1.Results of determining the content of some biologically active substances in compound herbal extract
Azzaya N ; Khandmaa D ; Naranchimeg E ; Batdorj D ; Khaliunsarnai B ; Badamtsetseg S ; Enkhsaikhan L ; Lkhaasuren R ; Khurelbaatar L ; Chimidtseren S
Mongolian Journal of Health Sciences 2025;85(1):85-90
Background:
Medicinal herbs have been used in traditional medicine to treat systemic inflammatory disease for many
years. For instance, Rhodiola rosea L extracts were used to enhance behavioural stresses for improving fatigue and
depression. Gallic acid, found in Rhodiola rosea L and Rhodiola quidrifida is, a natural polyphenol, exhibits multiple
therapeutic activities, including anti-inflammatory, anti-cancer, antioxidant, and anti-angiogenic effects. Saposhnikovia
divaricate (its ethanol extract mainly) notified to support function of musculoskeletal tissue and to enhance tissue regeneration by its anti-inflammatory effect. The Salsola laricifolia L has been studied for its strong antioxidant activity, improve
immune function, boost energy, and exhibit anti-inflammatory effects. This study allowed us to screen anti-inflammatory
effects of medicinal plants and future therapeutic possibility.
Aim:
To study the content of phenolic compounds (gallic acid) in the composition of complex products of plants widely
used in Mongolian traditional medicine, which have been found to have biological activity of the extracts
Materials and Methods:
The herbal extract was extracted from Rhodiola rosea L, Saposhnikovia divaricata (Tuscz)
Schischk, Rhodiola quidrifida Pall.Fisch, Salsola laricifolia Turcz.ex Litv in laboratory of the Drug Research Institute of
Monos Group, Mongolia.
We used solvents for HPLC grade was used to identify the bioactive components that Gallic acid in the compound plant
extract.
:
Results: The bioactive compounds in each of the Rhodiola rosea L, Rhodiola quadrifida Pall.Fisch and four medicinal
plant extracts were identified using HPLC, confirming the presence of Gallic acid.
Conclusion
Our research results showed that the quantitative content of Gallic acid in the composite plant extract was
high, at 1.02%.
2.A review of biologically active compounds and pharmacological activities of raw materials of Sugmel 3 tan
Sodgerel D ; Badamtsetseg S ; Enkhbold G ; Sugarmaa B ; Tsetsegmaa S ; Lkhaasuren R ; Khurelbaatar L
Mongolian Pharmacy and Pharmacology 2024;24(1):80-89
Sleep fulfills the vital physiological needs of the human body. However, 45 percent of the world’s population suffers from sleep problems.
In this article, Sugmel 3 tan /prescription/ widely used in traditional medicine for insomnia was selected and biologically active compounds and pharmacological activities of the plants included in the prescription were reviewed. Essential oils from fruits of Amomum kravanh Pierre ex Gagnep and Cuminum cyminum L. are considered to relax the body and mind to improve a night of sleep. Pharmacological and clinical studies of piperine isolated from Piper longum L. fruits demonstrated that the compound possessed anti-depression-like activity and cognitive enhancing effect.
3.Study of some bioactive substances contained in dry extracts of cultivated Inula helenium L. plant
Bujinlkham B ; Sugarmaa B ; Batdorj D ; Ganchimeg G ; Saikhanbayar P ; Munkhzaya B ; Maral L ; Badamtsetseg S ; Lkhaasuren R ; Akhtolkhyn T
Mongolian Pharmacy and Pharmacology 2024;25(2):29-37
Introduction:
Since 1993, the Inula helenium L. plant has been planted in the production area (Bulgan
Province, Dashinchilen Sum) of the Traditional Hatchery Science and Production Corporation’s medicinal
plant introduction and cultivation experience. At the Drug Research Institute, there is also a botanical institute
for medicinal plants where it is grown. In traditional Mongolian medicine, the roots and rhizomes of Inula
helenium L. are used to reduce inflammation, boost immunity, enhance hunger, and improve intestinal
motility. Inula helenium L. roots and rhizomes contain biologically active compounds such as monoterpenes,
sesquiterpenes, phenols, flavonoids, and polysaccharides.
