Background: Cold storage facilities are the most common workplaces that produce artificially cold work environments and are associated with different adverse effects on human health, work productivity and the occurrence of accidents and injuries. The aim of this study was to measure the antagonistic health effects on workers, so that common factors causing abnormal symptoms could be determined, and to gather basic information to monitor the associated health risks from the exposure to cold work environments. Material and Methods: A cross-sectional analytical study was conducted to investigate the occurrence of cold-related adverse health effects, musculoskeletal symptoms, skin problems, injuries, respiratory illnesses, general hygiene and occupational environment related to cold indoor workplaces, using the Standardized Nordic Questionnaire. A total of 200 subjects took part in this study, including 100 exposed and 100 unexposed to cold environments. A 1-way analysis of variance (ANOVA) and a t-test were applied to measure statistical differences and to differentiate the cases where variations occurred, using SPSS 16. Results: The study revealed that a longer and constant exposure to extremely cold indoor work environments significantly increased (p < 0.001) the cold-related symptoms and musculoskeletal disorders which ultimately reduced (p < 0.01) the efficiency, effectiveness, performance and work ability of the exposed workers. Conclusions: The study disclosed various adverse cold-related complaints of the studied subjects who were exposed to extreme cold conditions during a maximum number of working hours. The most consistent problems were related to musculoskeletal discomfort, skin problems and respiratory abnormalities.
Magnetic chicken bone-based biochar (MCBB) was successfully prepared and efficiently adsorbed rhodamine-B (RB) dye and tetracycline (TC) in multi-component systems. The magnetisation value, surface area, and pH of the MCBB were found to be 66.5 emu/g, 328 m/g, and 8.3, respectively. RB has higher saturation capacity (96.5 mg/g) and occupies more active sites on MCBB, thus limiting the sorption of TC with lower saturation capacity (63.3 mg/g). Langmuir isotherm suitably describes the sorption process in a single-component system; however, the multi-component system was well fitted to the Sheindorf-Rebhun-Sheintuch model. The selectivity factor values confirmed that MCBB had higher adsorption affinity toward RB than TC. The intraparticle diffusion model played a significant role in the sorption process. The MCBB can be easily desorbed with base-spiked HO and reused without loss in stability or structural integrity.
Purpose: To isolate thymoquinone (TQ) from Nigella sativa L. and Thymus vulgaris L., and investigate its anti-proliferative effect on HeLa cancer cells. Method: Pulverized dried samples of N. sativa seed (100 g) and aerial parts of T. vulgaris (1000 g) were subjected to Soxhlet extraction using methanol and n-hexane combined in different proportions. Thymoquinone (TQ) was then isolated from the extracts using high performance liquid chromatography (HPLC). The isolated TQ was further subjected to Fourier Transform Infrared (FTIR) spectroscopy to identify its functional groups. The anti-proliferative effect of TQ on HeLa cancer cells was evaluated using 3-[4, 5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide (MTT) assay. Results: Extract yield from N. sativa was significantly higher than from T. vulgaris, and also increased with increase in the proportion of methanol in the extraction solvent (p < 0.05). Methanol and n-hexane (4:1, v:v) yielded the highest amount of oil, with yields of 15.8 and 9.7 ml/25 g dry weight (d.wt.) from N. sativa and T. vulgaris, respectively. The results obtained from HPLC showed that the concentration of TQ isolated from N. sativa (388.61 µg/ml) was significantly higher than that from T. vulgaris (357.03 µg/ml, p < 0.05). The anti-proliferative effects of TQ standard and TQ isolated from N. sativa on HeLa cancer cells were dose-dependent, and was highest at the lowest concentration. The number of viable cells significantly decreased with increase in TQ concentration (p < 0.01). TQ from N. sativa significantly reduced the number of viable cells even at the lowest concentration when compared to TQ standard (p < 0.05). Cell death was significantly higher in TQ-treated groups than in untreated cancer cells. Conclusion: The results obtained in this study show that N. sativa is a potential source of TQ, with the yield enhanced by modifying the extraction procedure or solvent used. Furthermore, TQ isolated from N. sativa exerts a dose-dependent anti-proliferative effect on HeLa cancer cells.
AbstractCurrently, the green route for synthesis of silver nanoparticles (Ag NPs) using plants leaf extract is an emerging research area in nanotechnology. The present study was explored for synthesis, characterization and catalytic application of Ag NPs using Diospyros lotus fresh leaf extracts. Factors affecting the synthesis were optimized and optimum conditions were pH of 8.6, silver nitrate (AgNO3) concentration of 1.5 mM and 10 mL leaf extract. Formation of Ag NPs was observed by change in color of reaction mixture from pale yellow to reddish brown. The synthesized Ag NPs were characterized using UV-Vis spectrophotometer, EDX, XRD and SEM analyses. UV-Vis spectrophotometer showed maximum absorbance peak in the range of 407 nm at different time intervals indicating formation of Ag NPs. SEM and XRD analysis confirmed face centered cubic structure and crystalline nature of biologically synthesized Ag NPs with average particle size of 27 nm. The purity of synthesized Ag NPs was revealed by EDX. Finally, photo catalytic activity (PCA) of Ag NPs was studied and 72.91% decolorization of industrial waste water was obtained at 54 h. Some important parameters like pH, turbidity, conductance; TSS, TDS, sulphide, sulphates, etc. were also monitored before and after treatment with Ag NPs.
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