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一种用于角膜植入的简单的交联胶原组织替代物。

A simple, cross-linked collagen tissue substitute for corneal implantation.

作者信息

Liu Yuwen, Gan Lisha, Carlsson David J, Fagerholm Per, Lagali Neil, Watsky Mitchell A, Munger Rejean, Hodge William G, Priest David, Griffith May

机构信息

National Research Council Canada, Ottawa, Ontario, Canada.

出版信息

Invest Ophthalmol Vis Sci. 2006 May;47(5):1869-75. doi: 10.1167/iovs.05-1339.

Abstract

PURPOSE

To develop a simple corneal substitute from cross-linked collagen.

METHODS

Porcine type I collagen (10%; pH 5), was mixed with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and N-hydroxysuccinimide (NHS). The final homogenous solution was molded to corneal dimensions, cured, and then implanted into rabbits and minipigs by lamellar keratoplasty. The implants were followed for up to 6 months after surgery. Clinical examinations of the cornea included detailed slit lamp biomicroscopy, in vivo confocal microscopy, topography and esthesiometry for nerve function. Histopathologic examinations were also performed on rabbit corneas harvested after 6 months.

RESULTS

Cross-linked collagen (refractive index, 1.35) had optical clarity superior to human corneas. Implanted into rabbit and porcine corneas, only 1 of 24 of the surgical corneas showed a slight haze at 6 months after surgery. All other implants showed no adverse reactions and remained optically clear. Topography showed a smooth surface and a profile similar to that of the contralateral nonsurgical eye. The implanted matrices promoted regeneration of corneal cells, tear film, and nerves. Touch sensitivity was restored, indicating some restoration of function. The corneas with implants showed no significant loss of thickness and demonstrated stable host-graft integration.

CONCLUSIONS

Collagen can be adequately stabilized, using water soluble carbodiimides as protein cross-linking reagents, in the fabrication of corneal matrix substitutes for implantation. The simple cross-linking methodology would allow for easy fabrication of matrices for transplantation in centers where there is a shortage of corneas, or where there is need for temporary patches to repair perforations in emergency situations.

摘要

目的

利用交联胶原蛋白开发一种简单的角膜替代物。

方法

将猪I型胶原蛋白(10%;pH 5)与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)混合。将最终的均匀溶液模制成角膜尺寸,固化,然后通过板层角膜移植术植入兔子和小型猪体内。术后对植入物进行长达6个月的随访。角膜的临床检查包括详细的裂隙灯生物显微镜检查、体内共聚焦显微镜检查、地形图检查和神经功能的感觉测量。还对术后6个月采集的兔角膜进行了组织病理学检查。

结果

交联胶原蛋白(折射率为1.35)的光学清晰度优于人角膜。植入兔和猪角膜后,24只手术角膜中只有1只在术后6个月出现轻微混浊。所有其他植入物均未出现不良反应,保持光学清晰。地形图显示表面光滑,轮廓与对侧未手术眼相似。植入的基质促进了角膜细胞、泪膜和神经的再生。触觉敏感性恢复,表明功能有所恢复。植入物的角膜厚度没有明显损失,宿主-移植物整合稳定。

结论

使用水溶性碳二亚胺作为蛋白质交联剂,可以在制造用于植入的角膜基质替代物时充分稳定胶原蛋白。这种简单的交联方法将便于在角膜短缺的中心或紧急情况下需要临时修补穿孔的地方制造用于移植的基质。

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