Methods:
The roots and rhizomes of Inula helenium L. were extracted with water and 70% ethanol at the
following ratios 1:10 (2% of WAC), 1:8, and 1:6 by partial maceration at 700C for 2 hours each, extracted
and concentrated. The dry extract was obtained by the spray drying procedure. High-performance liquid
chromatography for determining the content of alantolactone, thin-layer chromatography for qualitative
analysis. Spectrophotometer for determining the content of polyphenolic compounds, colored compounds
with Folin-Ciocalteu reagent for qualitative analysis. Spectrophotometer for determining the content of inulin, and colored compounds with phenol and sulfuric acid solutions for qualitative analysis.
Conclusion
In determining the content of polyphenolic compounds, inulin, and alantolactone in the dry extract
taken from the roots and rhizomes of cultivated Inula helenium L., the content of polyphenolic compound in dry extract A was 2.50±0.08%, and alantolactone was 1.39±0.11% in the raw material of the plant, while B dry the extract had a high concentration of inulin of 58.51±0.66%.
4.Standardization of dried tuber of Jerusalem Artichoke (Helianthus tuberosus L.)
Batdorj D ; Maral L ; Maralgua A ; Nomin J ; Battulga B ; Tserenkhand G ; Lkhaasuren R ; Khurelbaatar L ; Badamtsetseg S
Mongolian Pharmacy and Pharmacology 2024;25(2):45-51
The Jerusalem Artichoke (JA) (Helianthus tuberosus L.) is an annual plant native to North America and widely distributed in Europe and Central Asia. The tuber of JA contains 80% water, 15% polysaccharide (Inulin etc.), 2% protein, and a small amount of starch and fat. Inulin is a polysaccharide that is widely used as a prebiotic, fat substitute, and sugar substitute. This substance has high biological activity and is contained in large quantities.
The purpose of this study was to standardize the quality and safety of dried tubers of JA. Standardization includes parameters such as microscopic analysis, identification, quantification, validation of methods following the guidelines issued by ICH guidelines, and quality, including safety analysis (appearance, moisture, mechanical impurities, heavy metals, microbiological purity).
The content of inulin was 64.17±1.25%. The mean relative standard deviation of method validation (RMS%) was 1.27%, 1.18%, 1.22%, and the relative mean standard deviation (RMS) of method precision was 1.94%. The specific absorbance was 307 nm. The correlation coefficient R2=0.9998 was obtained for the reference curve of the standard substance. The detection limit of the method was 2.64 μg/ml, and the detection limit was 7.99 μg/ml.
The method mentioned above has been confirmed to be suitable for the quantitative determination of inulin in the tuber of JA. Moreover, Microbiological purity and heavy metal requirements are met.
5.HPLC method for quantification of salidroside for quality control of golden root (Rhodiola Rosea L, Rhodiola Crenulata L.) dry extract
Battulga B ; Badamtsetseg S ; Lkhaasuren R ; Odontuya G ; Khurelbaatar L
Mongolian Pharmacy and Pharmacology 2024;25(2):52-57
Background:
The high-performance liquid chromatography (HPLC) method was developed to select
salidroside in tablet formulation dietary supplements, raw material containing other components. Further,
the proposed method was validated for linearity, precision (system precision, method precision, intermediate
or inter-day precision), and accuracy, stability in analytical solution, syst em suitability, and ruggedness.
The developed method exhibited the best results in terms of the validation above parameters. The other
components and additives did not interfere with their determinations. The method was found to be selective,
simple, economical, accurate, reproducible, rapid, and reliable for routine estimation purposes of salidroside
in golden root dry extract. The goal of this study was to develop the validation method of salidroside in the
dietary supplement.
