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Collagen-phosphorylcholine interpenetrating network hydrogels as corneal substitutes

  • Wenguang Liu
    ,
  • Chao Deng
    ,
  • Christopher R. McLaughlin
    ,
  • Per Fagerholm
    ,
  • Neil S. Lagali
    ,
  • Belinda Heyne
*Corresponding author for this work
  • University of Ottawa
    ,
  • Linköping University
    ,
  • University of Tennessee Health Science Center
    ,
  • Tokyo Dental College
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

A biointeractive collagen-phospholipid corneal substitute was fabricated from interpenetrating polymeric networks comprising 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide and N-hydroxysuccinimide crosslinked porcine atelocollagen, and poly(ethylene glycol) diacrylate crosslinked 2-methacryloyloxyethyl phosphorylcholine (MPC). The resulting hydrogels showed an overall increase in mechanical strength beyond that of either original component and enhanced stability against enzymatic digestion (by collagenase) or UV degradation. More strikingly, these hydrogels retained the full biointeractive, cell friendly properties of collagen in promoting corneal cell and nerve in-growth and regeneration (despite MPC's known anti-adhesive properties). Measurements of refractive indices, white light transmission and backscatter showed the optical properties of collagen-MPC are comparable or superior to those of the human cornea. In addition, the glucose and albumin permeability were comparable to those of human corneas. Twelve-month post-implantation results of collagen-MPC hydrogels into mini-pigs showed regeneration of corneal tissue (epithelium, stroma) as well as the tear film and sensory nerves. We also show that porcine collagen can be substituted with recombinant human collagen, resulting in a fully-synthetic implant that is free from the potential risks of disease transmission (e.g. prions) present in animal source materials.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1551-1559 (9 pages)

Journal (Volume, Issue Number)

Biomaterials (Volume 30, Issue 8)

Publication milestones

  • Published - 03/2009

Publication status

Published - 03/2009

ISSN

0142-9612

Publication IDs

  • Scopus: 58249089265
  • PubMed: 19097643

Publication metrics

Metrics

SciVal
FWCI
4.82
SciVal
Author count
13
SciVal
citations
142
SciVal
Paper percentile
97
SciVal
Top percentile
5
Scopus
citations
Fractional count
1
Fractional count
0.08
Fractional count
12
Fractional count
0.92
Fractional count
1
Fractional count
1

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Captures
184
Citation count
193

Funding Details

We thank Mr. Minoru Fukuda at Kyorin University for excellent TEM assistance and Subhadra Dravida for technical assistance with immunohistochemistry. Funding support from NSERC and CIHR Canada CHRP Grant No. 337436 to M. Griffith and J.C. Scaiano; NSERC studentship to C.R. McLaughlin.
FundersFunding number
CIHR
337436
NSERC
-