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胶原海绵

胶原海绵的相关文献在1994年到2022年内共计135篇,主要集中在基础医学、外科学、内科学 等领域,其中期刊论文74篇、会议论文9篇、专利文献29130篇;相关期刊49种,包括华东理工大学学报(自然科学版)、解剖学杂志、中华神经外科疾病研究杂志等; 相关会议8种,包括第十七届全国中西医结合疡科学术交流会、2016年中华中医药学会外治分会学术年会、第十一次全国中医外治学术年会等;胶原海绵的相关文献由406位作者贡献,包括姚昶、武继民、叶萍等。

胶原海绵—发文量

期刊论文>

论文:74 占比:0.25%

会议论文>

论文:9 占比:0.03%

专利文献>

论文:29130 占比:99.72%

总计:29213篇

胶原海绵—发文趋势图

胶原海绵

-研究学者

  • 姚昶
  • 武继民
  • 叶萍
  • 任伟业
  • 关静
  • 周青
  • 汪海波
  • 王玉新
  • Yao Chang
  • 冯雪莉
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 马也; 赵磊磊; 高建萍; 孔英俊; 张贵锋; 刘涛
    • 摘要: 针对胶原基生物材料,通过不同方法研究了基于牛胶原的海绵和脱细胞基质材料的降解过程,比较两种材料的降解规律,定量考察了胶原基材料体内降解周期.通过在SD大鼠脊柱两侧皮下分别植入胶原海绵与脱细胞基质,在不同周数取样,分别观察两种材料降解程度并称重建立降解曲线,利用高效液相色谱质谱联用技术筛选出牛I型胶原的特征多肽GEGGPQGPRG,并进行定量分析.分批次将大鼠体内残留部分进行酶解,再利用三重四极杆质谱对特征肽进行定量,建立降解曲线.结果 表明,脱细胞基质与胶原海绵体内降解趋势相似.胶原海绵降解8周特征肽浓度为(0.40±0.10)×10-5 mg/mL,表明胶原海绵降解较为完全.脱细胞基质降解16周特征肽浓度为(1.30±0.11)×10-5 mg/mL,表明脱细胞基质降解较为完全.
    • 韩刘君; 孙尧; 于晓龙; 谷玉
    • 摘要: 目的 观察CM-DIL体外标记兔骨髓来源的内皮祖细胞(EPCs)的可行性及其在胶原海绵上的生长情况.方法 用Percoll分离液的方法分离、培养EPCs,并进行鉴定;观察CM-DIL标记后的EPCs与胶原海绵的生物相容性,HE染色评价EPCs的生长情况.结果 CM-DIL标记EPCs的细胞膜为红色,分离培养的EPCs其表面标志物CD31和CD34表达均为阳性,种植于胶原海绵上的EPCs可存活,并沿胶原海绵支架生长.结论 CM-DIL可作为体外标记EPCs的方法,胶原海绵可作为一种较为理想的组织工程学支架材料.
    • 苗宗宁; 孙鸿丽; 薛一峰
    • 摘要: 探索人绒毛膜来源间充质干细胞与胶原海绵的生物相容性及复合培养向血管内皮细胞分化.应用IV型胶原酶消化的方法,从胎盘组织中分离人绒毛膜间充质细胞,培养第2代细胞,进行内皮诱导后,种植于Matrigel基质胶并观察成管情况;细胞与胶原海绵复合培养,通过HE染色以及免疫荧光染色,鉴定CD31和vWF的表达.人绒毛膜间充质干细胞向血管内皮定向诱导2周后,形态由长梭形、旋涡状生长逐步变为圆形、铺路石状,免疫荧光染色结果显示CD31和vWF阳性表达;种植于Matrigel胶12 h后表现出成管功能,与胶原海绵复合培养,经HE染色,可见细胞分布于材料内部,免疫荧光染色可见CD31和vWF阳性表达细胞.人绒毛膜间充质干细胞具有定向诱导分化为血管内皮细胞的潜能,胶原海绵具有良好的生物相容性,可以作为组织工程研究的支架材料.
    • 蒋斌; 郑明辉; 张斌; 郝朦尘; 张喜
    • 摘要: 目的:观察在不同大小离心力作用下三维载体上骨髓间充质干细胞(BMSCs)的生长情况.方法:取大鼠第3代BMSCs种植于胶原海绵支架,分为对照组(0 r/min)、200 r/min组、500 r/min以及800 r/min组;实验组给予相应转速的离心力刺激,对照组同步置于除离心外相同的环境中;利用CM-Dil活细胞膜染色观察BMSCs与海绵支架的相容性,检测不同时相下端粒酶浓度,H-E染色评价BMSCs的生长情况.结果:BMSCs种植后存活,沿胶原海绵支架表面和空洞生长;端粒酶浓度在第15天内均递增,在第57天内均下降,且200 r/min和500 r/min组增高值>对照组,800 r/min组<对照组;H-E染色显示200 r/min和500 r/min组细胞数量比对照组明显增多,以500 r/min组最多,而800 r/min组明显减少.结论:较低转速(200 r/min与500 r/min)的离心力可促进BMSCs增殖,而过高转速(800 r/min)的离心力抑制BMSCs增殖,且在500 r/min干预5d时细胞的生长活性最强.