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Poorabdian S.,Health Science University | Mirlohi A.H.,Esfahan University of Medical science | Habibi E.,Health Science University | Shakerian M.,Health Science University
International Journal of Occupational Medicine and Environmental Health | Year: 2013

Objective: One of the practical models for assessment of stressful working conditions due to job strain is "job demand and control" or Karasek's job strain model. This model explains how adverse physical and psychological effects including cardiovascular disease risk factors can be established due to high work demand. The aim was to investigate how certain cardiovascular risk factors including body mass index (BMI), heart rate, blood pressure, serum total cholesterol levels, and cigarette smoking are associated with job demand and control in workers. Materials and Methods: In this cohort study, 500 subjects completed "job demand and control" questionnaires. Factor analysis method was used in order to specify the most important "job demand and control" questions. Health check-up records of the workers were applied to extract data about cardiovascular disease risk factors. Ultimately, hypothesis testing, based on Eta, was used to assess the relationship between separated working groups and cardiovascular risk factors (hypertension and serum total cholesterol level). Results: A significant relationship was found between the job demand-control model and cardiovascular risk factors. In terms of chi-squared test results, the highest value was assessed for heart rate (Chi2 = 145.078). The corresponding results for smoking and BMI were Chi2 = 85.652 and Chi2 = 30.941, respectively. Subsequently, Eta result for total cholesterol was 0.469, followed by hypertension equaling 0.684. Moreover, there was a significant difference between cardiovascular risk factors and job demand-control profiles among different working groups including the operational group, repairing group and servicing group. Conclusion: Job control and demand are significantly related to heart disease risk factors including hypertension, hyperlipidemia, and cigarette smoking. © 2013 Versita Warsaw and Springer-Verlag Wien. Source

Eskandarian A.A.,Esfahan University of Medical science
Iranian Journal of Parasitology | Year: 2013

Background: Diagnosis of some diseases is difficult due to invasive sampling. Urine has been candidate as a non-invasive and convenient alternative. It has many advantages and easy accessibility but some technical ills should be removed. Finding a suitable extraction method for improving urine DNA quantity and quality in altering invasive specimens for molecular diagnosis of some infectious diseases, was the main object of present research. Method: Toxoplasmosis was selected as an experimental model, regarding the congenital and ocular forms, its abundance and requirement to invasive sample for diagnosis. Samples prepared by adding some defined Toxoplasma gondii (RH strain) tachyzoites to normal urine. Several urine DNA extraction and purification methods comparatively were tested for finding the best one. The amount of extracted DNA assessed using Nanodrope spectrophotometer and a multiplex semi-nested PCR were designed for evaluating the results. Results: Urine samples with known number of tachyzoites were purified comparatively by five better methods. The results reviled that Cinnagen kit performed with more efficacies. It works well up to 1-5tachyzoites μl-1 of urine. The amount and quality of extracted DNA of more than 100 urine samples with defined tachyzoites were analyzed using a nested PCR method. Finally methods were enough sensitive to detect one tachyzoite DNA in final PCR reaction. Conclusion: This method was enough eligible and sensitive to perform molecular tests for different purposes of instance detecting toxoplasmosis by urine sample as a convenience and non invasive method; although it is better to perform some more experiments using patients samples comparing gold methods. Source

Fallah A.A.,Shahrekord University | Saei-Dehkordi S.S.,Shahrekord University | Nematollahi A.,Shahrekord University | Jafari T.,Esfahan University of Medical science
Microchemical Journal | Year: 2011

The objective of this research was to determine the differences between farmed and wild rainbow trout in terms of heavy metal and trace element accumulation in edible tissues. The samples were analyzed for As, Ba, Cd, Co, Cr, Cu, Fe, Mn, Mo, Ni, Pb, Se, Sr and Zn by inductively coupled plasma-optical emission spectrometry (ICP-OES); and for Hg by cold vapor atomic absorption spectrometry (CVAAS). The results were expressed as μg/g of dry weight. With the exception of Ba and Sr, liver had significantly higher heavy metal and trace element concentrations compared to the muscle in farmed or wild fish. Higher levels of Ba, Cr, Fe, Mn and Zn, as well as lower levels of Cu and Sr were found in tissues of wild rainbow trout compared to its farmed relative. Levels of Cd in 41.6% of farmed fish samples and 45.8% of wild fish samples exceeded the European Commission regulation. Regarding the Pb, concentrations in 50% of farmed fish samples and 62.5% of wild ones were above the European Commission limit. However, levels of Hg and As in all of the examined samples were lower than the legislated limits. The differences in heavy metal and trace element accumulation observed between farmed and wild fish were probably related to the differences in their environmental conditions and dietary element concentrations. © 2011 Elsevier B.V. Source

Fallah A.A.,Shahrekord University | Rahnama M.,University of Zabol | Jafari T.,Esfahan University of Medical science | Saei-Dehkordi S.S.,Shahrekord University
Food Control | Year: 2011

This study aimed to determine the occurrence of aflatoxin M1 (AFM1) contamination in 682 dairy product samples consisting of raw milk of cow, goat and sheep; Lighvan cheese; and industrial and traditional yoghurt, Kashk and Doogh samples collected from popular markets and dairy ranches in four large Iranian cities. Thin layer chromatography (TLC) technique was used for analysis of the samples. Results showed that the incidence and levels of AFM1 contamination in raw cow milk and industrial products (manufactured from cow milk) were higher than raw goat or sheep milk, and traditional products (made from goat and sheep milk), respectively. Moreover, seasonal variations influenced the concentration of AFM1 in most of the analyzed dairy products. Owing to the abundance and popularity of the industrial products, contamination of these products in such a level could be a potential hazard for public health. © 2011 Elsevier Ltd. Source

Homayouni A.,Mashhad University of Medical Sciences | Sadeghi F.,Mashhad University of Medical Sciences | Varshosaz J.,Esfahan University of Medical science | Afrasiabi Garekani H.,Mashhad University of Medical Sciences | And 2 more authors.
Colloids and Surfaces B: Biointerfaces | Year: 2014

Poor solubility and dissolution of hydrophobic drugs have become a major challenge in pharmaceutical development. Drug nanoparticles have been widely accepted to overcome this problem. The aim of this study was to manufacture celecoxib nanoparticles using antisolvent precipitation and high pressure homogenization techniques in the presence of varying concentrations of soluplus® as a hydrophilic stabilizer. Antisolvent crystallization followed by freeze drying (CRS-FD) and antisolvent crystallization followed by high pressure homogenization and freeze drying (HPH-FD) were used to obtain celecoxib nanoparticles. The obtained nanoparticles were analyzed in terms of particle size, saturation solubility, morphology (optical and scanning electron microscopy), solid state (DSC, XRPD and FT-IR) and dissolution behavior. The results showed that celecoxib nanoparticle can be obtained when soluplus was added to the crystallization medium. In addition, the results showed that the concentration of soluplus and the method used to prepare nanoparticles can control the size and dissolution of celecoxib. Samples obtained in the presence of 5% soluplus through HPH technique showed an excellent dissolution (90%) within 4min. It is interesting to note that celecoxib samples with high crystallinity showed better dissolution than those celecoxib samples with high amorphous content, although they had the same concentration of soluplus. DSC and XRPD proved that samples obtained via HPH technique are more crystalline than the samples obtained through only antisolvent crystallization technique. © 2014 Elsevier B.V. Source

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