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Development of Perfluoro Decalin/Fluorinated Polyimide Core–Shell Microparticles via SPG Membrane Emulsification Using Methyl Perfluoropropyl Ether Cosolvent

机译:使用甲基全氟丙基醚助溶剂通过 SPG 膜乳化开发全氟十氢/氟化聚酰亚胺核壳微粒

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摘要

Red blood cell-inspired perfluorocarbon-encapsulated core–shell particles have been developed for biomedical applications. Although the use of perfluorodecalin (FDC) is expected for core–shell particles owing to its high oxygen solubility, the low solubility of FDC in any organic solvent, owing to its fluorous properties, prevents its use in core–shell particles. In this study, a new cosolvent system composed of dichloromethane (DCM) and heptafluoropropyl methyl ether (HFPME) was found to dissolve both FDC and fluorinated polyimide (FPI) based on a systematic study using a phase diagram, achieving a homogeneous disperse phase for emulsification composed of oxygen-permeable FPI and oxygen-soluble FDC. Using this novel cosolvent system and Shirasu porous glass (SPG) membrane emulsification, FDC-encapsulated FPI shell microparticles were successfully prepared for the first time. In addition to oxygenation, demonstrated using hypoxia-responsive HeLa cells, the fabricated core–shell microparticles exhibited monodispersity, excellent stability, biocompatibility, and oxygen capacity.
机译:红细胞启发的全氟化碳封装的核壳颗粒已开发用于生物医学应用。尽管由于全氟十氢萘 (FDC) 的高氧溶解度,预计会用于核壳颗粒,但由于其氟特性,FDC 在任何有机溶剂中的溶解度较低,因此无法在核壳颗粒中使用。在本研究中,基于使用相图的系统研究,发现一种由二氯甲烷 (DCM) 和七氟丙基甲基醚 (HFPME) 组成的新型助溶剂系统可以溶解 FDC 和氟化聚酰亚胺 (FPI),实现由透氧 FPI 和氧溶性 FDC 组成的均匀分散乳化相。使用这种新型助溶剂系统和 Shirasu 多孔玻璃 (SPG) 膜乳化,首次成功制备了 FDC 封装的 FPI 壳微粒。除了使用缺氧反应性 HeLa 细胞证明的氧合外,制造的核壳微粒还表现出单分散性、优异的稳定性、生物相容性和氧容量。

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