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软骨生物材料

软骨生物材料的相关文献在2014年到2020年内共计118篇,主要集中在基础医学、临床医学 等领域,其中期刊论文118篇、专利文献947077篇;相关期刊2种,包括中国组织工程研究、中国组织工程研究等; 软骨生物材料的相关文献由397位作者贡献,包括郭全义、陈伟、刘丰等。

软骨生物材料—发文量

期刊论文>

论文:118 占比:0.01%

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论文:947077 占比:99.99%

总计:947195篇

软骨生物材料—发文趋势图

软骨生物材料

-研究学者

  • 郭全义
  • 陈伟
  • 刘丰
  • 周建林
  • 周观金
  • 张永红
  • 方洪松
  • 杨建华
  • 翁金清
  • 袁琨

软骨生物材料

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    • 邱皓; 陈诗谋; 翁政; 朱云; 刘盾; 陈渝
    • 摘要: 背景:研究显示富血小板血浆具有很强的促进软骨细胞修复和增生作用.目的:探讨富血小板血浆在骨性关节炎中对软骨细胞修复及滑膜炎症抑制的疗效.方法:新西兰大白兔40只,于兔耳中央动脉取血后采用Hokugo等的方法制备富血小板血浆,同时检测外周血及富血小板血浆的血小板、血小板衍生生长因子、转化生长因子β和血管内皮生长因子水平.采用前交叉韧带切断法来制作动物模型后随机将兔分为实验组和对照组,实验组双侧膝关节每周注射1次0.3 mL富血小板血浆;对照组每周注射1次0.3 mL无菌生理盐水,共注射10周.注射后第2,4,6,8,10周对兔进行大体观察及膝关节组织学观察;检测关节软骨Ⅱ型胶原蛋白及基质金属蛋白酶13水平,并进行软骨组织Mankin评分.实验方案经重庆医科大学动物实验伦理委员会批准.结果 与结论:①富血小板血浆中血小板、血小板衍生生长因子、转化生长因子β和血管内皮生长因子水平分别是正常血中的5.5,4.8,7.7和6.2倍(均P<0.05);②注射后第6周实验组Mankin评分小于对照组(P<0.05);③实验组第4,6,8,10周时Ⅱ型胶原蛋白水平明显高于对照组(P<0.05);实验组第2,4,6,8,10周时基质金属蛋白酶13水平明显小于对照组(P<0.05);④结果表明,关节腔内注射富血小板血浆能通过缓解关节滑膜炎症及延缓甚至阻断软骨细胞的损伤来抑制骨性关节炎的进展.
    • 李文超; 许瑞江; 黄靖香; 李浩宇; 蔡刚; 陈辉
    • 摘要: 背景:骺板细胞外基质具有丰富的胶原、蛋白多糖及信号分子,其成分和特征最接近天然骺板组织,是构建织工程骺板的最理想原料之一.目的:采用骺板细胞外基质构建取向柱状仿生支架材料,并对其进行性能评估.方法:取胎牛膝关节标本,采用超湿法粉碎、差速离心及有机溶剂分离等技术联合处理获得细胞外基质微丝,利用定向结晶、冷冻干燥技术及物理/化学交联方法制备出骺板细胞外基质源性仿生柱状支架材料,扫描电镜观察支架的内部结构及孔径,检测支架的孔隙率及吸水膨胀率,同时对支架进行组织学观察.结果与结论:①苏木精-伊红染色显示,细胞外基质微丝呈纤维状,形状规则,均匀一致;甲苯胺蓝、番红O及Ⅱ型胶原免疫组织化学染色呈阳性,说明保留了天然骺板细胞外基质的有效成分;②显微镜显示支架横截面呈多孔蜂窝状结构,孔径均匀一致,形状规则,纵切面显示平行排列的柱状结构,均匀一致,孔径分布均匀,相互连通好,支架外壁纤维呈纵向取向排列,类似于天然骺板软骨的柱状分布结构.扫描电镜显示支架横切面呈多孔蜂窝状,均匀分布,形状规则,支架的横向孔径为(117.5±15.37)μm.支架孔隙率为(92.05±1.54)%,吸水膨胀率为(95.95±1.07)%;③结果表明,骺板细胞外基质源性仿生柱状组织工程支架材料在成分来源和结构特征方面均达到了模仿天然骺板软骨的特点.
    • 李文超; 许瑞江; 黄靖香; 李浩宇; 蔡刚; 陈辉
    • 摘要: 背景:骺板细胞外基质具有丰富的胶原、蛋白多糖及信号分子,其成分和特征最接近天然骺板组织,是构建织工程骺板的最理想原料之一。目的:采用骺板细胞外基质构建取向柱状仿生支架材料,并对其进行性能评估。方法:取胎牛膝关节标本,采用超湿法粉碎、差速离心及有机溶剂分离等技术联合处理获得细胞外基质微丝,利用定向结晶、冷冻干燥技术及物理/化学交联方法制备出骺板细胞外基质源性仿生柱状支架材料,扫描电镜观察支架的内部结构及孔径,检测支架的孔隙率及吸水膨胀率,同时对支架进行组织学观察。结果与结论:(1)苏木精-伊红染色显示,细胞外基质微丝呈纤维状,形状规则,均匀一致;甲苯胺蓝、番红O及Ⅱ型胶原免疫组织化学染色呈阳性,说明保留了天然骺板细胞外基质的有效成分;(2)显微镜显示支架横截面呈多孔蜂窝状结构,孔径均匀一致,形状规则,纵切面显示平行排列的柱状结构,均匀一致,孔径分布均匀,相互连通好,支架外壁纤维呈纵向取向排列,类似于天然骺板软骨的柱状分布结构。扫描电镜显示支架横切面呈多孔蜂窝状,均匀分布,形状规则,支架的横向孔径为(117.5±15.37)μm。支架孔隙率为(92.05±1.54)%,吸水膨胀率为(95.95±1.07)%;(3)结果表明,骺板细胞外基质源性仿生柱状组织工程支架材料在成分来源和结构特征方面均达到了模仿天然骺板软骨的特点。
