Pub Date : 2021-12-10DOI: 10.19163/2307-9266-2021-9-6-506-518
D. R. Imachueva, Фатима Казбековна Серебряная, E. Machs, V. Kotseruba
At the moment, a relevant objective in pharmacognosy, is the use of all kinds of the DNA analysis methods for identifying plant materials, detecting counterfeits, genetically modified crops and products.The aim of the research is to study the possibility of using molecular genetic research methods in the analysis of the genus Hedysarum L., for the identification of medicinal plant materials. This article presents the results of the application of molecular genetic research methods in the analysis of the genus Hedysarum L. in the flora of the North Caucasus.Materials and methods. The study material was the samples of the genus Hedysarum L. species collected in the North Caucasus: Hedysarum caucasicum M. Bieb. (in the fruiting phase in the territory of the Karachay-Cherkess Republic); Hedysarum grandiflorum Pall. (in the fruiting phase in the Volgograd region); Hedysarum daghestanicum Rupr. ex Boiss. (in the flowering phase in the Republic of Dagestan). Sequencing of the ITS1-5.8S-ITS2 marker region of gene 5.8S by the RNA ribosome was carried out according to the Sanger method on the AbiPrism 3130 genetic analyzer at the laboratory of biosystematics and cytology of Komarov Botanical Institute of the Russian Academy of Sciences.Results. Based on a comparative study of the marker region of the nuclear ribosomal gene 5.8S rRNA, marker nucleotide substitutions of Hedysarum caucasicum M. Bieb., Hedysarum daghestanicum Rupr. ex Boiss., Hedysarum grandiflorum Pall, have been identified. The most probable secondary structure of 5.8S rRNA has been constructed. It has been shown that based on the analysis performed, it is possible to predict additional raw material sources of mangiferin and other groups of xanthones using the molecular data exemplified by the Obscura section.Conclusion. Based on the data obtained, it can be concluded that the morphological classification of the genus Hedysarum L. can be confirmed within the Obscura section.
目前,生药学的一个相关目标是利用各种DNA分析方法鉴定植物材料,检测假冒伪劣产品,转基因作物和产品。本研究的目的是探讨利用分子遗传学方法对海丝兰属植物进行分析,以鉴别药用植物的可能性。本文介绍了分子遗传学研究方法在北高加索地区植物区系中的应用结果。材料和方法。研究材料为采集于北高加索地区的海苔属植物(Hedysarum caucasicum M. Bieb)。(在卡拉恰伊-切尔克斯共和国境内处于结果阶段);桔梗。(在伏尔加格勒地区处于结果阶段);大菱鲆。木香。(达吉斯坦共和国的花期)。在俄罗斯科学院科马罗夫植物研究所生物系统与细胞学实验室的AbiPrism 3130遗传分析仪上,按照Sanger法对基因5.8S的ITS1-5.8S-ITS2标记区进行了RNA核糖体测序。通过对核糖体基因5.8S rRNA标记区域的比较研究,研究了高加索海藓(Hedysarum caucasicum M. Bieb)的标记核苷酸替换。;大菱鲆;木香。一种名为Hedysarum grandflorum Pall的植物已被鉴定。构建了5.8S rRNA最可能的二级结构。结果表明,基于所进行的分析,可以利用暗丘切片所示的分子数据预测芒果苷和其他类群的口山酮的其他原料来源。根据所获得的资料,可以得出结论,在暗丘剖面内可以确定Hedysarum L.的形态分类。
{"title":"USE OF SEQUENCING METHODS FOR SPECIES IDENTIFICATION EXEMPLIFIED BY PHYLOGENETIC RELATIONSHIPS WITHIN GENUS HEDYSARUM L.","authors":"D. R. Imachueva, Фатима Казбековна Серебряная, E. Machs, V. Kotseruba","doi":"10.19163/2307-9266-2021-9-6-506-518","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-506-518","url":null,"abstract":"At the moment, a relevant objective in pharmacognosy, is the use of all kinds of the DNA analysis methods for identifying plant materials, detecting counterfeits, genetically modified crops and products.The aim of the research is to study the possibility of using molecular genetic research methods in the analysis of the genus Hedysarum L., for the identification of medicinal plant materials. This article presents the results of the application of molecular genetic research methods in the analysis of the genus Hedysarum L. in the flora of the North Caucasus.Materials and methods. The study material was the samples of the genus Hedysarum L. species collected in the North Caucasus: Hedysarum caucasicum M. Bieb. (in the fruiting phase in the territory of the Karachay-Cherkess Republic); Hedysarum grandiflorum Pall. (in the fruiting phase in the Volgograd region); Hedysarum daghestanicum Rupr. ex Boiss. (in the flowering phase in the Republic of Dagestan). Sequencing of the ITS1-5.8S-ITS2 marker region of gene 5.8S by the RNA ribosome was carried out according to the Sanger method on the AbiPrism 3130 genetic analyzer at the laboratory of biosystematics and cytology of Komarov Botanical Institute of the Russian Academy of Sciences.Results. Based on a comparative study of the marker region of the nuclear ribosomal gene 5.8S rRNA, marker nucleotide substitutions of Hedysarum caucasicum M. Bieb., Hedysarum daghestanicum Rupr. ex Boiss., Hedysarum grandiflorum Pall, have been identified. The most probable secondary structure of 5.8S rRNA has been constructed. It has been shown that based on the analysis performed, it is possible to predict additional raw material sources of mangiferin and other groups of xanthones using the molecular data exemplified by the Obscura section.Conclusion. Based on the data obtained, it can be concluded that the morphological classification of the genus Hedysarum L. can be confirmed within the Obscura section.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"63 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79502426","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-07DOI: 10.19163/2307-9266-2021-9-6-454-464
L. Balykova, O. Radaeva, K. Zaslavskaya, Y. Kostina, M. S. Iskandyarova, E. Negodnova, V. Eremeev, L. Sabirov, E. Semeleva
In many ways, arterial hypertension and obesity determine the likelihood of a severe course and lethal outcomes in COVID-19. This fact justifies the expediency of an early use of drugs with a direct antiviral action, the analysis of their efficacy not only in the acute, but also in the postcovid period.The aim of the research was to analyze the outpatient cards and case histories of the COVID-19 patients to study the effect of the early (up to the 5th day after the onset of the first symptoms of the disease) use of the drug based on favipiravir, on the frequency of patients’ hospitalizations with arterial hypertension and obesity, as well as to determine the cytokine status characteristics of this patient category in the postcovid period.Materials and methods. “An open prospective comparative study of the “Areplivir®” (favipiravir) efficacy in the debut of COVID-19 in comorbid patients” was carried out in the Republic of Mordovia (the analysis of the hospitalizations frequency and blood levels of M-CSF, EPO in 218 patients, in terms of the use of the antiviral preparation).Results. According to the results of the analysis, it was found out that, despite the presence of comorbid conditions that increase the risk of developing a severe course of COVID-19, i.e. obesity and essential arterial hypertension, in the group of patients taking favipiravir, the