BACKGROUND Esophageal cancer(EC)is an aggressive malignancy with low survival(10%-30%).Nutritional problems are present throughout the perioperative period and are key to prognosis.Home enteral nutrition appears to im...BACKGROUND Esophageal cancer(EC)is an aggressive malignancy with low survival(10%-30%).Nutritional problems are present throughout the perioperative period and are key to prognosis.Home enteral nutrition appears to improve the nutritional status of patients with EC.Few studies have addressed the experience of patients administering their own nutritional fluids and managing their own feeding tubes at home.The aim of this study was to explore the real-life experience of self-management of feeding tubes in patients at home after EC surgery in the first 3 months after discharge following surgery.AIM To explore feeding tube self-management experience of patients at home 3 months after discharge following EC surgery.METHODS Face-to-face semi-structured interviews were conducted with 18 patients using a feeding tube at home after EC surgery.Thematic analysis of the recordings identified themes related to feeding tube self-management.RESULTS Patients expressed similar feelings about their tube management experiences concerning three contextualized themes:Self-management dilemmas,distressing experiences,and self-management facilitators.CONCLUSION There are many dilemmas and problems in self-managing feeding tubes in postoperative homebound patients with EC.Clinical staff should provide guidance to promote a positive change in self-management behavior.展开更多
Searching for highly efficient catalysts toward dehydrogenation of hydrazine for chemical hydrogen storage is highly desirable for the development of hydrogen economy. Herein, we report a simple in situ co-reduction s...Searching for highly efficient catalysts toward dehydrogenation of hydrazine for chemical hydrogen storage is highly desirable for the development of hydrogen economy. Herein, we report a simple in situ co-reduction synthesis of NiPt nanoparticles supported on CeO_2 nanospheres and their superior catalytic performance for hydrogen generation from alkaline solution of hydrazine at room temperature. Thanks to the strong electronic interaction arising from synergistic effect at atomic lever and support-metal interaction between NiPt and CeO_2.The obtained Ni_5Pt_5-CeO_2 catalyst exhibits 100% hydrogen selectivity and superior catalytic performance for hydrogen generation from alkaline solution of hydrazine at room temperature, with a TOF value of 416 h 1.展开更多
As BiVO4 is one of the most popular visible-light-responding photocatalysts, it has been widely used for visiblelight-driven water splitting and environmental purification. However, the typical photocatalytic activity...As BiVO4 is one of the most popular visible-light-responding photocatalysts, it has been widely used for visiblelight-driven water splitting and environmental purification. However, the typical photocatalytic activity of unmodified BiVO4 for the degradation of organic pollutants is still not impressive. To address this limitation, we studied Fe2O3-modified porous BiVO4 nanoplates. Compared with unmodified BiVO4, the Fe2O3-modified porous Bi VO4 nanoplates showed significantly enhanced photocatalytic activities in decomposing both dye and colorless pollutant models, such as rhodamine B(Rh B) and phenol,respectively. The pseudo-first-order reaction rate constants for the degradation of RhB and phenol on Fe2O3-modified BiVO4 porous nanoplates are 27 and 31 times larger than that of pristine Bi VO4, respectively. We also found that the Fe2O3 may act as an efficient non-precious metal co-catalyst, which is responsible for the excellent photocatalytic activity of Fe2O3/BiVO4.Graphical Abstract Fe2O3, as a cheap and efficient co-catalyst, could greatly enhance the photocatalytic activity of Bi VO4 porous nanoplates in decomposing organic pollutants.展开更多
The development of highly active noble-metal-flee catalysts for catalytic hydrolysis of ammonia borane is mandatory for its application in hydrogen storage. Herein, Co-CeOx nanoclusters have been successfully anchored...The development of highly active noble-metal-flee catalysts for catalytic hydrolysis of ammonia borane is mandatory for its application in hydrogen storage. Herein, Co-CeOx nanoclusters have been successfully anchored on a three-dimensional nitrogen-doped graphene hydrogel （NGH） by a simple coreduction method and further used as efficient catalysts to catalytic hydrolysis of ammonia borane at room temperature. Thanks to the strong synergistic electronic effect between Co and CeOx, as well as the strong metal-support interaction between Co-CeOx and 3D NGH, the as-synthesized Co-（CeOx）0.91/NGH catalyst exhibits superior catalytic activity toward hydrolysis of ammonia borane, with the turnover frequency （TOF） value of 79.5 min 1, which is almost 13 times higher than that of Co]NGH, and higher than most of the reported noble-metal-free catalysts.展开更多
