Biointegration of corneal macroporous membranes based on poly(ethyl acrylate) copolymers in an experimental animal model. Issue 3 (18th June 2014)
- Record Type:
- Journal Article
- Title:
- Biointegration of corneal macroporous membranes based on poly(ethyl acrylate) copolymers in an experimental animal model. Issue 3 (18th June 2014)
- Main Title:
- Biointegration of corneal macroporous membranes based on poly(ethyl acrylate) copolymers in an experimental animal model
- Authors:
- Alió del Barrio, Jorge L.
Chiesa, Massimo
Gallego Ferrer, Gloria
Garagorri, Nerea
Briz, Nerea
Fernandez‐Delgado, Jorge
Sancho‐Tello Valls, Maria
Botella, Carmen Carda
García‐Tuñón, Ignacio
Bataille, Laurent
Rodriguez, Alejandra
Arnalich‐Montiel, Francisco
Gómez Ribelles, Jose L.
Antolinos‐Turpín, Carmen M.
Gómez‐Tejedor, Jose A.
Alió, Jorge L.
De Miguel, Maria P. - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p>Currently available keratoprosthesis models (nonbiological corneal substitutes) have a less than 75% graft survival rate at 2 years. We aimed at developing a model for keratoprosthesis based on the use of poly(ethyl acrylate) (PEA)‐based copolymers, extracellular matrix‐protein coating and colonization with adipose‐derived mesenchymal stem cells. Human adipose tissue derived mesenchymal stem cells (h‐ADASC) colonization efficiency of seven PEA‐based copolymers in combination with four extracellular matrix coatings were evaluated <italic>in vitro</italic>. Then, macroporous membranes composed of the optimal PEA subtypes and coating proteins were implanted inside rabbit cornea. After a 3‐month follow‐up, the animals were euthanized, and the clinical and histological biointegration of the implanted material were assessed. h‐ADASC adhered and survived when cultured in all PEA‐based macroporous membranes. The addition of high hydrophilicity to PEA membranes decreased h‐ADASC colonization <italic>in vitro</italic>. PEA‐based copolymer containing 10% hydroxyethyl acrylate (PEA‐HEA10) or 10% acrylic acid (PEA‐AAc10) monomeric units showed the best cellular colonization rates. Collagen plus keratan sulfate‐coated polymers demonstrated enhanced cellular colonization respect to fibronectin, collagen, or uncoated PEAs. <italic>In vivo</italic> implantation of membranes resulted in an extrusion rate of 72% for PEA, 50% for<abstract abstract-type="main"> <title>Abstract</title> <p>Currently available keratoprosthesis models (nonbiological corneal substitutes) have a less than 75% graft survival rate at 2 years. We aimed at developing a model for keratoprosthesis based on the use of poly(ethyl acrylate) (PEA)‐based copolymers, extracellular matrix‐protein coating and colonization with adipose‐derived mesenchymal stem cells. Human adipose tissue derived mesenchymal stem cells (h‐ADASC) colonization efficiency of seven PEA‐based copolymers in combination with four extracellular matrix coatings were evaluated <italic>in vitro</italic>. Then, macroporous membranes composed of the optimal PEA subtypes and coating proteins were implanted inside rabbit cornea. After a 3‐month follow‐up, the animals were euthanized, and the clinical and histological biointegration of the implanted material were assessed. h‐ADASC adhered and survived when cultured in all PEA‐based macroporous membranes. The addition of high hydrophilicity to PEA membranes decreased h‐ADASC colonization <italic>in vitro</italic>. PEA‐based copolymer containing 10% hydroxyethyl acrylate (PEA‐HEA10) or 10% acrylic acid (PEA‐AAc10) monomeric units showed the best cellular colonization rates. Collagen plus keratan sulfate‐coated polymers demonstrated enhanced cellular colonization respect to fibronectin, collagen, or uncoated PEAs. <italic>In vivo</italic> implantation of membranes resulted in an extrusion rate of 72% for PEA, 50% for PEA‐AAc10, but remarkably of 0% for PEA‐HEA10. h‐ADASC survival was demonstrated in all the membranes after 3 months follow‐up. A slight reduction in the extrusion rate of h‐ADASC colonized materials was observed. No significant differences between the groups with and without h‐ADASC were detected respect to transparency or neovascularization. We propose PEA with low hydroxylation as a scaffold for the anchoring ring of future keratoprosthesis. © 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 1106–1118, 2015.</p> </abstract> … (more)
- Is Part Of:
- Journal of biomedical materials research. Volume 103:Issue 3(2015:Mar.)
- Journal:
- Journal of biomedical materials research
- Issue:
- Volume 103:Issue 3(2015:Mar.)
- Issue Display:
- Volume 103, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 103
- Issue:
- 3
- Issue Sort Value:
- 2015-0103-0003-0000
- Page Start:
- 1106
- Page End:
- 1118
- Publication Date:
- 2014-06-18
- Subjects:
- Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1552-4965 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jbm.a.35249 ↗
- Languages:
- English
- ISSNs:
- 1549-3296
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4953.720000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4111.xml