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基于生物功能化纳米复合生物材料的小直径旁路移植物的原位内皮化潜力

In situ endothelialization potential of a biofunctionalised nanocomposite biomaterial-based small diameter bypass graft.

作者信息

de Mel Achala, Punshon Geoffrey, Ramesh Bala, Sarkar Sandip, Darbyshire Arnold, Hamilton George, Seifalian Alexander M

机构信息

Centre for Nanotechnology, Biomaterial and Tissue Engineering, UCL Division of Surgery and Interventional Science, University College London, London, UK.

出版信息

Biomed Mater Eng. 2009;19(4-5):317-31. doi: 10.3233/BME-2009-0597.

Abstract

Endothelial dysfunction or the lack of an endothelium associated with cardiovascular grafts is a major cause of graft failure which is linked to thrombosis and related complications. This study was aimed to (1) biofunctionalise a nanocomposite biomaterial, Polyhedral Oligomeric silsesquioxane modified polycarbonate urea-urethane (POSS-PCU), based small diameter vascular graft and to (2) induce endothelialization with EPC containing monocytes, which were extracted from peripheral blood. (1) Biofunctionalisation of the nanocomposite polymer: bioactive RGD peptide, which is a functional domain of an extracellular matrix component, fibronectin, was synthesised using fmoc chemistry. A lauric acid hydrophobic "tail" was attached to optimise the RGD orientation on the biomaterial. The peptide was cross linked to POSS-PCU. The presence of RGD on the nanocomposite was tested with water contact angle measurements and specificity tests were carried out with the peptide RAD (2) Progenitor cells were extracted from peripheral blood of adult healthy volunteers and cultured on porous biofunctionalised nanocomposite polymer under static conditions. Cells were also introduced to a circuit to which the grafts are connected and non static pulsatile flow conditions were introduced after 72 h following cell introduction. The degree of cell growth was tested with Alamar Blue assay. Endothelialization was confirmed with SEM and by immunostaining for endothelial cell markers, CD34, CD31 and eNOS. Water contact angle measurement indicated that biofunctionalisation had increased hydrophilicity of the nanocomposite polymer. Alamar blue indicated a greater presence of cells on biofunctionalised nanocomposite and this relative increase in cell viability was specific to RGD as confirmed with RAD peptides. SEM provided evidence for endothelial cell morphology and this was confirmed with endothelial cell markers with immunostaining. Biofunctionalised nanocomposite polymer-based small diameter bypass graft demonstrated the potential for relatively rapid endothelialization from cells extracted from peripheral blood.

摘要

内皮功能障碍或与心血管移植物相关的内皮缺失是移植物失败的主要原因,这与血栓形成及相关并发症有关。本研究旨在:(1)对基于纳米复合生物材料——多面体低聚倍半硅氧烷改性聚碳酸酯脲-聚氨酯(POSS-PCU)的小直径血管移植物进行生物功能化;(2)利用从外周血中提取的含单核细胞的内皮祖细胞诱导内皮化。(1)纳米复合聚合物的生物功能化:使用芴甲氧羰基化学合成生物活性RGD肽,其为细胞外基质成分纤连蛋白的功能域。连接月桂酸疏水“尾”以优化生物材料上RGD的取向。该肽与POSS-PCU交联。通过水接触角测量测试纳米复合材料上RGD的存在,并使用肽RAD进行特异性测试。(2)从成年健康志愿者的外周血中提取祖细胞,并在静态条件下在多孔生物功能化纳米复合聚合物上培养。还将细胞引入与移植物相连的回路中,并在细胞引入后72小时引入非静态脉动流条件。用阿拉玛蓝测定法测试细胞生长程度。通过扫描电子显微镜(SEM)和对内皮细胞标志物CD34、CD31和内皮型一氧化氮合酶(eNOS)的免疫染色来确认内皮化。水接触角测量表明生物功能化增加了纳米复合聚合物的亲水性。阿拉玛蓝表明生物功能化纳米复合材料上细胞的存在更多,并且如用RAD肽所证实的,这种细胞活力的相对增加对RGD具有特异性。SEM提供了内皮细胞形态的证据,并且通过免疫染色的内皮细胞标志物证实了这一点。基于生物功能化纳米复合聚合物的小直径旁路移植物显示出来自外周血提取细胞相对快速内皮化的潜力。

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