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| 1 | Effect of platinum on the photocatalytic degradation of chlorinated organic compound显示文摘TiO 2 nanoparticles, doped with different Pt contents, were prepared by a modified photodeposition method using Degussa P-25 TiO 2 , H 2 PtCl 6 ·6H 2 O and methanol as the solvents. The physicochemical properties of Pt/TiO 2 were investigated by the nitrogen adsorption and desorption isotherm measurement technique, X-ray diffraction analysis and photoluminescence spectra, respectively. Reaction rates from photocatalytic removal of dichloromethane over Degussa P-25 TiO 2 and Pt/TiO 2 were evaluated. The average diameter and BET surface area of the TiO 2 catalyst particles were 300 nm and 50 m 2 /g, respectively. The degradation efficiency was 99.0%, 82.7%, 55.2%, and 57.9% with TiO 2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. And the degradation efficiency was 99.3%, 79.7%, 76.5%, and 73.4% with a 0.005 wt.% Pt/TiO 2 at inlet concentrations of 50, 100, 200, and 300 ppm, respectively. In addition, we found that the photoluminescence emission peak intensities decreased with increases in the doping amount of Pt, which indicates that the irradiative recombination was weakened. Furthermore, the results showed that the UV/0.005 wt.% Pt/TiO 2 process was capable of efficiently decomposing gaseous DCM in air. | Chih Ming Ma Ya Wen Lee Gui Bing Hong Te Li Su Je Lueng Shie Chang Tang Chang | 2011 | Journal of Environmental Sciences2011，23，4： | 5 |
| 2 | Paris saponin Ⅶ,a direct activator of AMPK,induces autophagy and exhibits therapeutic potential in non-small-cell lung cancer显示文摘Paris saponinⅦ(PSⅦ),a bioactive constituent extracted from Trillium tschonoskii Maxim.,is cytotoxic to several cancer types.This study was designed to explore whether PSⅦprevents non-small-cell lung cancer(NSCLC)proliferation and to investigate its molecular target.AMP-activated protein kinase(AMPK)has been implicated in the activation of autophagy in distinct tissues.In cultured human NSCLC cell lines,PSⅦinduces autophagy by activating AMPK and inhibiting m TOR signaling.Furthermore,PSⅦ-induced autophagy activation was reversed by the AMPK inhibitor compound C.Computational docking analysis showed that PSⅦdirectly interacted with the allosteric drug and metabolite site of AMPK to stabilize its activation.Microscale thermophoresis assay and drug affinity responsive target stability assay further confirmed the high affinity between PSⅦand AMPK.In summary,PSⅦacts as a direct AMPK activator to induce cell autophagy,which inhibits the growth of NSCLC cells.In the future,PSⅦtherapy should be applied to treat patients with NSCLC. | XIANG Yu-Chen SHEN Jie SI Yuan LIU Xue-Wen ZHANG Liang WEN Jun ZHANG Te YU Qing-Qing LU Jun-Fei XIANG Ke LIU Ying | 2021 | Chinese Journal of Natural Medicines2021，19，3： | 4 |
| 3 | Effects of Maternal Screening and Universal Immunization to Prevent Mother-to-Infant Transmission of HBV显示文摘 | Huey–Ling Chen Lung–Huang Lin Fu–Chang Hu Jian–Te Lee Wen–Terng Lin Yao–Jung Yang Fu–Chen Huang Shu–Fen Wu Solomon Chih–Cheng Chen Wan–Hsin Wen Chia–Hsiang Chu Yen–Hsuan Ni Hong–Yuan Hsu Pei–Lin Tsai Cheng–Lun Chiang Ming–Kwang Shyu Ping–Ing Lee Feng–Yee | 2012 | Gastroenterology2012，，4： | 2 |
| 4 | Controlling plasmon‐exciton interactions through photothermal reshaping显示文摘We investigated the plasmon-exciton interactions in an individual gold nanorod(GNR)with monolayer MoS2 at room temperature with the single-particle spectroscopy technique.To control the plasmon-exciton interaction,we tuned the local surface plasmon resonance of an individual GNR in-situ by employing the photothermal reshaping effect.The scattering spectra of the GNR-MoS2 hybrids exhibited two dips at the frequencies of the A and B excitons of monolayer MoS2,which were caused by the plasmon-induced resonance energy transfer effect.The resonance energy transfer rate increased when the surface plasmon resonance of the nanorod matched well with the exciton transition energy.Also,we demonstrated that the plasmon-enhanced fluorescence process dominated the photoluminescence of the GNR-MoS2 hybrid.These results provide a flexible way to control the plasmon-exciton interaction in an all-solid-state operating system at room temperature. | Aiqin Hu Shuai Liu Jingyi Zhao Te Wen Weidong Zhang Qihuang Gong Yongqiang Meng Yu Ye Guowei Lu | 2020 | Opto-Electronic Advances2020，3，1： | 2 |
| 5 | Evaluation of chitosan/PVA blended hydrogel membranes显示文摘 | Jen Ming Yang Wen Yu Su Te Lang Leu | 2004 | Journal of Membrane Science2004，2236，： | 1 |
