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Ca-P仿生人工骨材料的设计与制备 被引量:1
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作者 王欣宇 韩颖超 《陶瓷学报》 CAS 2003年第2期107-110,共4页
本文设计了用磷酸钙生物陶瓷制备仿生人工骨的工艺路线 ,从原料合成。
关键词 Ca—p仿生人工材料 设计 制备 磷酸钙生物陶瓷 原料合成 材料成型 烧结
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新短肽P17-骨形态发生蛋白2/胶原基质矿化磷灰石材料生物活性的评价
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作者 张雪 张扬 崔福斋 《中国组织工程研究》 CAS 北大核心 2020年第22期3547-3552,共6页
背景:胶原基质矿化磷灰石材料具有仿生的化学组成及良好的生物学性能,已被用于某些骨缺损修复;新短肽P17-骨形态发生蛋白2具有良好的生物相容性和成骨诱导生物活性,因此将新短肽P17-骨形态发生蛋白2与胶原基质矿化磷灰石材料制备成复合... 背景:胶原基质矿化磷灰石材料具有仿生的化学组成及良好的生物学性能,已被用于某些骨缺损修复;新短肽P17-骨形态发生蛋白2具有良好的生物相容性和成骨诱导生物活性,因此将新短肽P17-骨形态发生蛋白2与胶原基质矿化磷灰石材料制备成复合支架材料可望提升骨修复效率和效果。目的:探讨新型P17-骨形态发生蛋白2/胶原基质矿化磷灰石复合材料的生物活性。方法:将兔骨髓间充质干细胞分别接种于新型P17-骨形态发生蛋白2/胶原基质矿化磷灰石复合材料与胶原基质矿化磷灰石材料上,培养3,7 d后,利用RT-PCR检测细胞碱性磷酸酶mRNA相对表达。将新型P17-骨形态发生蛋白2/胶原基质矿化磷灰石复合材料(实验组)与胶原基质矿化磷灰石材料(对照组)分别埋置于SD大鼠皮下,植入12,35 d后进行Masson染色后组织学分析。将新型P17-骨形态发生蛋白2/胶原基质矿化磷灰石复合材料(实验组)与胶原基质矿化磷灰石材料(对照组)分别植入日本大耳白兔下颌骨箱状缺损处,植入5,15周后进行大体与X射线检查。实验经中国医科大学附属口腔医院伦理委员会批准。结果与结论:①复合材料组培养7 d的碱性磷酸酶mRNA表达高于胶原基质矿化磷灰石组(P<0.05);②皮下埋植实验显示两组材料和组织界面均未引起明显的急性炎症反应,植入后35d实验组可见更多的纤维细胞与材料嵌合;③骨缺损修复实验中,大体观察显示两种材料均具有良好的骨修复能力,植入5周时缺损区已有缩小趋势,植入15周缺损表面比较平整;X射线检查显示与对照组相比,实验组缺损区缩小趋势更明显;④结果表明,新型P17-骨形态发生蛋白2/胶原基质矿化磷灰石复合支架材料具有比胶原基质矿化磷灰石更为优良的生物活性与骨缺损修复能力。 展开更多
关键词 胶原基质矿化磷灰石 髓间充质干细胞 p17-形态发生蛋白2 诱导分化 再生 组织工程 生物相容性 缺损
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筋骨力防治去势大鼠骨质疏松的研究
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作者 程丽芳 刘涛 +2 位作者 张玉芝 刘瑾 张维东 《中药药理与临床》 CAS CSCD 2000年第3期29-30,共2页
目的 :研究筋骨力对切除卵巢大鼠所造成骨质疏松的影响。方法 :用卵巢摘除方法 ,以己烯雌酚、钙尔奇D作为阳性对照 ,观察了筋骨力对骨质疏松大鼠子宫重量、骨Ca、骨P的含量及骨组织形态的改变。结果 :筋骨力可明显增加去卵巢大鼠子宫重... 目的 :研究筋骨力对切除卵巢大鼠所造成骨质疏松的影响。方法 :用卵巢摘除方法 ,以己烯雌酚、钙尔奇D作为阳性对照 ,观察了筋骨力对骨质疏松大鼠子宫重量、骨Ca、骨P的含量及骨组织形态的改变。结果 :筋骨力可明显增加去卵巢大鼠子宫重量 ,增加骨Ca含量 ,对股骨骨小梁宽度、面积及皮质骨厚度、面积均具有明显改善作用。结论 :筋骨力具有显著的防治骨质疏松作用。 展开更多
关键词 卵巢切除术 质疏松 Ca 骨p 组织形态计量学
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温针治疗肱骨外上髁炎 被引量:1
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作者 崔向华 《中国中医药咨讯》 2010年第36期282-282,共1页
目的:寻找治疗肱骨外上髁炎的有效办法;方法:用温针灸治疗肱骨外上髁炎68例;结果:用温针治疗肱骨外上髁炎有效率100%;结论:用温针灸治疗肱骨外上髁炎效果明显。
关键词 温针 p2外上髁炎 针刺疗法
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A MOF derived hierarchically porous 3D N‐CoP_(x)/Ni_(2)P electrode for accelerating hydrogen evolution at high current densities 被引量:1
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作者 Lan Wang Ning gong +5 位作者 Zhou Zhou Qicheng Zhang Wenchao Peng Yang Li Fengbao Zhang Xiaobin Fan 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第4期1176-1183,共8页
Hydrogen evolution reaction is a critical reaction in water splitting for hydrogen production.However,developing effective and stable non‐noble‐metal electrocatalysts which work well at high current densities demand... Hydrogen evolution reaction is a critical reaction in water splitting for hydrogen production.However,developing effective and stable non‐noble‐metal electrocatalysts which work well at high current densities demanded by industry still remain great challenge.Herein,taking advantage of the highly tunable metal‐organic