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Background and aims: Ocular traumas are among the most important causes of visual acuity loss and acquired unilateral blindness in children, with permanent effects on their psychological and social development. The epidemiology of ocular traumas, especially those of children in different societies, is affected by the culture and level of education, lifestyle, and socioeconomic level. Considering that no accurate statistics on these injuries have been reported in Hamadan, Iran, this study aimed to investigate the epidemiology of various types of injuries in children following ocular traumas in Hamadan. Methods: This cross-sectional study included 293 patients under 18 years of age with ocular trauma who were visited in Farshchian Sina hospital in 2019. A detailed medical history was obtained including demographic information, type of injury, initial and final visual acuity, cause of injury, mother’s occupational status, and the delay between trauma and the examination, and the examiner-recorded definitive care. Finally, the data were analyzed using Excel software, and a significance level of 0.05 was used. Results: Out of 293 patients examined, 38.91% were female, and 61.09% were male. Children aged 1-5 years (30.72%) were the most commonly affected group, followed by those aged 6-10 years (29.35%). There were 19 cases of chemical injury, 33 cases of penetrating trauma, and 241 cases of blunt trauma. The mean initial vision in patients was 0.31±0.347 logMAR, and the mean final vision was 0.06±0.084 logMAR. In 94 patients, it was impossible to check visual acuity due to their lower age. Besides, 49.83% of injuries happened at home. Conclusion: In this research, the most common type of ocular trauma was blunt trauma in male patients, which occurred at home in the presence of the mother. Therefore, it is obvious that the most effective way to prevent these incidents is that parents should pay more attention to their children, implement well-established safety precautions while playing at home, and use standard play equipment.

Abstract DFT calculations were used to study the quantum capacitance of pure, B/Al/Si/N/P-doped, and defective γ-graphyne. Due to the direct relationship between capacitance and electronic states around the Fermi level, structures' electronic properties were evaluated by DOS plots. The results of integrated specific quantum capacitance in the range of water stability potential show an improvement of capacity in each p and n-type doping. The calculated cohesive energies of doped structures reflect the stability enhancement. Also, the stability/capacitance of single and double vacancies in two distinct positions (sp and sp2) were examined. The results illustrate stability retention and quantum capacitance improvement of these defective structures. Among the doped structures, the maximum quantum capacitance is 2251.10 F/gr belonging to the aluminum doped structure (in the sp position). For the defective structures, the maximum quantum capacitance is 4221.69 F/gr belonging to removing two sp carbon atoms. These quantum capacitances significantly improved compared to the pristine structure (1216.87 F/gr) and many other structures. These stunning results can contribute to the design of appropriate structures as electrode materials for high-efficiency supercapacitors.

Abstract Spherical nanocarriers can lead to a bright future to lessen problems of virus infected people. Spherical polyethylene glycol (PEG) and spherical silica (SiO2) are novel attractive nanocarriers as drug delivery agents, especially they are recently noticed to be reliable for antiviral drugs like anti-HIV, anti-covid-19, etc. Lamivudine (3TC) is used as a first line drug for antiviral therapy and the atomic view of 3TC-PEG/SiO2 complexes enable scientist to help improve treatment of patients with viral diseases. This study investigates the interactions of 3TC with Spherical PEG/SiO2, using molecular dynamics simulations. The mechanism of adsorption, the stability of systems and the drug concentration effect are evaluated by analyzing the root mean square deviation, the solvent accessible surface area, the radius of gyration, the number of hydrogen bonds, the radial distribution function, and Van der Waals energy. Analyzed data show that the compression of 3TC is less on PEG and so the stability is higher than SiO2; the position and intensity of the RDF peaks approve this stronger binding of 3TC to PEG as well. Our studies show that PEG and also SiO2 are suitable for loading high drug concentrations and maintaining their stability; therefore, spherical PEG/SiO2 can reduce drug dosage efficiently.

Background: Aerobic and intense exercises with an increase in free radicals cause damages at the cellular level, heart disease, cancer, and the development of aging processes, which one of its symptoms is increased serum concentrations of liver enzymes. Objective: The purpose of this study was to investigate the concurrent effect of four weeks of aerobic training and propolis supplementation on the activity of liver enzymes, including ALT, AST, and SOD in endurance athletes. Methods: Thirty-two male athletes (age: 21±1.4 years) in track and field were randomly divided into three groups: exercise group, exercise with placebo group, and exercise with supplement group. Propolis supplementation was taken as two tablets (500 mg) twice a day and aerobic exercise was performed for 4 weeks and in 24 sessions with an intensity of 60 to 65% of heart rate. The statistical method was done using one-way ANOVA and Tukey post hoc test by SPSS v. 18 software. Findings: The results showed that there was a statistically significant difference between groups in serum levels of SOD, AST, and ALT (P0.05). Conclusion: The results showed that aerobic exercise alone can increase SOD levels and propolis supplementation with aerobic exercise can reduce AST and ALT serum levels and lead to improved liver cell function.

