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钛表面双层纳米管制备及生物活性的测定
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作者 孙磊 夏荣 +3 位作者 徐基亮 胡小晔 刘春 孙子环 《安徽医科大学学报》 CAS 北大核心 2014年第10期1492-1495,共4页
采用电化学两步阳极氧化法在钛表面制备纳米管,光滑纯钛作为对照组,通过场发射电镜、X射线能量色散谱和原子力显微镜观察分析试件表面微观形貌、元素组成和三维形貌并计算粗糙度。体外培养小鼠骨髓间质干细胞(BMSCs)进行生物活性的测定... 采用电化学两步阳极氧化法在钛表面制备纳米管,光滑纯钛作为对照组,通过场发射电镜、X射线能量色散谱和原子力显微镜观察分析试件表面微观形貌、元素组成和三维形貌并计算粗糙度。体外培养小鼠骨髓间质干细胞(BMSCs)进行生物活性的测定。结果显示在钛表面制备出有序的双层蜂窝状二氧化钛纳米管阵列,纳米管的表面由钛和氧元素组成,纳米管组粗糙度值大于光滑组,两组间比较差异有统计学意义(P<0.05),纳米管组试件促进了BMSCs的黏附、增殖和分化。 展开更多
关键词 阳极氧化 纳米管 骨髓间质干细胞 生物活性
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纯钛表面加载RGD多肽的体外实验研究 被引量:3
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作者 徐基亮 夏荣 +3 位作者 孙磊 胡小晔 刘春 孙子环 《安徽医科大学学报》 CAS 北大核心 2014年第11期1591-1595,共5页
目的探讨纯钛表面加载RGD多肽进行生物功能化修饰的可行性。方法借助电化学和分子自组装技术在纯钛表面构建TiO2纳米管-聚多巴胺-RGD多肽活性层,采用场发射扫描电镜(FESEM)、X射线光电子能谱(XPS)对各组钛片进行表面形貌和元素组成分析... 目的探讨纯钛表面加载RGD多肽进行生物功能化修饰的可行性。方法借助电化学和分子自组装技术在纯钛表面构建TiO2纳米管-聚多巴胺-RGD多肽活性层,采用场发射扫描电镜(FESEM)、X射线光电子能谱(XPS)对各组钛片进行表面形貌和元素组成分析。培养小鼠骨髓基质干细胞(BMSCs),对处理前后的钛片进行体外生物活性评价。结果 SEM和XPS显示,两步阳极氧化后在纯钛表面形成蜂窝多孔的TiO2纳米管,多巴胺在TiO2纳米管上自聚合成聚多巴胺涂层,同时向外接枝偶联RGD多肽,最终在纯钛表面成功形成了TiO2纳米管-聚多巴胺-RGD多肽活性层,体外细胞培养显示,该活性层有利于细胞黏附、增殖和分化。结论 RGD多肽功能化修饰的钛片有良好的生物相容性,这种钛表面功能化修饰法可望用于改善钛种植体,提高骨结合。 展开更多
关键词 TIO2纳米管 RGD多肽 多巴胺 骨髓基质干细胞
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二氧化钛纳米管阵列加载重组人骨形成蛋白2的体外生物活性研究 被引量:2
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作者 孙子环 夏荣 +3 位作者 孙磊 胡小晔 闵曦 徐基亮 《中华口腔医学杂志》 CAS CSCD 北大核心 2015年第8期478-482,共5页
目的 探讨二氧化钛纳米管阵列加载重组人骨形成蛋白2 (recombinant human bone morphogenetic protein-2,rhBMP-2)对小鼠骨髓间充质干细胞(bone mesenchymal stem cell,BMSC)早期活性的影响,为钛种植体表面生物化学改性提供实验依据... 目的 探讨二氧化钛纳米管阵列加载重组人骨形成蛋白2 (recombinant human bone morphogenetic protein-2,rhBMP-2)对小鼠骨髓间充质干细胞(bone mesenchymal stem cell,BMSC)早期活性的影响,为钛种植体表面生物化学改性提供实验依据.方法 利用阳极氧化技术在纯钛片表面制备双层二氧化钛纳米管阵列,化学接枝rhBMP-2(实验组),以机械抛光的纯钛为空白对照组,阴性对照A组为二氧化钛纳米管组、阴性对照B组为二氧化钛纳米管+羰基二咪唑组.用场发射扫描电镜观察各组形貌并用X射线光电子能谱仪检测各组元素.各组试件与BMSC共培养,检测第1天各组细胞黏附铺展情况(每组样本量为3),第1、3、5天各组细胞增殖A值及第5、7、11天各组碱性磷酸酶活性(每组每个时间点样本量为3).结果 场发射扫描电镜示实验组表面可见粟粒状颗粒物,X射线光电子能谱仪示实验组氮峰明显增高.场发射扫描电镜示第1天实验组细胞黏附铺展良好,细胞间连接广泛而紧密,均优于其他3组.第1天各组细胞增殖效果不明显;第3、5天实验组A值(3.295±0.153、3.823±0.059)均显著高于空白对照组(2.479±0.064、3.131±0.096)、阴性对照A组(2.715±0.075、3.371±0.047)及阴性对照B组(2.756±0.132、3.637±0.047) (P<0.05);第5、7、11天实验组碱性磷酸酶活性(0.0477±0.0287、0.0615±0.0016、0.0667±0.0018)均显著高于其他3组(P<0.05).结论 二氧化钛纳米管阵列可通过生物化学法加载rhBMP-2并具备良好的生物相容性. 展开更多
关键词 纳米管 间质干细胞 骨形成蛋白
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Highly Efficient and Selective Removal of Pb(II) ions by Sulfur-Containing Calcium Phosphate Nanoparticles 被引量:1
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作者 龚成云 耿志刚 +3 位作者 董安乐 叶新新 汪国忠 张云霞 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2016年第5期607-616,I0002,共11页
