中国组织工程研究

中国组织工程研究 ›› 2010, Vol. 14 ›› Issue (51): 9555-9558.doi: 10.3969/j.issn.1673-8225.2010.51.012

• 组织工程血管材料 tissue-engineered vascular materials • 上一篇    下一篇

组织工程血管基质的制备及保存

池一凡1，许  慧2，林明山1，侯文明1，孙忠东1，孙  龙1，牛兆倬1，孙  勇1，生  伟1   

  1. 1青岛大学医学院附属青岛市立医院心脏外科，山东省青岛市  266071；2青岛大学医学院附属医院麻醉科，山东省青岛市  266071
  • 出版日期:2010-12-17 发布日期:2010-12-17
  • 通讯作者: 林明山，硕士，医师，青岛大学医学院附属青岛市立医院心脏外科，山东省青岛市 266071 Lincoln3086@yahoo.com.cn
  • 作者简介:池一凡☆，男，1964年生，福建省龙岩市人，汉族，2001年法国马赛第二大学医学院毕业，博士，主任医师，教授，硕士生导师，主要从事心血管外科的基础及临床研究。 chiyf@hotmail.com
  • 基金资助:

    青岛市科技局基金项目(06-2-2-6-nsh)。

Preparation and preservation of tissue engineered vascular matrix

Chi Yi-fan1, Xu Hui2, Lin Ming-shan1, Hou Wen-ming1, Sun Zhong-dong1, Sun Long1, Niu Zhao-zhuo1, Sun Yong1, Sheng Wei1   

  1. 1 Department of Cardiovascular Surgery, Qingdao Municipal Hospital, Medical College of Qingdao University, Qingdao  266071, Shandong Province, China; 2 Department of Anesthesiology, Affiliated Hospital, Medical College of Qingdao University, Qingdao  266071, Shandong Province, China
  • Online:2010-12-17 Published:2010-12-17
  • Contact: Lin Ming-shan, Master, Physician, Department of Cardiovascular Surgery, Qingdao Municipal Hospital, Medical College of Qingdao University, Qingdao 266071, Shandong Province, China Lincoln3086@yahoo.com.cn
  • About author:Chi Yi-fan☆, Doctor, Chief physician, Professor, Master’s supervisor, Department of Cardiovascular Surgery, Qingdao Municipal Hospital, Medical College of Qingdao University, Qingdao 266071, Shandong Province, China chiyf@hotmail.com
  • Supported by:

    a grant by Science and Technology Bureau of Qingdao, No. 06-2-2-6-nsh*

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被引次数

1

摘要：

背景：为构建全生物化组织工程血管，制备及保存脱细胞血管基质。
目的：制备组织工程血管基质，观察其保存于液氮中的可行性。
方法：采用胰蛋白酶、低渗溶液、化学除垢剂法处理兔胸主动脉来制备组织工程血管基质，标本作大体、光镜及扫描电镜、透射电镜观察，并将制备的血管基质放入液氮中保存，3个月后取出作扫描电镜观察。
结果与结论：经该法处理的兔血管细胞全部脱除，胶原纤维、弹性纤维无断裂，细胞外基质保持完好，液氮保存3个月后扫描电镜观察与新鲜基质无明显差别。提示酶、低渗溶液、化学除垢剂联合法是制备组织工程血管基质的较好方法，制备的血管基质可放入液氮中进行短期保存。

关键词: 血管基质, 组织工程, 兔胸主动脉, 除垢剂, 液氮保存

Abstract:

BACKGROUND: Acellular vascular matrix is prepared and preserved in order to construct complete biological tissue engineered vessels.
OBJECTIVE: To prepare tissue engineered vascular matrix and to investigate the feasibility of preserving it in liquid nitrogen.
METHODS: Trypsin, hypertonic solutions and chemical detergent were applied for a multi-step process to prepare acellular tissue engineered vascular matrix from rabbit thoracic aorta. The specimen was observed with macroscopic observation, light microscope, scanning electron microscope and transmission electron microscope. Then the specimen was observed by scanning electron microscope after preserved in liquid nitrogen for 3 months.
RESULTS AND CONCLUSION: The cells were removed completely after this processing in rabbit blood vessels, the elastic fibers and collagen fibers were preserved well, extracellular matrix maintained intact. There were no obvious differences in scanning electron microscopy observation between the specimen preserved in liquid nitrogen for 3 months and the fresh matrix. A combined method of trypsin, hypertonic solution and chemical detergent can be a better method to prepare tissue engineered vascular matrix, and the vascular matrix could be preserved in liquid nitrogen for a short time.

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