April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Degradable Polyesteramides: A Novel Platform for Ophthalmic Drug Delivery
Author Affiliations & Notes
  • Astrid Franken
    DSM Biomedical, Geleen, The Netherlands
  • Anja Kemp
    DSM Biomedical, Geleen, The Netherlands
  • Ken Messier
    DSM Biomedical, Geleen, The Netherlands
  • Aylvin Dias
    DSM Biomedical, Geleen, The Netherlands
  • George Mihov
    DSM Biomedical, Geleen, The Netherlands
  • Anna K. Salz
    Department of Ophthalmology, University Hospital RWTH Aachen, Aachen, Germany
  • Gabriele Thumann
    Department of Ophthalmology, University Hospital RWTH Aachen, Aachen, Germany
  • Footnotes
    Commercial Relationships  Astrid Franken, DSM Biomedical-sponsor (E); Anja Kemp, DSM Biomedical-sponsor (E); Ken Messier, DSM Biomedical-sponsor (E); Aylvin Dias, DSM Biomedical-sponsor (E); George Mihov, DSM Biomedical-sponsor (E); Anna K. Salz, University hospital RWTH Aachen, Department of Ophthalmology (F); Gabriele Thumann, University hospital RWTH Aachen, Department of Ophthalmology (F)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 3262. doi:
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    • Get Citation

      Astrid Franken, Anja Kemp, Ken Messier, Aylvin Dias, George Mihov, Anna K. Salz, Gabriele Thumann; Degradable Polyesteramides: A Novel Platform for Ophthalmic Drug Delivery. Invest. Ophthalmol. Vis. Sci. 2011;52(14):3262.

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

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Abstract
 
Purpose:
 

DSM’s amino acid-based polyesteramides (‘PEAs’) are being developed as a novel degradable biomaterial for applications in ocular drug delivery. PEAs are highly versatile with respect to physico-chemical properties and processability, and hold promise as a multi-month sustained release delivery system. Biodegradation and inflammatory response is tested by subconjunctival and intravitreal implantation into rabbit eyes.

 
Methods:
 

PEAs are based on α-amino acids, aliphatic dicarboxylic acids and aliphatic α-ω diols. These PEAs have been processed into fibrils with a fluorescent dye. In Biodegradation and initial tissue response are assessed by clinical photo-documentation, fluorescent microscopy and histological examination based on H&E staining.

 
Results:
 

PEAs have been processed into fibrils of approximately 100 µm diameter for delivery through small gauge needles (≤ 26G) to subconjunctival and intravitreal spaces. PEAs degrade enzymatically as demonstrated in vitro with chymotrypsin, esterases, lipases as well as macrophage meditated degradation. In-vivo degradation profiles and tissue response of fibril implants are on-going.

 
Conclusions:
 

Amino acid based biodegradable polymers represent a next generation platform for sustained release drug delivery and hold promise for utility in ophthalmology.  

 
Keywords: injection • vitreous • development 
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