Material and Methods:
The Rhodiola rosae L. dry extract was supplied Arshin Co.ltd in People’s Republic of
China. The standard salidroside was supplied from Sigma Aldrich Co Ltd. We used solvents for HPLC grade
(methanol, acetonitrile). Chromatographic conditions: A gradient HPLC (Shimadzu CBM20AD) with serial
dual plunger pump; analytical column: Shimadzu GIST С18 150 x 4.6 mm, particle size 5 μm; flow rate: 1
ml/min; column temperature: 400C, detection: UV 275 nm. Chromatographic procedure: 20 μl of the mixed
standard preparation and assay (sample) preparation were separately injected into the chromatography, the
chromatograms were recorded, and the responses for the major peaks were measured. The run time was
approximately 15 minutes.
Results
The calibration curves for the salidroside were made by plotting the peak area versus the
concentration for each analyte using regression analysis. Each calibration curve was obtained using six levels
of concentrations in the range of 100-800 µg/mL. The linear correlation coefficient (r2=1) for all calibration
curves was higher than 1 for all analytes. The LOD and LOQ for salidroside were golden root dry extract
in 8.788 µg/mL and 26.61 µg/mL, respectively. Accuracy and precision were assessed by analyzing five
samples independently prepared at low, middle, and high concentrations. The RSD values of repeatability
and intermediate precision were below 1.12%, 1.19 and 1.79%. The accuracy remains between 91 to 109%.
The resulting accuracy data were satisfactory for the quantitative analysis of salidroside in golden root dry
extract. This article presents a simple, accurate, reproducible, and thoroughly validated HPLC-based method
for qualitative and quantitative analysis of salidroside, as part of the quality assessment of golden root dry
extract.
6.A brief review on rat models of myocardial infraction
Davaasambuu T ; Oyunchimeg B ; Enkhbold G ; Badamtsetseg S ; Lkhaasuren L ; Khurelbaatar L
Mongolian Pharmacy and Pharmacology 2024;25(2):85-94
Myocardial infarction (Ml) is necrosis and death of heart muscle secondary to ischemia and acute coronary artery thrombosis. Ml, commonly known as a heart attack, happens when the oxygen rich blood flow to a part of the heart muscle is blocked for a prolonged period, causing damage or death to the heart tissue. This blockage is most often caused by a buildup of fat, cholesterol, and other substances, which form a plaque in the coronary arteries. Furthermore, patients with cancer constitute a high-risk population for cardiovascular disease and as of the last 5 years, 50% of patients with cardiovascular disease have been diagnosed with cancer, according to World Health Organization. The provision of complete insight into Ml complications along with designing ajpreventive program against Ml seems necessary. The use of medications has been practiced over the years for the prevention of HF. However, some of these medications produce adverse effects and due to high cost are not easily available to every patient. Over the past decades, there has been a significant rise in the use of herbal supplements based on traditional medicine to prevent, avoid, and/or treat different conditions, including cardiovascular disease; this rise results from a natural source, efficiency
with few or no adverse effects and low cost. In vivo models of heart failure (HF) and myocardial infarction (Ml) are essential for understanding the pathophysiology of these conditions and for developing new treatments.
These models typically involve inducing heart failure or myocardial infarction in animals, such as rodents to study disease mechanisms and evaluate potential therapies.
In this review, we discuss the most common preclinical models of Ml currently employed in cardiovascular research. Among them, Ml induced heart failure is a method of ligation of the left anterior descending artery of coronary an experimental animal. Its physiological relevance, cost-effective, uncomplicated, and suitable
method for evaluating research results. The rat model of myocardial infarction offers numerous advantages that make it a valuable tool for cardiovascular research.
