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  • Enhanced regeneration of corneal tissue via a bioengineered collagen construct implanted by a nondisruptive surgical technique.

Enhanced regeneration of corneal tissue via a bioengineered collagen construct implanted by a nondisruptive surgical technique.

Tissue engineering. Part A (2014-11-21)
Marina Koulikovska, Mehrdad Rafat, Goran Petrovski, Zoltán Veréb, Saeed Akhtar, Per Fagerholm, Neil Lagali
ABSTRACT

Severe shortage of donor corneas for transplantation, particularly in developing countries, has prompted the advancement of bioengineered tissue alternatives. Bioengineered corneas that can withstand transplantation while maintaining transparency and compatibility with host cells, and that are additionally amenable to standardized low-cost mass production are sought. In this study, a bioengineered porcine construct (BPC) was developed to function as a biodegradable scaffold to promote corneal stromal regeneration by host cells. Using high-purity medical-grade type I collagen, high 18% collagen content and optimized EDC-NHS cross-linker ratio, BPCs were fabricated into hydrogel corneal implants with over 90% transparency and four-fold increase in strength and stiffness compared with previous versions. Remarkably, optical transparency was achieved despite the absence of collagen fibril organization at the nanoscale. In vitro testing indicated that BPC supported confluent human epithelial and stromal-derived mesenchymal stem cell populations. With a novel femtosecond laser-assisted corneal surgical model in rabbits, cell-free BPCs were implanted in vivo in the corneal stroma of 10 rabbits over an 8-week period. In vivo, transparency of implanted corneas was maintained throughout the postoperative period, while healing occurred rapidly without inflammation and without the use of postoperative steroids. BPC implants had a 100% retention rate at 8 weeks, when host stromal cells began to migrate into implants. Direct histochemical evidence of stromal tissue regeneration was observed by means of migrated host cells producing new collagen from within the implants. This study indicates that a cost-effective BPC extracellular matrix equivalent can incorporate cells passively to initiate regenerative healing of the corneal stroma, and is compatible with human stem or organ-specific cells for future therapeutic applications as a stromal replacement for treating blinding disorders of the cornea.

MATERIALS
Product Number
Brand
Product Description

Tetracaine hydrochloride, European Pharmacopoeia (EP) Reference Standard
Corning® Costar® TC-Treated Multiple Well Plates, size 24 wells, flat bottom wells, case of 100 (20 Bulk Packs of 5), sterile, lid
Supelco
Tetracaine hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
Tetracaine for system suitability, European Pharmacopoeia (EP) Reference Standard
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Acetone, Pharmaceutical Secondary Standard; Certified Reference Material
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Acetone, analytical standard
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Chloroform, analytical standard
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Propidium iodide, ≥94% (HPLC)
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Acetone, ≥99%, meets FCC analytical specifications
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Chloroform, anhydrous, ≥99%, contains 0.5-1.0% ethanol as stabilizer
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Glutaraldehyde solution, 50 wt. % in H2O
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Chloroform, anhydrous, contains amylenes as stabilizer, ≥99%
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Acetone, ACS spectrophotometric grade, ≥99.5%
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Glutaraldehyde solution, technical, ~50% in H2O (5.6 M)
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Diethyl azodicarboxylate solution, 40 wt. % in toluene
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Glutaraldehyde solution, 50% in H2O, suitable for photographic applications
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Glutaraldehyde solution, Grade II, 25% in H2O
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Glutaraldehyde solution, Grade I, 25% in H2O, specially purified for use as an electron microscopy fixative
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Xylazine, ≥99%
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Propidium iodide, ≥94.0% (HPLC)
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Glutaraldehyde solution, Grade I, 50% in H2O, specially purified for use as an electron microscopy fixative or other sophisticated use
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Chloroform, contains 100-200 ppm amylenes as stabilizer, ≥99.5%
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