need for hospitalization was twice as low (p < 0.05), in relation to the comparison group. The analysis of the cytokine status revealed that in the postcovid period, in the group that took the drug based on favipiravir at the outpatient stage, the average level of M-CSF was significantly lower (p> 0.05), and EPO was higher (p> 0.05) than in the patients from the group “without antiviral drugs at the outpatient stage”. Indirectly, according to the previously obtained data, that acts as a potential marker for reducing the risk of long-term cardiovascular complications of COVID-19.Conclusion. This study showed that an early prescription of favipiravir contributes to a decrease in the rate of COVID-19 patients’ hospitalization even against the background of concomitant hypertension and obesity, due to a decrease in the likelihood of moderate and severe courses of the disease, and also leads to an earlier objective and subjective recovery. The results demonstrated a high potential benefit of an early favipiravir use in the novel coronavirus infection and in the prevention of postcovid complications.
{"title":"STUDY OF CLINICAL AND PATHOGENETIC EFFECTS OF ANTI-VIRAL DRUG BASED ON FAVIPIRAVIR IN COMORBID PATIENTS WITH COVID-19 AT THE OUTPATIENT STAGE OF TREATMENT","authors":"L. Balykova, O. Radaeva, K. Zaslavskaya, Y. Kostina, M. S. Iskandyarova, E. Negodnova, V. Eremeev, L. Sabirov, E. Semeleva","doi":"10.19163/2307-9266-2021-9-6-454-464","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-454-464","url":null,"abstract":"In many ways, arterial hypertension and obesity determine the likelihood of a severe course and lethal outcomes in COVID-19. This fact justifies the expediency of an early use of drugs with a direct antiviral action, the analysis of their efficacy not only in the acute, but also in the postcovid period.The aim of the research was to analyze the outpatient cards and case histories of the COVID-19 patients to study the effect of the early (up to the 5th day after the onset of the first symptoms of the disease) use of the drug based on favipiravir, on the frequency of patients’ hospitalizations with arterial hypertension and obesity, as well as to determine the cytokine status characteristics of this patient category in the postcovid period.Materials and methods. “An open prospective comparative study of the “Areplivir®” (favipiravir) efficacy in the debut of COVID-19 in comorbid patients” was carried out in the Republic of Mordovia (the analysis of the hospitalizations frequency and blood levels of M-CSF, EPO in 218 patients, in terms of the use of the antiviral preparation).Results. According to the results of the analysis, it was found out that, despite the presence of comorbid conditions that increase the risk of developing a severe course of COVID-19, i.e. obesity and essential arterial hypertension, in the group of patients taking favipiravir, the need for hospitalization was twice as low (p < 0.05), in relation to the comparison group. The analysis of the cytokine status revealed that in the postcovid period, in the group that took the drug based on favipiravir at the outpatient stage, the average level of M-CSF was significantly lower (p> 0.05), and EPO was higher (p> 0.05) than in the patients from the group “without antiviral drugs at the outpatient stage”. Indirectly, according to the previously obtained data, that acts as a potential marker for reducing the risk of long-term cardiovascular complications of COVID-19.Conclusion. This study showed that an early prescription of favipiravir contributes to a decrease in the rate of COVID-19 patients’ hospitalization even against the background of concomitant hypertension and obesity, due to a decrease in the likelihood of moderate and severe courses of the disease, and also leads to an earlier objective and subjective recovery. The results demonstrated a high potential benefit of an early favipiravir use in the novel coronavirus infection and in the prevention of postcovid complications.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"39 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78763439","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-07DOI: 10.19163/2307-9266-2021-9-6-465-475
Y. Petukhova, E. Eliseeva, A. Petukhova
The aim of the study is to assess the clinical and economic effectiveness of the practical implementation results of programmed screening for colorectal cancer (CRC) in the Primorsky Territory using clinical and economic research methods.Materials and methods. In the study, the following kinds of data were used: the statistical data from the regional clinic’s cancer registry on the structure of the morbidity and average life expectancy of CRC patients in the Primorsky Territory; the data on the cost of screening studies and the stages of anticancer therapy in accordance with the “Territorial Tariff Agreement on Payment for Medical Care (Medical Services) in the System of Compulsory Health Insurance in the Territory of Primorsky Krai”, 2021. Two methods of clinical and economic analysis with the corresponding calculation formulas have been applied. The cost of medical interventions were estimated in accordance with the screening standards and clinical guidelines for the treatment of malignant neoplasms of the colon and rectum, approved by the Scientific and Practical Council of the Ministry of Health of the Russian Federation, 2020.Results. The evidence-based substantiation of screening clinical effects has been obtained: the structure redistribution of colorectal cancer incidence towards the prevalence of early forms by 16.81%; the average increase in the life expectancy of patients with the studied disease is 12.8 months. A natural consequence of these events is the predicted decrease in the mortality rate from CRC in the territory of the subject in the subsequent years. The economic justification of CRC screening software which guarantees a significant saving in health care resources amounting to 23% compared to an alternative strategy, has been demonstrated. It can influence the management decisions on the further strategy of the mass introduction of this medical technology.Conclusion. Currently, CRC screening is the most effective way to reduce morbidity and mortality from this disease. The predominance of the early diagnosis of the disease is extrapolated to significant savings in public health care. A promising direction for further research in the field of CRC screening is the study of its long-term effects, in particular, a detailed clinical and economic analysis of the diagnostics effectiveness and the elimination of premalignant neoplasms.