7.A review of clinical research on the five medicinal herb soak therapy
Enkhbold G ; Badamtsetseg S ; Munkhzaya B ; Lkhaasuren R ; Khurelbaatar L
Mongolian Pharmacy and Pharmacology 2024;25(2):100-110
Introduction:
The Five Medicinal Herb Soak Therapy, as described in the 23rd chapter of “The Secret
Quintessential Instructions on the Eight Branches of the Ambrosia Essence Tantra,” a key text in traditional medicine, is noted for its therapeutic applications. It is recommended for conditions such as joint stiffness, tumors, acute and chronic wound swelling, sores, abscesses, hunchback, muscle rheumatism, anthrax, scattered heat and wind disorders. The Five Medicinal Herb Soak consists of Ledum palustre L., Juniperus pseudosabia Fisch.Et M., Myricaria alopecuroides Schrenk., Ephedra Przewalskii Stapf., and Artemisia frigida Willd. This therapy is widely practiced in Mongolia, China, the Inner Mongolia Autonomous Region, the Tibetan Autonomous Region, the Qinghai Province, and the Gansu Province. This clinical observational study review aims to predict treatment outcomes, establish treatment guidelines, and facilitate the development of other pharmaceutical forms. It is anticipated that this review will serve as a scientific reference for the application of the Five Medicinal Herb Soak Therapy.
Objective:
The objective of this review is to analyze and synthesize clinical studies on the Five Medicinal
Herb Soak Therapy.
Methods:
Keywords “五味甘露” (Wu wei gan lu), “Tibetan medicine five-flavor Manna” were used to search
for relevant research articles and theses in biomedical databases, including PubMed (https://pubmed.ncbi.
nlm.nih.gov/) and the China National Knowledge Infrastructure CNKI (https://www.cnki.net/). The collected
data were systematically analyzed and reviewed.
Conclusion
The Five Medicinal Herb Soak Therapy demonstrates significant therapeutic value in treating
conditions such as gout, rheumatic joint inflammations, digestive disorders, female reproductive system
diseases, spinal herniation, arthritis, varicose veins, and scurvy. Integrating this therapy with Mongolian,
Tibetan, Chinese, and European medical practices can enhance treatment efficacy by reducing treatment
duration, alleviating symptoms, and preventing recurrence. Furthermore, developing more efficient
pharmaceutical forms of the Five Medicinal Herb Soak could improve its effectiveness and reduce potential
side effects.
8.Effects of some syrups on citric acid induced cough in rat
Munkh-Erdene R ; Davaasambuu V ; Bat-Oyun U ; Ahsholpan B ; Badamtsetseg S ; LKhaasuren R ; Hurelbaatar L
Mongolian Pharmacy and Pharmacology 2023;23(2):20-25
Abstract:
In Mongolia, flu and flu-like diseases affect many people, and pneumonia is a public health concern. Therefore, we have an urgent need to research and develop a new medicinal syrup to replace imported products using raw materials grown in Mongolia and to compare it with similar products. There are imported cough syrup products on the pharmaceutical market of Mongolia, but there are domestic pharmaceutical products. Moreover, there is limited research data on cough relief. The main goal of the research team is to compare the experimentally obtained syrup containing Plantago asiatica L, Malva Sylvestris L. and syrup containing Plantago major L. Juice, honey that produced by Monos Pharm LLC whish the cough relieving drug Gerbion syrup.
Material and methods:
The vivarium of the pharmacology laboratory, Drug research institute,
TPC7062Ti mark IVC system (Shanghai Pretty Industries Co.,Ltd, China) in a special environment
with one care and one feeding regimen (Lab Mice Diet, Constant Formula Balanced Nutrition,
Jiangsu Xietong Pharmaceutical Bio- Engineering Co., LTD, China, www.jsxtsw.com ) used 64
non-WISTAR white rats weighing 180-218 g. Experimental rats were smoked with an aerosol of
17% citric acid aqueous solution for 5 minutes. The statistical processing of the research results
was done using the One-Way ANOVA/Multiple comparisons data of the GraphPad Prism 8 program.
Results and conclusion
Expressing the number of coughs produced in the experimental rats as
a percentage (%), the control group showed 3.95% cough relief, and the experimental group-1 by
48.4%, experimental group-2 by 71.1%, comparison group by 74.6%, respectively has reduced.
Experimental group -2 and comparison group for dry cough caused by citric acid 17%, it affects
the cough receptors in the mucous membrane of the respiratory tract and relaxes the bronchial
muscles (A and C fiber).
