4.8 Article

Stable oxime-crosslinked hyaluronan-based hydrogel as a biomimetic vitreous substitute

Journal

BIOMATERIALS
Volume 271, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2021.120750

Keywords

Hydrogel; Retinal tamponade; Retinal detachment; Vitreous substitute; Hyaluronan

Funding

  1. Krembil Foundation
  2. Canada First Research Excellence Fund through Medicine by Design at the University of Toronto
  3. Natural Sciences and Engineering Research Council of Canada
  4. Canadian Foundation for Innovation [19119]
  5. Ontario Research Fund

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The study developed a new hyaluronan-oxime crosslinked hydrogel as a vitreous substitute, which has similar physical properties to the native vitreous. It showed good cytocompatibility and biocompatibility in vitro with mouse retinal explants and in rabbit eyes, demonstrating stability and limited swelling.
Vitreous substitutes are clinically used to maintain retinal apposition and preserve retinal function; yet the most used substitutes are gases and oils which have disadvantages including strict face-down positioning post-surgery and the need for subsequent surgical removal, respectively. We have engineered a vitreous substitute comprised of a novel hyaluronan-oxime crosslinked hydrogel. Hyaluronan, which is naturally abundant in the vitreous of the eye, is chemically modified to crosslink with poly(ethylene glycol)-tetraoxyamine via oxime chemistry to produce a vitreous substitute that has similar physical properties to the native vitreous including refractive index, density and transparency. The oxime hydrogel is cytocompatible in vitro with photoreceptors from mouse retinal explants and biocompatible in rabbit eyes as determined by histology of the inner nuclear layer and photoreceptors in the outer nuclear layer. The ocular pressure in the rabbit eyes was consistent over 56 d, demonstrating limited to no swelling. Our vitreous substitute was stable in vivo over 28 d after which it began to degrade, with approximately 50% loss by day 56. We confirmed that the implanted hydrogel did not impact retina function using electroretinography over 90 days versus eyes injected with balanced saline solution. This new oxime hydrogel provides a significant improvement over the status quo as a vitreous substitute.

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