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Electrospun gelatin/hyaluronic acid nanofibers as a platform for uric acid delivery to neural tissue

  • Reva M. Street
  • , Frank H. Kung
  • , Laura T. Beringer
  • , Daniel B. Amchin
  • , Bonnie L. Firestein
  • , Caroline L. Schauer

Producción científica: Articlerevisión exhaustiva

2 Citas (Scopus)

Resumen

Uric acid (UA) is an antioxidant that has been reported to be a neuroprotective compound for injuries and diseases, and specifically, diseases of the central nervous system. However, uric acid is highly insoluble in aqueous solutions, and high levels in the serum lead to gout, which limits its use in humans. Here, we develop a novel drug delivery platform that will release uric acid in a sustained manner for application to neural tissue. We demonstrate that one-step incorporation of UA into an electrospun gelatin/hyaluronic acid nanofiber mat results in controlled release of UA in culture medium. Taking a unique approach, we made solutions of 12% gelatin and 1% hyaluronic acid in a formic acid solvent and added UA for production of nanofiber mats. We then dehydrothermally crosslinked the mats and tested for release of UA into physiological cell culture medium. To test whether the mats have any detrimental effects on healthy nervous system tissue, we cultured spinal cord explants on the mats extended and assessed extensions from the explants. We observed that comparable numbers and lengths of dendrites are extended from the spinal cord tissue, regardless of the amount UA content in the mats. Our results suggest that electrospun gelatin/hyaluronic acid nanofibers can be used as a platform for sustained uric acid delivery to neural tissue without detrimental effects.

Idioma originalEnglish
Número de artículoe3517
PublicaciónBiotechnology Progress
Volumen41
N.º2
DOI
EstadoPublished - mar 1 2025

Nota bibliográfica

Publisher Copyright:
© 2024 American Institute of Chemical Engineers.

Financiación

This work is funded in part by Funding for research provided by the New Jersey Commission on Spinal Cord Research (NJCSCR) grant CSCR14IRG005 (to B.L.F.). Researcher support for R.M.S. was provided by the Graduate Assistance in Areas of National Need (GAANN) Fellowship (Award # P200A120253) and the Drexel University Freshman Design Fellowship. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

FinanciadoresNúmero del financiador
Drexel University
New Jersey Commission on Spinal Cord ResearchCSCR14IRG005, P200A120253

    ASJC Scopus subject areas

    • Biotechnology

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