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        Polydopamine-Coated Fe3O4 Nanoparticles as Synergistic Redox Mediators for Catalytic Reduction of Azo Dyes

        Sinan Du,Yang Luo,FANG ZUO,XINHUA LI,Dong Liu 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2017 NANO Vol.12 No.3

        Polydopamine-coated Fe3O4 (Fe3O4@PDA) nanoparticles (NPs) were prepared as synergistic redox mediators for the catalytic reduction, by NaBH4, of azo dyes such as methyl orange (MO) and methyl red (MR). Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) were applied to determine their surface morphology, surface chemistry and detailed chemical composition, respectively. The latter technique confirmed the presence of quinone moieties. Moreover, a vibrating sample magnetometer (VSM) was used to confirm the superparamagnetic properties of these NPs. The characteristic optical absorption maximum of MO at 462 nm was used to monitor the decolorization process. This was employed to determine the catalytic activity in the reaction. An enhancement of the catalytic activity of the magnetic-separable Fe3O4@PDA nanocatalyst over that of PDA microspheres (MPs) was observed. Moreover, their reusability and stability were also investigated. A synergistic electron transfer mechanism involving both Fe3O4 and PDA moieties was proposed as follows: the quinone moieties and Fe (III) species in Fe3O4@PDA NPs served as systematic redox mediators, with quinone receiving an electron from NaBH4. The reduced quinone next transfers an electron to the Fe (III) moiety, generating an Fe (II) species that in turn transfers an electron to the azo dye. We determined that this process resulted in enhanced reductive degradation of azo dyes when compared with PDA MPs. Moreover, Fe3O4@PDA NPs could be magnetically separated and recycled. We therefore concluded that these NPs show great potential in the immobilization of homogeneous catalysts in the chemical reduction processes of azo dyes.

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        The Presence of Fragmented QRS on 12-Lead Electrocardiography in Patients with Coronary Artery Ectasia

        Fatih Sen,Samet Yılmaz,Mevlüt Serdar Kuyumcu,Özcan Özeke,Mustafa Mücahit Balcı,Sinan Aydog˘du 대한심장학회 2014 Korean Circulation Journal Vol.44 No.5

        Background and Objectives: Coronary artery ectasia (CAE) is an angiographic finding characterized by dilation of an arterial segment with a diameter at least 1.5 times that of its adjacent normal coronary artery. Fragmented QRS (fQRS) complexes are electrocardiographic signals which reflect altered ventricular conduction around regions of a myocardial scar and/or ischaemia. In the present study, we aimed to evaluate the presence of fQRS in patients with CAE. Subjects and Methods: The study population included 100 patients with isolated CAE without coronary artery disease (CAD) and 80 angiographically normal controls. fQRS was defined as the presence of an additional R wave or notching of R or S wave or the presence of fragmentation in two contiguous leads corresponding to a major coronary artery territory. Results: The two groups were similar in terms of age, sex, hypertension, dyslipidemia, and family history of CAD. The presence of fQRS was significantly (p<0.05) higher in the CAE group than that in the normal coronary artery group (29% vs. 6.2%, p=0.008). Isolated CAE were detected most commonly in the right coronary artery (61%), followed by left anterior descending artery (52%), left circumflex artery (36%), and left main artery (9%). Multivariate stepwise logistic regression analysis showed that CAE {odds ratio (OR) 1.412; 95% confidence interval (CI) 1.085–1.541; p=0.003} and diabetes (OR 1.310; 95% CI 1.025–1.482; p=0.041) were independently associated with fQRS. Conclusion: The presence of fragmented QRS associated with increased risk for arrhythmias and cardiovascular mortality was significantly higher in patients with CAE than in patient with normal coronary artery. Further studies are needed to determine whether the presence of fragmented QRS is a possible new risk factor for patients with CAE.

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