Jingyan Shi , Jianing Li , Jingyun Ma , Xiaoling Yang , Chang Xue , Yuan Zhang , Xinghua Gao
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引用次数: 0
Abstract
Microphysiological systems, including organ-on-a-chip systems, can achieve in vitro biomimicry of tissues and organs using microfluidic three-dimensional cell culture devices. These technologies can compensate for the shortcomings of animal models in basic disease research, and can even replace them in some cases. For example, they have demonstrated significant advantages and potential in the evaluation and screening of drugs for diabetes. In this study, we developed an islet microphysiological system based on a fibrous material and microfluidic spinning. This system includes pancreatic islet-loaded microfibers prepared using controllable pneumatic valves combined with microfluidic spinning technology and a microfluidic system comprising microfibers assembled with vascular endothelial cells. The results showed that the prepared microfibers loaded a large number of monodisperse pancreatic islet clusters with good cell activity and function. Microfibers were assembled with vascular endothelial cells in a microfluidic system, providing a 3D environment that mimicked natural blood vessels and supported high-throughput cell loading. Microfibers are vascularized by endothelial cells that grow on their surfaces. The microfluidic system simulated capillary blood flow and nutrient exchange, thereby enhancing the physiological relevance of the model. We evaluated the diabetes treatment drug Glucagon-like peptide-1 (GLP-1) using this system. Immunofluorescence staining, RT-qPCR, and ELISA confirmed the glucose-lowering and cardiovascular protective effects of GLP-1. This islet microphysiological system provides a novel platform for studying diabetes, screening new drugs, and promoting personalized medicine. The ability of this system to simulate physiological conditions through the synergy of biophysical and biochemical factors makes it a powerful tool for biomedical research.
期刊介绍:
Biomaterials is an international journal covering the science and clinical application of biomaterials. A biomaterial is now defined as a substance that has been engineered to take a form which, alone or as part of a complex system, is used to direct, by control of interactions with components of living systems, the course of any therapeutic or diagnostic procedure. It is the aim of the journal to provide a peer-reviewed forum for the publication of original papers and authoritative review and opinion papers dealing with the most important issues facing the use of biomaterials in clinical practice. The scope of the journal covers the wide range of physical, biological and chemical sciences that underpin the design of biomaterials and the clinical disciplines in which they are used. These sciences include polymer synthesis and characterization, drug and gene vector design, the biology of the host response, immunology and toxicology and self assembly at the nanoscale. Clinical applications include the therapies of medical technology and regenerative medicine in all clinical disciplines, and diagnostic systems that reply on innovative contrast and sensing agents. The journal is relevant to areas such as cancer diagnosis and therapy, implantable devices, drug delivery systems, gene vectors, bionanotechnology and tissue engineering.