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乙交酯-丙交酯共聚物与神经生长因子复合支架的细胞相容性及缓释作用

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李继业[1] 万虹[1] 杨飞[2] 历俊华[1] 李德志[1] 王亚杰[3] 王身国[2]

[1]首都医科大学附属北京市神经外科研究所,北京市100050 [2]中国科学院化学研究所高分子物理与化学国家重点实验室,北京市100080 [3]首都医科大学附属北京天坛医院检验科,北京市100050

中国组织工程研究与临床康复
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国际标准刊号:ISSN 1673-8225
国内统一刊号:CN 11-5516/R

摘  要:

目的:体外实验观察生物可降解材料乙交酯-丙交酯共聚物与神经生长因子复合支架的细胞相容性及其缓释作用. 方法:实验于2005-05/09在首都医科大学附属北京市神经外科研究所损伤修复实验室完成.①实验方法:乙交酯-丙交酯共聚物采用专利技术(200510011350.9)制备,体外将许旺细胞和神经干细胞与乙交酯-丙交酯共聚物共培养.②实验评估:扫描电镜下观察许旺细胞和神经干细胞在乙交酯-丙交酯共聚物内生长状况;应用组织工程技术将神经生长因子整合入乙交酯-丙交酯共聚物内,0.02 g乙交酯-丙交酯共聚物(干质量)中含有1μg神经生长因子,ELISA法检测每天神经生长因子释放的质量浓度. 结果:①扫描电镜下乙交酯-丙交酯共聚物横断面可见其为网格状,纵断面可见其直孔道.②许旺细胞和神经干细胞在乙交酯-丙交酯共聚物支架上生长良好,与其紧密贴附.③培养后第4天神经生长因子释放的质量浓度达峰值,第7天趋于平稳,稳定释放的质量浓度为100μg/L. 结论:①乙交酯-丙交酯共聚物与许旺细胞和神经干细胞具有良好的生物相容性及细胞亲和性.②按神经生长因子(1μg)与乙交酯-丙交酯共聚物(干质量0.02 g)的比例合成的神经生长因子-乙交酯-丙交酯共聚物组织工程材料可缓慢稳定释放神经生长因子,达到其可以发挥生物学活性的质量浓度100μg/L.[著者文摘]

栏目信息:

研究与报告

分 类 号:

R318.08

文献标识码:

A

文章编号:

1673-8225(2007)31-06161-04

相关文章:

参考文献(20篇) 耦合文献(30篇)  主题相关

[参考文献]

Cell compatibility and release of poly (lactide-co-glycolide acid) scaffold with nerve growth factor

Li JY,Wan H,Yang F,Li JH,Li DZ,Wang YJ,Wang SG(1Beijing Institute of Neurosurgery, Capital Medical University, Beijing 100050, China; 2State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, China; 3Department of Clinical Laboratory, Beijing Tiantan Hospital, Capital Medical University, Beijing 100050, China)

Abstract:

AIM: To in vitro observe the cell compatibility and release of biodegradable poly (lactide-co-glycolide acid) (PLGA) scaffold integrated with nerve growth factor (NGF). METHODS: The experiment was carried out in the Laboratory of Injury Repairs, Beijing Institute of Neuresurgery Affiliated to Capital Medical University from May to September in 2005. ①The production of PLGA was made by technology of patent (200510011350.9). Schwann cells and neural stem cells were cultured within PLGA scaffold in vitro. ②The growth of Schwann cells and neural stem cells were observed by scanning electron microscope; NGF was integrated into PLGA by tissue engineering technology, 1 μg NGF for 0.02 g PLGA (dry weight); The release concentration of NGF was tested with ELISA. RESULTS:①Scanning electron microscope examination: Plenty of meshes on T-sect and straight channels on longitudinal section were observed on PLGA. ②Schwann cells and neural stem cells grew well and touched tightly in PLGA scaffold.③The concentrations of NGF reached the peak amplitude on the 4^th day, and released steadily on the 7^th day with the value was 100 μg/L. CONCLUSION: ①PLGA scaffold has well biological compatibility and cellular affinity with Schwann cells and neural stem cells.②With the ratio of 1μg NGF in 0.02 g PLGA, NGF can constantly release on the level of 100 μg/L, which displays the biological activity.[著者文摘]

收稿日期: 2007-04-25
修订日期: 2007-06-06

基金资助:

国家自然科学基金国际合作研究项目(30540450581);九七三课题(1005CB522704)

作者简介:

李继业,男,1981年生,山东省潍坊市人,汉族,2006年首都医科大学毕业,硕士,医师,主要从事脊髓损伤修复方面研究.lijiye1981@163.com 通讯作者:万虹,研究员,硕士生导师,首都医科大学附属北京市神经外科研究所,北京市 100050 wanhong50@hotmail.com

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