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Core-Shell Electrospun Fibers with an Improved Open Pore Structure for Size-Controlled Delivery of Nanoparticles

  • University of Montana
  • New Jersey Institute of Technology

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Electrospun fiber meshes with controlled drug delivery properties have great potential for applications such as wound dressings, tissue engineering, and cancer treatment. However, controlling the drug release, especially from core-shell fibers, remains the main challenge. In this study, core-shell fibers were developed with silver nanoparticles (Ag NPs, as an antibacterial agent) loaded inside the core. The fiber shell was composed of polycaprolactone (PCL, shell matrix), polyethylene glycol (PEG, porogen), and zinc oxide nanoparticles (ZnO NPs). ZnO NPs were used in this study to improve the structure of pores in the shell (which serve as a diffusion pathway for Ag NPs) and thus to control the release rate. ZnO NPs associated with PCL, resulting in the formation of the PEG phase deeper in the fiber shell during the electrospinning process. Moreover, the diffusion/release rate of Ag NPs from electrospun fibers was fine-tuned with variation in particle size. Fibers were loaded with three size compositions of 20, 110 nm, or a mix of the two Ag NPs inside the fiber core. Release studies showed fast, slow, and intermediate delivery rates obtained with the defined Ag NPs. Fine-tuned release of Ag NPs confirmed the formation of open pores within a stable shell structure because controlling the release rate was only possible through this well-defined release pathway. Furthermore, tensile strength analysis revealed excellent mechanical stability of the fibers after pore formation.

Original languageEnglish
Pages (from-to)4004-4015
Number of pages12
JournalACS Applied Polymer Materials
Volume2
Issue number9
DOIs
StatePublished - Sep 11 2020

Funding

We acknowledge Kevin L. Trout for fabricating the electrospinning instrument; Jim Driver for technical support on the electron microscopy; Monica Serban for technical support on the mechanical testing; Samar Azizighannad for technical support on the BET analyses; Lou Herritt for technical support on the confocal microscopy; and Sarah Elizabeth Totten for technical support on the antibacterial analyses. We thank Gretchen McCaffrey for her editorial guidance. The authors acknowledge the resources and support provided by the BioSpectroscopy Core Research Laboratory at the University of Montana, which is supported by the National Institute of General Medical Sciences (NIGMS) of the National Institutes of Health CoBRE award P20 GM103546 to the Center for Biomolecular Structure and Dynamics. Additional funding was provided by the National Institutes of Health (NIGMS) CoBRE award P30 GM103338 and the National Institute of Environmental Health Sciences (NIEHS) award R01 ES023209. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Funder number
P20 GM103546, P30 GM103338
R01 ES023209

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • coaxial electrospinning
    • drug delivery
    • pore structure
    • porogen
    • silver nanoparticle
    • zinc oxide nanoparticle

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