    • 周勇; 王大平; 贾兆锋; 刘威; 朱伟民; 崔家鸣; 何勇; 陈洁琳; 王大明; 彭亮权
    • 摘要: 背景:混合技术可增强材料的热敏性、机械性能、黏弹性和结构性能,还可改善混合材料的生物降解性、生物相容性和其他生物医学性质.目的:制备聚乙烯醇/壳聚糖多孔水凝胶材料,观察其修复软骨缺损的效果.方法:在加入与不加入表面活性剂聚山梨酯80的情况下,通过冷冻-解冻循环及乳化发泡-冷冻冰晶相分离法制备不同组分的聚乙烯醇/壳聚糖多孔水凝胶材料(聚乙烯醇与壳聚糖的质量比分别为5:5、6:4、7:3、8:2及9:1),以含水率、溶胀度、热行为、力学性能及细胞相容性实验筛选聚乙烯醇与壳聚糖最佳质量比,进行动物体内实验.取18只新西兰大白兔,制作双侧膝关节软骨缺损模型,随机分3组干预,实验组缺损处植入负载骨髓间充质干细胞的聚乙烯醇/壳聚糖多孔水凝胶材料,对照组植入聚乙烯醇/壳聚糖水凝胶,空白对照组未植入任何材料,植入12周后,组织学观察修复效果.结果与结论:①成功制备了聚乙烯醇/壳聚糖多孔复合水凝胶,以加入聚山梨酯80、聚乙烯醇与壳聚糖质量比为6:4的水凝胶含水量≥90%,力学性能良好,理化性能稳定,孔隙率≥90%,内部疏松多孔的网状结构更利于细胞生长增殖,具有良好细胞相容性,选择其进行动物体内植入实验.②空白对照组软骨缺陷完全没有再生,表面只有一层薄薄的纤维覆盖.对照组软骨缺陷由类软骨组织填充,表面欠光滑,填充不完整,但可见大量类软骨细胞长入.实验组修复效果最好,表面平整,由大量细胞填充.③结果表明,复合骨髓间充质干细胞的聚乙烯醇/壳聚糖多孔水凝胶材料可促进软骨缺损的修复.%BACKGROUND:By mixing technology, various materials are mixed and complemented each other to enhance heat sensitivity, mechanical properties, viscoelasticity of the materials and improve their biocompatibility, biodegradability and other biomedical properties.OBJECTIVE:To prepare polyvinyl alcohol (PVA)/chitosan (CS) porous hydrogel and to observe its effects on the repair of articular cartilage defects.METHODS: PVA, CS and polysorbate-80 were used as raw materials to prepare the hydrogels at the PVA/CS ratio of 5:5, 6:4, 7:3, 8:2 and 9:1 by freezing-thawing cycle and emulsification-frostice phase separation, and the physical and chemical properties, mechanical properties, and biocompatibility of the hydrogels were detected to find out the best PVA/CS ratio. Eighteen New Zealand rabbits were enroled to make models of bilateral articular cartilage defects, and then randomized into three groups: blank control group; control group; experimental group. The prepared hydrogel was compounded with rabbit bone marrow mesenchymal stem cells (BMSCs) and then implanted into the rabbit articular cartilage defect in the experimental group, the PVA/CS hydrogel was implanted in the control group, and nothing was implanted in the blank control group. After 12 weeks, the animals were killed and the repairing effect was observed by gross observation and histological examination.RESULTS AND CONCLUSION:The PVA/CS porous composite hydrogel was successfully prepared, and PVA:CS=6:4 was the best in the presence of good mechanical properties, stable physical and chemical properties, and water