9.Effect of “shilajit+golden rosa” or vitos preparation on immune response cells (CD4, CD8, IGG, CD64) by azathioprine induced immunosuppression in mice
Batchimeg B ; Davaasambuu T ; Badamtsetseg S ; Bayanmunkh A ; Odongerel A ; Tsetsegmaa S ; Choijamts G ; Lkhagva L ; Khurelbaatar L
Mongolian Pharmacy and Pharmacology 2022;20(1):39-44
Introduction:
During many decides, compounds derived from natural raw materials have demonstrated their effectiveness as therapeutic agents in different areas, such as metabolic disorder, immune system diseases and its regulations. Natural based products, like herbal medicines and minerals are implicated in the regulation of immune function. They control the immune system in a pleiotropic manner and participate in various processes of the adaptive/innate immunity. Therefore, natural raw material has great potential for targeted immune modulators, in the treatment of certain types of immunologic and inflammatory diseases, like rheumatoid arthritis, plaque psoriasis, ankylosing spondylitis and immune deficiency. The purpose of this survey was to study influence of “Shilajit +Golden Rosa” combined shot preparation named by Vitos on immune system in the experimental and preclinical circumstances.
Goal:
The purpose of this survey was to study influence of “Shilajit +Golden Rosa” Vitos shot preparation
on immune system in the experimental and preclinical circumstances.
Material and Methods:
The immune deficiency was to created by Azathioprine through 5 days in the Balb/c mice after that control group, preparation of “Shilajit +Golden Rosa” Vitos shot were administrated appropriate doses by oral during 10 days. Then we collected blood and quantified amount of CD4+, CD8+, IgG and CD64 (Mouse Elisa Kit Assay: Catalog.No:WAM-568, Elisa Reader, 450 <b>нмb>, Melsin Medical Co.LTD, www. melsin.com) on the 5th, 10th days.
Results:
All statistical analyses were conducted with SPSS version 20.0 software (IBM, Armonk, NY). Oneway ANOVA was used to assess statistical significance between “Shilajit +Golden Rosa” Vitos shot group and days of observation. Mean values of CD4+, CD8+, CD4/CD8 ratio, IgG, CD64 levels determined in the control and sample group. CD4+, CD8+, CD4/CD8 ratio, IgG and CD64 levels were significantly increased in the “Shilajit +Golden Rosa” Vitos shot group compared with control group by 20.8-67.8 per cent (p<0.05, p<0.01).
Conclusion
It’s concluded that, “Shilajit +Golden Rosa” Vitos shot preparation shows immune-stimulator activity not only in the level of cellular (T cells:CD4+, CD8+) but also humoral immunity (B cells: IgG, CD64) in the previously using Azathioprine (75mg/kg) to provoke pathological model of immunosuppression
10.Technological study to convert traditional powder medicine into modern dosage formulation
Ganchimeg G ; Lkhaasuren R ; Odchimeg B ; Badamtsetseg S ; Sugarmaa B ; Bayanmunkh A ; Lkhagva L ; Tsetsegmaa S ; Khurelbaatar L
Mongolian Medical Sciences 2021;195(1):38-42
Introduction:
The Mongolian people have been using traditional medicine for hundreds of years. However, there is
a need to produce traditional medicinal dosage forms such as capsules, tablets, decoctions easier to
drink, store and transport, and to standardize not only finished product, but the raw materials used for
traditional medicines in line with the current drug production, drug quality and safety requirements.
Therefore, in this study, we aim to standardize five ingredients of a traditional powder medicine,
which have been widely used for colds and flu in Mongolian, Chinese and Tibetan traditional medicine
practice, and to convert the powder drug into tablet form using qualified raw materials.
Materials and Methods:
The study to convert multi-ingredient traditional powder into tablet was carried out at the Experimental
production pharmaceutical technology unit and Pharmaceutical chemistry Laboratory of the Drug
research institute, Monos Group, and the Quality control laboratory of medicine of Monos Pharm LLC.
Result
All raw materials were standardized and wet granulation method was used to prepare granules for
the tableting with qualified raw materials. 4 different models of the tablet form was prepared and
investigated. It was determined that model X-2 fully meets the general requirements for the tablet
form.
Result Analysis
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