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《材料导报》期刊社  2017, Vol. 31 Issue (2): 20-24    https://doi.org/10.11896/j.issn.1005-023X.2017.02.004
  材料研究 |
多巴胺表面修饰胶原膜促进细胞粘附和增殖的研究*
崔国廉, 但年华, 但卫华
四川大学皮革化学与工程教育部重点实验室,四川大学生物医学工程技术研究中心, 成都 610065;
Surface Modification of Collagen Films with Dopamine to Promote Cell Adhesion and Proliferation
CUI Guolian, DAN Nianhua, DAN Weihua
Key Laboratory of Leather Chemistry and EngineeringSichuan University,Ministry of Education;The Research Center of Biomedical Engineering and Technology, Sichuan University, Chengdu 610065;
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摘要 多巴胺已经被广泛地用于材料的表面修饰改性,能够提高材料的生物相容性,赋予材料新的反应活性。为了考察多巴胺表面修饰胶原膜对其机械强度、湿热稳定性、亲水性和生物相容性的影响,对多巴胺自组装表面修饰胶原膜不同时间形成的膜材料进行研究,结果发现,经过多巴胺自组装表面修饰后,胶原保持完整的三股螺旋结构,膜材料的机械强度、湿热稳定性和亲水性均得到提高,而且成纤维细胞更易于在膜上粘附和增殖。
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崔国廉
但年华
但卫华
关键词:  多巴胺  胶原膜  表面修饰  细胞粘附    
Abstract: Dopamine has been widely used to surface modify materials due to its multi-functional reactivity and biocompatibility. Herein, in order to investigate whether the mechanical strength, hydrothermal stability, hydrophilic property and biocompatibility of collagen films are influenced, dopamine was used to surface-modify collagen films, and then the films were characterized. Results showed that the triple helix structure of collagen remains intact, and mechanical strength, hydrothermal stability and hydrophi-lic property of the films are enhanced. Besides, the films can promote adhesion and proliferation of fibroblasts.
Key words:  dopamine    collagen film    surface modification    fibroblast adhesive
               出版日期:  2017-01-25      发布日期:  2018-05-02
ZTFLH:  O636.9  
基金资助: *国家自然科学基金(51473001)
作者简介:  崔国廉:男,1988年生,硕士研究生,研究方向为胶原基生物医学材料 但卫华:通讯作者,男,1956年生,教授,博士研究生导师,研究方向为生物质医用材料 E-mail:dwh5607@263.net
引用本文:    
崔国廉, 但年华, 但卫华. 多巴胺表面修饰胶原膜促进细胞粘附和增殖的研究*[J]. 《材料导报》期刊社, 2017, 31(2): 20-24.
CUI Guolian, DAN Nianhua, DAN Weihua. Surface Modification of Collagen Films with Dopamine to Promote Cell Adhesion and Proliferation. Materials Reports, 2017, 31(2): 20-24.
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http://www.mater-rep.com/CN/10.11896/j.issn.1005-023X.2017.02.004  或          http://www.mater-rep.com/CN/Y2017/V31/I2/20
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