35 research outputs found

    Determination of the sulphur balance in coal during combustion in small and large fuel beds

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    U toku ovih ispitivanja eksperimentalno smo provjeravali uobičajeni proračun emisije sumpora na osnovu tzv. »sagorivog sumpora« u uglju. Mjerenja sadržaja sumpora u dimnim plinovima su pokazala da se ovakvim proračunima, koji se baziraju na određivanju tzv. »vezanog sumpora« u laboratorijskim uslovima spaljivanjem goriva do 800°C, može načiniti greška i do 100%. Emisija sumpora iz velikih ložišta za centralno grijanje kreće se otprilike 90%, dok je pretpostavljena emisija iz podataka o »sagorivom sumporu« trebala da iznosi otprilike 50%. Emisije sumpora iz sobnih peći kretale su se od 56 do 88% zavisno od konstrukcije, te od načina loženja i režima rada peći. I u ovom su slučaju emisije redovno bile više od očekivanih emisija »sagorivog sumpora«. Rezu!tati ovih mjerenja nam pokazuju da se prilikom projektovanja i proračuna emisije i visine dimnjaka ne možemo osloniti samo na podatke o sadržaju »sagorivog sumpora« u gorivu nego na eksperimentalne podatke o bilansu sumpora, koji se sve češće mogu naći u stranoj tehničkoj literaturi.The usual rough estimate of sulphur emission was checked experimentally on the basis of the sulphur content in coal known as »burnt sulphur«. The measurements of the content of sulphur in stack gases proved that such an estimate based on the measuring of sulphur in ash known as »bound sulphur« under laboratory conditions of burning fuel up to 800°C, can result in an error of up to 100%. The emission of sulphur from solid fuel beds used for central heating comes to 90% while the supposed emission based on »burnt sulphur« should be about 50%. The sulphur emission from domestic stoves reached 56% to 88% depending on stove design, coal burning and on operating conditions. The emissions were always greater than the expected emissions of »burnt sulphur«. The results of these measurements indicate that we cannot rely only on the information concerning »burnt sulphur« content when the design and calculation of chimney emission and height is carried out, but the experimental data on sulphur balance should also be taken into account. Such data can be more and more often found in foreign technical literature

    Advanced glycoxidation and lipoxidation end products (AGEs and ALEs): an overview of their mechanisms of formation

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    Advanced lipoxidation end products (ALEs) and advanced glycation end products (AGEs) have a pathogenetic role in the development and progression of different oxidative-based diseases including diabetes, atherosclerosis, and neurological disorders. AGEs and ALEs represent a quite complex class of compounds that are formed by different mechanisms, by heterogeneous precursors and that can be formed either exogenously or endogenously. There is a wide interest in AGEs and ALEs involving different aspects of research which are essentially focused on set-up and application of analytical strategies (1) to identify, characterize, and quantify AGEs and ALEs in different pathophysiological conditions ; (2) to elucidate the molecular basis of their biological effects ; and (3) to discover compounds able to inhibit AGEs/ALEs damaging effects not only as biological tools aimed at validating AGEs/ALEs as drug target, but also as promising drugs. All the above-mentioned research stages require a clear picture of the chemical formation of AGEs/ALEs but this is not simple, due to the complex and heterogeneous pathways, involving different precursors and mechanisms. In view of this intricate scenario, the aim of the present review is to group the main AGEs and ALEs and to describe, for each of them, the precursors and mechanisms of formation

    DNA damage by lipid peroxidation products: implications in cancer, inflammation and autoimmunity