content≥ 90%. In additional, scanning electron microscopy showed a porous network structure, with the porosity≥ 90%. The results of cell counting kit-8 assay and the results of cell death and survival showed that the hydrogel was non-cytotoxic and beneficial to the cell proliferation. In the blank control group, knee articular cartilage defects were not repaired within 12 weeks after surgery, showing significant granulation tissue filling. In the control group, knee articular cartilage defects were full of cartilage-like tissues with no smooth surface, but there were a great amount of chondrocyte-like cells. In the experimental group, knee articular cartilage defects were well repaired and full of a great amount of chondrocytes with the smooth surface. To conclude, the PVA/CS porous composite hydrogel could repair articular cartilage defects as an ideal tissue-engineered cartilage material.
    • 周丽斌1; 徐冰心2; 丁瑞英2; 韩浩伦2; 王刚2; 李保卫2; 王鸿南2; 吴玮2
    • 摘要: 背景:寻找理想的组织工程支架材料,仍然是软骨组织工程学的重要课题之一。目的:探讨微纤维胶原应用于软骨组织工程支架的可行性。方法:手术切取兔耳软骨,提取原代软骨细胞,并进行扩增培养。将海绵状微纤维胶原用无菌刀片切割成小方块,取第2代软骨细胞混悬液接种于微纤维胶原支架材料上。体外培养1周后,植入裸鼠体内,观察8周后取材,进行大体、组织学、免疫组织化学等方法观察。结果与结论:(1)在细胞接种过程中,湿水之后的微纤维胶原支架无明显缩水,仍然能够保持其立体形态;(2)体外培养1周以及植入体内8周后,无明显体积和形态变化;(3)裸鼠体内培养8周后形成白色半透明且富有弹性的成熟软骨块;(4)组织学观察可见所构建的软骨组织成熟,基质分泌旺盛,组织内仍可见未完全降解的微纤维胶原材料;(5)结果表明,微纤维胶原蛋白是一种良好的软骨组织工程支架材料。
    • 周丽斌; 徐冰心; 丁瑞英; 韩浩伦; 王刚; 李保卫; 王鸿南; 吴玮
    • 摘要: BACKGROUND:To seek for ideal scaffold materials is still an important task for cartilage tissue engineering.OBJECTIVE:To investigate the application of the AviteneTM microfibrillar collagen hemostat sponge in cartilage tissue engineering.METHODS:Rabbit auricular cartilage was harvested via surgical operation,and primary chondrocytes were isolated and amplified.Microfibrillar collagen hemostat sponge was cut into small bricks.The passage 2 chondrocytes were suspended and seeded onto the spongy bricks.After 1 week of in vitro culture,the constructs were then implanted into nude mice.After 8 weeks,the specimens were collected and evaluated using gross,histological and immunohistochamical observation.RESULTS AND CONCLUSION:During the cell seeding,the scaffold maintained its dimensions.No shrinkage was observed when the cell suspension was added.There was no considerable change in dimensions during the 1-week in vitro