framework(MOF)templates,nitrogen doped binary transition metal phosphides electrocatalysts(N‐CoP_(x)/Ni_(2)P)with three‐dimensional(3D)conductive network structure were successfully synthesized.The 3D open porous channels could expose more catalytically active sites;nitrogen doping and the synergistic effect between CoP and Ni_(2)P can increase the electron density of Co atoms at active sites,further optimizing the Gibbs free energy of hydrogen(ΔGH*)and water(ΔG_(H_(2)O*)).As a result,the obtained N‐CoP_(x)/Ni_(2)P catalyst exhibits extraordinary electrocatalytic activity in a wide pH range.Especially,it requires an extremely low overpotential of 152 mV to deliver a high current density of 650 mA cm^(–2) in alkaline media.This work may shed some light on the rational design of cheap electrocatalysts and electrode materials that work well at high current densities. 展开更多
关键词 Hydrogen evolution reaction MOF templates N‐Cop_(x)/Ni_(2)p Three‐dimensional conductive network High current density
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Substance P stimulates differentiation of mice osteoblast through up-regulating Osterix expression 被引量:4
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作者 孙海飚 陈君长 +2 位作者 刘强 郭敏锋 张华平 《Chinese Journal of Traumatology》 CAS 2010年第1期46-50,共5页
Objective: To investigate the molecular pathway of substance P (SP) to induce osteoblastic differentiation. Methods: Mesenchymal stem cells were isolated and cultured. The cultures were divided into four groups w... Objective: To investigate the molecular pathway of substance P (SP) to induce osteoblastic differentiation. Methods: Mesenchymal stem cells were isolated and cultured. The cultures were divided into four groups with Group A (control group) cultured without any factors, Group B cultured with SP, Group C cultured with SP and SP receptor neurokinin-1 (NK1) antagonist, and Group D cultured with SP NK1 antagonist respectively to induce osteoblastic cells differentiation. Osterix gene expression was detected by reverse transcription-polymerase chain reaction (RT-PCR) for three times after 1-2 weeks of cultivation and the results were analyzed by one-way analysis of variance (ANOVA). Results: The log phase of bone marrow stromal cells appeared at 4-6 days. ALP staining revealed that the majority of cells, more than 95%, were positive and small bluepurple granules were found in the cytoplasm. And Group B, treated with SP, showed a higher level of ALP activity than the other three groups. Meanwhile, RT-PCR found that Osterix expression in Group B was obviously up-regulated, compared with other groups. But Osterix expression in Group D had no remarkable differences, compared with the controls. Conclusions: SP can up-regulate Osterix gene expression to stimulate differentiation of mesenchymal stem cells into osteoblastic cells at the final stage. The regulatory effect of SP on Osterix expression was dependant on SP NK1 receptors. 展开更多
关键词 Substance p OSTEOBLASTS Osterix protein rat Runx2 protein rat Cell differentiation
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