{"title":"CLINICAL AND ECONOMIC JUSTIFICATION OF SOFTWARE SCREENING PERFORMANCE OF COLORECTAL CANCER AT THE REGION LEVEL","authors":"Y. Petukhova, E. Eliseeva, A. Petukhova","doi":"10.19163/2307-9266-2021-9-6-465-475","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-465-475","url":null,"abstract":"The aim of the study is to assess the clinical and economic effectiveness of the practical implementation results of programmed screening for colorectal cancer (CRC) in the Primorsky Territory using clinical and economic research methods.Materials and methods. In the study, the following kinds of data were used: the statistical data from the regional clinic’s cancer registry on the structure of the morbidity and average life expectancy of CRC patients in the Primorsky Territory; the data on the cost of screening studies and the stages of anticancer therapy in accordance with the “Territorial Tariff Agreement on Payment for Medical Care (Medical Services) in the System of Compulsory Health Insurance in the Territory of Primorsky Krai”, 2021. Two methods of clinical and economic analysis with the corresponding calculation formulas have been applied. The cost of medical interventions were estimated in accordance with the screening standards and clinical guidelines for the treatment of malignant neoplasms of the colon and rectum, approved by the Scientific and Practical Council of the Ministry of Health of the Russian Federation, 2020.Results. The evidence-based substantiation of screening clinical effects has been obtained: the structure redistribution of colorectal cancer incidence towards the prevalence of early forms by 16.81%; the average increase in the life expectancy of patients with the studied disease is 12.8 months. A natural consequence of these events is the predicted decrease in the mortality rate from CRC in the territory of the subject in the subsequent years. The economic justification of CRC screening software which guarantees a significant saving in health care resources amounting to 23% compared to an alternative strategy, has been demonstrated. It can influence the management decisions on the further strategy of the mass introduction of this medical technology.Conclusion. Currently, CRC screening is the most effective way to reduce morbidity and mortality from this disease. The predominance of the early diagnosis of the disease is extrapolated to significant savings in public health care. A promising direction for further research in the field of CRC screening is the study of its long-term effects, in particular, a detailed clinical and economic analysis of the diagnostics effectiveness and the elimination of premalignant neoplasms.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"40 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77472508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-07DOI: 10.19163/2307-9266-2021-9-6-495-505
E. V. Kazakova, V. Trukhin, I. Narkevich, I. I. Basakina
The biotechnology industry is currently one of the most dynamically developing sectors of the pharmaceutical industry, that is why it requires improvement in the personnel management system aimed at increasing the flexibility and adaptability of the organization.The aim of the research is to determine the degree of readiness of the organization’s employees for innovations as illustrated by the example of an export-oriented enterprise.Materials and methods. The source information was collected from the employees of the biotechnological enterprise through a questionnaire survey. The representative sample included 588 respondents. The statistical processing of data was carried out using the specialized software IBM SPSS STATISTICS (IBM, USA, 2017). The consistent readiness of the organization’s employees for innovations was determined using I.O. Zagashev’s methods. To assess the reliability of the psychological test, an internal consistency model with Cronbach’s alpha was applied. Statistical hypotheses were tested by comparing the central tendencies of two independent samples using Student’s t-test and the Mann–Whitney nonparametric test.Results. The distribution results of key motivating factors for personnel showed that motivating factors such as an adequate salary and sustainable employment took the leading positions. However, the assessment of the employees’ consistent readiness for innovations according to I.O. Zagashev’s methods shows a high degree of the personnel’s readiness for changes due to positive emotional perception of any innovations.Conclusion. The results obtained make it possible to arrive at the conclusion that the established team favorably responds to all innovations, and is ready to support them in the future being aware of the organization’s desire for innovations. In the future, the results will be used to determine the required management functions and goals and to develop the personnel management strategy in the context of the knowledge transfer, technology and export policy of the pharmaceutical enterprise.
