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设计并制备聚氨酯-胶原/肝素接枝聚己内酯双层仿生小口径血管移植物及其初步动物试验。

Design and preparation of polyurethane-collagen/heparin-conjugated polycaprolactone double-layer bionic small-diameter vascular graft and its preliminary animal tests.

机构信息

Department of Pediatric Cardiac Surgery, Beijing Children Hospital, Capital Medical University, Beijing 100045, China.

出版信息

Chin Med J (Engl). 2013 Apr;126(7):1310-6.

Abstract

BACKGROUND

People recently realized that it is important for artificial vascular biodegradable graft to bionically mimic the functions of the native vessel. In order to overcome the high risk of thrombosis and keep the patency in the clinical small-diameter vascular graft (SDVG) transplantation, a double-layer bionic scaffold, which can offer anticoagulation and mechanical strength simultaneously, was designed and fabricated via electrospinning technique.

METHODS

Heparin-conjugated polycaprolactone (hPCL) and polyurethane (PU)-collagen type I composite was used as the inner and outer layers, respectively. The porosity and the burst pressure of SDVG were evaluated. Its biocompatibility was demonstrated by the 3-(4,5-dimethyl-2-thiazol)-2,5-diphenyl-2H tetrazolium bromide (MTT) test in vitro and subcutaneous implants in vivo respectively. The grafts of diameter 2.5 mm and length 4.0 cm were implanted to replace the femoral artery in Beagle dog model. Then, angiography was performed in the Beagle dogs to investigate the patency and aneurysm of grafts at 2, 4, and 8 weeks post-transplantation. After angiography, the patent grafts were explanted for histological analysis.

RESULTS

The double-layer bionic SDVG meet the clinical mechanical demand. Its good biocompatibility was proven by cytotoxicity experiment (the cell's relative growth rates (RGR) of PU-collagen outer layer were 102.8%, 109.2% and 103.5%, while the RGR of hPCL inner layer were 99.0%, 100.0% and 98.0%, on days 1, 3, and 5, respectively) and the subdermal implants experiment in the Beagle dog. Arteriography showed that all the implanted SDVGs were patent without any aneurismal dilatation or obvious anastomotic stenosis at the 2nd, 4th, and 8th week after the operation, except one SDVG that failed at the 2nd week. Histological analysis and SEM showed that the inner layer was covered by new endothelial-like cells.

CONCLUSION

The double-layer bionic SDVG is a promising candidate as a replacement of native small-diameter vascular graft.

摘要

背景

人们最近意识到,人工血管生物可降解移植物仿生模拟天然血管的功能非常重要。为了克服临床小直径血管移植物(SDVG)移植中高血栓风险并保持通畅性,通过静电纺丝技术设计并制造了一种双层仿生支架,该支架可以同时提供抗凝和机械强度。

方法

使用肝素化聚己内酯(hPCL)和聚氨酯(PU)-I 型胶原复合材料分别作为内层和外层。评估 SDVG 的孔隙率和爆裂压力。通过体外 3-(4,5-二甲基-2-噻唑)-2,5-二苯基-2H 四唑溴盐(MTT)试验和体内皮下植入物分别证明了其生物相容性。将直径为 2.5mm、长度为 4.0cm 的移植物植入 Beagle 犬模型以替代股动脉。然后,在移植后 2、4 和 8 周对 Beagle 犬进行血管造影以研究移植物的通畅性和动脉瘤。血管造影后,取出通畅的移植物进行组织学分析。

结果

双层仿生 SDVG 满足临床力学需求。细胞毒性实验(PU-胶原外层的细胞相对生长率(RGR)分别为 102.8%、109.2%和 103.5%,而 hPCL 内层的 RGR 分别为 99.0%、100.0%和 98.0%,在第 1、3 和 5 天)和 Beagle 犬皮下植入实验证明了双层仿生 SDVG 的良好生物相容性。血管造影显示,所有植入的 SDVG 在手术后第 2、4 和 8 周均保持通畅,没有任何动脉瘤扩张或明显吻合口狭窄,除了一个在第 2 周失败的 SDVG。组织学分析和 SEM 显示内层被新的内皮样细胞覆盖。

结论

双层仿生 SDVG 是一种有前途的天然小直径血管移植物替代品。

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