ACS Appl Mater Interfaces. 2018 Aug 1;10(30):25069-25079. doi: 10.1021/acsami.8b06386. Epub 2018 Jul 20.
Nanofiber microspheres have attracted a lot of attention for biomedical applications because of their injectable and biomimetic properties. Herein, we report for the first time a new method for fabrication of nanofiber microspheres by combining electrospinning and electrospraying and explore their potential applications for cell therapy. Electrospraying of aqueous dispersions of electrospun nanofiber segments with desired length obtained by either cryocutting or homogenization into liquid nitrogen followed by freeze-drying and thermal treatment can form nanofiber microspheres. The microsphere size can be controlled by varying the applied voltage during the electrospray process. A variety of morphologies were achieved including solid, nanofiber, porous and nanofiber microspheres, and hollow nanofiber microspheres. Furthermore, a broad range of polymer and inorganic bioactive glass nanofiber-based nanofiber microspheres could be fabricated by electrospraying of their short nanofiber dispersions, indicating a comprehensive applicability of this method. A higher cell carrier efficiency of nanofiber microspheres as compared to solid microspheres was demonstrated with rat bone marrow-derived mesenchymal stem cells, along with the formation of microtissue-like structures in situ, when injected into microchannel devices. Also, mouse embryonic stem cells underwent neural differentiation on the nanofiber microspheres, indicated by positive staining of β-III-tubulin and neurite outgrowth. Taken together, we developed a new method for generating nanofiber microspheres that are injectable and have improved viability and maintenance of stem cells for potential application in cell therapy.
纳米纤维微球因其可注射和仿生特性而在生物医学应用中引起了广泛关注。在此,我们首次报道了一种通过静电纺丝和静电喷雾相结合制备纳米纤维微球的新方法,并探索了其在细胞治疗中的潜在应用。通过将通过冷冻切割或匀浆到液氮中获得的所需长度的静电纺纳米纤维段的水性分散体进行静电喷雾,然后进行冷冻干燥和热处理,可以形成纳米纤维微球。通过改变静电喷雾过程中的施加电压,可以控制微球的尺寸。实现了多种形态,包括实心、纳米纤维、多孔和纳米纤维微球,以及中空纳米纤维微球。此外,通过静电喷雾其短纳米纤维分散体,可以制备出多种聚合物和无机生物活性玻璃纳米纤维基纳米纤维微球,表明该方法具有广泛的适用性。与实心微球相比,纳米纤维微球作为细胞载体的效率更高,当将其注入微通道装置时,体内原位形成微组织样结构。此外,在纳米纤维微球上,小鼠胚胎干细胞经历了神经分化,β-III-微管蛋白的阳性染色和神经突的生长表明了这一点。总之,我们开发了一种新的方法来生成可注射的纳米纤维微球,提高了干细胞的活力和维持能力,为细胞治疗的潜在应用提供了可能。