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Small M, Faglie A, Craig AJ, et al. Nanostructure-Enabled and Macromolecule-Grafted Surfaces for Biomedical Applications. Micromachines (Basel). 2018;9(5)doi: 10.3390/mi9050243.
Small, M., Faglie, A., Craig, A. J., Pieper, M., Fernand Narcisse, V. E., Neuenschwander, P. F., & Chou, S. F. (2018). Nanostructure-Enabled and Macromolecule-Grafted Surfaces for Biomedical Applications. Micromachines, 9(5), . https://doi.org/10.3390/mi9050243
Small, Madeline, et al. "Nanostructure-Enabled and Macromolecule-Grafted Surfaces for Biomedical Applications." Micromachines vol. 9,5 (2018). doi: https://doi.org/10.3390/mi9050243
Small M, Faglie A, Craig AJ, Pieper M, Fernand Narcisse VE, Neuenschwander PF, Chou SF. Nanostructure-Enabled and Macromolecule-Grafted Surfaces for Biomedical Applications. Micromachines (Basel). 2018 May 17;9(5). doi: 10.3390/mi9050243. PMID: 30424176; PMCID: PMC6187347.
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Micromachines (Basel). 2018 May 17;9(5). doi: 10.3390/mi9050243.

Nanostructure-Enabled and Macromolecule-Grafted Surfaces for Biomedical Applications.

Micromachines

Madeline Small, Addison Faglie, Alexandra J Craig, Martha Pieper, Vivian E Fernand Narcisse, Pierre F Neuenschwander, Shih-Feng Chou

Affiliations

  1. Department of Mechanical Engineering, College of Engineering, The University of Texas at Tyler, 3900 University Blvd., Tyler, TX 75799, USA. [email protected].
  2. Department of Mechanical Engineering, College of Engineering, The University of Texas at Tyler, 3900 University Blvd., Tyler, TX 75799, USA. [email protected].
  3. Department of Mechanical Engineering, College of Engineering, The University of Texas at Tyler, 3900 University Blvd., Tyler, TX 75799, USA. [email protected].
  4. Department of Mechanical Engineering, College of Engineering, The University of Texas at Tyler, 3900 University Blvd., Tyler, TX 75799, USA. [email protected].
  5. Department of Chemistry and Physics, School of Arts and Sciences, LeTourneau University, Longview, TX 75607, USA. [email protected].
  6. Department of Cellular and Molecular Biology, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, USA. [email protected].
  7. Department of Mechanical Engineering, College of Engineering, The University of Texas at Tyler, 3900 University Blvd., Tyler, TX 75799, USA. [email protected].

PMID: 30424176 PMCID: PMC6187347 DOI: 10.3390/mi9050243

Abstract

Advances in nanotechnology and nanomaterials have enabled the development of functional biomaterials with surface properties that reduce the rate of the device rejection in injectable and implantable biomaterials. In addition, the surface of biomaterials can be functionalized with macromolecules for stimuli-responsive purposes to improve the efficacy and effectiveness in drug release applications. Furthermore, macromolecule-grafted surfaces exhibit a hierarchical nanostructure that mimics nanotextured surfaces for the promotion of cellular responses in tissue engineering. Owing to these unique properties, this review focuses on the grafting of macromolecules on the surfaces of various biomaterials (e.g., films, fibers, hydrogels, and etc.) to create nanostructure-enabled and macromolecule-grafted surfaces for biomedical applications, such as thrombosis prevention and wound healing. The macromolecule-modified surfaces can be treated as a functional device that either passively inhibits adverse effects from injectable and implantable devices or actively delivers biological agents that are locally based on proper stimulation. In this review, several methods are discussed to enable the surface of biomaterials to be used for further grafting of macromolecules. In addition, we review surface-modified films (coatings) and fibers with respect to several biomedical applications. Our review provides a scientific update on the current achievements and future trends of nanostructure-enabled and macromolecule-grafted surfaces in biomedical applications.

Keywords: grafting; macromolecules; surfaces; thrombosis; wound healing

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