340 research outputs found

    Ultrasound palpation sensor for tissue thickness and elasticity measurement - assessment of transverse carpal ligament

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    Author name used in this publication: Y. P. ZhengAuthor name used in this publication: A. P. C. ChoiAuthor name used in this publication: M. H. LuAuthor name used in this publication: X. ChenAuthor name used in this publication: Q. H. Huang2006-2007 > Academic research: refereed > Publication in refereed journalAccepted ManuscriptPublishe

    Bounded solutions for the nonlinear wave equation

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    Interface modification of clay and graphene platelets reinforced epoxy nanocomposites: a comparative study

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    The interface between the matrix phase and dispersed phase of a composite plays a critical role in influencing its properties. However, the intricate mecha-nisms of interface are not fully understood, and polymer nanocomposites are no exception. This study compares the fabrication, morphology, and mechanical and thermal properties of epoxy nanocomposites tuned by clay layers (denoted as m-clay) and graphene platelets (denoted as m-GP). It was found that a chemical modification, layer expansion and dispersion of filler within the epoxy matrix resulted in an improved interface between the filler mate-rial and epoxy matrix. This was confirmed by Fourier transform infrared spectroscopy and transmission electron microscope. The enhanced interface led to improved mechanical properties (i.e. stiffness modulus, fracture toughness) and higher glass transition temperatures (Tg) compared with neat epoxy. At 4 wt% m-GP, the critical strain energy release rate G1c of neat epoxy improved by 240 % from 179.1 to 608.6 J/m2 and Tg increased from 93.7 to 106.4 �C. In contrast to m-clay, which at 4 wt%, only improved the G1c by 45 % and Tg by 7.1 %. The higher level of improvement offered by m-GP is attributed to the strong interaction of graphene sheets with epoxy because the covalent bonds between the carbon atoms of graphene sheets are much stronger than silicon-based clay

    Fabrication of a Highly Sensitive Chemical Sensor Based on ZnO Nanorod Arrays

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    We report a novel method for fabricating a highly sensitive chemical sensor based on a ZnO nanorod array that is epitaxially grown on a Pt-coated Si substrate, with a top–top electrode configuration. To practically test the device, its O2 and NO2 sensing properties were investigated. The gas sensing properties of this type of device suggest that the approach is promising for the fabrication of sensitive and reliable nanorod chemical sensors

    Metal organic framework nanosheets in polymer composite materials for gas separation

