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Novel methodology based on biomimetic superhydrophobic substrates to immobilize cells in hydrogel spheres for tissue engineering applications

机译:基于仿生超疏水底物的新型方法,可将细胞固定在水凝胶球体中,用于组织工程应用

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摘要

The low retention/integration of injected cells by host structures representsan important challenge in cell based therapies for regenerativemedicine purposes. Cell immobilization in hydrogels for target celldelivery has been developed to circumvent this issue. However, theexisting immobilization methodologies sometimes have several stepsunder wet conditions and present some drawbacks, including poorencapsulation efficiency and the use of harmful conditions for cells orother fragile molecules, such as proteins or growth factors. In order tosurpass these problems mesenchymal stem cells isolated from rats(rMSCs) bone marrow and fibronectin (FN) were immobilized in alginatebeads to mimic extracellular matrix environment using an innovativeapproach involving the jellification of the liquid precursor dropletsonto superhydrophobic surfaces. The alginate drops with cells and FNhardened very fast, at room temperature, into hydrogels spheres in anisolated environment which avoided the loss of FN and any contaminationor exchange of molecules with other liquid phase. The process forparticle fabrication employed allowed a very high efficiency on FNencapsulation and also the mild conditions prevented the loss of cellviability. Encapsulated rMSCs remained viable and were slowlyreleased from the beads during more than 20 days.
机译:宿主结构对被注射细胞的低保留/整合性代表了基于细胞的再生医学目的疗法的一项重要挑战。已经开发出将水凝胶中的细胞固定化以用于靶细胞递送来解决这个问题。然而,现有的固定化方法有时在潮湿条件下具有多个步骤,并且存在一些缺点,包括封装效率低下以及对细胞或其他易碎分子(例如蛋白质或生长因子)使用有害条件。为了克服这些问题,使用一种创新的方法将从大鼠(rMSCs)分离的骨髓间充质干细胞和纤连蛋白(FN)固定在藻酸盐珠中,以模拟细胞外基质环境,这种方法涉及将液体前体dropletson胶凝成超疏水性表面。在室温下,藻酸盐与细胞一起滴落,并且FN在隔离环境中非常快速地硬化进入水凝胶球体,从而避免了FN的损失以及任何与其他液相的分子的污染或交换。所采用的颗粒制造方法可以使FN封装的效率非常高,而且温和的条件也可以防止细胞活力的丧失。封装的rMSC保持活力,并在超过20天的时间内从珠粒中缓慢释放。

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