Design and fabrication of an artificial cornea based on a photolithographically patterned hydrogel construct

David Myung, Wongun Koh, Amit Bakri, Fan Zhang, Amanda Marshall, Jungmin Ko, Jaan Noolandi, Michael Carrasco, Jennifer R. Cochran, Curtis W. Frank, Christopher N. Ta

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88 Citations (Scopus)

Abstract

We describe the design and fabrication of an artificial cornea based on a photolithographically patterned hydrogel construct, and demonstrate the adhesion of corneal epithelial and fibroblast cells to its central and peripheral components, respectively. The design consists of a central "core" optical component and a peripheral tissue-integrable "skirt." The core is composed of a poly(ethylene glycol)/poly(acrylic acid) (PEG/PAA) double-network with high strength, high water content, and collagen type I tethered to its surface. Interpenetrating the periphery of the core is a microperforated, but resilient poly(hydroxyethyl acrylate) (PHEA) hydrogel skirt that is also surface-modified with collagen type I. The well-defined microperforations in the peripheral component were created by photolithography using a mask with radially arranged chrome discs. Surface modification of both the core and skirt elements was accomplished through the use of a photoreactive, heterobifunctional crosslinker. Primary corneal epithelial cells were cultured onto modified and unmodified PEG/PAA hydrogels to evaluate whether the central optic material could support epithelialization. Primary corneal fibroblasts were seeded onto the PHEA hydrogels to evaluate whether the peripheral skirt material could support the adhesion of corneal stromal cells. Cell growth in both cases was shown to be contingent on the covalent tethering of collagen. Successful demonstration of cell growth on the two engineered components was followed by fabrication of core-skirt constructs in which the central optic and peripheral skirt were synthesized in sequence and joined by an interpenetrating diffusion zone.

Original languageEnglish
Pages (from-to)911-922
Number of pages12
JournalBiomedical Microdevices
Volume9
Issue number6
DOIs
Publication statusPublished - 2007 Dec

Bibliographical note

Funding Information:
Acknowledgments This research was supported by the Bio-X Program and the Office of Technology Licensing at Stanford University. Instrument support was provided by the shared facilities at the Center on Polymer Interfaces and Macromolecular Assemblies (CPIMA) at Stanford University. The authors thank Stacey Bent and Jungsic Hong for use of the X-ray spectrometer and Beinn Muir for use of his high-resolution digital camera. Additional external support was also received from VISX, Incorporated (now VISX Technology) and the Fight for Sight Foundation.

All Science Journal Classification (ASJC) codes

  • Biomedical Engineering
  • Molecular Biology

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