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    [EN] Composites incorporating two-dimensional nanostructures within polymeric matrices have potential as functional components for several technologies, including gas separation. Prospectively, employing metal-organic frameworks (MOFs) as versatile nanofillers would notably broaden the scope of functionalities. However, synthesizing MOFs in the form of freestanding nanosheets has proved challenging. We present a bottom-up synthesis strategy for dispersible copper 1,4-benzenedicarboxylate MOF lamellae of micrometre lateral dimensions and nanometre thickness. Incorporating MOF nanosheets into polymer matrices endows the resultant composites with outstanding CO2 separation performance from CO2/CH4 gas mixtures, together with an unusual and highly desired increase in the separation selectivity with pressure. As revealed by tomographic focused ion beam scanning electron microscopy, the unique separation behaviour stems from a superior occupation of the membrane cross-section by the MOF nanosheets as compared with isotropic crystals, which improves the efficiency of molecular discrimination and eliminates unselective permeation pathways. This approach opens the door to ultrathin MOF-polymer composites for various applications.The research leading to these results has received funding (J.G., B.S.) from the European Research Council under the European Union’s Seventh Framework Programme (FP/2007-2013)/ERC Grant Agreement no. 335746, CrystEng-MOF-MMM. T.R. is grateful to TUDelft for funding. G.P. acknowledges the A. von Humboldt Foundation for a research grant. A.C., I.L. and F.X.L.i.X. thank Consolider-Ingenio 2010 (project MULTICAT) and the ‘Severo Ochoa’ programme for support. I.L. also thanks CSIC for a JAE doctoral grant.Ródenas Torralba, T.; Luz Mínguez, I.; Prieto González, G.; Seoane, B.; Miro, H.; Corma Canós, A.; Kapteijn, F.... (2015). Metal organic framework nanosheets in polymer composite materials for gas separation. Nature Materials. 14(1):48-55. https://doi.org/10.1038/nmat4113S4855141Stankovich, S. et al. Graphene-based composite materials. Nature 442, 282–286 (2006).Wang, Q. H., Kalantar-Zadeh, K., Kis, A., Coleman, J. N. & Strano, M. S. Electronics and optoelectronics of two-dimensional transition metal dichalcogenides. Nature Nanotech. 7, 699–712 (2012).Choi, S. et al. Layered silicates by swelling of AMH-3 and nanocomposite membranes. Angew. Chem. Int. Ed. 47, 552–555 (2008).Varoon, K. et al. Dispersible exfoliated zeolite nanosheets and their application as a selective membrane. Science 334, 72–75 (2011).Corma, A., Fornes, V., Pergher, S. B., Maesen, Th. L. M. & Buglass, J. G. Delaminated zeolite precursors as selective acidic catalysts. 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Ethane/ethene separation turned on its head: Selective ethane adsorption on the metal-organic framework ZIF-7 through a gate-opening mechanism. J. Am. Chem. Soc. 132, 17704–17706 (2010).Deng, H. et al. Multiple functional groups of varying ratios in metal-organic frameworks. Science 12, 846–850 (2010).Khaletskaya, K. et al. Integration of porous coordination polymers and gold nanorods into core-shell mesoscopic composites toward light-induced molecular release. J. Am. Chem. Soc. 135, 10998–11005 (2013).Corma, A., Garcia, H. & Llabrés i Xamena, F. X. Engineering metal organic frameworks for heterogeneous catalysis. Chem. Rev. 110, 4606–4655 (2010).Mueller, U. et al. Metal-organic frameworks-prospective industrial applications. J. Mater. Chem. 16, 626–636 (2006).Gascon, J. & Kapteijn, F. Metal-organic framework membranes-high potential, bright future? Angew. Chem. Int. Ed. 49, 1530–1532 (2010).Li, Y. S. et al. Controllable synthesis of metal-organic frameworks: From MOF nanorods to oriented MOF membranes. Adv. Mater. 22, 3322–3326 (2010).Gascon, J. et al. Practical approach to zeolitic membranes and coatings: State of the art, opportunities, barriers, and future perspectives. Chem. Mater. 24, 2829–2844 (2012).Bae, T-H. et al. A high-performance gas-separation membrane containing submicrometer-sized metal-organic framework crystals. Angew. Chem. Int. Ed. 49, 9863–9866 (2010).Zornoza, B. et al. Functionalized flexible MOFs as fillers in mixed matrix membranes for highly selective separation of CO2 from CH4 at elevated pressures. Chem. Commun. 47, 9522–9524 (2011).Zornoza, B., Tellez, C., Coronas, J., Gascon, J. & Kapteijn, F. Metal organic frameworks based mixed matrix membranes: An increasingly important field of research with a large application potential. Microp. Mesop. Mater. 166, 67–78 (2013).Zhang, C., Dai, Y., Johnson, J. R., Karvan, O. & Koros, W. High performance ZIF-8/6FDA-DAM mixed matrix membrane for propylene/propane separations. J. Mem. Sci. 389, 34–42 (2012).Li, T., Pan, Y., Peinemann, K-V. & Lai, Z. Carbon dioxide selective mixed matrix composite membrane containing ZIF-7 nano-fillers. J. Mem. Sci. 425–426, 235–242 (2013).Makiura, R. et al. Surface nano-architecture of a metal-organic framework. Nature Mater. 9, 565–571 (2010).Mori, W. et al. Synthesis of new adsorbent copper(II) terephthalate. Chem. Lett. 26, 1219–1220 (1997).Xin, Z., Bai, J., Shen, Y. & Pan, Y. Hierarchically micro- and mesoporous coordination polymer nanostructures with high adsorption performance. Cryst. Growth Des. 10, 2451–2454 (2010).Adams, R., Carson, C., Ward, J., Tannenbaum, R. & Koros, W. Metal organic framework mixed matrix membranes for gas separations. Micropor. Mesopor. Mater. 131, 13–20 (2010).Carson, C. G. et al. Synthesis and structure characterization of copper terephthalate metal-organic framework. Eur. J. Inorg. 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Predictive models for mixed-matrix membrane performance: A review. Chem. Rev. 113, 4980–5028 (2013)

