Liu Wenguang, Merrett Kimberley, Griffith May, Fagerholm Per, Dravida Subhadra, Heyne Belinda, Scaiano Juan C, Watsky Mitchell A, Shinozaki Naoshi, Lagali Neil, Munger Rejean, Li Fengfu
Deptartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Biomaterials. 2008 Mar;29(9):1147-58. doi: 10.1016/j.biomaterials.2007.11.011.
We successfully fabricated transparent, robust hydrogels as corneal substitutes from concentrated recombinant human type I and type III collagen solutions crosslinked with 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide (EDC) and N-hydroxysuccinimide (NHS). White light transmission through these gels is comparable or superior to that of human corneas. Hydrogels from both type I and type III collagens supported in vitro epithelium and nerve over-growth. While both these biocompatible hydrogels have adequate tensile strength and elasticity for surgical manipulation, type III collagen hydrogels tended to be mechanically superior. Twelve-month post-implantation results of type I recombinant collagen-based corneal substitutes into mini-pigs showed retention of optical clarity, along with regeneration of corneal cells, nerves and tear film. For clinical use, implants based on fully characterized, recombinant human collagen eliminate the risk of pathogen transfer or xenogeneic immuno-responses posed by animal collagens.
我们成功地用1-乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)和N-羟基琥珀酰亚胺(NHS)交联的浓缩重组人I型和III型胶原溶液制备了透明、坚固的水凝胶作为角膜替代物。透过这些凝胶的白光透射率与人类角膜相当或更高。I型和III型胶原水凝胶都支持体外上皮细胞和神经的过度生长。虽然这两种生物相容性水凝胶都具有足够的拉伸强度和弹性以进行手术操作,但III型胶原水凝胶在机械性能上往往更优越。将基于I型重组胶原的角膜替代物植入小型猪12个月后的结果显示,其光学清晰度得以保持,同时角膜细胞、神经和泪膜也得以再生。对于临床应用,基于充分表征的重组人胶原的植入物消除了动物胶原带来的病原体转移或异种免疫反应的风险。