109 research outputs found
Impact of copeptin on diagnosis of acute coronary syndrome
AbstractBackgroundAcute coronary syndrome remains the principal cause of death, so the early diagnosis is of great importance. Cardiac troponin is the preferred biomarker for acute myocardial infarction. Cardiac chest pain immediately increased copeptin secretion. The combination of copeptin and cardiac troponin I is being suggested for early diagnosis of acute coronary syndrome.SubjectIt was done to emphasize the importance of association of copeptin, cardiac troponin I and high sensitive C reactive protein to confirm the diagnosis of acute myocardial infarction or unstable angina pectoris in patients with a cardiac chest pain.MethodThe current study enrolled 22 patients with acute myocardial infarction as group i and 33 patients with unstable angina pectoris as group ii. The third group consisted of 23 apparently healthy persons. Patients and controls were subjecting to laboratory investigations, which include the levels of copeptin, high-sensitivity cardiac troponin high sensitive C reactive protein creatine kinase MB fraction, lipid and I profile.ResultsWe found a significant increase of copeptin in group i when compared to group iii (30.01±12.92) (9.54±3.55), respectively, p value=0.000 and group ii (30.01±12.92) (11.16±4.58) respectively, p value 0.000, but a non-significant difference in group ii when compared to group iii (11.16±4.58) (9.54±3.55) respectively, p value=0.160. Also cardiac troponin I showed a significant increase in group i when compared to group ii (136.73±26.07) (11.18±3.79), p value=0.000, and group iii (136.73±26.07) (9.61±3.70) respectively, p value=0.000, but a non-significant difference between group ii (11.18±3.79), and group iii (9.61±3.70), p value=0.129. There was a positive correlation between copeptin and cardiac troponin I within group i, r=0.718, p value=0.000.ConclusionIn suspected acute coronary syndrome, determination of copeptin and cardiac troponin I provides a remarkable negative predictive value, which aids in early and safe ruling out of myocardial infarction
Assessment of the grinding wheel active surface condition using SEM and image analysis techniques
Targeting poly(ADP-ribose) polymerase activity for cancer therapy
Poly(ADP-ribosyl)ation is a ubiquitous protein modification found in mammalian cells that modulates many cellular responses, including DNA repair. The poly(ADP-ribose) polymerase (PARP) family catalyze the formation and addition onto proteins of negatively charged ADP-ribose polymers synthesized from NAD+. The absence of PARP-1 and PARP-2, both of which are activated by DNA damage, results in hypersensitivity to ionizing radiation and alkylating agents. PARP inhibitors that compete with NAD+ at the enzyme’s activity site are effective chemo- and radiopotentiation agents and, in BRCA-deficient tumors, can be used as single-agent therapies acting through the principle of synthetic lethality. Through extensive drug-development programs, third-generation inhibitors have now entered clinical trials and are showing great promise. However, both PARP-1 and PARP-2 are not only involved in DNA repair but also in transcription regulation, chromatin modification, and cellular homeostasis. The impact on these processes of PARP inhibition on long-term therapeutic responses needs to be investigated
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IN-SITU MINING OF PHOSPHATE ORES
Presently the mining of Florida phosphate requires the movement of over a 100-ton of materials (overburden, sand, clay) for every ton of phosphate concentrate recovered. Not only is this energy intensive, but it also causes significant stress on the environment. In 2003, the Department of Energy solicited ideas for innovative mining ideas that could significantly improve the efficiency of mining. An award was made to the University of Florida Engineering Research Center to evaluate the in situ mining of phosphates using an aqueous CO{sub 2} solution. Tests were carried out in a 15.2 cm (6-inch) diameter column, 1.83 meter (6 feet) long at pressures up to 117.2 kg/cm{sup 2} (40 psi). Results to date demonstrate that initially the MgO is leached from the ore and then the phosphate. While the tests are continuing, so far they have not demonstrated P{sub 2}O{sub 5} concentrations that are economically attractive
ADSORPTION MECHANISM OF TOXIC METAL IONS BY CLAY (ATTAPULGITE)
A series of adsorption tests were conducted to analyze the sorption capacity of attapulgite. Ions such as cobalt, nickel, lead and cadmium were adsorbed from waste solutions onto attapulgite surface. Adsorption depletion tests were performed as a function of solid to liquid ratio, conditioning time, heavy metal ion concentration, and pH to identify the mode and extent of interactions in the system. Conditioning time data confirm that ion exchange is nearly complete after 30 seconds indicating the fast kinetics of the ion exchange process. Solid to liquid ratio data suggest that optimum ratio is 50g/Liter. The adsorption isotherms constructed as function of heavy metal concentration and pH reveal that adsorption of metal ions increase in the order of Co> Ni> Cd> Pb. The attapulgite was found to be rather receptive to the adsorption of heavy metal ions, and fairly high amounts of calcium, potassium and magnesium ions were desorbed from the attapulgite into the solution. A quantitative analysis of the adsorption results indicates that a one-to-one ion exchange mechanism is responsible for the incorporation of cations into the structure of attapulgite. The results show that attapulgite. Similar to sepiolite, is a potential clay mineral for the removal of toxic metal ions from wastewater streams
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