生物技术行业目前是制药行业中最具活力的发展部门之一,这就是为什么它需要改善人事管理系统,旨在增加组织的灵活性和适应性。本研究的目的是确定组织雇员对创新的准备程度,并以出口导向型企业为例加以说明。材料和方法。本研究通过问卷调查的方式,从该生物技术企业的员工中收集源信息。代表性样本包括588名受访者。使用专业软件IBM SPSS STATISTICS (IBM, USA, 2017)对数据进行统计处理。利用扎加舍夫的方法确定了组织员工对创新的持续准备。为了评估心理测试的信度,采用了内部一致性模型与Cronbach 's alpha。通过比较两个独立样本的集中趋势,采用学生t检验和Mann-Whitney非参数检验来检验统计假设。人员关键激励因素的分布结果显示,充分的薪酬和可持续就业等激励因素占据主导地位。然而,根据I.O.扎加舍夫的方法对员工持续创新准备的评估显示,由于对任何创新的积极情感感知,员工对变化的准备程度很高。所获得的结果使我们有可能得出这样的结论:已建立的团队对所有的创新都有良好的反应,并且在意识到组织对创新的渴望后,准备在未来支持他们。在未来,研究结果将用于确定制药企业在知识转移、技术和出口政策背景下所需的管理职能和目标,并制定人员管理战略。
{"title":"ANALYSIS OF THE PERSONNEL’S CONSISTENT READINESS FOR CHANGES AS ILLUSTRATED BY THE EXAMPLE OF AN EXPORT-ORIENTED BIOTECHNOLOGICAL ENTERPRISE","authors":"E. V. Kazakova, V. Trukhin, I. Narkevich, I. I. Basakina","doi":"10.19163/2307-9266-2021-9-6-495-505","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-495-505","url":null,"abstract":"The biotechnology industry is currently one of the most dynamically developing sectors of the pharmaceutical industry, that is why it requires improvement in the personnel management system aimed at increasing the flexibility and adaptability of the organization.The aim of the research is to determine the degree of readiness of the organization’s employees for innovations as illustrated by the example of an export-oriented enterprise.Materials and methods. The source information was collected from the employees of the biotechnological enterprise through a questionnaire survey. The representative sample included 588 respondents. The statistical processing of data was carried out using the specialized software IBM SPSS STATISTICS (IBM, USA, 2017). The consistent readiness of the organization’s employees for innovations was determined using I.O. Zagashev’s methods. To assess the reliability of the psychological test, an internal consistency model with Cronbach’s alpha was applied. Statistical hypotheses were tested by comparing the central tendencies of two independent samples using Student’s t-test and the Mann–Whitney nonparametric test.Results. The distribution results of key motivating factors for personnel showed that motivating factors such as an adequate salary and sustainable employment took the leading positions. However, the assessment of the employees’ consistent readiness for innovations according to I.O. Zagashev’s methods shows a high degree of the personnel’s readiness for changes due to positive emotional perception of any innovations.Conclusion. The results obtained make it possible to arrive at the conclusion that the established team favorably responds to all innovations, and is ready to support them in the future being aware of the organization’s desire for innovations. In the future, the results will be used to determine the required management functions and goals and to develop the personnel management strategy in the context of the knowledge transfer, technology and export policy of the pharmaceutical enterprise.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79939545","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-07DOI: 10.19163/2307-9266-2021-9-6-441-453
Y. Kostyro, K. Alekseev
An original heparinoid, sulfated arabinogalactan in the form of potassium salt, possessing anticoagulant and hypolipidemic activities, has been developed at the A.E. Favorsky Irkutsk Institute of Chemistry Siberian Branch of the Russian Academy of Sciences.The aim was to develop solid peroral dose forms (capsules and film-coated tablets) for the prevention and treatment of atherosclerotic lesion of blood vessels on the basis of potassium salt of sulfated arabinogalactan which would be suitable for further clinical trials of these forms.Materials and methods. The following materials were used in the work: sulfated arabinogalactan in the form of potassium salt, obtained at the A.E. Favorsky Irkutsk Institute of Chemistry Siberian Branch of the Russian Academy of Sciences; Ludipress®; AEROSIL® 200 Pharma; calcium stearate; Aquacoat ECD. The powder mixtures were briquetted followed by tableting and application of the finished film coating Aquacoat ECD, and encapsulation in hard gelatin capsules.Results. Composition and technological characteristics of capsules and film-coated tablets were determined using physico-chemical and technological properties of sulfated arabinogalactan in the form of potassium salt. Technological parameters and quality indicators were determined for the solid pharmaceutical dose forms in accordance with the requirements of the State Pharmacopoeia of the Russian Federation of the XIVth edition. Conclusion. The optimum compositions and technology for the preparation of capsules and film-coated tablets based on potassium salt of sulfated arabinogalactan for the prevention and treatment of atherosclerotic lesion of blood vessels, were developed. The data obtained were used for the regulatory documentation design.
{"title":"DEVELOPMENT OF PERORAL HYPOLIPIDEMIC FORMULATION BASED ON SULFATED ARABINOGALACTAN IN THE FORM OF POTASSIUM SALT","authors":"Y. Kostyro, K. Alekseev","doi":"10.19163/2307-9266-2021-9-6-441-453","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-441-453","url":null,"abstract":"An original heparinoid, sulfated arabinogalactan in the form of potassium salt, possessing anticoagulant and hypolipidemic activities, has been developed at the A.E. Favorsky Irkutsk Institute of Chemistry Siberian Branch of the Russian Academy of Sciences.The aim was to develop solid peroral dose forms (capsules and film-coated tablets) for the prevention and treatment of atherosclerotic lesion of blood vessels on the basis of potassium salt of sulfated arabinogalactan which would be suitable for further clinical trials of these forms.Materials and methods. The following materials were used in the work: sulfated arabinogalactan in the form of potassium salt, obtained at the A.E. Favorsky Irkutsk Institute of Chemistry Siberian Branch of the Russian Academy of Sciences; Ludipress®; AEROSIL® 200 Pharma; calcium stearate; Aquacoat ECD. The powder mixtures were briquetted followed by tableting and application of the finished film coating Aquacoat ECD, and encapsulation in hard gelatin capsules.Results. Composition and technological characteristics of capsules and film-coated tablets were determined using physico-chemical and technological properties of sulfated arabinogalactan in the form of potassium salt. Technological parameters and quality indicators were determined for the solid pharmaceutical dose forms in accordance with the requirements of the State Pharmacopoeia of the Russian Federation of the XIVth edition. Conclusion. The optimum compositions and technology for the preparation of capsules and film-coated tablets based on potassium salt of sulfated arabinogalactan for the prevention and treatment of atherosclerotic lesion of blood vessels, were developed. The data obtained were used for the regulatory documentation design.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"32 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84563346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-06DOI: 10.19163/2307-9266-2021-9-6-426-440
E. Privalova
The aim of the article was to analyze the state of knowledge of the following plants: Heteropappus altaicus (Willd.) Novopokr., Solidago dahurica L., Leucanthemum vulgare Lam., Tripleurospermum inodorum (L.), Antennaria dioica (L.) Gaertn., Leontopodium conglobatum (Turcz.) Hand.-Mazz. and Geranium eriostemon Fischer., G. pratense L., G. wlassowianum Fisch. ex Link. (Geraniaceae).Materials and methods. To compile the review, the information from the following scientific open and available literature sources placed in scientific libraries of institutions, in electronic databases and search systems, was used: floristic summaries “Flora of Siberia”; “Flora of Central Siberia”; Electronic library of the Siberian branch of the Russian Academy of Sciences; Elibrary; PubMed; Scopus; CyberLeninka, Google Academy; The Plant List, Global Compositae Checklist. The search carried out, was based on the publications for the period of 2009-2020, on the information requests for names of families and subfamilies, names of plant species, biologically active compounds in English, Latin and Russian.Results. A comparative analysis of morphological characters, common species names and the synonyms for the listed species, has been carried out. The studied objects are characterized by the presence of polyphenolic compounds and substances of a triterpene structure, in particular, flavonoids, hydroxycinnamic acids, tannides. In addition, the representatives of the Asteroideae subfamily (Asteraceae) show the accumulation of essential oils, and the representatives of the Geranium genus (geranium) show the accumulation of anthocyanins. The spectrum of the pharmacological activity includes anti-inflammatory, choleretic, antimicrobial, antispasmodic and other types of effects.Conclusion. The presented review makes it possible to arrive at the conclusion about a certain knowledge level of the regional representatives of the Asteroideae subfamily and the Geranium genus. This determines the prospects of these plant objects for further pharmacognostic and pharmacological research and the creation of drugs on their basis – the sources of polyphenolic compounds.