%Objective:To observe the growth of bone mesenchymal stem cells (BMSCs) cultured in the three-dimensional carrier under different centrifugal forces.Methods:The third-generation BMSCs were seeded into the collagen sponges and divided into control group,200 r/min group,500 r/min group and 800 r/min group with each experimental group being given corresponding centrifugal force.The control group was exposed to the same environment except for the centrifugal force.The compatibility of BMSCs with collagen sponge was observed by CM-Dil staining and the growth of BMSCs was assessed by telomerase concentration detection at different time points (1 d,3 d,5 d,7 d) and H-E staining of paraffin section on the 7th day.Results:BMSCs survived in the collagen sponges and proliferated well.Telomerase concentration of all groups gradually increased from day 1 to day 5 and decreased from day 5 to day 7.The concentration of 200 r/min group and 500 r/min group was higher than the control group,while that of the 800 r/min group was lower than the control group.H-E staining showed that the cell number of 200 r/min group and 500 r/min group was significantly higher than the control group,with the highest in the 500 r/min group.However,the cell number of 800 r/min group was significantly lower than the control group.Conclusion:Lower rotation speed (200 r/min and 500 r/min) promotes proliferation of BMSCs,while higher rotation speed (800 r/min) inhibits the proliferation.The growth activity of BMSCs is the strongest in the 500 r/min group on the 5th day.
    • 薛静娴; 陈绪; 许岩磊; 任伟业; 李燕; 张宇轩; 姚昶
    • 摘要: BACKGROUND:Studies have found that adipose-derived stem cells (ADSCs)/collagen complexes can promote the ADSCs differentiation and maturation into mature adipocytes and promote angiogenesis.OBJECTIVE:To explore the biological properties of the ADSCs/collagen sponge composite material and to detect its effect on angiogenesis.METHODS:(1) ADSCs were cultured on collagen sponge (experimental group) or cultured alone (control group).After 24 hours of culture,cell adhesive rate of ADSCs was determined with flow cytometry.After 2,4,6 days of culture,cell proliferation and level of vascular endothelial growth factor (VEGF) in the culture medium were detected.(2) Chick embryo chorioallantoic membranes were exposed and incubated for 7 days and then divided into four groups:0.2 mL of sterile PBS was added in the blank group,0.2 mL of 2× 108/L passage 3 ADSCs suspension was added in the ADSCs group,collagen sponge was added in the collagen sponge group,and collagen sponge with 0.2 mL of 2× 108/L passage 3 ADSCs suspension was added in the composite group.After 7 days of incubation,the microvessel count around the chorioallantoic membrane was measured.RESULTS AND CONCLUSION:(1) The cell adhesive rate of ADSCs to collagen sponge reached to (93.04±0.67)%.