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聚乳酸/聚羟基乙酸共聚物网管支架体外预血管化及体内植入的实验研究 被引量:7

A STUDY ON IN VITRO FORCE-VASCULARIZATION AND IN VIVO VASCULARIZATION OF POROUS POLYLACTIC/GLYCOLIC ACID COPOLYMER SCAFFOLDS WITH INTERNAL NETWORK CHANNELS
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摘要 目的研究预血管化对含网管的多孔可降解聚乳酸/聚羟基乙酸共聚物(polylacticl/glycolicacidcopolymer,PLGA)支架血管化的影响。方法将含网管的多孔可降解PLGA支架由小鼠微血管内皮细胞预血管化,分为体外预血管化组(A组)和单纯支架组(B组)。将两组支架植入12只雌性NIH小鼠肠系膜间,分别于术后2、4周取材,行组织学及免疫组织化学观察血管化情况,并应用图像分析软件计算支架血管化面积。结果支架体外预血管化后,其网管内可见微血管内皮细胞均匀贴壁。支架植入体内2周,切片血管化面积A组为2260.91±242.35μm2与B组823.64±81.29μm2比较,差异有统计学意义(P<0.01);4周时A组为17284.36±72.67μm2与B组17041.14±81.51μm2比较,差异无统计学意义(P>0.05)。植入2周支架切片肌动蛋白阳性染色面积A组为565.22±60.58μm2与B组205.91±16.25μm2比较,差异有统计学意义(P<0.01);4周时A组为4321.09±19.82μm2与B组4260.28±27.17μm2比较,差异无统计学意义(P>0.05)。结论含网管的多孔可降解PLGA支架是一种良好的简易血管化支架模型;预血管化可以明显增强支架植入早期的血管化。 Objective To study the influence of in vitro force-vascularization on in vivo vascularization of porous polylactic glycolic acid copolymer(PLGA) scaffolds with internal network channels (PPSINC). Methods After the in vitro force-vascularization of PPSINCs covered with microvessel endothelial cells (MVEC) of mice, they were divided into two groups: the force-vascularization group (group A) and the control group with only PSINCs (group B). All the PPSINCs were planted in the mesentery of 12 mice for 2 and 4 weeks, the PPSINCs were cut out, the vascularization of PPSINCs was investigated by histology and immunohistochemistry, and the vascularization area of the histologic section of the PPSINCs was measured with the computer assistant image analysis system. Results After the in vitro force vascularization of PPSINCs, the MVEC of the mice sticking on the channel wall could be seen. After the scaffold was implanted into the mice for 2 weeks, the vascularization area of the histologic section of PPSINCs (VA) in group A (2 260. 91± 242.35 μm^2) was compared with that in group B (823.64± 81.29μm^2),and the difference was significant in statistics(P〈0.01). The VA for 4 weeks in group A (17 284.36±72.67μm^2) was compared with that in group B (17 041.14±81.51μm^2),and the difference was not significant in statistics(P〉0.05). The area of the actin positive staining (AA) in the histologic section of PPSINCs for 2 weeks' implantation in group A (565.22±60.58μm^2) was compared with that in group B (205.91±16.25μm^2), and the difference was significant in statistics (P〈0.01). After the implantation for 4 weeks, the VA in group A (4 321.09±19. 82 μm^2) was compared with group B (4 260. 28±27.17μm^2), and the difference was not significant in statistics(P〉0.05). Conclusion The PPSINC is a good simple scaffold model of vasculariazation. The in vitro force-vascularization can increase the in vivo vascularization of PPSINCs in the early stage.
出处 《中国修复重建外科杂志》 CAS CSCD 北大核心 2006年第2期181-184,共4页 Chinese Journal of Reparative and Reconstructive Surgery
基金 军队医药卫生科研基金"十五"计划面上资助项目(01MB084)~~
关键词 预血管化 聚乳酸/聚羟基乙酸共聚物 支架 血管化 Force-vascularization Polylactic/glycolic acid copolymer Scaffold Vascularization
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参考文献14

  • 1吴仕和,徐迎新,阎锡蕴,宋旭华,尹太,王金晶,李荣.纤维蛋白凝胶立体培养诱导血管样结构的形成[J].中华实验外科杂志,2004,21(3):337-338. 被引量:12
  • 2Langer RS, Vacanti JP. Tissue engineering: the challenges ahead.Sci Am,1999,280(4):86-89.
  • 3Vacanti JP, Langer R. Tissue engineering: the design and fabrication of living replacement devices for surgical reconstruction and transplantation. Lancet, 1999,354 (Suppl) : 32-34.
  • 4Langer R, Vancanti JP. Tissue Engineering. Science, 1993, 260(5110) : 920-926.
  • 5徐迎新,吴仕和,阎锡蕴,宋旭华,尹太,王金晶,李荣.预制微血管样结构凝胶的植入研究[J].中华实验外科杂志,2005,22(8):954-955. 被引量:8
  • 6Hasirei V, Berthiaume F, Bondre SP, et al. Expression of liver-specific functions by rat hepatocytes seeded in treated poly (lactic co-glycolic) acid biodegradable foams. Tissue Eng, 2001,7 (4):385-394.
  • 7Kim SS,Utsunomiya H,Koski JA,et al. Survival and function of hepatocytes on novel three-dimensional synthetic biodegradable polymer scaffolds with an intrinsic network of channels. Ann Surg, 1998,228 (1) :8-13.
  • 8Seal BL, Otero TC, Pahitch A, et al. Polymeric biomaterials for tissue and organ regeneration. Mater Sci Eng,2001,34: 147-230.
  • 9Mayer J, Karamuk E, Akaike T, et al. Matrices of tissue engineering scaffold structure for a bioartifical liver support system. J Control Res,2000,64(2) ..81-89.
  • 10Kaufman PM,Heimrath S, Kim BS,et al. Highly porous matrices as a three-dimensional culture system for hepatocytes. Cell Transplant, 1997,6 (5) : 463-468.

二级参考文献6

  • 1Kahalibmarzouk JF, Kooper T. Allograft replacement of the tracheal. J Thorac Cardiovasc Surg, 1993, 105:242-246.
  • 2Dan F. Lab-grown organs begin to take shape. Sclece, 1999, 284:422-425.
  • 3Breat R, Zanger DE, Sassaoki T, et al. Methods in laboratory investigation: assessment of a method of isolation, purification, and cultivation of rat liver sinusoidal endothelial cells. Laboratory Investigation, 1994, 70:944-995.
  • 4Mconey DJ, Kaufman PM, Sano K, et al. Transplantation of hepatocytes using porous, biodegradable sponges. Transplantation Proceeding, 1994,26:3425-3426.
  • 5陈慧梅,廖红,高静.肝细胞培养方法研究进展[J].细胞生物学杂志,2002,24(3):163-166. 被引量:22
  • 6吴仕和,徐迎新,阎锡蕴,宋旭华,尹太,王金晶,李荣.纤维蛋白凝胶立体培养诱导血管样结构的形成[J].中华实验外科杂志,2004,21(3):337-338. 被引量:12

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