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Toward Better Biointegration of Boston KPro

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Kyung Jae Jeong, Ph.D., Claes H. Dohlman, M.D., Ph.D., and Daniel S. Kohane, M.D., Ph.D. Harvard-MIT Health Sciences and Technology, Department of Anesthesiology ... – PowerPoint PPT presentation

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Title: Toward Better Biointegration of Boston KPro


1
Toward Better Biointegration of Boston KPro
  • Kyung Jae Jeong, Ph.D., Claes H. Dohlman, M.D.,
    Ph.D., and Daniel S. Kohane, M.D., Ph.D.

Harvard-MIT Health Sciences and
Technology, Department of Anesthesiology,
Childrens Hospital Boston, Harvard Medical
School Massachusetts Eye and Ear Infirmary,
Harvard Medical School
The authors have no financial interest in the
subject matter of this poster.
2
Boston Kpro and Biointegration
  • Cell migration
  • Cell proliferation with minimal immune response
  • ECM Production
  • Adhesion
  • Good biointegration will also reduce the danger
    of bacterial/fungal infection.

Khan et al. (2008)
3
Advantages of Dopamine-Based Surface Chemistry
  • Dopamine (or DOPA) is a major component of mussel
    adhesive protein and has good adhesive
    properties.
  • Polydopamine coating can form on virtually all
    surfaces.
  • Polydopamine coating can further be used to
    immobilize biological molecules which contain
    either thiol or amine groups at a high density.
  • Chemistry is very simple.

Lee et al. Nature (2007)
Lee et al. Adv. Materials (2009)
4
Corneal Epithelial Cells on Various Surfaces
PMMA
PMMA-RGD
MTS assay on corneal epithelial cells
Dopa-PMMA-RGD
Dopa-PMMA
Fluorescence micrographs of epithelial cells.
Nucleus (blue) and actin cytoskeleton (red)
5
Keratocytes on Various Surfaces
PMMA
PMMA-RGD
MTS assay on keratocytes
Dopa-PMMA
Dopa-PMMA-RGD
6
Biological Effect of Polydopamine Coating
Calcium assay. on human aortic smooth muscle
cells (HASMC). Red point corresponds to
polydopamine coating. Higher fluorescence
response corresponds to higher cell contraction.
IL-6 concentration from the cells seeded on
various surfaces after 24 hours. TNF- a was not
detected from neither cell types.
  • Polydopamine coating does not release dopamine
    monomer (mass spectrometry)
  • Minimal contraction of the aortic smooth muscle
    cells (Calcium Flux Assay).
  • Not significantly high level of proinflammatory
    cytokines released from the cells seeded on the
    polydopamine surface (ELISA, IL-6 and TNF-a).

7
SEM Images
PMMA-RGD
PMMA
Dopa-PMMA
Dopa-RGD-PMMA
8
Adhesion of Polydopamine Coated PMMA to Collagen
Gel
A small PMMA cylinder was pressed onto collagen
gel over night to see if there is any adhesion at
the interface.
PMMA Cylinder
Collagen Gel
PMMA
Dopa-PMMA
9
Summary
  • Polydopamine coating enhanced the proliferation
    of corneal epithelial cells and keratocytes in
    vitro.
  • Polydopamine coating is not proinflammatory and
    is not expected to cause vascular constriction as
    its monomer would do.
  • SEM images show ECM secretion from all surfaces.
  • Both polydopamine-coated surfaces exhibited firm
    adhesion to collagen gel.
  • Polydopamine coating may enhance the
    biointegration of Boston KPro when applied to the
    stem of the device.
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