| 6 | Effect of storage and gamma irradiation on ( japonica ) waxy rice 显示文摘 | Wen Chieh Sung Mei Chu Hong Te Sheng Chang | 2008 | Radiation Physics Chemistry2008，，77： | 1 |
| 7 | Erythropoietin structure-function relationships: high degree of sequence homology among mammals显示文摘 | WEN D BOISSEL J-P R TRACY TE | 1993 | Blood1993，82，5： | 1 |
| 8 | Adoptive transfer of metabolically reprogrammed macrophages for atherosclerosis treatment in diabetic ApoE^(-/-) mice显示文摘Atherosclerosis is characterized by inflammation in the arterial wall,which is known to be exacerbated by diabetes.Therapeutic repression of inflammation is a promising strategy for treating atherosclerosis.In this study,we showed that diabetes aggravated atherosclerosis in apolipoproteinE knockout(ApoE^(-/-))mice,in which increased expression of long-chain acyl-CoA synthetase 1(Acsl1)in macrophages played an important role.Knockdown of Acsl1 in macrophages(Mφ^(shAcsl1))reprogrammed macrophages to an anti-inflammatory phenotype,especially under hyperglycemic conditions.Injection of Mφ^(shAcsl1) reprogrammed macrophages into streptozotocin(STZ)-induced diabetic ApoE^(-/-) mice(ApoE^(-/-)+STZ)alleviated inflammation locally in the plaque,liver and spleen.Consistent with the reduction in inflammation,plaques became smaller and more stable after the adoptive transfer of reprogrammed macrophages.Taken together,our findings indicate that increased Acsl1 expression in macrophages play a key role in aggravated atherosclerosis of diabetic mice,possibly by promoting inflammation.Adoptive transfer of Acsl1 silenced macrophages may serve as a potential therapeutic strategy for atherosclerosis. | Tingting Wang Yan Dong Li Yao Fan Lu Chenxi Wen Zhuo Wan Li Fan Zhelong Li Te Bu Mengying Wei Xuekang Yang Yi Zhang | 2022 | Bioactive Materials2022，7，10： | 1 |
| 9 | Specialized sorting of GLUT4 and its recruitment to the cell surface are independently regulated by distinct Rabs显示文摘 | Sadacca LA Bruno J Wen J Xiong W Mcgraw TE | 2013 | Mol Biol Cell2013，24，16： | 1 |
| 10 | Cloning and characterization of protease-activated receptor 4显示文摘 | Wen FU Anderson H Whitmore TE | 1998 | Proc Natl Acad Sci USA1998，95，： | 1 |
| 11 | Evaluation of chitosan/PVA blended hydrogel membranes显示文摘 | Yang Jen Ming Su Wen Yu Leu Te Lang | 2004 | J Mem Sci2004，236，12： | 1 |
| 12 | Pharmacokinetics and metabolic profile of free, conjugated and total silymarin flavonolignans in human plasma after oral administration of milk thistle extract显示文摘 | WEN Z DUMAS TE SCHRIEBER SJ | 2008 | Drug Metab Dispos2008，36，1： | 1 |
| 13 | Novel green-emitting Na2CaP O4F:Eu2+phosphors for near-ultraviolet white light-emitting diodes显示文摘 | HUANG Chien Hao CHEN Yen Chi KUO Te Wen | 2011 | Journal of Luminescence2011，131，： | 1 |
| 14 | Estrogen prevents oxidative damagc to the mitochondria in Friedreich's atax ia skin fibroblasts显示文摘 | Richardson TE Yu AE Wen Y | 2012 | PLoS One2012，7，34： | 1 |
| 15 | Synthesis and characterization of polyimide/multi - walled carbon nanotube nanocomposites 显示文摘 | MO TE - CHENG WANG HONG - WEN CHEN SAN - YAN | 2008 | Polymer Composites2008，29，4： | 1 |
| 16 | Quantities of grains of aluminum and those of TiB2 and Al3Ti partides added in the grain-refining processes 显示文摘 | Lee Cheng Te and Chen Sinn Wen | 2002 | Materials Science and Engineering2002，325，： | 1 |
| 17 | Evaluation of chitosan/PVA blended hydrogel membranes显示文摘 | Jen Ming Yang Wen Yu Su Te Lang Leu | 2004 | Journal of Membrane Science2004，236，： | 1 |
| 18 | POLYMERIZATION OF ETHYLENE METHYL PHOSPHATE IN THE PRESENCE OF SODIUM POLY(ETHYLENE GLYCOL)ATE显示文摘Poly(ethylene methyl phosphate)-poly(ethylene glycol)-poly(ethylene methyl phosphate) triblockcopolymers carrying hydroxyl group at both chain ends were synthesized with sodium poly(ethyleneglycol)ate as initiator. The effects of the factors such as solvent, amount of the initiator and reaction timewere investigated. The copolymers were characterized by IR, 1H-NMR, 1H{31P}-NMR, 13C-NMR, 31P{1H}-NMR, and DSC. High molecular weight of the copolymer and high yield of the polymerization were achievedwithin 3 min at 25℃. The polymerization process was studied by 31P{1H}-NMR and transesterification wasfound during longer polymerization time. | Jie Wen Ren-xi Zhuo Lu Wang Laboratory of Biomedical Materials of the State te Education Commission of China, Department of Chemistry, Wuhan University, Wuhan 430072, China | 1999 | Chinese Journal of Polymer Science1999，17，3： | 0 |
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