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Acrylate-based materials for heart valve scaffold engineering

机译:基于丙烯酸酯的心脏阀脚手架工程材料

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摘要

Calcific aortic valve disease (CAVD) is the most frequent cardiac valve pathology. Its standard treatment consists of surgical replacement either with mechanical (metal made) or biological (animal tissue made) valve prostheses, both of which have glaring deficiencies. In the search for novel materials to manufacture artificial valve tissue, we have conducted a high-throughput screening with subsequent up-scaling to identify non-degradable polymer substrates that promote valve interstitial cells (VICs) adherence/growth and, at the same time, prevent their evolution toward a pro-calcific phenotype. Here, we provide evidence that one of the two identified 'hit' polymers, poly(methoxyethylmethacrylate-co-diethylaminoethylmethacrylate), provided robust VICs adhesion and maintained the healthy VICs phenotype without inducing pro-osteogenic differentiation. This ability was also maintained when the polymer was used to coat a non-woven poly-caprolactone (PCL) scaffold using a novel solvent coating procedure, followed by bioreactor- assisted VICs seeding. Since we observed that VICs had an increased secretion of the elastinmaturing component MFAP4 in addition to other valve-specific extracellular matrix components, we conclude that valve implants constructed with this polyacrylate will drive the biological response of human valve-specific cells.
机译:钙化主动脉瓣病(CAVD)是最常见的心脏瓣膜病理学。其标准治疗包括用机械(金属制造)或生物(动物组织制造)阀假肢的手术替代品组成,这两者都具有辉煌的缺陷。在寻找制造人造瓣膜组织的新材料中,我们已经进行了高通量筛选,随后上缩放,以鉴定促进瓣膜间质细胞(VIC)粘附/生长的不可降解的聚合物基材,同时防止他们对促钙化表型的进化。这里,我们提供了两种鉴定的“击中”聚合物中的一种,聚(甲氧基甲基丙烯酸甲酯 - 二乙基氨基甲基丙烯酸甲基丙烯酸甲酯)中的一种,提供了鲁棒的VICS粘附,并保持健康的VICS表型而不诱导促骨析分化。当使用新的溶剂涂层程序使用聚合物来涂覆非织造聚己内酯(PCL)支架时,也保持这种能力,然后是生物反应器辅助的伴侣播种。由于我们观察到除了其他瓣膜特异性细胞外基质组分之外,VICS的分泌物增加了弹性蛋白染色组分MFAP4,我们得出结论,用该聚丙烯酸酯构建的阀门植入物将驱动人瓣膜特异性细胞的生物响应。

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  • 来源
    《Biomaterials Science》 |2018年第1期|共14页
  • 作者单位

    Unita di Ingegneria Tissutale Cardiovascolare Centro Cardiologico Monzino IRCCS Milan Italy;

    School of Chemistry EaStCHEM University of Edinburgh Edinburgh UK;

    Unita di Ingegneria Tissutale Cardiovascolare Centro Cardiologico Monzino IRCCS Milan Italy;

    School of Chemistry EaStCHEM University of Edinburgh Edinburgh UK;

    Unita di Proteomica Centro Cardiologico Monzino IRCCS Milan Italy;

    Institute for Bioengineering School of Engineering University of Edinburgh Edinburgh UK;

    Dipartimento Di Scienze Cliniche e di Comunita (Sez. Cardiovascolare) Universita di Milano Milan Italy;

    Unita di Proteomica Centro Cardiologico Monzino IRCCS Milan Italy;

    School of Chemistry EaStCHEM University of Edinburgh Edinburgh UK;

    Unita di Ingegneria Tissutale Cardiovascolare Centro Cardiologico Monzino IRCCS Milan Italy;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 计量学;
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