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染料介导光氧化法处理的同种异体动脉体内近期生物稳定性和细胞毒性研究

Research on Short-term Biological Stability and Cytotoxicity of Allogenic Arteries Cross-linked by Dye-mediated Photooxidation In Vivo
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摘要 观察染料介导光氧化(DMP)法处理的家兔胸主动脉用于同种异体腹主动脉置换后,在体内血流环境下的生物稳定性和细胞毒性。以经染料介导的光氧化反应处理的家兔胸主动脉为研究对象,以戊二醛(GA)处理的家兔胸主动脉以及自体腹主动脉原位移植作为对照,建立家兔胸-腹主动脉移植模型;实验动物观察饲养1个月后,取出标本观察,通过光学显微镜半定量计数观察移植血管的体内生物稳定性;通过扫描电镜半定量计数观察移植血管内皮覆盖情况,以此评价移植血管的细胞毒性。结果显示:DMP组生物稳定性指数较自体动脉移植组低,差异不具统计学意义(P>0.05),DMP组生物稳定性指数较GA组高,差异具显著统计学意义(P<0.01);DMP组内皮覆盖率较GA组高,差异具显著统计学意义(P<0.01)。表明:光氧化反应处理的家兔胸主动脉在家兔胸-腹主动脉移植的动物模型中,生物稳定性高,细胞毒性低。 This study evaluated the biological stability and cytotoxicity of rabbit thoracic aorta cross-linked by dye-mediated photooxidation in vivo environment of blood flow. Rabbits, whose allogenic thoracic aorta was cross- linked by dye-mediated pbotooxidation (DMP, n=6) and glutaraldehyde (GA, n=6), were in the DMP group and GA group, respectively; rabbits, whose homogenic abdominal aorta was orthotopic transplanted (OT, n=6), were in the OT group. Then the donor arteries were transplanted into the position of the abdominal arteries of rabbits. After operation, the animals were fed for 1 month, then each of graft arteries was removed for observation. Biological stability was evaluated through histological analysis under optical microscope. Cytotoxicity was evaluated through ratio of coverage of endothelial cell (ES) under scanning-electron microscope. The results showed that no statistically significant difference was noted between DMP group and OT group (P〉0.05)3 however, there was a significant difference between DMP group and GA group (P〈0.01). The stability index in DMP group was much higher than that in GA group. There was a statistically significant difference between DMP group and GA group (P〈0.01). Ratio was much higher in DMP group than in GA group. In conclusion, the arteries cross-linked by dye-mediated photooxidation treatment appeared to have higher biological stability and lower cytotoxicity in rabbit allogenic transplation model.
出处 《生物医学工程学杂志》 EI CAS CSCD 北大核心 2009年第2期390-393,共4页 Journal of Biomedical Engineering
基金 山东省自然科学基金资助项目(Y2007C011)
关键词 染料介导光氧化 同种异体动脉 移植 生物稳定性 细胞毒性 Dye-mediated photooxidation (DMP) Allogenic artery Transplantation Biologicalstability Cytotoxieity
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参考文献10

  • 1田鹏,陈剑秋.小口径人工血管材料的研究进展[J].透析与人工器官,2004,15(3):32-38. 被引量:5
  • 2蔡小满,刘锦纷.血管组织工程的进展[J].中国胸心血管外科临床杂志,2003,10(4):290-293. 被引量:3
  • 3BENGTSSON L A, PHILLIPS R, HAEGERSTRAND A N. In vitro endothelialization of photooxidatively stabilized xenogeneic pericardium[J]. Ann Thorac Surg, 1995,60(2 suppl) : s365-s368.
  • 4MOORE M A, PHILLIPS R E Jr, MCLLROY B K, et al. Evaluation of porcine valves prepared by dye-mediated photooxidation[J]. Ann Thorae Surg,1998,66(6 suppl) :s245-s248.
  • 5WESTABY S, BIANCO R W, KATSUMATA T, et al. The carbomedics "Oxford"photofix stentless valve (PSV)[J]. Semin Thorac Cardiovasc Surg, 1999,11 (4 suppl 1) :206-209.
  • 6MOORE M A, PHILIPS R E. Bioeompatibility and immunologic properties of pericardial tissue stabilized by dye-mediated photooxidation[J]. J Heart Valve Dis, 1997,6 (3) : 307-315.
  • 7谷志涛,刘鲁祁.染料介导光氧化法处理的同种异体动脉体内近期抗钙化性能评价[J].山东大学学报(医学版),2007,45(10):1050-1053. 被引量:1
  • 8MOORE M A, ADAMS A K. Calcification resistance, biostability and low immunogenic potential of porcine heart valves modified by dye-mediated photooxidation[J]. J Biomed Mater Res, 2001 ;56(1) :24-30.
  • 9冯耀光,吴忠仕,胡建国,胡铁辉,张竟超,徐朝军,王晖,马忠夏.光氧化反应处理牛颈静脉带瓣管道的形态学与理化性能研究[J].中南大学学报(医学版),2004,29(4):429-431. 被引量:13
  • 10VESELY I. Analysis of the medtronic intact bioprosthetie valve : Effects of "zero-pressure" fixation[J]. Thorac Cardiovasc Surg, 1991,101(1) :90-99.

二级参考文献65

  • 1田鹏,陈剑秋.小口径人工血管材料的研究进展[J].透析与人工器官,2004,15(3):32-38. 被引量:5
  • 2Kim BS, Baez CE, Atala A. Biomaterials for tissue engineering.World J Urol, 2000, 18(1):2-9.
  • 3Weinberg CB, Bell E. A blood vessel model constructed from collagen and cultured vascular cells. Science, 1986, 231(4736):397 400.
  • 4Berglund JD, Mohseni MM, Nerem RM, et al. A biological hybrid model for collagen-based tissue engineered vascular constructs. Biomaterials, 2003, 24(7) :1241-1254.
  • 5Girton TS, Oegema TR, Grassl ED, et al. Mechanisms of stiffening and strengthening in media-equivalents fabricated using glyeation. J Biomech Eng, 2000, 122(3):216-223.
  • 6L'Heureux N. Paquet S, Labbe R, et al. A completely biological tissue-engineered human blood vessel. FASEB J,1998.12(1):47-56.
  • 7Shinoka T, Shum-Tim D, Ma PX, et al. Creation of viable pulmonary artery autografts through tissue engineering. J Thorae Cardiovase Surg, 1998, 115(3):536-545.
  • 8Shum-Tim D, Stock U, Hrkach J, et al. Tissue engineering of autologous aorta using a new biodegradable polymer. Ann Thorac Surg, 1999, 68(6):2298-2304.
  • 9Niklason LE, Gao J, Abbott WM, et al. Functional arteries grown in vitro. Science, 1999, 284(5413):489-493.
  • 10Hoerstrup SP, Zund G, Sodlan R, et al. Tissue engineering of small caliber vascular grafts. Eur J Cardlothorac Surg, 2001, 20(1) : 164-169.

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