culture and at 8 weeks after implantation in nude mice.At 8 weeks post-implantation,mature cartilage blocks were harvested,which were white,translucent,and flexible.Histologically,the constructs appeared to have typical mature cartilaginous tissues,with robust extracellular matrix secretion,in which the microfibrillar collagen was incompletely degraded.We conclude that the microfibrillar collagen is a favorable scaffold material for cartilage tissue engineering.%背景:寻找理想的组织工程支架材料,仍然是软骨组织工程学的重要课题之一.目的:探讨微纤维胶原应用于软骨组织工程支架的可行性.方法:手术切取兔耳软骨,提取原代软骨细胞,并进行扩增培养.将海绵状微纤维胶原用无菌刀片切割成小方块,取第2代软骨细胞混悬液接种于微纤维胶原支架材料上.体外培养1周后,植入裸鼠体内,观察8周后取材,进行大体、组织学、免疫组织化学等方法观察.结果与结论:①在细胞接种过程中,湿水之后的微纤维胶原支架无明显缩水,仍然能够保持其立体形态;②体外培养1周以及植入体内8周后,无明显体积和形态变化;③裸鼠体内培养8周后形成白色半透明且富有弹性的成熟软骨块;④组织学观察可见所构建的软骨组织成熟,基质分泌旺盛,组织内仍可见未完全降解的微纤维胶原材料;⑤结果表明,微纤维胶原蛋白是一种良好的软骨组织工程支架材料.
    • 肖统光; 郝春香; 荆晓光; 刘雪剑; 郭岗岗; 杨建华; 郭全义
    • 摘要: 背景:软骨组织工程主要包括种子细胞、支架材料、细胞因子及生物反应器等,其中支架材料是构建组织工程软骨的关键环节.目的:制备关节软骨细胞外基质/人脐带Wharton胶复合多孔支架,评估其理化特性及细胞相容性.方法:采用物理法分别制备猪关节软骨细胞外基质及人脐带Wharton胶,然后以冻融干燥法制备关节软骨细胞外基质/人脐带Wharton胶复合多孔支架,检测支架的孔隙率、吸水率、组织成分及纵向压缩弹性模量,并进行组织学染色.将关节软骨细胞外基质/人脐带Wharton胶复合多孔支架与兔软骨细胞共培养7d,进行扫描电镜观察、活-死细胞染色及苏木精-伊红染色;分别采用关节软骨细胞外基质/人脐带Wharton胶复合多孔支架浸提液与细胞培养液培养兔软骨细胞6d,MTT法检测细胞增殖.结果与结论:①关节软骨细胞外基质/人脐带Wharton胶复合多孔支架横断面为均匀的多孔网状结构,孔壁上密布软骨纤维,纵断面为垂直管状结构,支架苏木精-伊红红染、番红O及甲苯胺蓝染色均呈阳性,含有胶原和糖胺多糖成分,支架的吸水率、孔隙率和纵向压缩弹性模量分别为(17.418 8±0.909 0)%、(81.495 1±6.621 0)%和(2.833 3±0.456 4)kPa;②共培养7d,兔软骨细胞在支架上黏附和增殖,并均匀长入支架孔隙内;③关节软骨细胞外基质/人脐带Wharton胶复合多孔支架浸提液对软骨细胞无毒性;④结果表明,关节软骨细胞外基质/人脐带Wharton胶复合多孔支架的理化性能及生化成分与天然软骨相似,具有良好的细胞相容性.%BACKGROUND:Soft tissue engineering mainly includes seed cells,scaffolds,cytokines and bioreactors,among which,the scaffolds are the key link in the construction of tissue-engineered cartilage.OBJECTIVE:To prepare an articular cartilage extracellular matrix/human umbilical cord Wharton gel porous scaffold,and to evaluate its physicochemical properties and biocompatibility.METHODS:The articular cartilage extracellular matrix/human umbilical cord Wharton gel porous scaffold was prepared by freeze thawing drying method using porcine articular cartilage extracellular matrix and human umbilical cord Wharton glue as raw materials.The porosity,water absorption,tissue composition and longitudinal compressive elastic modulus of the scaffold were measured and histologically