A 3D‐Printed Assemblable Bespoke Scaffold as a Versatile Microcryogel Carrier for Site‐Specific Regenerative Medicine

间充质干细胞 材料科学 血管生成 脚手架 生物医学工程 骨形态发生蛋白2 脐静脉 生物陶瓷 再生医学 血管内皮生长因子 纳米技术 干细胞 细胞生物学 体外 生物 医学 癌症研究 血管内皮生长因子受体 生物化学
作者
Seunghun S. Lee,Nicole Kleger,Gisela Kuhn,Helen Greutert,Xiaoyu Du,Thijs Smit,André R. Studart,Stephen J. Ferguson
出处
期刊:Advanced Materials [Wiley]
卷期号:35 (44) 被引量:6
标识
DOI:10.1002/adma.202302008
摘要

Advances in additive manufacturing have led to diverse patient-specific implant designs utilizing computed tomography, but this requires intensive work and financial implications. Here, Digital Light Processing is used to fabricate a hive-structured assemblable bespoke scaffold (HIVE). HIVE can be manually assembled in any shape/size with ease, so a surgeon can create a scaffold that will best fit a defect before implantation. Simultaneously, it can have site-specific treatments by working as a carrier filled with microcryogels (MC) incorporating different biological factors in different pockets of HIVE. After characterization, possible site-specific applications are investigated by utilizing HIVE as a versatile carrier with incorporated treatments such as growth factors (GF), bioceramic, or cells. HIVE as a GF-carrier shows a controlled release of bone morphogenetic protein/vascular endothelial growth factor (BMP/VEGF) and induced osteogenesis/angiogenesis from human mesenchymal stem cells (hMSC)/human umbilical vein endothelial cells (HUVECs). Furthermore, as a bioceramic-carrier, HIVE demonstrates enhanced mineralization and osteogenesis, and as a HUVEC carrier, it upregulates both osteogenic and angiogenic gene expression of hMSCs. HIVE with different combinations of MCs yields a distinct local effect and successful cell migration is confirmed within assembled HIVEs. Finally, an in vivo rat subcutaneous implantation demonstrates site-specific osteogenesis and angiogenesis.

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