Ultrafine Ru nanoparticles are successfully deposited on MCM-41 by using a simple liquid impregnation- reduction method, and further investigated for catalytic hydrolysis of ammonia borane and methylamine borane. Amon...Ultrafine Ru nanoparticles are successfully deposited on MCM-41 by using a simple liquid impregnation- reduction method, and further investigated for catalytic hydrolysis of ammonia borane and methylamine borane. Among all the catalysts tested, 1.12wt% Ru/MCM-41 exhibits the highest catalytic activity, with turnover frequency value of 288 min^-1展开更多
The complex model of Thermus thermophilus xylose isomerase （TtXI） with D-xylose was constructed, and molecular dynamics （MD） simulations were carried out at 300 and 360 K for 10 ns by NAMD2.5. The radius of gyrati...The complex model of Thermus thermophilus xylose isomerase （TtXI） with D-xylose was constructed, and molecular dynamics （MD） simulations were carried out at 300 and 360 K for 10 ns by NAMD2.5. The radius of gyration （Rg）, subunit interactions, and residue flexibility were analyzed. The results show that residues 60-69, 142-148, 169-172, and 332-340 have high flexibility at 300 and 360 K. Residues with higher flexibility at 360 K than that at 300 K can mainly be divided into two groups： one locates in the helix-loophelix region consisting of residues 55-80 in catalytic domain; the other at subunit interfaces. The Rg of catalytic domain at 360 K shows 0.16 A higher than that at 300 K, but Rg of small C-terminal domain has no obvious difference. The results indicate that enhanced Rg of catalytic domain may lead to the intense motion of the active site of TtXI and promote the D-xylose isomization reaction. Eight hydrogen bonds and five ion pairs are reduced at subunit interfaces at 360 K compared with 300 K, that may be the main reason for the decrease in rigidity and increase in activity at high temperature of TtXI. This result also help to explain the cold-adaption phenomenon of TtXI E372G mutant reported previously. Our results reveal the relationship between temperature and structure flexibility of TtXI, and play an important role in understanding the thermostability of thermophile protein with multiple subunits.展开更多
文摘BACKGROUND Esophageal cancer(EC)is an aggressive malignancy with low survival(10%-30%).Nutritional problems are present throughout the perioperative period and are key to prognosis.Home enteral nutrition appears to improve the nutritional status of patients with EC.Few studies have addressed the experience of patients administering their own nutritional fluids and managing their own feeding tubes at home.The aim of this study was to explore the real-life experience of self-management of feeding tubes in patients at home after EC surgery in the first 3 months after discharge following surgery.AIM To explore feeding tube self-management experience of patients at home 3 months after discharge following EC surgery.METHODS Face-to-face semi-structured interviews were conducted with 18 patients using a feeding tube at home after EC surgery.Thematic analysis of the recordings identified themes related to feeding tube self-management.RESULTS Patients expressed similar feelings about their tube management experiences concerning three contextualized themes:Self-management dilemmas,distressing experiences,and self-management facilitators.CONCLUSION There are many dilemmas and problems in self-managing feeding tubes in postoperative homebound patients with EC.Clinical staff should provide guidance to promote a positive change in self-management behavior.
基金financially supported by the National Natural Science Foundation of China (No. 21571145)Large-scale Instrument and Equipment Sharing Foundation of Wuhan University
文摘Searching for highly efficient catalysts toward dehydrogenation of hydrazine for chemical hydrogen storage is highly desirable for the development of hydrogen economy. Herein, we report a simple in situ co-reduction synthesis of NiPt nanoparticles supported on CeO_2 nanospheres and their superior catalytic performance for hydrogen generation from alkaline solution of hydrazine at room temperature. Thanks to the strong electronic interaction arising from synergistic effect at atomic lever and support-metal interaction between NiPt and CeO_2.The obtained Ni_5Pt_5-CeO_2 catalyst exhibits 100% hydrogen selectivity and superior catalytic performance for hydrogen generation from alkaline solution of hydrazine at room temperature, with a TOF value of 416 h 1.