(2)The absorbance value (at 6 days of culture) and level of VEGF (at 4 and 6 days of culture) in the experimental group were significantly higher than those in the control group (P < 0.01 or P < 0.05).(3) Compared with the blank group,the number of microvessels was significantly higher in the ADSCs,collagen sponge and composite groups (P < 0.05).Moreover,higher amount of microvessels were found in the composite group than the ADSCs and collagen sponge groups (P < 0.05).To conclude,ADSCs can adhere well to the collagen sponge with good biocompatibility and their combined use can improve angiogenesis further by enhancing cell proliferation and VEGF secretion of ADSCs.%背景:研究发现,脂肪干细胞胶原复合物可促进脂肪干细胞向成熟脂肪细胞分化、成熟,并可促进血管新生.目的:探查胶原海绵复合脂肪干细胞的生物学特性及其对血管新生的影响.方法:①实验组将人脂肪干细胞接种于胶原海绵上,以细胞单独培养为阴性对照组,培养24 h后,检测细胞黏附率;培养第2,4,6天,检测细胞增殖与培养液中血管内皮生长因子水平;②鸡胚绒毛尿囊膜实验:暴露孵育7d的鸡胚尿囊膜,分4组,空白组向尿囊膜加入0.2 mL无菌PBS,脂肪干细胞组加入0.2 mL 2×108 L-1第3代脂肪干细胞悬液,胶原海绵组加入胶原海绵,复合组加入2×108 L-1第3代脂肪干细胞悬液0.2 mL与胶原海绵.孵育7d后,测定尿囊膜周围微血管计数.结果与结论:①细胞黏附率:脂肪干细胞在胶原海绵上的黏附率为(93.04±0.67)%;②细胞增殖与培养液中血管内皮细胞生长因子水平:实验组培养第6天的细胞增殖A值高于对照组(P<0.01),培养第4,6天的血管内皮生长因子水平高于对照组(P<0.05);③鸡胚绒毛尿囊膜实验:脂肪干细胞组、胶原海绵组、复合组微血管计数高于空白组(P<0.05),复合组高于脂肪干细胞组、胶原海绵组(P<0.05);④结果表明:脂肪干细胞与胶原海绵具有良好的生物相容性,两者复合有良好的促进血管新生作用,其机制可能与促进脂肪干细胞增殖与分泌血管内皮生长因子相关.
    • 薛静娴1; 陈绪1; 许岩磊1; 任伟业2; 李燕2; 张宇轩1; 姚昶1
    • 摘要: 背景:研究发现,脂肪干细胞胶原复合物可促进脂肪干细胞向成熟脂肪细胞分化、成熟,并可促进血管新生。目的:探查胶原海绵复合脂肪干细胞的生物学特性及其对血管新生的影响。方法:(1)实验组将人脂肪干细胞接种于胶原海绵上,以细胞单独培养为阴性对照组,培养24 h后,检测细胞黏附率;培养第2,4,6天,检测细胞增殖与培养液中血管内皮生长因子水平;(2)鸡胚绒毛尿囊膜实验:暴露孵育7 d的鸡胚尿囊膜,分4组,空白组向尿囊膜加入0.2 mL无菌PBS,脂肪干细胞组加入0.2 mL 2×108 L-1第3代脂肪干细胞悬液,胶原海绵组加入胶原海绵,复合组加入2×108 L-1第3代脂肪干细胞悬液0.2 mL与胶原海绵。孵育7 d后,测定尿囊膜周围微血管计数。结果与结论:(1)细胞黏附率:脂肪干细胞在胶原海绵上的黏附率为(93.04±0.67)%;(2)细胞增殖与培养液中血管内皮细胞生长因子水平:实验组培养第6天的细胞增殖A值高于对照组(P〈0.01),培养第4,6天的血管内皮生长因子水平高于对照组(P〈0.05);(3)鸡胚绒毛尿囊膜实验:脂肪干细胞组、胶原海绵组、复合组微血管计数高于空白组(P〈0.05),复合组高于脂肪干细胞组、胶原海绵组(P〈0.05);(4)结果表明:脂肪干细胞与胶原海绵具有良好的生物相容性,两者复合有良好的促进血管新生作用,其机制可能与促进脂肪干细胞增殖与分泌血管内皮生长因子相关。
    • 卢静; 王雨佳; 凌炜诗; 陈旻骁; 李长红; 关爽; 邓旭明
    • 摘要: 背景:林蛙是中国珍稀的药用动物,林蛙皮是林蛙取油后的废弃物,其胶原蛋白含量丰富且量大、无污染和疫病危险,具有开发成为胶原海绵的潜力,但目前尚未见林蛙皮胶原海绵制备工艺方面的研究.目的:对林蛙皮胶原海绵的制备工艺进行优化,考察林蛙皮胶原海绵的物理性质及体外细胞相容性.方法:利用壳聚糖和戊二醛对林蛙皮胶原蛋白海绵进行改性,以壳聚糖与胶原蛋白质量比(1:1、1:2、1:4)、戊二醛浓度(1%、1.5%、2%)为实验因子,以具有显著性差异的吸水倍数、机械性能和热变性温度为指标,采用正交实验设计对林蛙皮胶原蛋白海绵的制备工艺进行优化,观察林蛙皮胶原蛋白海绵表观形貌.将9种林蛙皮胶原蛋白海绵分别与人包皮成纤维细胞共培养,检测细胞增殖.结果与结论:①确定林蛙皮胶原海绵的最佳工艺条件为:壳聚糖与林蛙胶原蛋白质量为1:1,戊二醛浓度为1%,在该条件下,林蛙皮胶原海绵的吸水倍数为5.22,断裂伸长率为10.96%,热变性温度为81.24°C;此条件下的林蛙皮胶原海绵孔径200-400μm,网孔大小基本一致,排列有序;②除壳聚糖与胶原蛋白为1:4、戊二醛浓度为1%或5%的林蛙皮胶原海绵外,其他林蛙皮胶原海绵对人包皮成纤维细胞的细胞活性均有促进作用,有利于细胞的活性和生长;③结果表明,林蛙皮胶原海绵具有良好的生物相容性.