stained.Rabbit chondrocytes were co-cultured with the articular cartilage extracellular matrix/human umbilical cord Wharton gel porous scaffold for 7 days.Then,scanning electron microscopy,live-dead cell staining and hematoxylin-eosin staining were performed.In addition,rabbit chondrocytes were cultured in the extract of the articular cartilage extracellular matrix/human umbilical cord Wharton gel porous scaffold and cell culture medium for 6 days,respectively;and MTT assay was used to detect cell proliferation.RESULTS AND CONCLUSION:The articular cartilage extracellular matrix/human umbilical cord Wharton gel porous scaffolds had a cross-section of uniform porous network structure and a vertical cross-section of the vertical tubular structure,and the pore wall was densely covered with cartilage fibers.The composite porous scaffold was positive for hematoxylin-eosin staining,safranin O staining and toluidine blue staining,and contained collagen and glycosaminoglycan ingredients.The water absorption,porosity and longitudinal compressive elastic modulus of the scaffolds were (17.418 8±0.909 0)%,(81.495 1±6.621 0)% and (2.833 3±0.456 4) kPa,respectively.After 7 days of co-culture,rabbit chondrocytes adhered to the scaffold and proliferated,and further grew into the pores of the scaffold.Moreover,the scaffold was non-toxic to the rabbit chondrocytes.To conclude,the physiochemical properties and biochemical components of articular cartilage extracellular matrix/human umbilical cord Wharton gel porous scaffolds are similar to those of natural cartilage,and the scaffold has good biocompatibility.
    • 姜良斌12; 韦标方2; 冯志2; 岳永彬12
    • 摘要: 背景:骨髓间充质干细胞在软骨组织工程研究中作为一种常见的种子细胞被广泛应用于软骨缺损修复.目的:以人脱细胞羊膜作为细胞支架负载兔骨髓间充质干细胞用以修复兔股骨髁间窝软骨缺损.方法:将兔骨髓间充质干细胞接种于人脱细胞羊膜上,体外共培养2周.建立兔股骨髁间窝区关节软骨缺损模型,右膝软骨缺损处设为空白对照组,不植入任何材料,左膝软骨缺损处为实验侧,分别植入人脱细胞羊膜-骨髓间充质干细胞和单纯人脱细胞羊膜.术后第8,12周,取膝关节软骨缺损部位新生组织,行大体观察、组织学检测,评估新生软骨质量.结果与结论:①大体观察结果:人脱细胞羊膜-骨髓间充质干细胞组有类软骨形成,质地较软,与周围正常软骨结合良好;人脱细胞羊膜组未形成软骨组织.空白对照组缺损区只由纤维样组织填充;②组织学观察结果:人脱细胞羊膜-骨髓间充质干细胞组新生出软骨细胞及软骨陷窝,并形成软骨基质,Ⅱ型胶原免疫组织化学染色呈阳性.软骨基质甲苯胺蓝染色较深.人脱细胞羊膜组仅有极少量的软骨细胞,甲苯胺蓝染色较浅,Ⅱ型胶原免疫组织化学染色呈阴性,无软骨基质形成.空白对照组为纤维组织修复,甲苯胺蓝染色较浅;③结果表明,人脱细胞羊膜有利于骨髓间充质干细胞的软骨化,软骨缺损处由类软骨组织填充,能够有效修复关节软骨缺损.
    • 姜良斌; 韦标方; 冯志; 岳永彬
