Background: Honey is a natural biologically active substance with antibacterial, antioxidant, anti-inflammatory, and tissue regeneration–promoting properties, and it has traditionally been used in wound treatment for centuries. Numerous studies have confirmed that the phenolic compounds, enzymes, hydrogen peroxide, and amino acids contained in honey inhibit bacterial growth and accelerate wound healing. Wound infections are commonly caused by pathogenic bacteria such as Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Escherichia coli which are major factors that delay wound healing and lead to complications. However, the direct application of honey to wounds presents challenges such as adhesiveness, absorption, dose stability, and sterility. Therefore, it is necessary to formulate honey into a suitable pharmaceutical dosage form to facilitate its use and introduce natural raw materials into therapeutic practice. Thus, incorporating honey as the main active ingredient into a hydrogel dressing could enable the development of a novel therapeutic wound dressing that is physically and chemically stable and capable of maintaining an optimal moist wound environment, which is essential for wound healing. Honey-containing hydrogel dressings differ from other dressings in their ability to balance the wound environment, absorb and retain moisture, provide antibacterial and anti-inflammatory effects, and support tissue regeneration. The significance of this study lies not only in investigating the antibacterial activity of honey but also in determining the bacterial killing time, thereby providing useful data for future studies. Aim: To investigate the antibacterial activity of honey and determine its bacterial killing time. Materials and Methods: Domestic honey samples were compared with imported honey samples in terms of antibacterial activity and bacterial killing time. Domestic honey samples were coded as D1, D2, D3, C1, and C2, while the imported honey sample was coded as M. A total of six honey samples were evaluated. Using the broth microdilution method, the antibacterial activity against four bacterial strains commonly associated with burn wound infections Staphylococcus aureus ATCC 25923, Pseudomonas aeruginosa ATCC 28583, Klebsiella pneumoniae ATCC 1706, and Escherichia coli ATCC 25218 was determined and compared. Subsequently, bacterial killing time was evaluated using the broth dilution method with honey concentrations prepared at ratios of 7:3 (70%), 5:5 (50%), and 4:6 (40%). Results: The antibacterial activities of D1, D2, D3, C1, C2, and M honey samples against S. aureus, P. aeruginosa, K. pneumoniae, and E. coli were determined. Among them, D3, C2, and M honey samples showed stronger antibacterial activity. Therefore, these three honey samples were further investigated by determining bacterial killing time over an 18-hour period. For D3 honey diluted at a 7:3 ratio, the killing time was 15 hours for S. aureus and 7 hours for P. aeruginosa, while the killing times for K. pneumoniae and E. coli exceeded 18 hours. D3 honey diluted at a 5:5 ratio showed bacterial killing times exceeding 18 hours for all tested bacteria. For C2 honey diluted at a 7:3 ratio, the killing times were 16 hours for S. aureus, 12 hours for P. aeruginosa, 16 hours for K. pneumoniae, and 17 hours for E. coli. C2 honey diluted at a 5:5 ratio killed E. coli in 18 hours, whereas the killing times for S. aureus, P. aeruginosa, and K. pneumoniae exceeded 18 hours. For M honey diluted at a 7:3 ratio, the killing times were 8 hours for S. aureus, 7 hours for P. aeruginosa, 9 hours for K. pneumoniae, and 8 hours for E. coli. M honey diluted at a 5:5 ratio killed S. aureus in 9 hours, P. aeruginosa in 10 hours, K. pneumoniae in 10 hours, and E. coli in 9 hours. Conclusions 1. The antibacterial activity of honey against Staphylococcus aureus, Pseudomonas aeruginosa, Klebsiella pneumoniae, and Escherichia coli varied depending on honey concentration, with honey concentrations of 40–45% demonstrating the highest antibacterial activity. Furthermore, M honey exhibited the strongest antibacterial activity compared to the other honey samples. 2. In determining bacterial killing time, the domestic honey samples killed bacteria within 9 hours, whereas the imported honey sample killed bacteria within 7 hours.