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    Oxidative stress and lipid peroxidation (LPO) induced by inflammation, excess metal storage and excess caloric intake cause generalized DNA damage, producing genotoxic and mutagenic effects. The consequent deregulation of cell homeostasis is implicated in the pathogenesis of a number of malignancies and degenerative diseases. Reactive aldehydes produced by LPO, such as malondialdehyde, acrolein, crotonaldehyde and 4-hydroxy-2-nonenal, react with DNA bases, generating promutagenic exocyclic DNA adducts, which likely contribute to the mutagenic and carcinogenic effects associated with oxidative stress-induced LPO. However, reactive aldehydes, when added to tumor cells, can exert an anticancerous effect. They act, analogously to other chemotherapeutic drugs, by forming DNA adducts and, in this way, they drive the tumor cells toward apoptosis. The aldehyde-DNA adducts, which can be observed during inflammation, play an important role by inducing epigenetic changes which, in turn, can modulate the inflammatory process. The pathogenic role of the adducts formed by the products of LPO with biological macromolecules in the breaking of immunological tolerance to self antigens and in the development of autoimmunity has been supported by a wealth of evidence. The instrumental role of the adducts of reactive LPO products with self protein antigens in the sensitization of autoreactive cells to the respective unmodified proteins and in the intermolecular spreading of the autoimmune responses to aldehyde-modified and native DNA is well documented. In contrast, further investigation is required in order to establish whether the formation of adducts of LPO products with DNA might incite substantial immune responsivity and might be instrumental for the spreading of the immunological responses from aldehyde-modified DNA to native DNA and similarly modified, unmodified and/or structurally analogous self protein antigens, thus leading to autoimmunity

    Evaluation of Apoptotic, Antiproliferative, and Antimigratory Activity of Origanum syriacum against Metastatic Colon Cancer Cells

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    The effect of an ethanolic extract of fresh leaves of Origanum syriacum (OSEE) on the proliferative, apoptotic, and migratory capacities of LoVo and SW620 colon cancer cells was investigated. OSEE showed a concentration-dependent apoptotic and antiproliferative effect on LoVo and SW620 cells at 500 μg mL−1 or higher after 48 h of exposure. Additionally, OSEE inhibited the migration of both LoVo and SW620 cells by decreasing (50–75%) wound-healing capacity at 500 and 1,000 μg mL−1. The results suggest that OSEE may have potential anticarcinogenic activity in metastatic colon cancer cells through the dual effect of inhibiting cell proliferation and migration and induction of apoptosis.Scopu

    Biocompatibility of oxygen-plasma-treated polystyrene substrates

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    The biocompatibility of polystyrene (PS) samples has been improved by treatment with weakly ionized highly non-equilibrium oxygen plasma. Samples were exposed to plasma for 30 s for which they have received a dose of ions of 4.5 × 1017 m−2 and a neutral oxygen atom dose of 3 × 10−23 m−2. Both untreated and plasma-treated samples were tested for biocompatibility according to the same procedure. Proliferation of human mammary epithelial cells (HMECs) on samples revealed a dramatically improved biocompatibility of polystyrene treated by oxygen plasma. The HMECs were deposited on all samples and incubated for 1, 2 and 6 days. MTT test revealed about two times higher activity of cell enzymes after 48 h incubation. The activity for plasma-treated samples remained much higher than for untreated samples even after 6 days of incubation when the samples were already covered with a dense film of HMECs

    Determination of multiple mycotoxins in Qatari population serum samples by LC-MS/MS

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    Human exposure to mycotoxins is almost inevitable as mycotoxins are naturally occurring contaminants of large portion of food and feed. Depending on the type of mycotoxins, inter-individual mycotoxin adsorption, bioaccumulation, distribution, metabolism and excretion, can cause serious adverse health effects. Therefore, continuous biomonitoring studies of population exposure to mycotoxins are needed. Here we describe a multi-analyte approach for the detection and quantification of 20 mycotoxins in human serum using ultra-performance liquid chromatography-electrospray/tandem mass spectrometry operated in targeted multiple reaction monitoring mode. The validated method was used to assess occurrence of mycotoxins in serum samples of 46 residents of Qatar. Mycotoxins that were detected with high incidence were HT-2 toxin (13.0%), sterigmatocystin (10.9%) and 3-acetyldeoxynivalenol (6.5%). Also, co-exposure to several mycotoxins was noticed in the analysed samples. Our results show that strict food quality control is needed to remove mycotoxin contaminated food from the market in order to minimise human exposure to mycotoxins
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