Composite Hydrogels With Controlled Degradation in 3D Printed Scaffolds

乙二醇 活力测定 自愈水凝胶 材料科学 PEG比率 细胞包封 复合数 组织工程 脚手架 聚酯纤维 乳酸 化学工程 纳米技术 高分子化学 化学 细胞 生物医学工程 复合材料 生物化学 生物 工程类 经济 医学 细菌 遗传学 财务
作者
Zhongliang Jiang,Rajib K. Shaha,Kun Jiang,Ralph McBride,Carl P. Frick,John Oakey
出处
期刊:IEEE Transactions on Nanobioscience [Institute of Electrical and Electronics Engineers]
卷期号:18 (2): 261-264 被引量:16
标识
DOI:10.1109/tnb.2019.2905510
摘要

Controlled cell delivery has shown some promising outcomes compared with traditional cell delivery approaches over the past decades, and strategies focused on optimization or engineering of controlled cell delivery have been intensively studied. In this paper, we demonstrate the fabrication of a 3D printed hydrogel scaffold infused with degradable PEGPLA/NB composite hydrogel core for controlled cell delivery with improved cell viability and facile tunability. The 3D printed poly (ethylene glycol) diacrylate (PEGDA) scaffold with specifically designed architectures can provide mechanical support while allowing bidirectional diffusion of small molecules, thus permitting structural integrity and long-term cell viability. Poly(lactic acid)-poly(ethylene glycol)-poly(lactic acid) (PLA-PEG-PLA), which is highly susceptible to hydrolysis, however, the acrylation reactions it utilizes for chain growth have been reported as toxic to cells. Poly(ethylene glycol) norbornene (PEGNB), validated for its excellent cytocompatibility, was therefore mixed and infused together with PLA-PEG-PLA into the printed PEGDA scaffold. Cells encapsulated microfluidically into PEGNB microspheres and then polymerized within PEGPLA/NB composite hydrogel maintained excellent viability over a week. Controlled cell release was achieved via the manipulation of PEGPLA/NB composition. By increasing PEGNB proportion in the core, cell release was significantly slowed while increasing PLA-PEG-PLA proportion eventually resulted in a very robust cell release within a short time frame. The functionality of released cells was validated by their cell viability and proliferation potential. In summary, we have shown this droplet-microencapsulation technique coupled with composite degradable hydrogel and 3D printing could offer an alternative route for controlled cell delivery.

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