%BACKGROUND: Forest frog is a rare medicinal animal in China, but the skin of forest frog is waste after Oviductus Ranae production. The forest frog skin is rich of collagen, and is large in quantity without pollution and disease risk. So the forest frog skin has potential to be developed into collagen sponge; however, there is no research on collagen sponge preparation as yet.OBJECTIVE: To optimize the preparation of collagen sponge from forest frog skin, and to investigate the physical properties and in vitro cell compatibility.METHODS: Chitosan and glutaraldehyde were used to modify collagen sponge from forest frog skin. Chitosan/collagen (w/w) (1:1, 1:2, 1:4) and glutaraldehyde concentration (1%, 1.5% and 2%) were selected as the experimental factors.The significant water absorbency, mechanical properties and thermal denaturation temperature were chosen as the indexes. Using the orthogonal experimental design, we optimized collagen sponge preparation process. We also investigated the in vitro cell compatibility and surface morphology of the collagen sponge. The nine kinds of collagen sponges from forest frog skins were co-cultured with human foreskin fibroblasts to detect cell proliferation.RESULTS AND CONCLUSION: When the chitosan/collagen was 1:1 and the glutaraldehyde concentration was 1%, we could get the collagen sponge with ideal water absorbency (water absorption capacity=5.22), mechanical properties (elongation at break=10.96%) and thermal denaturation temperature (81.24 °C). The aperture of the forest frog skin collagen sponge was 200-400 μm, and the pores were consistent in the size and arranged regularly. Except the chitosan/collagen of 1:4 and the glutaraldehyde concentration of 1% or 5%, all kinds of forest frog skin collagen sponges could promote the viability of human foreskin fibroblasts and exerted benefits to cell viability and growth. To conclude,the forest frog skin collagen sponge has good biocompatibility and apparent morphology, in aggreement with the requirements of biological materials.
    • 田茂伟
    • 摘要: 目的 观察分析胶原海绵人工硬脑膜在颅脑损伤硬脑膜修补术中的应用效果.方法 120例行硬脑膜修补术的颅脑损伤患者,随机分为A组和B组,各60例.A组患者采用胶原海绵人工硬脑膜修补,B组患者采用自体膜修补.观察比较两组手术时间、术中出血量、硬膜外总引流量以及术后并发症发生率.结果 A组并发症发生率为5.00%,明显低于B组的18.33%,差异有统计学意义(P0.05).结论 与自体膜相比较,胶原海绵人工硬脑膜用于颅脑损伤后硬脑膜修补术可以减少术后并发症发生率,并能为二期颅骨修补创造有利的条件,是硬脑膜修补的理想材料.