{"title":"A FEW REPRESENTATIVES OF ASTEROIDAE (ASTERACEAE) SUBFAMILY AND GERANIUM (GERANIACEAE) GENUS IN THE BAIKAL REGION (REVIEW","authors":"E. Privalova","doi":"10.19163/2307-9266-2021-9-6-426-440","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-426-440","url":null,"abstract":"The aim of the article was to analyze the state of knowledge of the following plants: Heteropappus altaicus (Willd.) Novopokr., Solidago dahurica L., Leucanthemum vulgare Lam., Tripleurospermum inodorum (L.), Antennaria dioica (L.) Gaertn., Leontopodium conglobatum (Turcz.) Hand.-Mazz. and Geranium eriostemon Fischer., G. pratense L., G. wlassowianum Fisch. ex Link. (Geraniaceae).Materials and methods. To compile the review, the information from the following scientific open and available literature sources placed in scientific libraries of institutions, in electronic databases and search systems, was used: floristic summaries “Flora of Siberia”; “Flora of Central Siberia”; Electronic library of the Siberian branch of the Russian Academy of Sciences; Elibrary; PubMed; Scopus; CyberLeninka, Google Academy; The Plant List, Global Compositae Checklist. The search carried out, was based on the publications for the period of 2009-2020, on the information requests for names of families and subfamilies, names of plant species, biologically active compounds in English, Latin and Russian.Results. A comparative analysis of morphological characters, common species names and the synonyms for the listed species, has been carried out. The studied objects are characterized by the presence of polyphenolic compounds and substances of a triterpene structure, in particular, flavonoids, hydroxycinnamic acids, tannides. In addition, the representatives of the Asteroideae subfamily (Asteraceae) show the accumulation of essential oils, and the representatives of the Geranium genus (geranium) show the accumulation of anthocyanins. The spectrum of the pharmacological activity includes anti-inflammatory, choleretic, antimicrobial, antispasmodic and other types of effects.Conclusion. The presented review makes it possible to arrive at the conclusion about a certain knowledge level of the regional representatives of the Asteroideae subfamily and the Geranium genus. This determines the prospects of these plant objects for further pharmacognostic and pharmacological research and the creation of drugs on their basis – the sources of polyphenolic compounds.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82934943","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-06DOI: 10.19163/2307-9266-2021-9-6-476-484
A. S. Sheremetyeva, A. Napsheva, N. Durnova
The aim of research is to study the antitumor activity of aqueous and alcoholic extracts of Thymus marschallianus Willd. on male outbreed white rats with transplanted liver tumor PC-1. Materials and methods. The object of study is crushed grass of Thymus marschallianus Willd. collected in the Saratov vicinity in the flowering phase. Extracts from the specified plant material were made in two different ways: first way, water was used as an extractant, in the other, ethyl alcohol 95%. 15 male outbreed white laboratory rats weighing 200±50 were used in experiment. The subcutaneous injections of alveolar liver cancer RS-1 were made in scapula area. Animals with transplanted tumor were randomly divided into 3 groups of 5 rats: the first was a control (negative control) that did not receive extract; the second was an experimental one that receiving alcoholic extract of Thymus marschallianus Willd.; the third was an experimental one that receiving aqueous extract of Thymus marschallianus Willd. To study the pathomorphosis of the tumor, morphological and morphometric methods were used standard histological staining with hematoxylin and eosin. Results It has been established that alcoholic and aqueous extracts of Thymus marschallianus Willd. have antitumor activity. Morphological examination of animal tumors showed a decrease in the number of preserved tumor cells in the view field, pronounced necrobiotic and atrophic changes in tumor cells, absence of mitosis, proliferation of connective tissue fibers corresponding to the II-III degree of tumor pathomorphosis. Conclusion. Thymus marschallianus Willd. aqueous extract showed more potent antitumor activity. Introduction into tumor tissue revealed morphological signs of apoptosis: the appearance of apoptotic bodies, karyopycnosis, and condensation of nuclear chromatin in tumor cells. It can be assumed that the more pronounced antitumor effect of the aqueous extract is due to the higher yield of flavonoids.
