April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Optimisation of Polymer Scaffolds for Ocular Cell Transplantation
Author Affiliations & Notes
  • H. A. Thomson
    Clinical Neurosciences,
    University of Southampton, Southampton, United Kingdom
  • A. Treharne
    School of Chemistry,
    University of Southampton, Southampton, United Kingdom
  • P. Walker
    School of Chemistry,
    University of Southampton, Southampton, United Kingdom
  • M. Grossel
    School of Chemistry,
    University of Southampton, Southampton, United Kingdom
  • A. J. Lotery
    Clinical Neurosciences,
    University of Southampton, Southampton, United Kingdom
    Eye Unit, Southampton General Hospital, Southampton, United Kingdom
  • Footnotes
    Commercial Relationships  H.A. Thomson, None; A. Treharne, None; P. Walker, None; M. Grossel, None; A.J. Lotery, None.
  • Footnotes
    Support  Gift of Sight, Foresight RP, Lord Sandberg
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 6230. doi:
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    • Get Citation

      H. A. Thomson, A. Treharne, P. Walker, M. Grossel, A. J. Lotery; Optimisation of Polymer Scaffolds for Ocular Cell Transplantation. Invest. Ophthalmol. Vis. Sci. 2009;50(13):6230.

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

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Abstract

Purpose: : The retinal pigment epithelium would be the primary target for cellular replacement in degenerative ocular diseases such as age related macular degeneration. Transplantation of cells into the eye as a suspension has a number of disadvantages including cell death and incorrectly localised or disorganised grafts. Recent studies have demonstrated that growth of RPE cells on polymer scaffolds can facilitate the transplantation of cells as an intact monolayer which may reduce cell death by up to 10 fold (1). However there have only been limited investigations to determine the optimal polymer composition for such scaffolds.

Methods: : Using a technique described by (2). We manufactured and evaluated five different blends of poly(L-lactic acid) (PLLA) with poly(D, L-lactic-glycolic acid) (PLGA). Scanning electron microscopy (SEM) and 13C Nuclear magnetic resonance spectroscopy were used to characterise the polymer surface and verify the ratios produced. Polymer surface chemistry was modified using the extracellular matrix protein laminin. The polymer blends were then seeded with ARPE-19 cells and maintained in culture for up to 4 weeks. Cell adherence and proliferation were assessed using SEM and immunofluorescence. Cell survival was quantified by measurement of apoptosis and cell membrane integrity. Maintenance of phenotypic characteristics was also investigated using immunocytochemistry.

Keywords: transplantation • retinal pigment epithelium • cell survival 
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