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Antimicrobial Expanded Polytetrafluoroethylene Film Prepared by 3-ray Radiation Induced Grafting of Poly(acrylic acid) 被引量:4
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作者 王运龙 汪谟贞 +2 位作者 吴启超 周晓 葛学武 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2015年第1期107-112,I0002,共7页
The simultaneous γ-ray-radiation-induced grafting polymerization of acrylic acid on ex- panded polytetrafluoroethylene (ePTFE) film was investigated. It was found that the degree of grafting (DG) of poly(acrylic... The simultaneous γ-ray-radiation-induced grafting polymerization of acrylic acid on ex- panded polytetrafluoroethylene (ePTFE) film was investigated. It was found that the degree of grafting (DG) of poly(acrylic acid) (PAA) can be controlled by the monomer concentration, absorbed dose, and dose rate under an optimal inhibitor concentration of [Fe2+]=18 mmol/L. SEM observation showed that the macroporous structure in ePTFE films would be covered gradually with the increase of the DG of PAA. The prepared ePTFE-g-PAA film was im- mersed in a neutral silver nitrate solution to fabricate an ePTFE-g-PAA/Ag hybrid film after the addition of NaBH4 as a reduction agent of Ag+ to Ag atom. SEM, XRD, and XPS results proved that Ag nanoparticles with a size of several tens of nanometers to 100 nanometers were in situ immobilized on ePTFE film. The loading capacity of Ag nanoparticles could be tuned by the DG of PAA, and determined by thermal gravimetric analysis. The quart- titative antibacterial activity of the obtained ePTFE-g-PAA/Ag hybrid films was measured using counting plate method. It can kill all the Escherichia coli in the suspension in 1 h. Moreover, this excellent antibacterial activity can last at least for 4 h. This work provides a facile and practical way to make ePTFE meet the demanding antimicrobial requirement in more and more practical application areas. 展开更多
关键词 Expanded polytetrafluoroethylene film Radiation grafting Poly(acrylic acid) Silver nanoparticles Antibacterial property
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Magnetic Nano-Amorphous-Iron-Oxide-Based Drug Delivery System with Dual Therapeutic Mechanisms
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作者 Shan Lei Li-an Wang +3 位作者 Fu-xing Lin Kun Zeng Mo-zhen Wang Xue-wu Ge 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2020年第3期376-384,I0003,共10页
Smart nanoparticles that respond to pathophysiological parameters,such as p H,GSH,and H2O2,have been developed with the huge and urgent demand for the high-efficient drug delivery systems(DDS)for cancer therapy.Herein... Smart nanoparticles that respond to pathophysiological parameters,such as p H,GSH,and H2O2,have been developed with the huge and urgent demand for the high-efficient drug delivery systems(DDS)for cancer therapy.Herein,cubic poly(ethylene glycol)(PEG)-modified mesoporous amorphous iron oxide(AFe)nanoparticles(AFe-PEG)have been successfully prepared as p H-stimulated drug carriers,which can combine doxorubicin(DOX)with a high loading capacity of 948 mg/g,forming a novel multifunctional AFe-PEG/DOX nanoparticulate DDS.In an acidic microenvironment,the AFe-PEG/DOX nanoparticles will not only release DOX efficiently,but also release Fe ions to catalyze the transformation of H2O2 to·OH,acting as fenton reagents.In vitro experimental results proved that the AFe-PEG/DOX nanoparticles can achieve combination of chemotherapeutic(CTT)and chemodynamic therapeutic(CDT)effects on Hela tumor cells.Furthermore,the intrinsic magnetism of AFePEG/DOX makes its cellular internalization efficiency be improved under an external magnetic field.Therefore,this work develops a new and promising magnetically targeted delivery and dual CTT/CDT therapeutic nano-medicine platform based on amorphous iron oxide. 展开更多
关键词 Cubic amorphous iron oxide nanoparticles p H-responsive CHEMOTHERAPY Chemodynamic therapy Magnetically targeted delivery
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多重响应性超支化星形聚合物的合成与组装以及控制释放研究 被引量:9
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作者 张文建 范溦 +2 位作者 李敏 洪春雁 潘才元 《化学学报》 SCIE CAS CSCD 北大核心 2012年第16期1690-1696,共7页
含二硫键的自引发单体与2-(2-甲氧基乙氧基)乙基甲基丙烯酸酯(MEO2MA)进行自缩合乙烯基共聚合得到超支化PMEO2MA(H-PMEO2MA).以它作大分子引发剂,引发二甲氨基乙基甲基丙烯酸酯(DMAEMA)进行原子转移自由基聚合,合成了具有温度、pH以及... 含二硫键的自引发单体与2-(2-甲氧基乙氧基)乙基甲基丙烯酸酯(MEO2MA)进行自缩合乙烯基共聚合得到超支化PMEO2MA(H-PMEO2MA).以它作大分子引发剂,引发二甲氨基乙基甲基丙烯酸酯(DMAEMA)进行原子转移自由基聚合,合成了具有温度、pH以及氧化还原多重响应性的超支化星形聚合物H-PMEO2MA-star-PDMAEMA.证明了H-PMEO2MA有低临界溶液温度(LCST);研究了PDMAEMA链段的长度和溶液的pH值对超支化星形聚合物的LCST的影响.当H-PMEO2MA-star-PDMAEMA水溶液温度从2℃升高至室温,H-PMEO2MA变成疏水性而发生聚集,形成以H-PMEO2MA为核,PDMAEMA为壳的胶束.在胶束形成过程中,将尼罗红装载到这种聚合物胶束中,形成释药系统,研究了pH、氧化还原响应性释药性能. 展开更多
关键词 自缩合乙烯基聚合 原子转移自由基聚合 超支化星形聚合物 多重响应性 控制释放
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网络结构对多层聚乙烯共混物界面扩散行为的影响 被引量:4
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作者 李文林 牛艳华 +1 位作者 王志刚 张军 《高分子学报》 SCIE CAS CSCD 北大核心 2012年第9期1007-1014,共8页
通过溶液法制备超高分子量聚乙烯(UHMWPE)/乙烯-己烯共聚物(PEH)共混物,采用动态流变学方法研究了UHMWPE/PEH共混物多层膜在熔点以上的界面扩散行为,结合Double-Reptation理论计算得到了UHMWPE/PEH共混物多层膜的自扩散系数.研究表明UHM... 通过溶液法制备超高分子量聚乙烯(UHMWPE)/乙烯-己烯共聚物(PEH)共混物,采用动态流变学方法研究了UHMWPE/PEH共混物多层膜在熔点以上的界面扩散行为,结合Double-Reptation理论计算得到了UHMWPE/PEH共混物多层膜的自扩散系数.研究表明UHMWPE在浓度c=1.0 wt%以上可以在PEH基体中形成网络结构.UHMWPE/PEH共混物多层膜界面扩散不符合严格的菲克扩散定律,扩散系数具有时间依赖性.扩散曲线显示扩散过程在到达平台值之前分为2个区域,区域I接近于菲克扩散;然而由于引入UHMWPE,区域II扩散显著偏离菲克扩散行为,特别是当UHMWPE在PEH基体中形成网络结构以后,偏离菲克扩散行为更加显著. 展开更多
关键词 聚乙烯共混物 网络结构 界面扩散 流变学
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