State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Int J Artif Organs. 2021 May;44(5):340-349. doi: 10.1177/0391398820959345. Epub 2020 Sep 24.
The study aimed to develop a biocompatible microcapsule for hepatocytes and create a bio-mimic microenvironment for maintaining hepatic-specific functions of hepatocytes in vitro. The work is proposed for the bioartificial liver system in the treatment of liver failure. In this study, microcapsules were prepared with hyaluronate (HA)/sodium alginate (SA) as an inner core and an outer chitosan (CS) shell via one-step spraying method. C3A cells were encapsulated in microcapsules to examine the biocompatibility of HA-SA-CS microcapsules. MTT and fluorescence microscopy indicated that C3A cells had high viability in the HA-SA-CS microcapsules. The liver-specific functions, such as urea and albumin synthesis, and CYP1A2 and CYP3A4 activities from encapsulated cells were increased in the HA-SA-CS microcapsules compared to the SA-CS microcapsules. The gene expressions of CYP450 related genes were also increased by HA on day 3. The study suggests that HA-SA-CS microcapsules have good biocompatibility and can maintain a favorable environment for hepatocytes. This approach has improved the preservation of liver cells' metabolic functions and could be a candidate for the bioartificial liver system.
本研究旨在开发一种用于肝细胞的生物相容性微胶囊,并为体外维持肝细胞的肝特异性功能创建一种仿生微环境。这项工作是为肝衰竭的生物人工肝系统提出的。在这项研究中,通过一步喷涂法将透明质酸(HA)/海藻酸钠(SA)作为内芯和壳聚糖(CS)外壳制备微胶囊。将 C3A 细胞包封在微胶囊中,以检查 HA-SA-CS 微胶囊的生物相容性。MTT 和荧光显微镜观察表明,C3A 细胞在 HA-SA-CS 微胶囊中具有高活力。与 SA-CS 微胶囊相比,包封细胞的尿素和白蛋白合成以及 CYP1A2 和 CYP3A4 活性等肝特异性功能在 HA-SA-CS 微胶囊中增加。第 3 天,HA 还增加了 CYP450 相关基因的表达。研究表明,HA-SA-CS 微胶囊具有良好的生物相容性,并能为肝细胞维持良好的环境。这种方法提高了肝细胞代谢功能的保存,可能成为生物人工肝系统的候选方案。