibacterial activity in relation to E. faecalis, A. baumannii and B. cereus, which have an antibacterial effect superior to the comparison drug eucalyptus tincture.
Conclusion. Thus, it was determined that the tincture of Tatar maple leaves and ginnalin A in 70% ethyl alcohol have a more pronounced antibacterial activity against Enterococcus faecalis, Acinetobacter baumannii and B. cereus strains, compared with the comparison drug eucalyptus tincture.



Solid-phase product based on dihydroquercetin and glycine: preparation and physico-chemical properties
Abstract
Introduction. Alzheimer's disease is the most common cause of dementia and imposes a heavy financial burden on society in developed countries. According to scientific information, flavonoids prevent the formation of β-amyloid plaques and tau aggregates, proteins that play a key role in the pathogenesis of Alzheimer's disease. To overcome the biopharmaceutical limitations of flavonoids, it is proposed to obtain crystals with amino acids. Assuming a possible pharmacological synergism, the amino acid glycine, which is also capable of influencing links in the biochemical mechanisms of neurodegenerative diseases, was chosen as a conformer to dihydroquercetin flavanonol.
Objective is to obtain and to characterize a solid-phase product of dihydroquercetin and glycine.
Material and methods. The dihydroquercetin-glycine composition was obtained by lyophilization of their aqueous solution. The morphology was characterized by scanning electron microscopy. The crystallinity was demonstrated by X-ray powder diffraction spectra. The thermal analysis was performed by differential scanning calorimetry and thermogravimetry. The solubility in water was evaluated, according to SP RF XV.
Results. Lyophilizate is a light-yellow powder. The form of these particles is thin flakes with a perforated surface, which have a significantly lower degree of crystallinity compared to the initial components. Crystallization of the amorphous flavonoid impurity in the composition is not observed, but we can see the phase transition from γ-glycine to α-glycine. According to SP RF XV, the solubility of resulting product is more than raw dihydroquercetin.
Conclusion. The solid monophase dihydroquercetin-glycine system can be used to develop a new dosage form “Lyophilizate” (SP RF XV, PM.1.4.1.0031) and further preclinical study of safety and efficacy of neurodegenerative diseases.



Evaluation of the effectiveness of herbal medicine in the complex treatment of urolithiasis
Abstract
Introduction. Based on research of scientific data, to conduct a comprehensive review and comparative characteristics of the effectiveness of the use of herbal medicines for the treatment of urolithiasis.
Aim. Study of scientific works on the analysis of their influence on stones and clinical outcomes at the stages of preparation for remote lithotripsy and in the postoperative period, as well as comparison of their therapeutic activity with the use of only antispasmodics or lithotripsy without additional pharmacotherapy.
Methods. The following information resources were used to search for relevant studies: electronic databases PubMed, Google Scholar, elibrary, CyberLeninka and Cochrane Library. The following key queries were used in the work: “urolithiasis”, “phytotherapy”, “rowatinex”, “canephron”, “urolesan”, “phytolysin”, “cystone”. The search depth was 33 years (1992–2025). A total of 2330 publications were found, after excluding duplicates, invalid works, publications with no free access to the full text, the final number of works included in this literature review in the direction of “herbal medicine” and “urolithiasis” was 16. The total number of sources in the article is 34.
Results. The conducted analysis of scientific literature allowed to establish that medicinal herbal preparations demonstrate significant efficiency in the treatment of urolithiasis. Combined use of herbal preparations with remote lithotripsy showed advantages in decreasing the frequency of complications, decreasing the size of stones, facilitating their passage and decreasing the need for repeated procedures. The review confirms the advisability of including herbal medicine in complex treatment regimens for urolithiasis.
Conclusion. Analysis of literary data confirmed the effectiveness of herbal medicines in the treatment of urolithiasis, in combination with lithotripsy.



Technology of medicines
Ustification of technology and analysis of liquid extract of garlic scales
Abstract
Introduction. Disposal of food industry waste is an urgent problem that requires a solution. Hundreds of tons of meal from the food and pharmaceutical industries remain unclaimed, although they could become the basis for the creation of new medicines and biologically active food additives. One of the waste products of the food industry is the integumentary scales of garlic, which contain natural antioxidants – polyphenols. However, at present, in scientific medicine, garlic scales have been studied little and are not used in pharmacy. Purpose of the study: development of technology for extract of garlic scales of the winter variety “Petrovsky”.
Material and methods. The material was dried winter garlic scales, harvested from cultivated garlic in the Stavropol Territory in 2023. Identification of anthocyanins in the raw material and extract was carried out by thin-layer chromatography and by the characteristic maximum in the light absorption spectrum. Quantitative determination of anthocyanins was carried out by spectrophotometry, after establishing the optimal parameters for their extraction from raw materials (degree of grinding, extraction time, type of extractant, type of extraction). The extract was obtained by repercolation with a completed cycle in a battery of three percolators using the countercurrent principle. The assessment of quality indicators (appearance, dry residue, alcohol concentration in the extract, content of active substances) and functional characteristics of the finished extract was carried out in accordance with the requirements of the Global Fund.
Results. As a result of the experiments, the optimal parameters for the extraction of anthocyanins from scales were established, and a comparative assessment was carried out using 1% solutions of hydrochloric acid and citric acid as extractants in the quantitative determination method. The developed spectrophotometric method for the quantitative determination of anthocyanins in raw materials made it possible to establish their content as 0.501±0.012%, using a specific absorption index of cyanidin 3-5-diglycoside equal to 453. The determination error did not exceed ±2.5%. The commodity and technological indicators of the raw materials were determined, the concentration of the extractant (ethyl alcohol), and the conditions for extracting the raw materials were substantiated. A technology has been developed for liquid extract of garlic scales using the repercolation method, dividing the raw material into equal parts with a completed cycle. The analysis of the obtained extract was carried out according to pharmacopoeial indicators: appearance, dry residue, alcohol concentration in the extract, content of active substances.
Conclusion. The results of the research can serve as a basis for further studies of the biological activity of the obtained extract as a remedy with antioxidant and anti-inflammatory activity.