{"title":"ANTITUMOR ACTIVITY IN VIVO OF AQUEOUS AND ALCOHOLIC EXTRACTS OF THYMUS MARSCHALLIANUS WILLD","authors":"A. S. Sheremetyeva, A. Napsheva, N. Durnova","doi":"10.19163/2307-9266-2021-9-6-476-484","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-476-484","url":null,"abstract":"The aim of research is to study the antitumor activity of aqueous and alcoholic extracts of Thymus marschallianus Willd. on male outbreed white rats with transplanted liver tumor PC-1. Materials and methods. The object of study is crushed grass of Thymus marschallianus Willd. collected in the Saratov vicinity in the flowering phase. Extracts from the specified plant material were made in two different ways: first way, water was used as an extractant, in the other, ethyl alcohol 95%. 15 male outbreed white laboratory rats weighing 200±50 were used in experiment. The subcutaneous injections of alveolar liver cancer RS-1 were made in scapula area. Animals with transplanted tumor were randomly divided into 3 groups of 5 rats: the first was a control (negative control) that did not receive extract; the second was an experimental one that receiving alcoholic extract of Thymus marschallianus Willd.; the third was an experimental one that receiving aqueous extract of Thymus marschallianus Willd. To study the pathomorphosis of the tumor, morphological and morphometric methods were used standard histological staining with hematoxylin and eosin. Results It has been established that alcoholic and aqueous extracts of Thymus marschallianus Willd. have antitumor activity. Morphological examination of animal tumors showed a decrease in the number of preserved tumor cells in the view field, pronounced necrobiotic and atrophic changes in tumor cells, absence of mitosis, proliferation of connective tissue fibers corresponding to the II-III degree of tumor pathomorphosis. Conclusion. Thymus marschallianus Willd. aqueous extract showed more potent antitumor activity. Introduction into tumor tissue revealed morphological signs of apoptosis: the appearance of apoptotic bodies, karyopycnosis, and condensation of nuclear chromatin in tumor cells. It can be assumed that the more pronounced antitumor effect of the aqueous extract is due to the higher yield of flavonoids.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79435272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-12-06DOI: 10.19163/2307-9266-2021-9-6-485-494
A. Yasenyavskaya, A. Tsibizova, L. Andreeva, N. Myasoedov, O. Bashkina, M. Samotrueva
The aim of the article was to study the effect of glyproline neuropeptide compounds Thr–Lys–Pro–Arg–Pro–Gly–Pro (Selank), Pro–Gly–Pro and Pro–Gly–Pro–Leu, on the level of apoptotic factors (caspase-3, caspase-8, the tumor necrosis factor) and neurotrophic factors (the nerve growth factor and the brain neurotrophic factor) in the blood serum of white rats under the experimental modeling of “social” stress.Materials and methods. The experimental studies were carried out on 90 nonlinear white male rats aged 6 months. By the type of behavior, in the process of “social” stress modeling, all the rats were divided into “aggressors” and “victims”. In the study, the following experimental groups (n=10) were formed: control individuals; groups of the rats exposed to stress for 20 days; groups of the animals treated intraperitoneally at the dose of 100 μg/kg/day, starting from the 1st day of the stress factor exposure, with a course of 20 days of glyproline compounds Thr–Lys–Pro–Arg–Pro–Gly–Pro (Selank), Pro–Gly–Pro and Pro–Gly–Pro–Leu. The effect of the compounds on the level of apoptotic and neurotrophic factors was assessed by determining the level of caspase-3, caspase-8, the tumor necrosis factor, the nerve growth factor and the brain neurotrophic factor of white rat blood serum by enzyme immunoassay.Results. According to the results of the study, it was found out that under the conditions of “social” stress, there was an increase in the apoptotic processes accompanied by an increase in the level of caspase-3, caspase-8, TNF-α in the blood serum of white rats, as well as a decrease in the concentration of neurotrophic factors – BDNF and NGF. The administration of giproline compounds against the background of stress, contributed to the restoration of the studied indicators level, which is most likely due to the presence of antiapoptotic and neuroprotective effects in giprolines due to the inhibition of the caspase-dependent cascade of apoptosis reactions, as well as the induction of the synthesis of neurotrophic factors with the antiapoptotic activity.Conclusion. Thus, the administration of glyproline neuropeptide compounds Thr–Lys–Pro–Arg–Pro–Gly–Pro (Selank), Pro–Gly–Pro and Pro–Gly–Pro–Leu under stress conditions, contributes to the restoration of the initiating and effector caspases level, as well as of neurotrophic factors. As a result of the experiment, an anti-apoptotic effect is observed due to the inhibition of the caspase-dependent cascade of reactions, as well as a stress-protective effect is observed due to the restoration of the brain neurotrophic factors level.
