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Fibrin-based tissue engineering: Comparison of different methods of autologous fibrinogen isolation

机译:基于纤维蛋白的组织工程:自体纤维蛋白原分离的不同方法的比较

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Objective: This study is focussed on the optimal method of autologous fibrinogen isolation with regard to the yield and the use as a scaffold material. This is particularly relevant for pediatric patients with strictly limited volumes of blood. Materials and Methods: The following isolation methods were evaluated: cryoprecipitation, ethanol (EtOH) precipitation, ammonium sulfate [(NH4)2SO4)] precipitation, ammonium sulfate precipitation combined with cryoprecipitation, and polyethylene glycol precipitation combined with cryoprecipitation. Fibrinogen yields were quantified spectrophotometrically and by electrophoretic analyses. To test the influence of the different isolation methods on the microstructure of the fibrin gels, scanning electron microscopy (SEM) was used and the mechanical strength of the cell-free and cell-seeded fibrin gels was tested by burst strength measurements. Cytotoxicity assays were performed to analyze the effect of various fibrinogen isolation methods on proliferation, apoptosis, and necrosis. Tissue development and cell migration were analyzed in all samples using immunohistochemical techniques. The synthesis of collagen as an extracellular matrix component by human umbilical cord artery smooth muscle cells in fibrin gels was measured using hydroxyproline assay. Results: Compared to cryoprecipitation, all other considered methods were superior in quantitative analyses, with maximum fibrinogen yields of ??80% of total plasma fibrinogen concentration using ethanol precipitation. SEM imaging demonstrated minor differences in the gel microstructure. Ethanol-precipitated fibrin gels exhibited the best mechanical properties. None of the isolation methods had a cytotoxic effect on the cells. Collagen production was similar in all gels except those from ammonium sulfate precipitation. Histological analysis showed good cell compatibility for ethanol-precipitated gels. Conclusion: The results of the present study demonstrated that ethanol precipitation is a simple and effective method for isolation of fibrinogen and a suitable alternative to cryoprecipitation. This technique allows minimization of the necessary blood volume for fibrinogen isolation, particularly important for pediatric applications, and also has no negative influence on microstructure, mechanical properties, cell proliferation, or tissue development. ? 2013, Mary Ann Liebert, Inc.
机译:目的:本研究着眼于自体纤维蛋白原分离的最佳方法,涉及产量和用作支架材料的方面。这对于血液量严格受限的小儿患者尤其重要。材料和方法:评价了以下分离方法:低温沉淀,乙醇(EtOH)沉淀,硫酸铵[(NH4)2SO4)]沉淀,硫酸铵沉淀与低温沉淀结合以及聚乙二醇沉淀与低温沉淀结合。通过分光光度法和电泳分析定量纤维蛋白原的产量。为了测试不同分离方法对血纤蛋白凝胶微观结构的影响,使用了扫描电子显微镜(SEM),并通过破裂强度测量测试了无细胞和接种细胞的血纤蛋白凝胶的机械强度。进行了细胞毒性测定,以分析各种纤维蛋白原分离方法对增殖,凋亡和坏死的影响。使用免疫组织化学技术分析了所有样品的组织发育和细胞迁移。使用羟脯氨酸测定法测量了人脐带动脉平滑肌细胞在纤维蛋白凝胶中胶原蛋白作为细胞外基质成分的合成。结果:与冷冻沉淀相比,所有其他考虑的方法在定量分析方面均优于其他方法,使用乙醇沉淀时最大的纤维蛋白原产率为血浆总纤维蛋白原浓度的80%。 SEM成像显示出凝胶微结构的微小差异。乙醇沉淀的纤维蛋白凝胶表现出最佳的机械性能。分离方法均未对细胞产生细胞毒性作用。除了来自硫酸铵沉淀的凝胶外,所有凝胶的胶原蛋白生产均相似。组织学分析显示乙醇沉淀凝胶具有良好的细胞相容性。结论:本研究结果表明乙醇沉淀是分离纤维蛋白原的一种简单有效的方法,是冷冻沉淀的合适替代方法。该技术可将血纤蛋白原分离所需的最小血容量降至最低,这对儿科应用尤为重要,并且对微结构,机械性能,细胞增殖或组织发育没有负面影响。 ? 2013年,玛丽·安·利伯特(Mary Ann Liebert,Inc.)

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