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Adhesive cryogel particles for bridging confined and irregular tissue defects
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作者 Yao-Ting Xue Ming-Yu Chen +14 位作者 Jia-Sheng Cao Lei Wang Jia-Hao Hu Si-yang Li Ji-Liang Shen Xin-Ge Li Kai-Hang Zhang Shu-Qiang Hao Sarun Juengpanich Si-Bo Cheng Tuck-Whye Wong xu-xu yang Tie-Feng Li Xiu-Jun Cai Wei yang 《Military Medical Research》 SCIE CAS CSCD 2023年第6期763-777,共15页
Background Reconstruction of damaged tissues requires both surface hemostasis and tissue bridging.Tissues with damage resulting from physical trauma or surgical treatments may have arbitrary surface topographies,makin... Background Reconstruction of damaged tissues requires both surface hemostasis and tissue bridging.Tissues with damage resulting from physical trauma or surgical treatments may have arbitrary surface topographies,making tissue bridging challenging.Methods This study proposes a tissue adhesive in the form of adhesive cryogel particles(ACPs) made from chitosan,acrylic acid,1-ethyl-3-(3-dimethylaminopropyl) carbodiimide(EDC) and N-hydroxysuccinimide(NHS).The adhesion performance was examined by the 180-degree peel test to a collection of tissues including porcine heart,intestine,liver,muscle,and stomach.Cytotoxicity of ACPs was evaluated by cell proliferation of human normal liver cells(LO2)and human intestinal epithelial cells(Caco-2).The degree of inflammation and biodegradability were examined in dorsal subcutaneous rat models.The ability of ACPs to bridge irregular tissue defects was assessed using porcine heart,liver,and kidney as the ex vivo models.Furthermore,a model of repairing liver rupture in rats and an intestinal anastomosis in rabbits were established to verify the effectiveness,biocompatibility,and applicability in clinical surgery.Results ACPs are applicable to confined and irregular tissue defects,such as deep herringbone grooves in the parenchyma organs and annular sections in the cavernous organs.ACPs formed tough adhesion between tissues[(670.9±50.1) J/m^(2) for the heart,(607.6±30.0) J/m^(2) for the intestine,(473.7±37.0) J/m^(2) for the liver,(186.1±13.3) J/m^(2) for the muscle,and(579.3±32.3) J/m^(2) for the stomach].ACPs showed considerable cytocompatibility in vitro study,with a high level of cell viability for 3 d[(98.8±1.2)%for LO2 and(98.3±1.6)%for Caco-2].It has comparable inflammation repair in a ruptured rat liver(P=0.58 compared with suture closure),the same with intestinal anastomosis in rabbits(P=0.40 compared with suture anastomosis).Additionally,ACP-based intestinal anastomosis(less than 30 s) was remarkably faster than the conventional suturing process(more than 10 min).When ACPs degrade after surgery,the tissues heal across the adhesion interface.Conclusions ACPs are promising as the adhesive for clinical operations and battlefield rescue,with the capability to bridge irregular tissue defects rapidly. 展开更多
关键词 Tissue reconstruction Wet adhesion Adhesive hydrogel BIOADHESIVE
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Mono-top signature from stop decay at the HE-LHC
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作者 xu-xu yang Hang Zhou +1 位作者 Tian-Peng Tang Ning Liu 《Communications in Theoretical Physics》 SCIE CAS CSCD 2021年第2期82-88,共7页
Searching for the top squark(stop)is a key task to test the naturalness of SUSY.Different from stop pair production,single stop production relies on its electroweak properties and can provide some unique signatures.Fo... Searching for the top squark(stop)is a key task to test the naturalness of SUSY.Different from stop pair production,single stop production relies on its electroweak properties and can provide some unique signatures.Following the single production process pp→t^(~)1X(~)1→tX^(~)1^(0)X^(~)1^(-),the top quark has two decay channels:leptonic channel and hadronic channel.In this paper,we probe the observability of these two channels in a simplified minimal supersymmetric standard model scenario.We find that,at the 27 TeV LHC with the integrated luminosity of L=15 ab^(-1),mt^(-)1<1900 GeV andμ<750 GeV can be excluded at 2σthrough the leptonic mono-top channel,while m_(t^(-)1)<1200 GeV andμ<350 GeV can be excluded at 2σthrough the hadronic channel. 展开更多
关键词 top squark mono-top signature HE-LHC
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