Literature DB >> 14530070

A model for the preliminary biological screening of potential keratoprosthetic biomaterials.

S R Sandeman1, A W Lloyd, B J Tighe, V Franklin, J Li, F Lydon, C S C Liu, D J Mann, S E James, R Martin.   

Abstract

A series of in vitro screening assays for the preliminary selection of biomaterials for use in the fabrication of artificial corneas (keratoprostheses) (KPros) have been investigated. These screening assays assessed the initial binding of inflammatory and cell adhesive proteins, activation of inflammatory proteins, adhesion of keratocytes, epithelial cells and macrophages and the production of inflammatory cytokines by keratocytes contacting biomaterials. Central optic biomaterials were selected on the basis of low-inflammatory and cell adhesion potential. Peripheral skirt materials were selected on the basis of low-inflammatory potential but good cell adhesion to anchor the implant within the host cornea. Green fluorescent protein (GFP) gene transfer was used in a novel context to investigate cell invasion in the absence of external staining techniques. Confocal laser scanning microscopy and scanning electron microscopy were used to investigate GFP positive keratocyte invasion of porous materials. The results of in vitro assays were compared to a corneal organ culture system in which the biomaterials were assessed within a stromal environment. A range of polyurethane-based interpenetrating polymers with a range of water contents were screened. All materials showed low-inflammatory potential. A reduction in biomaterial water content induced an increase in complement C3 and fibronectin binding and in cell adhesion to materials, whilst differences in co-monomer formulation had little impact. The screening methods used in the current study provide a suitable preliminary assessment regime for the in vitro evaluation of potential KPro materials.

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Year:  2003        PMID: 14530070     DOI: 10.1016/s0142-9612(03)00370-3

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  6 in total

1.  Cardiomyocytes in vitro adhesion is actively influenced by biomimetic synthetic peptides for cardiac tissue engineering.

Authors:  Alessandro Gandaglia; Rocio Huerta-Cantillo; Marina Comisso; Roberta Danesin; Francesca Ghezzo; Filippo Naso; Alessandra Gastaldello; Eleonora Schittullo; Edward Buratto; Michele Spina; Gino Gerosa; Monica Dettin
Journal:  Tissue Eng Part A       Date:  2011-12-05       Impact factor: 3.845

2.  Hydroxyapatite promotes superior keratocyte adhesion and proliferation in comparison with current keratoprosthesis skirt materials.

Authors:  J S Mehta; C E Futter; S R Sandeman; R G A F Faragher; K A Hing; K E Tanner; B D S Allan
Journal:  Br J Ophthalmol       Date:  2005-10       Impact factor: 4.638

3.  Control of scar tissue formation in the cornea: strategies in clinical and corneal tissue engineering.

Authors:  Samantha L Wilson; Alicia J El Haj; Ying Yang
Journal:  J Funct Biomater       Date:  2012-09-18

4.  Keeping an eye on decellularized corneas: a review of methods, characterization and applications.

Authors:  Samantha L Wilson; Laura E Sidney; Siobhán E Dunphy; James B Rose; Andrew Hopkinson
Journal:  J Funct Biomater       Date:  2013-07-10

5.  Evaluation of stability and biocompatibility of PHEMA-PMMA keratoprosthesis by penetrating keratoplasty in rabbits.

Authors:  Yawon Hwang; Gonhyung Kim
Journal:  Lab Anim Res       Date:  2016-12-23

6.  Biomimetic bone-like composites as osteo-odonto-keratoprosthesis skirt substitutes.

Authors:  Venkata Avadhanam; Ganesh Ingavle; Yishan Zheng; Sandeep Kumar; Christopher Liu; Susan Sandeman
Journal:  J Biomater Appl       Date:  2020-11-11       Impact factor: 2.646

  6 in total

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