基金partial financial support from NSFC(51372173,51002107,and21173159)NSFC for Distinguished Young Scholars(51025207)+3 种基金Research Climb Plan of ZJED(pd2013383)Opening Project of State Key Laboratory of High Performance Ceramics and Superfine Microstructure(SKL201409SIC)Xinmiao talent project of Zhejiang Province(2013R424060)College Students Research Project of Wenzhou University(14xk193)
文摘As BiVO4 is one of the most popular visible-light-responding photocatalysts, it has been widely used for visiblelight-driven water splitting and environmental purification. However, the typical photocatalytic activity of unmodified BiVO4 for the degradation of organic pollutants is still not impressive. To address this limitation, we studied Fe2O3-modified porous BiVO4 nanoplates. Compared with unmodified BiVO4, the Fe2O3-modified porous Bi VO4 nanoplates showed significantly enhanced photocatalytic activities in decomposing both dye and colorless pollutant models, such as rhodamine B(Rh B) and phenol,respectively. The pseudo-first-order reaction rate constants for the degradation of RhB and phenol on Fe2O3-modified BiVO4 porous nanoplates are 27 and 31 times larger than that of pristine Bi VO4, respectively. We also found that the Fe2O3 may act as an efficient non-precious metal co-catalyst, which is responsible for the excellent photocatalytic activity of Fe2O3/BiVO4.Graphical Abstract Fe2O3, as a cheap and efficient co-catalyst, could greatly enhance the photocatalytic activity of Bi VO4 porous nanoplates in decomposing organic pollutants.
基金financially supported by the National Natural Science Foundation of China (No. 21571145)Large-scale Instrument and Equipment Sharing Foundation of Wuhan University
文摘The development of highly active noble-metal-flee catalysts for catalytic hydrolysis of ammonia borane is mandatory for its application in hydrogen storage. Herein, Co-CeOx nanoclusters have been successfully anchored on a three-dimensional nitrogen-doped graphene hydrogel （NGH） by a simple coreduction method and further used as efficient catalysts to catalytic hydrolysis of ammonia borane at room temperature. Thanks to the strong synergistic electronic effect between Co and CeOx, as well as the strong metal-support interaction between Co-CeOx and 3D NGH, the as-synthesized Co-（CeOx）0.91/NGH catalyst exhibits superior catalytic activity toward hydrolysis of ammonia borane, with the turnover frequency （TOF） value of 79.5 min 1, which is almost 13 times higher than that of Co]NGH, and higher than most of the reported noble-metal-free catalysts.
基金financially supported by the National Natural Science Foundation of China(No.21201134)the Natural Science Foundation of Jiangsu Province(No.BK20130370)+1 种基金the Natural Science Foundation of Hubei Province(No.2013CFB288)Large-scale Instrument and Equipment Sharing Foundation of Wuhan University
文摘Ultrafine Ru nanoparticles are successfully deposited on MCM-41 by using a simple liquid impregnation- reduction method, and further investigated for catalytic hydrolysis of ammonia borane and methylamine borane. Among all the catalysts tested, 1.12wt% Ru/MCM-41 exhibits the highest catalytic activity, with turnover frequency value of 288 min^-1
基金This work was supported by the National Natural Science Foundation of China （No.20336010） and the State Key Basic Research and Development Plan of China （No.2003CB716000）.
文摘The complex model of Thermus thermophilus xylose isomerase （TtXI） with D-xylose was constructed, and molecular dynamics （MD） simulations were carried out at 300 and 360 K for 10 ns by NAMD2.5. The radius of gyration （Rg）, subunit interactions, and residue flexibility were analyzed. The results show that residues 60-69, 142-148, 169-172, and 332-340 have high flexibility at 300 and 360 K. Residues with higher flexibility at 360 K than that at 300 K can mainly be divided into two groups： one locates in the helix-loophelix region consisting of residues 55-80 in catalytic domain; the other at subunit interfaces. The Rg of catalytic domain at 360 K shows 0.16 A higher than that at 300 K, but Rg of small C-terminal domain has no obvious difference. The results indicate that enhanced Rg of catalytic domain may lead to the intense motion of the active site of TtXI and promote the D-xylose isomization reaction. Eight hydrogen bonds and five ion pairs are reduced at subunit interfaces at 360 K compared with 300 K, that may be the main reason for the decrease in rigidity and increase in activity at high temperature of TtXI. This result also help to explain the cold-adaption phenomenon of TtXI E372G mutant reported previously. Our results reveal the relationship between temperature and structure flexibility of TtXI, and play an important role in understanding the thermostability of thermophile protein with multiple subunits.
