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用于提高体积水凝胶中细胞活力的多孔可灌注微管状网络的构建。

Creation of Porous, Perfusable Microtubular Networks for Improved Cell Viability in Volumetric Hydrogels.

机构信息

Department of Biomedical Engineering, Stevens Institute of Technology, Hoboken, New Jersey 07030, United States.

Semcer Center for Healthcare Innovation, Stevens Institute of Technology, Hoboken, New Jersey 07030, United States.

出版信息

ACS Appl Mater Interfaces. 2024 Apr 17;16(15):18522-18533. doi: 10.1021/acsami.4c00716. Epub 2024 Apr 2.

Abstract

The creation of large, volumetric tissue-engineered constructs has long been hindered due to the lack of effective vascularization strategies. Recently, 3D printing has emerged as a viable approach to creating vascular structures; however, its application is limited. Here, we present a simple and controllable technique to produce porous, free-standing, perfusable tubular networks from sacrificial templates of polyelectrolyte complex and coatings of salt-containing citrate-based elastomer poly(1,8-octanediol--citrate) (POC). As demonstrated, fully perfusable and interconnected POC tubular networks with channel diameters ranging from 100 to 400 μm were created. Incorporating NaCl particulates into the POC coating enabled the formation of micropores (∼19 μm in diameter) in the tubular wall upon particulate leaching to increase the cross-wall fluid transport. Casting and cross-linking gelatin methacrylate (GelMA) suspended with human osteoblasts over the free-standing porous POC tubular networks led to the fabrication of 3D cell-encapsulated constructs. Compared to the constructs without POC tubular networks, those with either solid or porous wall tubular networks exhibited a significant increase in cell viability and proliferation along with healthy cell morphology, particularly those with porous networks. Taken together, the sacrificial template-assisted approach is effective to fabricate tubular networks with controllable channel diameter and patency, which can be easily incorporated into cell-encapsulated hydrogels or used as tissue-engineering scaffolds to improve cell viability.

摘要

由于缺乏有效的血管化策略,长期以来,大型、体积较大的组织工程构建物的创建一直受到阻碍。最近,3D 打印技术已成为创建血管结构的可行方法;然而,其应用受到限制。在这里,我们提出了一种简单且可控的技术,可从聚电解质复合物的牺牲模板和含盐柠檬酸酯弹性体聚(1,8-辛二醇-柠檬酸)(POC)的涂层中生产出多孔、独立、可灌注的管状网络。结果表明,成功制备了具有 100 至 400μm 通道直径的完全可灌注和相互连通的 POC 管状网络。将 NaCl 颗粒掺入 POC 涂层中,可在颗粒浸出时在管状壁中形成微孔(直径约 19μm),从而增加跨壁流体传输。将悬浮有人骨肉瘤细胞的明胶甲基丙烯酰(GelMA)浇铸和交联在独立的多孔 POC 管状网络上,可制造出 3D 细胞包封的构建体。与没有 POC 管状网络的构建体相比,具有实心或多孔壁管状网络的构建体的细胞活力和增殖显著增加,同时具有健康的细胞形态,尤其是具有多孔网络的构建体。总之,牺牲模板辅助方法可有效地制造具有可控通道直径和通畅性的管状网络,可轻松地将其纳入细胞包封的水凝胶中或用作组织工程支架,以提高细胞活力。

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