    Methylation profiling of Epstein-Barr virus immediate-early gene promoters, BZLF1 and BRLF1 in tumors of epithelial, NK- and B-cell origins

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    <p>Abstract</p> <p>Background</p> <p>Epstein-Barr virus (EBV) establishes its latency in EBV-associated malignancies, accompanied by occasionally reactivated lytic cycle. Promoter CpG methylation of EBV genome plays an essential role in maintaining viral latency. Two immediate-early (IE) genes, BZLF1 and BRLF1, induce the switch from latent to lytic infection. Studies of methylation-dependent binding of BZLF1 and BRLF1 to EBV promoters have been well reported, but little is known about the methylation status of <it>BZLF1 </it>and <it>BRLF1 </it>promoters (Zp and Rp) in tumor samples.</p> <p>Methods</p> <p>We evaluated the methylation profiles of Zp and Rp by methylation-specific PCR (MSP) and bisulfite genomic sequencing (BGS), as well as <it>BZLF1 </it>and <it>BRLF1 </it>expression by semiquantitative reverse transcription (RT)-PCR in tumors of epithelial, NK- and B-cell origins.</p> <p>Results</p> <p>We found that both Zp and Rp were hypermethylated in all studied EBV-positive cell lines and tumors of lymphoid (B- or NK cell) or epithelial origin, while unmethylated Zp and Rp alleles were detected in cell lines expressing <it>BZLF1 </it>and <it>BRLF1</it>. Following azacytidine treatment or combined with trichostatin A (TSA), the expression of <it>BZLF1 </it>and <it>BRLF1 </it>was restored along with concomitant promoter demethylation, which subsequently induced the reactivation of early lytic gene <it>BHRF1 </it>and late lytic gene <it>BLLF1</it>.</p> <p>Conclusions</p> <p>Hypermethylation of Zp and Rp mediates the frequent silencing of <it>BZLF1 </it>and <it>BRLF1 </it>in EBV-associated tumors, which could be reactivated by demethylation agent and ultimately initiated the EBV lytic cascade.</p

    The overmethylated genes in Helicobacter pylori-infected gastric mucosa are demethylated in gastric cancers

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    <p>Abstract</p> <p>Background</p> <p>The transitional-CpG sites between weakly methylated genes and densely methylated retroelements are overmethylated in the gastric mucosa infected with <it>Helicobacter pylori </it>(<it>H. pylori</it>) and they are undermethylated in the gastric cancers depending on the level of loss of heterozygosity (LOH) events. This study delineated the transitional-CpG methylation patterns of CpG-island-containing and -lacking genes in view of the retroelements.</p> <p>Methods</p> <p>The transitional-CpG sites of eight CpG-island-containing genes and six CpG-island-lacking genes were semi-quantitatively examined by performing radioisotope-labelling methylation-specific PCR under stringent conditions. The level of LOH in the gastric cancers was estimated using the 40 microsatellite markers on eight cancer-associated chromosomes. Each gene was scored as overmethylated or undermethylated based on an intermediate level of transitional-CpG methylation common in the <it>H. pylori</it>-negative gastric mucosa.</p> <p>Results</p> <p>The eight CpG-island genes examined were overmethylated depending on the proximity to the nearest retroelement in the <it>H. pylori</it>-positive gastric mucosa. The six CpG-island-lacking genes were similarly methylated in the <it>H. pylori</it>-positive and -negative gastric mucosa. In the gastric cancers, long transitional-CpG segments of the CpG-island genes distant from the retroelements remained overmethylated, whereas the overmethylation of short transitional-CpG segments close to the retroelements was not significant. Both the CpG-island-containing and -lacking genes tended to be decreasingly methylated in a LOH-level-dependent manner.</p> <p>Conclusions</p> <p>The overmethylated genes under the influence of retroelement methylation in the <it>H. pylori</it>-infected stomach are demethylated in the gastric cancers influenced by LOH.</p
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