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Generating nanotopography on PCL microfiber surface for better cell-scaffold interactions

  • Jie Sun*
  • , Linzhi Jing
  • , Hang Liu
  • , Dejian Huang
  • *Corresponding author for this work
    • National University of Singapore

    Research output: Contribution to journal › Conference article › peer-review

    8 Citations (Scopus)

    Abstract

    To understand the behavior of cells in natural environment, 3D scaffolds are needed to provide biomimetic environment for routine cell growth in vitro. Electrohydrodynamic jet (EHDJ) printing, one of the emerging 3D printing techniques, is capable of fabricating 3D scaffolds with oriented fibers and customized microscale structures. However, most of the EHDJ-printed scaffolds lack of hierarchical structures such as nanotopographies present in native tissues. In this study, we propose a novel approach that combine EHDJ printing of poly(e-caprolactone) (PCL)/gliadin composite inks to produce scaffolds with oriented microfibers. The nanoscale pores and flaws (fiber nanotopography) could be generated on the printed fibers by simply leaching the gliadin phase from the printed PCL/gliadin scaffolds. The density and size of nanotopographical features could be controlled by adjusting the gliadin ratio. Furthermore, by seeding mouse embryonic fibroblasts (NIH/3T3) cells, it clearly manifested that such scaffolds are favorable to cell adhesion, migration and proliferation efficiently. Thus, the newly designed PCL scaffolds with both micro- and nano-scale topographies can be a promising 3D cell culture platform with improved cell-scaffold interactions.

    Original languageEnglish
    Pages (from-to)619-624
    Number of pages6
    Journal48th SME North American Manufacturing Research Conference, NAMRC 48
    Volume48
    DOIs
    Publication statusPublished - 2020
    Event48th SME North American Manufacturing Research Conference, NAMRC 48 - Cincinnati, United States
    Duration: 22 Jun 2020 → 26 Jun 2020

    Keywords

    • Bioscaffold
    • Electrohydrodynamic jet printing
    • Gliadin
    • Nanotopography
    • PCL

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