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采用可生物吸收弹性植入物的原位心脏瓣膜组织工程 - 从材料设计到绵羊 12 个月的随访。

In situ heart valve tissue engineering using a bioresorbable elastomeric implant - From material design to 12 months follow-up in sheep.

机构信息

Department of Cardiothoracic Surgery, Academic Medical Center, Amsterdam, The Netherlands; Department of Cardiothoracic Surgery, University Medical Center, Utrecht, The Netherlands.

Department of Biomedical Engineering, Eindhoven University of Technology, The Netherlands; Institute for Complex Molecular Systems (ICMS), Eindhoven University of Technology, The Netherlands.

出版信息

Biomaterials. 2017 May;125:101-117. doi: 10.1016/j.biomaterials.2017.02.007. Epub 2017 Feb 8.

Abstract

The creation of a living heart valve is a much-wanted alternative for current valve prostheses that suffer from limited durability and thromboembolic complications. Current strategies to create such valves, however, require the use of cells for in vitro culture, or decellularized human- or animal-derived donor tissue for in situ engineering. Here, we propose and demonstrate proof-of-concept of in situ heart valve tissue engineering using a synthetic approach, in which a cell-free, slow degrading elastomeric valvular implant is populated by endogenous cells to form new valvular tissue inside the heart. We designed a fibrous valvular scaffold, fabricated from a novel supramolecular elastomer, that enables endogenous cells to enter and produce matrix. Orthotopic implantations as pulmonary valve in sheep demonstrated sustained functionality up to 12 months, while the implant was gradually replaced by a layered collagen and elastic matrix in pace with cell-driven polymer resorption. Our results offer new perspectives for endogenous heart valve replacement starting from a readily-available synthetic graft that is compatible with surgical and transcatheter implantation procedures.

摘要

制造活心脏瓣膜是目前瓣膜假体的理想替代品,因为目前的瓣膜假体存在耐久性有限和血栓栓塞并发症等问题。然而,目前制造此类瓣膜的策略需要使用细胞进行体外培养,或者使用去细胞化的人源或动物源性供体组织进行原位工程。在这里,我们提出并证明了使用合成方法进行原位心脏瓣膜组织工程的概念验证,其中使用无细胞、缓慢降解的弹性瓣膜植入物来填充内源性细胞,以在心脏内形成新的瓣膜组织。我们设计了一种纤维状瓣膜支架,由一种新型的超分子弹性体制成,使内源性细胞能够进入并产生基质。在绵羊的肺动脉瓣中的原位植入证明了其可持续功能长达 12 个月,而随着细胞驱动的聚合物吸收,植入物逐渐被分层的胶原和弹性基质取代。我们的结果为从易于获得的合成移植物开始的内源性心脏瓣膜置换提供了新的视角,这种移植物与手术和经导管植入程序兼容。

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