{"title":"EFFECT OF GLYPROLINES ON THE LEVEL OF APOPTOTIC AND NEUROTROPHIC FACTORS UNDER CONDITIONS OF “SOCIAL” STRESS","authors":"A. Yasenyavskaya, A. Tsibizova, L. Andreeva, N. Myasoedov, O. Bashkina, M. Samotrueva","doi":"10.19163/2307-9266-2021-9-6-485-494","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-6-485-494","url":null,"abstract":"The aim of the article was to study the effect of glyproline neuropeptide compounds Thr–Lys–Pro–Arg–Pro–Gly–Pro (Selank), Pro–Gly–Pro and Pro–Gly–Pro–Leu, on the level of apoptotic factors (caspase-3, caspase-8, the tumor necrosis factor) and neurotrophic factors (the nerve growth factor and the brain neurotrophic factor) in the blood serum of white rats under the experimental modeling of “social” stress.Materials and methods. The experimental studies were carried out on 90 nonlinear white male rats aged 6 months. By the type of behavior, in the process of “social” stress modeling, all the rats were divided into “aggressors” and “victims”. In the study, the following experimental groups (n=10) were formed: control individuals; groups of the rats exposed to stress for 20 days; groups of the animals treated intraperitoneally at the dose of 100 μg/kg/day, starting from the 1st day of the stress factor exposure, with a course of 20 days of glyproline compounds Thr–Lys–Pro–Arg–Pro–Gly–Pro (Selank), Pro–Gly–Pro and Pro–Gly–Pro–Leu. The effect of the compounds on the level of apoptotic and neurotrophic factors was assessed by determining the level of caspase-3, caspase-8, the tumor necrosis factor, the nerve growth factor and the brain neurotrophic factor of white rat blood serum by enzyme immunoassay.Results. According to the results of the study, it was found out that under the conditions of “social” stress, there was an increase in the apoptotic processes accompanied by an increase in the level of caspase-3, caspase-8, TNF-α in the blood serum of white rats, as well as a decrease in the concentration of neurotrophic factors – BDNF and NGF. The administration of giproline compounds against the background of stress, contributed to the restoration of the studied indicators level, which is most likely due to the presence of antiapoptotic and neuroprotective effects in giprolines due to the inhibition of the caspase-dependent cascade of apoptosis reactions, as well as the induction of the synthesis of neurotrophic factors with the antiapoptotic activity.Conclusion. Thus, the administration of glyproline neuropeptide compounds Thr–Lys–Pro–Arg–Pro–Gly–Pro (Selank), Pro–Gly–Pro and Pro–Gly–Pro–Leu under stress conditions, contributes to the restoration of the initiating and effector caspases level, as well as of neurotrophic factors. As a result of the experiment, an anti-apoptotic effect is observed due to the inhibition of the caspase-dependent cascade of reactions, as well as a stress-protective effect is observed due to the restoration of the brain neurotrophic factors level.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87131595","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-10-25DOI: 10.19163/2307-9266-2021-9-5-334-345
N. Surya, S. Bhattacharyya
Polymers have become an integral part of novel drug delivery system. One such successful biodegradable polymer is poly lactic-co-glycolic acid (PLGA) which consists of polyesters of lactic acid and glycolic acid. It is one of the FDA-approved biodegradable polymers which is extensively used for therapeutic purposes in recent times.The aim. To illuminate researchers on the chemistry, novel properties and applications of PLGA in pharmaceutical fields.Materials and methods. Various internet sources like Science Direct, Scopus, Web of Science, PubMed and google scholar were used as the data source. The key words search was carried out for the following words and combinations: PLGA, Novel drug delivery, PLGA Nano particles, biomedical applications of PLGA.Results. Pharmaceutical and biomedical industries are flooded with the use of synthetic and natural polymers. The mechanical and viscoelastic properties of the polymers make them suitable for the temporal and spatial delivery of therapeutic agents for an extended period. Employment of copolymerization techniques lead to the modification of water solubility of the polymers and make them suitable for various applications of drug delivery systems. Biodegradable polymers due to their biocompatibility and biodegradable property have attracted their use in novel drug delivery systems. PLGA is one of them. PLGA is versatile as it can be fabricated into any size, shape, and can be used to encapsulate small molecules, tissue engineering, and bone repair, etc.Conclusion. The sensitivity and biodegradability of PLGA makes it a smart polymer for targeted and sustained delivery of drugs and in various biomedical applications.
聚合物已成为新型给药系统的重要组成部分。其中一种成功的生物可降解聚合物是聚乳酸-羟基乙酸(PLGA),它由乳酸和羟基乙酸的聚酯组成。它是fda批准的生物可降解聚合物之一,近年来广泛用于治疗目的。的目标。阐明PLGA的化学性质、新特性及其在制药领域的应用。材料和方法。各种互联网资源,如Science Direct, Scopus, Web of Science, PubMed和google scholar被用作数据源。关键词检索:PLGA、新型药物递送、PLGA纳米颗粒、PLGA的生物医学应用。制药和生物医学行业充斥着合成和天然聚合物的使用。聚合物的机械和粘弹性特性使它们适合于延长时间的治疗剂的时间和空间递送。共聚技术的应用导致聚合物水溶性的改变,并使其适用于药物输送系统的各种应用。可生物降解聚合物由于其生物相容性和可生物降解的特性,在新型给药系统中得到了广泛的应用。PLGA就是其中之一。PLGA具有多种用途,可制成任何尺寸、形状,可用于小分子包封、组织工程、骨修复等领域。PLGA的敏感性和可生物降解性使其成为一种智能聚合物,用于靶向和持续递送药物以及各种生物医学应用。
{"title":"PLGA – THE SMART POLYMER FOR DRUG DELIVERY","authors":"N. Surya, S. Bhattacharyya","doi":"10.19163/2307-9266-2021-9-5-334-345","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-5-334-345","url":null,"abstract":"Polymers have become an integral part of novel drug delivery system. One such successful biodegradable polymer is poly lactic-co-glycolic acid (PLGA) which consists of polyesters of lactic acid and glycolic acid. It is one of the FDA-approved biodegradable polymers which is extensively used for therapeutic purposes in recent times.The aim. To illuminate researchers on the chemistry, novel properties and applications of PLGA in pharmaceutical fields.Materials and methods. Various internet sources like Science Direct, Scopus, Web of Science, PubMed and google scholar were used as the data source. The key words search was carried out for the following words and combinations: PLGA, Novel drug delivery, PLGA Nano particles, biomedical