    • 摘要: 背景:骨髓间充质干细胞在软骨组织工程研究中作为一种常见的种子细胞被广泛应用于软骨缺损修复.目的:以人脱细胞羊膜作为细胞支架负载兔骨髓间充质干细胞用以修复兔股骨髁间窝软骨缺损.方法:将兔骨髓间充质干细胞接种于人脱细胞羊膜上,体外共培养2周.建立兔股骨髁间窝区关节软骨缺损模型,右膝软骨缺损处设为空白对照组,不植入任何材料,左膝软骨缺损处为实验侧,分别植入人脱细胞羊膜-骨髓间充质干细胞和单纯人脱细胞羊膜.术后第8,12周,取膝关节软骨缺损部位新生组织,行大体观察、组织学检测,评估新生软骨质量.结果与结论:①大体观察结果:人脱细胞羊膜-骨髓间充质干细胞组有类软骨形成,质地较软,与周围正常软骨结合良好;人脱细胞羊膜组未形成软骨组织.空白对照组缺损区只由纤维样组织填充;②组织学观察结果:人脱细胞羊膜-骨髓间充质干细胞组新生出软骨细胞及软骨陷窝,并形成软骨基质,Ⅱ型胶原免疫组织化学染色呈阳性.软骨基质甲苯胺蓝染色较深.人脱细胞羊膜组仅有极少量的软骨细胞,甲苯胺蓝染色较浅,Ⅱ型胶原免疫组织化学染色呈阴性,无软骨基质形成.空白对照组为纤维组织修复,甲苯胺蓝染色较浅;③结果表明,人脱细胞羊膜有利于骨髓间充质干细胞的软骨化,软骨缺损处由类软骨组织填充,能够有效修复关节软骨缺损.%BACKGROUND: Bone marrow mesenchymal stem cells (BMSCs) as common seed cells have been widely used in tissue-engineered cartilage repair.OBJECTIVE: To use human amniotic membrane as a cell scaffold to carry rabbit BMSCs in order to repair articular cartilage defects in the femoral intercondylar fossa of rabbits.METHODS: Rabbit BMSCs were inoculated onto the human acellular amniotic membrane (HAAM) and co-cultured for 2 weeks. Articular defect models were made in the femoral intercondylar fossa of rabbits. The defects of the right knees served as blank control. BMSCs/HAAM composite was transplanted into the defect of the left knee joint as composite group, and HAAM was implanted into the defect of the left knee joint as HAAM group. These rabbits were killed at 8 and 12 weeks after implantation and the newly cartilage samples were evaluated grossly and histologically and then graded.RESULTS AND CONCLUSION: Gross observation showed the defects were filled with cartilaginous tissues in the composite group, and there were no cartilage tissues in the HAAM group, while only fibrous tissues were seen in the blank control group. Histologically, the defect region was full of chondrocytes in the composite group,immunohistochemistry staining indicated that collagen II was rich in the tissue, and furthermore, the cartilage matrix was stained deeply by toluidine blue. In the the HAAM group, there were few chondrocytes, toluidine blue staining was weakly positive, and immunohistochemistry staining was negative, indicating there was no cartilage matrix. In the blank control group, the defects were filled of fibroblasts and toluidine blue staining was weakly positive. To conclude, the BMSCs/HAAM is a good scaffold for BMSCs chondrogenic differentiation to effectively repair articular cartilage defects.
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