May 2007
Volume 48, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2007
Drug Delivery Systems to Promote Electrode-Host Integration in Retinal Prostheses
Author Affiliations & Notes
  • J. Winter
    Chemical Engineering, Ohio State University, Columbus, Ohio
  • M. N. Gokhale
    Chemical Engineering, Ohio State University, Columbus, Ohio
  • S. F. Cogan
    EIC Laboratoris, Norwood, Massachusetts
  • J. F. Rizzo
    Center for Innovative Visual Rehabilitation, Boston VA Hospital, Boston, Massachusetts
  • Footnotes
    Commercial Relationships J. Winter, None; M.N. Gokhale, None; S.F. Cogan, EIC Laboratories, E; J.F. Rizzo, None.
  • Footnotes
    Support Department of Veterans Affairs, Rehabilitation Research and Development Service, Project C-2726-C and NIH Grant No. R43 NS04968701
Investigative Ophthalmology & Visual Science May 2007, Vol.48, 2566. doi:
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    • Get Citation

      J. Winter, M. N. Gokhale, S. F. Cogan, J. F. Rizzo; Drug Delivery Systems to Promote Electrode-Host Integration in Retinal Prostheses. Invest. Ophthalmol. Vis. Sci. 2007;48(13):2566.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose:: To improve neuron-electrode integration in retinal prostheses through the incorporation of drug delivery and tissue engineered surfaces. The ultimate goal is to lower perceptual thresholds by reducing the separation distance between excitable elements (neurites) and electrodes.

Methods:: This study examined neurite extension from PC12 cells and retinal explants in response to neurotrophin (either NGF or BDNF) delivery from polymeric poly(ethylene glycol)-poly(lactic acid) hydrogels applied to the retinal prosthesis surface. Additionally, because of the expected limited duration of drug release, the effect of cell adhesion molecules (e.g., laminin, collagen, and poly-L-lysine) on promoting chronic neurite extension/attachment following acute neurotrophin administration was examined. Neurite length and density was measured at time points up to 2 weeks following bolus exposure using optical microscopy, immunochemistry, fluorescence microscopy, and Image J image analysis software.

Results:: PEGPLA drug release rates averaged less than < 2 weeks, but were improved through incorporation of poly(lactic-co-glycolic) acid microspheres. Increased neurite extension was evidenced in both PC12 and retinal explants during the initial 1 week study, with results comparable to a positive control receiving neurotrophin directly in cell culture medium. However, in a two week study conducted with retinal explants, it was determined that drug delivery slowed and extended neurites began to retract. The use of cell adhesion molecules appeared to not only mitigate this effect, but also to promote further neurite extension, even after neurotrophin delivery from polymer hydrogels was largely complete.

Conclusions:: Drug delivery applied to neural prostheses may induce neurite extension to electrode surfaces; however, additional modifications, such as the incorporation of cell adhesion molecules, are required to support a chronic interface between the electrode and neuron extensions.

Keywords: retina • growth factors/growth factor receptors • wound healing 
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