applications of PLGA.Results. Pharmaceutical and biomedical industries are flooded with the use of synthetic and natural polymers. The mechanical and viscoelastic properties of the polymers make them suitable for the temporal and spatial delivery of therapeutic agents for an extended period. Employment of copolymerization techniques lead to the modification of water solubility of the polymers and make them suitable for various applications of drug delivery systems. Biodegradable polymers due to their biocompatibility and biodegradable property have attracted their use in novel drug delivery systems. PLGA is one of them. PLGA is versatile as it can be fabricated into any size, shape, and can be used to encapsulate small molecules, tissue engineering, and bone repair, etc.Conclusion. The sensitivity and biodegradability of PLGA makes it a smart polymer for targeted and sustained delivery of drugs and in various biomedical applications.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"166 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77919776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2021-10-25DOI: 10.19163/2307-9266-2021-9-5-346-355
V. M. Pokrovsky, E. A. Patrakhanov, O. V. Antsiferov, I. Kolesnik, A. V. Belashova, V. Soldatova, O. N. Pokopeiko, A. Karagodina, I. Arkhipov, D. G. Voronina, D. N. Sushkova
Heat shock protein Hsp70 is one of the main cytoprotection components under the action of various external stimuli. The analysis of the literature data shows that nowadays, the researches’ overwhelming evidence has proven the role of Hsp70 as a biological target for the drug development; however, the ideas about its use as a drug are often multidirectional.The aim of the article is to analyze and generalize the literature data on the features of the physiological functions of heat shock protein Hsp 70, and indicate the possibilities of its use for the pharmacological correction of various pathological conditions.Materials and methods. In the process of selecting material for writing this review article, such databases as Google Patents, Science Research Portal, Google Scholar, ScienceDirect, CiteSeer, Publications, ResearchIndex, Ingenta, PubMed, KEGG, etc. were used The following words and word combinations were selected as markers for identifying the literature: Hsp70, Hsp70 stroke, Hsp70 neuroprotection, Hsp70 cytoprotection, recombinant drugs.Results. In this review, the pharmacology of one of the key members of this family, Hsp70, was focused on. The literary analysis confirms that this molecule is an endogenous regulator of many physiological processes and demonstrates tissue protective effects in modeling ischemic, neurodegenerative and inflammatory processes. The use of recombinant exogenous Hsp70 mimics the endogenous function of the protein, indicating the absence of a number of typical limitations characteristic of pharmacotherapy with high molecular weight compounds, such as immunogenicity, a rapid degradation by proteases, or a low penetration of histohematogenous barriers.Conclusion. Thus, Hsp70 may become a promising agent for clinical trials as a drug for the treatment of patients with neurological, immunological, and cardiovascular profiles.
热休克蛋白Hsp70是多种外界刺激作用下的主要细胞保护成分之一。通过对文献资料的分析,目前研究的压倒性证据已经证明了Hsp70作为药物开发的生物学靶点的作用;然而,关于它作为药物使用的想法往往是多方面的。本文的目的是对热休克蛋白hsp70的生理功能特点的文献资料进行分析和总结,并指出其在各种病理状况的药理纠正方面的可能性。材料和方法。在撰写这篇综述文章的材料选择过程中,使用了Google Patents、Science Research Portal、Google Scholar、ScienceDirect、CiteSeer、Publications、researchchindex、Ingenta、PubMed、KEGG等数据库,选择以下单词和单词组合作为文献识别的标记:Hsp70、Hsp70卒中、Hsp70神经保护、Hsp70细胞保护、重组药物。本文对该家族重要成员之一的Hsp70的药理作用进行了综述。文献分析证实,该分子是许多生理过程的内源性调节剂,并在模拟缺血、神经退行性和炎症过程中显示出组织保护作用。重组外源性Hsp70的使用模拟了该蛋白的内源性功能,表明不存在高分子量化合物药物治疗的一些典型局限性,如免疫原性、蛋白酶的快速降解或组织血液屏障的低穿透性。因此,Hsp70可能成为临床试验中有前景的药物,用于治疗神经、免疫和心血管疾病。
{"title":"HEAT SHOCK PROTEIN HSP70: PREREQUISITES FOR USE AS A MEDICINAL PRODUCT","authors":"V. M. Pokrovsky, E. A. Patrakhanov, O. V. Antsiferov, I. Kolesnik, A. V. Belashova, V. Soldatova, O. N. Pokopeiko, A. Karagodina, I. Arkhipov, D. G. Voronina, D. N. Sushkova","doi":"10.19163/2307-9266-2021-9-5-346-355","DOIUrl":"https://doi.org/10.19163/2307-9266-2021-9-5-346-355","url":null,"abstract":"Heat shock protein Hsp70 is one of the main cytoprotection components under the action of various external stimuli. The analysis of the literature data shows that nowadays, the researches’ overwhelming evidence has proven the role of Hsp70 as a biological target for the drug development; however, the ideas about its use as a drug are often multidirectional.The aim of the article is to analyze and generalize the literature data on the features of the physiological functions of heat shock protein Hsp 70, and indicate the possibilities of its use for the pharmacological correction of various pathological conditions.Materials and methods. In the process of selecting material for writing this review article, such databases as Google Patents, Science Research Portal, Google Scholar, ScienceDirect, CiteSeer, Publications, ResearchIndex, Ingenta, PubMed, KEGG, etc. were used The following words and word combinations were selected as markers for identifying the literature: Hsp70, Hsp70 stroke, Hsp70 neuroprotection, Hsp70 cytoprotection, recombinant drugs.Results. In this review, the pharmacology of one of the key members of this family, Hsp70, was focused on. The literary analysis confirms that this molecule is an endogenous regulator of many physiological processes and demonstrates tissue protective effects in modeling ischemic, neurodegenerative and inflammatory processes. The use of recombinant exogenous Hsp70 mimics the endogenous function of the protein, indicating the absence of a number of typical limitations characteristic of pharmacotherapy with high molecular weight compounds, such as immunogenicity, a rapid degradation by proteases, or a low penetration of histohematogenous barriers.Conclusion. Thus, Hsp70 may become a promising agent for clinical trials as a drug for the treatment of patients with neurological, immunological, and cardiovascular profiles.","PeriodicalId":20025,"journal":{"name":"Pharmacy & Pharmacology","volume":"45 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88421558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}