Electrospun nanoyarn scaffold and its application in tissue engineering
Highlights
► We prepared a novel nanoyarn scaffold using electrospinning. ► The scaffold has excellent surface properties and porous structures. ► L929 cells show an oriented growth pattern and improved cell infiltration on the nanoyarn scaffold.
Introduction
Recent approaches using electrospun scaffolds for tissue repair demonstrate the superiority of electrospinning in the fabrication of engineered scaffolds for tissue engineering applications [1]. Electrospun scaffolds have been widely investigated as substitutes for bone [2], cartilage [3] and tendon [4] regeneration. However, some limitations appeared in the applications due to the layer-by-layer process of electrospinning [5]. One of the problems encountered in the use of electrospun scaffolds is the limited infiltration of cells [6]. This is attributed to the smaller pore size of electrospun scaffold compared with that of cell diameter.
Many efforts have been addressed to improve pore size of the electrospun scaffolds so as to facilitate cell infiltration into electrospun scaffolds. One of the efforts relates to the optimizing of scaffold structures. For example, selecting of special materials for the scaffold fabrication was described to be a desirable approach to improve cell infiltration [7]. In this approach, water-soluble poly(ethylene oxide) (PEO) polymer was served as sacrificial fibers and leached out from nanofiber scaffolds to improve pore size. Leong et al. [8] reported a cryogenic electrospinning technique which utilized ice crystals as porogens to create larger pores within nanofiber scaffolds. Bryan et al. [5] designed a novel collection system for electrospinning to prepare cotton-like, uncompressed scaffold, which supported significantly enhanced cell in-growth penetration. However, the improved cell infiltration attained by those approaches inevitably compromise scaffold integrity or mechanical properties.
This study aims to fabricate a novel nanoyarn scaffold and evaluate its applications in tissue engineering. Electrospun SF/P(LLA-CL) nanofibers were deposited in a water vortex and bonded into nanoyarns and then collected by a rotating mandrel. The nanoyarn made up by nanofibers might have improved surface properties and porous structure. The nanoyarn scaffolds, composed of aligned nanoyarns, were seeded with mouse fibroblasts. The results showed that the nanoyarn scaffolds supported significantly accelerated proliferation, organized morphology and improved infiltration of cells compared with that of the random-oriented nanofibrous scaffolds.
Section snippets
Experimental
Materials: P(LLA-CL) (Mw=300 kDa; LA:CL=75:25) was obtained from Nara Medical University, Japan. Bombyx mori silkworm cocoons were kindly given by Jiaxing Silk Co. Ltd. (Jiaxing, China). L929 cells were obtained from institute of biochemistry and cell biology (Chinese Academy of Sciences, China). All reagents and medium for cell culture and seeding were purchased from Invitrogen.
Scaffold fabrication: Regenerative silk fibroin was prepared as our previously used method [9]. SF and P(LLA-CL) were
Results and discussion
The nanoyarn scaffold was prepared using a dynamic liquid electrospinning (Fig. 1). It is the vortex in water that twists electrospun nanofibers into nanoyarns. When the nanofibers arrive at the water surface, they flow with the whirly water in the vortex and form nanoyarns which are collected by the rotating mandrel. The obtained scaffold (Fig. 2A), made up of aligned nanoyarns (∼20 μm), shows a porous structure with large pores (20–50 μm in diameter) and grooves on the surface. However, the
Conclusion
We have developed a novel nanoyarn scaffold by dynamic liquid electrospinning. The scaffold has excellent surface properties and porous structures. L929 cells show an oriented growth pattern and enhanced cell infiltration on the nanoyarn scaffold. This scaffold is beneficial for cell growth and may be served as tendon or cartilage substitutes in tissue engineering applications. Further studies will be focused on its implantation into animal models for the investigation of biocompatibility in
Acknowledgments
This work is supported by the National Nature Science Foundation of China (31070871).
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