Abstract Background: Hepatitis B virus infection (HBV) is a significant global health problem and is a major cause of morbidity and mortality worldwide. Therefore, currently, introducing novel anti Hepatitis B drugs is taken into consideration. This study was planned to in silico screening novel Hepatitis B virus DNA polymerase inhibitors from two medicinal plants Terminalis chebula and Caesalpinia sappan. Materials and Methods: This is a descriptive-analytic study. In the study, three-dimensional structure of the Hepatitis B virus DNA polymerase was predicted using homology modeling method. A set of phytochemicals from mentioned plants were retrieved from Pubchem database in SDF format. In silico screening was carried out using molecular docking between mentioned phytochemicals and modeled polymerase by iGemdock 2.1 software. Results: Results of the study confirmed that all evaluated ligands have appropriate interactions to the polymerase with least toxicity and without genotoxicity potential. Results also showed that most interactions occur in reverse transcriptase domain which located in 354-694 area in the amino acid sequence of tested polymerase. Analysis of energy and amino acids involved in ligand-polymerase interaction revealed that Terchebin, Chebulinic Acid and Terflavin A have more effective interaction with the polymerase in compared to other ligands. Conclusion: Based on the results it can be concluded that evaluated compounds could be good candidates for in vitro and in vivo research in order to develop novel anti- Hepatitis B drugs.

Abstract Background: In the recent years, introducing plant materials with the ability to destroy or control of biofilm formation of Streptococcus mutans is highly regarded.This study was planned to investigate the anti-bacterial activity and biofilm inhibition of Satureja Khuzestanica Jamzad against biofilm and single form of S.mutans. Materials and Methods: The plant material collected, air dried and powdred. Then thier methanolic extract prepared by maceration method.The concentrated extract then diluted by sterile phosphate buffer.The anti-bacterial and biofilm inhibition activity of the extracts evaluated by dick diffiusion and micro titeration method respectively. Also, bioinformatic study of glucansucrase inhibition by dominant plant compounds of S.Khuzestanica Jamzad investigated by molecular docking method using Auto dock4 software. Results: The results revalued that all tested extracts especially leaf ectract had significant antibacterial activity against single form of S.mutans.Results also showed that leaf and stem extract had most and least biofilm inhibition with 70 and 13 presend inhibition, respectively. The bioinformatics results also confirmed that studied phytochemicals especially gama-terpinen, carvacrol and beta-bisabolene can effectively inhibit the glucansucrase. Conclusion: The results of present study showed that S.Khuzestanica Jamzad had significant antibacterial activity against single form of S.mutans and gama-terpinen, carvacrol and beta-bisabolene are most effective compounds in biofilm inhibition.

Abstract Background: Medicinal plants are primery source of many drugs to cure different diseases. The genus Prangos, (Umbelliferae family) consists of several medicinal plants that their desirable dffects have been approved. The aim of this study is to investigate the effectiveness of methanol extract in different parts of prangos ferulacea and prangos acaualis on human lymphocytes proliferation and their mutagenicity in salmonella typhimurium TA98. Materials and Methods: In this experimental study, the plants were collected from different areas of Kurdistan. Then, samples were air dried and powdered and methanol material of plants was extracted. The extracts were diluted to give concentrations of 10, 100, 500, 1000, 1500, 2000, 2500 μg/ml. Finally, the effects of these extracts on human lymphocytes proliferation and their mutagenecity have been investigated by the MTT and Ames test. Results: The results showed that different organs extract from both tested plants caused a significant increase in lymphocytes proliferation, specially in concentrations of 500 to 2500 μg/ml. Of studied excrtacts, the highest and lowest effect on lymphocytes proliferation was obtained in presence of flower and seed, respectively. In total, the levels of proliferation resulted of prangos ferulacea as compared with prangos acaulis were higher. Also, the results of study showed no mutagenicity of studied plant exctracts with considered concentrations. Conclusion: The findings revealed that both species of prangos can increase immune system function and were used as an safe medicinal plant to cure patients with immune deficiencies and microbial infections.

Abstract Background: Because of the reported high ability of virulence and medicinal resistance of HIV-1 virus during the last decades, many investigations have been performed concerning discovery and the introduction of anti-HIV-1 drugs. The results of numerous researches have shown that drugs and protease inhibitory compounds mainly containing plant derivatives specially terpenoids may control HIV-1 infection very effectively. The aim of this research is the bioinformatical study of HIV-1 protease inhibition by standard drugs and triterpenoides from plant and mushroom. Materials and Methods: This is a descriptive-analytic study. In the present study , the structure of drugs, triterpene comounds, and HIV-1 protease enzyme was received from the databases such as Chem Spider, PubChem, Human Metabolome Database (HMDB), and Protein Data Bank (PDB). After that, molecular docking was performed by iGRMDOCK 2.1 software Results: The results confirmed that the interactions of the triterpene compounds like the standard drugs were in three safeguarded and catalytic areas including central domain, flap and carboxylic terminal domain specially amino acids Asp25, Asp27, Ala28, Asp29 and Asp30 in active sites of HIV-1 protease. Also, The study of the interactions of these areas showed that there is a direct correlation between the strength of the interactions and IC50 values of these compounds. Conclusion: Finally, with due attention to the high effectiveness and the proprietary function of triterpenoids, we can conclude that these compounds may be considered as effectire HIV-1 antiprotease drugs.