http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Doped Sol-gel TiO<sub>2</sub> Films for Biological Applications
Gartner, M.,Trapalis, C.,Todorova, N.,Giannakopoulou, T.,Dobrescu, G.,Anastasescu, M.,Osiceanu, P.,Ghita, A.,Enache, M.,Dumitru, L.,Stoica, T.,Zaharescu, M.,Bae, J.Y.,Suh, S.H. Korean Chemical Society 2008 Bulletin of the Korean Chemical Society Vol.29 No.5
Mono and multilayer TiO2(Fe, $PEG_{600}$) films were deposited by the dip-coating on $SiO_2$/glass substrate using sol-gel method. In an attempt to improve the antibacterial properties of doped $TiO_2$ films, the influence of the iron oxides and polyethilenglycol ($PEG_{600}$) on the morphological, optical, surface chemical composition and biological properties of nanostructured layers was studied. Complementary measurements were performed including Spectroscopic Ellipsometry (SE), Scanning Electron Microscopy (SEM) coupled with the fractal analysis, X-Ray Photoelectron Spectroscopy (XPS) and antibacterial tests. It was found that different concentrations of Fe and $PEG_{600}$ added to coating solution strongly influence the porosity and morphology at nanometric scale related to fractal behaviour and the elemental and chemical states of the surfaces as well. The thermal treatment under oxidative atmosphere leads to films densification and oxides phase stabilization. The antibacterial activity of coatings against Escherichia Coli bacteria was examined by specific antibacterial tests.
Doped Sol-gel TiO₂Films for Biological Applications
M. Gartner*,C. Trapalis,N. Todorova,T. Giannakopoulou,G. Dobrescu,M. Anastasescu,P. Osiceanu,A. Ghita,M. Enache,L. Dumitru,T. Stoica,§ M. Zaharescu,J. Y. Bae,S.-H. Su* 대한화학회 2008 Bulletin of the Korean Chemical Society Vol.29 No.5
Mono and multilayer TiO₂(Fe, PEG600) films were deposited by the dip-coating on SiO₂/glass substrate using sol-gel method. In an attempt to improve the antibacterial properties of doped TiO₂films, the influence of the iron oxides and polyethilenglycol (PEG600) on the morphological, optical, surface chemical composition and biological properties of nanostructured layers was studied. Complementary measurements were performed including Spectroscopic Ellipsometry (SE), Scanning Electron Microscopy (SEM) coupled with the fractal analysis, X-Ray Photoelectron Spectroscopy (XPS) and antibacterial tests. It was found that different concentrations of Fe and PEG600 added to coating solution strongly influence the porosity and morphology at nanometric scale related to fractal behaviour and the elemental and chemical states of the surfaces as well. The thermal treatment under oxidative atmosphere leads to films densification and oxides phase stabilization. The antibacterial activity of coatings against Escherichia Coli bacteria was examined by specific antibacterial tests.
Lee, J,Hwang, Y J,Boo, J H,Han, D,Kwon, O K,Todorova, K,Kowall, N W,Kim, Y,Ryu, H Macmillan Publishers Limited 2011 Cell death and differentiation Vol.18 No.11
Huntington's disease (HD) is an autosomal-dominant neurological disorder caused by expanded CAG repeats in the Huntingtin (Htt) gene, but it is not known how this mutation causes neurodegeneration. Herein, we found that dysfunction of upstream binding factor-1 (UBF-1) is linked to reduced ribosomal DNA (rDNA) transcription in HD. We identified that UBF1 acetylation at Lys (K) 352 by CREB binding protein (CBP) is crucial for the transcriptional activity of rDNA. UBF1 mutation (K352A, K352Q, and K352R) decreased rDNA transcriptional activity. Moreover, both CBP–dHAT mutant and knockdown of CBP by siRNA reduced acetylation of UBF1 and resulted in the decreased transcription of rDNA into rRNA. ChIP analysis showed a significant reduction of UBF1 occupancy in the promoter of rDNA in STHdh<SUP>Q111</SUP> cell line model of HD. These results demonstrate that abnormal activity of UBF1 and its acetylation by CBP are linked to impaired rDNA transcription in HD. This novel mechanism suggests that modulation of UBF-mediated rDNA synthesis by CBP may be a therapeutic target for improving neuronal rDNA transcription in HD.