Background: Osteoporosis is a systemic skeletal disease characterized by reduced bone mineral density (BMD) and deterioration of bone microarchitecture, resulting in decreased bone strength and an increased risk of fragility fractures. Early assessment of BMD is essential for identifying skeletal abnormalities and supporting clinical decision-making. Dual-energy X-ray absorptiometry (DXA) is a widely used, non-invasive method for evaluating BMD at clinically relevant skeletal sites. Aim: To assess bone mineral density using DXA and describe the corresponding T-score and Z-score measurements in adult patients. Materials and Methods: This descriptive observational study was conducted from June to October 2026 at the Department of Trauma and Orthopedic Surgery, Mongolia–Japan Hospital, Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia. Eight patients aged 18 years or older without fractures were included. According to the study records, participants were selected using a random sampling method. Demographic characteristics, height, weight, body mass index (BMI), and DXA measurements were recorded. BMD, bone mineral content (BMC), T-scores, and Z-scores were assessed at the lumbar spine, hip, and forearm. Continuous variables were summarized as means and standard deviations, and categorical variables as frequencies and percentages. Results: A total of eight patients were included, comprising five males (62.5%) and three females (37.5%). The mean age was 52.65±7.95 years, and the mean BMI was 31.59±6.32 kg/m². The mean lumbar spine (L1–L4) T-score was 0.35±1.49, and the mean Z-score was 0.97± .36. The lowest reported mean T-score was observed at the left forearm (−1.29±4.34), followed by the right forearm (−1.25±3.87). Measurements were also recorded at the left and right hip regions. The findings were descriptive and were not intended to establish population-level prevalence. Conclusions The demographic and anthropometric characteristics of the eight patients included in the study were assessed. The mean age was 52.65±7.95 years, and the mean body mass index (BMI) was 31.59±6.32 kg/m². Of the participants, 5 (62.5%) were male and 3 (37.5%) were female. The mean BMI of the participants fell within the obesity category. Bone mineral density (BMD) was assessed using dual-energy X-ray absorptiometry (DEXA) at the lumbar spine, both hips, and both forearms. The results showed variations in BMD measurements across the different anatomical sites examined. An analysis of the T-scores and Z-scores for each measurement site revealed a mean T-score of 0.35±1.49 and a mean Z-score of 0.97±1.36 at the lumbar spine. At the left hip, the mean T-score was −0.63±1.29 and the mean Z-score was 0.34±1.52, while at the right hip, the mean T-score was −0.63±1.15 and the mean Z-score was 0.31±1.09. The mean T-scores of the forearm were comparatively lower, at −1.29± 4.34 on the left side and −1.25±3.87 on the right side.

Introduction: According to World Health Organization, air pollution is a major environmental risk to health and is estimated to cause approximately 1.6 million premature deaths worldwide per year. The air pollution of Ulaanbaatar city is rising year after year.Goal: The aim of this study was to define the lung function of adults in Ulaanbaatar.Materials and Methods: 1196 adults were randomly chosen aged over 20 years of Ulaanbaatar city. Of them 238 subjects were excluded because they had at least one of the following: a history of lung diseases including asthma, COPD, pulmonary tuberculosis, lung fibrosis; symptoms of chronic cough, wheeze, or dyspnea; history of thoracic surgery; history of major acute illness in the past 3 months; or a history of respiratory tract infection in the past 4 weeks. Besides demographic data, information on smoking habits was collected. The lung ventilation function of subjects was checked using a spirometry EasyOne, calculating the indexes Forced expiratory volume 1sec (FEV1), forced vital capacity (FVC), FEV1/FVC ratio. Lung function measurements followed a standardized protocol and fulfilled the ATS criteria.Results: Of the respondents, 486 were males (50.7%) and 472 were females (49.3%). There was a negative correlation between each lung function and age (p<0.05). The lung function was significantly lower in female than in male, for FEV1, FVC (male - FEV1 3.66±0.659 L, FVC 4.467±0.716 L, female-FEV1 2.663+0.559 L, FVC 3.237+0.586 L). In overall, FVC, FEV1 was decreased by 34.5, 37.2 percent, respectively compared with European LLN value.Conclusion: The mean value for FEV1, FVC, FEV1/FVC ratio was 3.17±0.78 L, 3.86+0.89 L and 82.02±6.75 % in overall, respectively.