Modern aspects of the development of bioadhesive dosage forms for the oral cavity (review)
Abstract
The creation of dosage forms with the ability to bioadhesive is an urgent direction in the development of pharmaceutical technology. This review systematizes modern developments of bioadhesive drugs for use in the oral cavity, including films, gels, tablets and micro-/nanoparticles. Special attention is paid to bioadhesive polymers, their systematization and description of properties and methods of inclusion in the composition of dosage forms. The key aspects of the structure of the oral mucosa that determine the effectiveness of bioadhesion and methods for measuring mucoadhesive properties (in vitro and in vivo), including stretching tests, rheological methods, the use of flow systems, etc. are considered. Examples of commercial drugs available on the Russian market and variants of formulations of dosage forms described in scientific publications are given. The review also addresses the issue of standardization of testing methods for these dosage forms, including the use of synthetic and natural mucosal analogues. In general, the development of bioadhesive medicines for the oral cavity opens up new opportunities for the treatment of local and systemic diseases, combining ease of use, prolonged effect and reduction of systemic adverse reactions.



Organization and economy
Current issues of regulating the development of the Russian pharmaceutical market
Abstract
Introduction. The relevance of regulating the pharmacy sector in Russia is growing against the backdrop of a dynamic pharmaceutical market facing problems with the availability of drugs and the influence of network structures.The study aims to analyze the legal regulation and prospects of the pharmacy sector.
Objective of the study. Conducting an analysis of the directions and features of legal regulation of the Russian pharmaceutical market, taking into account the existing risks and prospects for the development of the pharmacy sector, the availability of drug supply.
Material and methods. The materials were regulatory legal acts, results of analytical research of the pharmaceutical market, data from the register of licenses of Roszdravnadzor. The research methods included content analysis of regulatory legal acts and literature sources in the field of drug circulation, regulation of competitive markets, methods of retrospective, statistical, comparative and forecast analysis.
Results. The analysis of the pharmaceutical market revealed problems associated with its monopolization and reduced availability of drug care for some categories of citizens. The main problems include imbalance among market participants, territorial unevenness of pharmacy infrastructure and the lack of unified mechanisms for approaches to regulation for the state segment. The article presents an analysis of changes in legislation on regulating the pharmaceutical market, taking into account the main trends in the development of the pharmacy sector and the availability of drug provision. The vector of legal regulation aimed at increasing the availability of drug care and counteracting the monopolization of the market is noted. The problems of regulating pharmacy chains are identified due to the imperfect terminology, the lack of a differentiated approach when introducing the proposed antimonopoly restrictions. The risks of negative consequences for the development of individual market participants, including in the state segment, the availability of drug care in remote and sparsely populated areas are predicted.
Conclusion. The key problems associated with the specifics of the current stage of development of the pharmaceutical market have been identified. Recommendations for improving legislation can contribute to the development of the pharmacy sector and increase the availability of drug care.



Drug provision for ischemic heart disease and arterial hypertension in the Republic of Tajikistan
Abstract
Introduction. The increase in the incidence of coronary heart disease (CHD) and arterial hypertension (AH) in the Republic of Tajikistan, as well as the lack of social programs for drug provision, highlight the need to study the views of doctors regarding the prescription of drugs.
Objective. To study the preferences and opinions of physicians regarding drug provision for coronary heart disease and arterial hypertension in the Republic of Tajikistan to identify ways to optimize and improve pharmaceutical care for these patients.
Material and methods. The source for the research work were questionnaires of doctors of the Republican Clinical Center of Cardiology of the Republic of Tajikistan of all departments, the department of cardiorheumatology of the City Clinical Hospital No. 2 named after K. Tadjiev in Dushanbe, the National Diagnostic Center of the Republic of Tajikistan and City Health Centers No.1, 8, 10, 14, Dushanbe.
The work uses methods of content analysis, systematization, generalization, descriptive statistics using the program MS Office Excel 2017".
Results. 64% of physicians prefer fixed combinations or their combination with monotherapy. In 69% of cases, the choice of drug is influenced by the patient's ability to pay. Physicians generally follow clinical protocols, but only 52% systematically comply with them. An assessment of the availability of the latest drugs showed that almost half of physicians have only partial access to them. Most physicians have a positive attitude towards involving pharmacy workers in a multidisciplinary team of healthcare professionals in providing services to patients with coronary heart disease and hypertension.
Conclusion. Fixed combinations are considered more effective, especially by younger and middle-aged cardiologists. Doctors choose drugs mainly without reference to the manufacturer, focusing on effectiveness. The patient's solvency is an important criterion when prescribing therapy. The physician respondents acknowledge the importance of interprofessional interaction with pharmacists, in particular in terms of polypharmacy, consultation and coordination of actions. The obtained results can be used to improve pharmaceutical care and expand the functionality of pharmacists within the team model of care.