    • 江颖; 邓明霞; 汪海婴; 张含俊; 汪海波
    • 摘要: In this paper,native collagen (NC)was extracted from skin of grass carp,and it was proved typeⅠcollagen with intact triple helix structure via the DSC and circular dichroism and SDS-PAGE analysis.Low ther-mal denaturation (LD),high thermal denaturation (HD)and complete thermal denaturation(CD)collagen sam-ples were obtained by heat treatment of NC under different conditions,and the degrees of thermal denaturation of them were 16.9%,57.9 and 100% respectively,according to the changes of thermal denaturation enthalpy from DSC determination.On this basis,the research focused on the influences of heat treatment on the collagen structure and the corresponding properties of collagen sponges.The results show that the onset endothermic temperature (To )is the threshold temperature for the molecule structure and sponges properties stability. When subj ected to temperatures above this threshold temperature even in a short time,the triple helix structure of collagen would completely or partially unfold.At the same time,the ordering of material structure,mechani-cal properties and enzymatic sensitivities of collagen sponges reduced,the cell proliferation ability enhanced a-long with the rise of degrees of thermal denaturation of collagen.The findings demonstrate To is the crucial temperature and this temperature should not be exceeded during the production and utilization of native colla-gens.%以草鱼皮为原料提取天然胶原蛋白,经DSC、圆二色谱和 SDS-PAGE 分析证实为具有完整三螺旋分子结构的Ⅰ型胶原.在不同条件下对该胶原进行热处理后分别获得了低变性、高变性和完全变性的胶原样品,热变性焓测定结果表明热变性程度分别为16.9%,57.9%和100%.在此基础上,重点研究了热变性处理后胶原结构和胶原海绵材料性能的变化.结果表明,草鱼皮胶原变性的起始温度(To,33°C)是其分子结构和胶原海绵材料性能改变的阀值温度.高于该温度条件下的短暂受热历史即可导致胶原三螺旋结构的部分或完全解离.同时,胶原变性程度的增加,材料结构的有序性、材料力学性能和耐酶解能力也随之降低,但是促细胞增殖能力有所提升.可见,低于胶原热变性的起始温度是天然胶原提取和胶原材料应用的安全温度条件.
    • 宋唯一; 刘国民; 袁海波; 彭传刚; 徐坤; 殷德辉; 曹洪倩; 李娟
    • 摘要: 目的:探讨浸提时间、乙酸浓度及料液比对鼠尾腱胶原提取的影响,建立并优化鼠尾腱胶原的提取工艺,提高胶原提取效率.方法:选取健康SD大鼠鼠尾,采取酸溶法提取鼠尾腱胶原,观察不同浸提时间(12、24、48、72和96 h)、乙酸浓度(0.10、0.25、0.50、0.75和1.00 mol·L-1)及料液比(g∶mL)(1∶5、1∶10、1∶20、1∶40和1∶80)对胶原提取率的影响,利用正交试验判断浸提时间、乙酸浓度及料液比等影响因素的最佳工艺参数.通过SDS-PAGE电泳实验、单宁酸沉淀实验和傅里叶红外光谱实验等对提取的胶原进行鉴定.结果:单因素分析,胶原提取率在一定参数范围内随浸提时间、乙酸浓度及料液比的增加而增加.正交试验,鼠尾腱胶原提取的最佳工艺参数为浸提时间72 h、乙酸浓度0.5mol· L-1、料液比为1∶40.SDS-PAGE电泳显示,样品为Ⅰ型胶原,单宁酸沉淀实验显示胶原降解程度低,傅里叶红外光谱显示胶原结构完整.样品氨基酸含量测定符合胶原蛋白的成分特征.中性胶原溶液在37°C时能够形成固态胶原凝胶,胶原凝胶经过碳化二亚胺(EDC)交联后,扫描电镜下显示内部相互连接,构成孔径适中的蜂窝状多孔结构.结论:成功建立并优化鼠尾腱胶原蛋白的提取工艺,得出浸提时间、乙酸浓度及料液比等因素的最佳工艺参数,有效提高了鼠尾腱胶原的提取效率.
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