May 2008
Volume 49, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2008
Suprachoroidal Drug Delivery Using Microneedles
Author Affiliations & Notes
  • S. Patel
    Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia
  • H. F. Edelhuaser
    Department of Ophthalmology, Emory University, Atlanta, Georgia
  • J. M. Nickerson
    Department of Ophthalmology, Emory University, Atlanta, Georgia
  • M. R. Prausnitz
    Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia
  • Footnotes
    Commercial Relationships  S. Patel, None; H.F. Edelhuaser, None; J.M. Nickerson, None; M.R. Prausnitz, None.
  • Footnotes
    Support  NEI Grant R24-EY017045
Investigative Ophthalmology & Visual Science May 2008, Vol.49, 5006. doi:
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      S. Patel, H. F. Edelhuaser, J. M. Nickerson, M. R. Prausnitz; Suprachoroidal Drug Delivery Using Microneedles. Invest. Ophthalmol. Vis. Sci. 2008;49(13):5006.

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

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Abstract

Purpose: : Currently practiced ocular drug delivery methods, such as topical application, systemic administration and intravitreal injection, are either inefficient or invasive for posterior segment delivery. Microneedles have the potential to provide a minimally invasive, targeted method of drug delivery to the suprachoroidal space. In this work, we examine (1) whether microneedles can selectively deliver particles to the suprachoroidal space, and (2) the pressures and (3) insertion depth required for suprachoroidal delivery. The particles in the suprachoroidal space can provide sustained delivery directly to the choroid and retina for diseases that affect the posterior of the eye.

Methods: : Hollow glass microneedles were used to infuse nano- and micro-particle suspensions into the suprachoroidal space by inserting across the sclera. Experiments were performed on whole rabbit, pig, and human eyes in-vitro. Delivery was verified visually, as well as using florescence microscopy using whole eyes and histological cross sections.

Results: : Microneedles were shown to deliver nano- and micro-particle suspensions into the suprachoroidal space of rabbit, pig, and human eyes. Particle diameters used include 20 nm, 100 nm, 500 nm, and 1 µm. The particles can be designed to provide controlled drug delivery from the suprachoroidal space. Volumes of 15-30 µL were delivered into the space using a single microneedle; volumes delivered to rabbit eyes were lower compared to pig and human which were similar. Pressures required for delivery ranged from 150 kPa to 300 kPa with a small dependence on particle size. Insertion depth for suprachoroidal delivery was 500-700 µm in rabbit and 700-1000 µm in pig and human.

Conclusions: : Microneedles have shown for the first time to deliver nano- and micro- particle suspensions into the suprachoroidal space of rabbit, pig and human eyes. As a result, microneedles may provide a minimally invasive way for controlled drug delivery to the posterior of the eye, thus reducing dosing frequency and also allowing for better therapeutic control.

Keywords: choroid • retina 
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