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工程模块化、产氧微球,用于原位缓解细胞缺氧。

Engineering Modular, Oxygen-Generating Microbeads for the In Situ Mitigation of Cellular Hypoxia.

机构信息

J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL, 32610, USA.

Department of Immunology and Pathology, College of Medicine, University of Florida, Gainesville, FL, 32610, USA.

出版信息

Adv Healthc Mater. 2023 Jul;12(19):e2300239. doi: 10.1002/adhm.202300239. Epub 2023 Apr 20.

DOI:10.1002/adhm.202300239
PMID:36971050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10522802/
Abstract

Insufficient oxygenation is a key obstacle in the design of clinically scalable tissue-engineered grafts. In this work, an oxygen-generating composite material, termed OxySite, is created through the encapsulation of calcium peroxide (CaO ) within polydimethylsiloxane and formulated into microbeads for ease in tissue integration. Key material parameters of reactant loading, porogen addition, microbead size, and an outer rate-limiting layer are modulated to characterize oxygen generation kinetics and their suitability for cellular applications. In silico models are developed to predict the local impact of different OxySite microbead formulations on oxygen availability within an idealized cellular implant. Promising OxySite microbead variants are subsequently coencapsulated with murine β-cells within macroencapsulation devices, resulting in improved cellular metabolic activity and function under hypoxic conditions when compared to controls. Additionally, the coinjection of optimized OxySite microbeads with murine pancreatic islets within a confined transplant site demonstrates ease of integration and improved primary cell function. These works highlight the broad translatability delivered by this new oxygen-generating biomaterial format, whereby the modularity of the material provides customization of the oxygen source to the specific needs of the cellular implant.

摘要

氧合不足是临床可扩展组织工程移植物设计的关键障碍。在这项工作中,通过将过氧化钙 (CaO ) 封装在聚二甲基硅氧烷中并制成微珠,以方便组织整合,创建了一种称为 OxySite 的供氧复合材料。通过调节反应物负载、造孔剂添加、微珠大小和外部限速层等关键材料参数,来表征氧生成动力学及其在细胞应用中的适用性。开发了计算机模型来预测不同 OxySite 微珠配方对理想细胞植入物内氧气供应的局部影响。随后,将有前途的 OxySite 微珠与鼠 β 细胞共同包封在大微囊中,与对照相比,在缺氧条件下可提高细胞代谢活性和功能。此外,在受限移植部位中将优化的 OxySite 微珠与鼠胰岛共同注射,可证明其易于整合和提高原代细胞功能。这些工作突出了这种新型供氧生物材料格式带来的广泛转化潜力,其中材料的模块化可根据细胞植入物的具体需求定制氧气来源。

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