December 2002
Volume 43, Issue 13
Free
ARVO Annual Meeting Abstract  |   December 2002
Development of a Wide Bandgap Microfluidic Neural Stimulating Device for Vision
Author Affiliations & Notes
  • MR Safadi
    Ligon Research Center of Vision Wayne State University Detroit MI
    Biomedical Engineering/Elec and Comp Engineering
  • CA Jaboro
    Ligon Research Center of Vision Wayne State University Detroit MI
    Biomedical Engineering/Elec and Comp Engineering
  • AL Lagman
    Ligon Research Center of Vision Wayne State University Detroit MI
    Biomedical Engineering/Elec and Comp Engineering
  • GW Abrams
    Kresge Eye Institute
    Ligon Research Center of Vision Wayne State University Detroit MI
  • R Iezzi
    Kresge Eye Institute
    Ligon Research Center of Vision Wayne State University Detroit MI
  • JP McAllister
    Dept of Neurosurgery
    Ligon Research Center of Vision Wayne State University Detroit MI
  • GW Auner
    Ligon Research Center of Vision Wayne State University Detroit MI
    Biomedical Engineering/Elec and Comp Engineering
  • Footnotes
    Commercial Relationships   M.R. Safadi, None; C.A. Jaboro, None; A.L. Lagman, None; G.W. Abrams, None; R. Iezzi, None; J.P. McAllister, None; G.W. Auner, None. Grant Identification: Support: Research to Prevent Blindness, NSF Grant #98770720, Ligon Research Fund, WSU SSIM
Investigative Ophthalmology & Visual Science December 2002, Vol.43, 4466. doi:
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    • Get Citation

      MR Safadi, CA Jaboro, AL Lagman, GW Abrams, R Iezzi, JP McAllister, GW Auner; Development of a Wide Bandgap Microfluidic Neural Stimulating Device for Vision . Invest. Ophthalmol. Vis. Sci. 2002;43(13):4466.

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

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Abstract

Abstract: : Purpose: We have developed a microfluidic retinal prosthesis, using wide bandgap semiconductor thin film waveguides, to facilitate spatial and quantitative photactivation of caged neurotransmitter to microfluidic channels. Methods: Novel waveguide materials and micromachining technology is necessary to fabricate 360 nanometer capable waveguides for the microfluidic device. Single crystal wide bandgap semiconductor thin films are grown on sapphire with high refractive index buffer layer by plasma source molecular beam epitaxy (PSMBE). 248 nanometer KrF Excimer laser micromachining technology is employed to micro-fabricate wave-guiding channels and microfluidic structures. Results: A waveguide which allows for spatial and temporal drug delivery within the retina was fabricated. Wave-guiding channels were precisely fabricated to form a cavity to maximize the intensity of ultraviolet light. Wave-guiding properties were efficiently characterized as a function of thickness, geometry and crystalline quality. Conclusion: There is a need for a waveguide structure that may be used in physiological drug delivery systems. A device that may deliver ultraviolet light in precise amounts and to selective areas of a microfluidic implant without direct ultraviolet exposure to the biological cells is much needed in retinal and cortical implants. Results of a prototype microfluidic waveguide system will be presented.

Keywords: 554 retina • 490 neurotransmitters/neurotransmitter systems • 556 retina: neurochemistry 
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