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用于细胞培养和生物制剂递送的凝血因子Xa响应材料的开发与表征

Development and characterization of Factor Xa-responsive materials for applications in cell culture and biologics delivery.

作者信息

Doron Gilad, Pearson Joseph J, Guldberg Robert E, Temenoff Johnna S

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia, USA.

Knight Campus for Accelerating Scientific Impact, 6231 University of Oregon, Eugene, Oregon, USA.

出版信息

J Biomed Mater Res A. 2023 May;111(5):634-643. doi: 10.1002/jbm.a.37513. Epub 2023 Feb 16.

Abstract

Stimuli-responsive biomaterials may be used to better control the release of bioactive molecules or cells for applications involving drug delivery and controlled cell release. In this study, we developed a Factor Xa (FXa)-responsive biomaterial capable of controlled release of pharmaceutical agents and cells from in vitro culture. FXa-cleavable substrates were formed as hydrogels that degraded in response to FXa enzyme over several hours. Hydrogels were shown to release both heparin and a model protein in response to FXa. Additionally, RGD-functionalized FXa-degradable hydrogels were used to culture mesenchymal stromal cells (MSCs), enabling FXa-mediated cell dissociation from hydrogels in a manner that preserved multicellular structures. Harvesting MSCs using FXa-mediated dissociation did not influence their differentiation capacity or indoleamine 2,3-dioxygenase (IDO) activity (a measure of immunomodulatory capacity). In all, this FXa-degradable hydrogel is a novel responsive biomaterial system that may be used for on-demand drug delivery, as well as for improving processes for in vitro culture of therapeutic cells.

摘要

刺激响应性生物材料可用于更好地控制生物活性分子或细胞的释放,以用于药物递送和可控细胞释放等应用。在本研究中,我们开发了一种能响应凝血因子Xa(FXa)的生物材料,它能够从体外培养物中可控释放药剂和细胞。可被FXa切割的底物形成水凝胶,这种水凝胶会在数小时内响应FXa酶而降解。已证明水凝胶会响应FXa释放肝素和一种模型蛋白。此外,用RGD功能化的可被FXa降解的水凝胶来培养间充质基质细胞(MSC),使得FXa介导细胞从水凝胶中解离,且能保持多细胞结构。使用FXa介导的解离方法收获MSC不会影响其分化能力或吲哚胺2,3-双加氧酶(IDO)活性(一种免疫调节能力的衡量指标)。总之,这种可被FXa降解的水凝胶是一种新型的响应性生物材料系统,可用于按需给药,以及改进治疗性细胞的体外培养方法。

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