A facile one-step co-precipitation method was demonstrated to fabricate amorphous sulfurcontaining calcium phosphate (SCP) nanoparticles, in which the sulfur group was in-situ introduced into calcium phosphate. The ... A facile one-step co-precipitation method was demonstrated to fabricate amorphous sulfurcontaining calcium phosphate (SCP) nanoparticles, in which the sulfur group was in-situ introduced into calcium phosphate. The resulting SCP exhibited a noticeable enhanced performance for Pb(II) removal in comparison with hydroxyapatite (HAP), being capable of easily reducing 20 ppm of Pb(II) to below the acceptable standard for drinking water within less than 10 min. Remarkably, the saturated removal capacities of Pb(II) on SCP were as high as 1720.57 mg/g calculated by the Langmuir isotherm model, exceeding largely that of the previously reported absorbents. Significantly, SCP displayed highly selective removal ability toward Pb(II) ions in the presence of the competing metal ions (Ni(II), Co(II), Zn(II), and Cd(II)). Further investigations indicated that such ultra-high removal efficiency and preferable affinity of Pb(II) ions on SCP may be reasonably ascribed to the formation of rodlike hydroxypyromorphite crystals on the surface of SCP via dissolution-precipitation and ion exchange reactions, accompanied by the presence of lead sulfide precipitates. High removal efficiency, fast removal kinetics and excellent selectivity toward Pb(II) made the obtained SCP material an ideal candidate for Pb(II) ions decontamination in practical application. 展开更多
关键词 Sulfur-containing calcium phosphate Pb(II) ions Selective removal
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NH_(2)-MIL-53(Al)for Simultaneous Removal and Detection of Fluoride Anions
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作者 Dong-hua Xie Xiao Ge +1 位作者 Wen-xiu Qin Yun-xia Zhang 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2021年第2期227-237,I0002,I0003-I0010,共20页
To address the limitations of the separate fluoride removal or detection in the existing materials,herein,amino-decorated metal organic frameworks NH_(2)-MIL-53(Al)have been succinctly fabricated by a sol-hydrothermal... To address the limitations of the separate fluoride removal or detection in the existing materials,herein,amino-decorated metal organic frameworks NH_(2)-MIL-53(Al)have been succinctly fabricated by a sol-hydrothermal method for simultaneous removal and determination of fluoride.As a consequence,the proposed NH_(2)-MIL-53(Al)features high uptake capacity(202.5 mg/g)as well as fast adsorption rate,being capable of treating 5 ppm of fluoride solution to below the permitted threshold in drinking water within 15 min.Specifically,the specific binding between fluoride and NH_(2)-MIL-53(Al)results in the release of fluorescent ligand NH2-BDC,conducive to the determination of fluoride via a concentration-dependent fluorescence enhancement effect.As expected,the resulting NH_(2)-MIL-53(Al)sensor exhibits selective and sensitive detection(with the detection limit of 0.31μmol/L)toward fluoride accompanied with a wide response interval(0.5-100μmol/L).More importantly,the developed sensor can be utilized for fluoride detection in practical water systems with satisfying recoveries from 89.6% to 116.1%,confirming its feasibility in monitoring the practical fluoride-contaminated waters. 展开更多
关键词 NH_(2)-MIL-53(Al) FLUORIDE REMOVAL DETECTION
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