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A novel serum: Electrophoresis method to prepare acellular corneal matrix as an artificial corneal scaffold

机译:一种新型血清:电泳方法,用于制备无细胞角膜基质作为人造角膜脚手架

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Introduction: The aim of this study was to develop a novel decellularization method in order to obtain an ideal scaffold with good biocompatibility. Methods: The porcine corneas were treated with human serum for 5 days or serum-electrophoresis respectively. The electrophoresis (100 V/cm) was performed in sterilized buffer containing 40-mM tris base, 18-mM glacial acetic acid, and antibiotics for 1 h at 4 degrees C. The properties of artificial corneal scaffolds were characterized by morphological and histological examinations. The biocompatibility and biological safety were examined by subcutaneous implant test and lamellar keratoplasty. Results and conclusions: The transparency and appearance of serum-electrophoresis acellular porcine corneal matrix were better than serum acellular porcine corneal matrix. DNA and alpha-gal in serum-electrophoresis acellular porcine corneal matrix were more efficiently removed than those in serum acellular porcine corneal matrix (p < 0.05). The subcutaneous and corneal implantation experiments showed serum-electrophoresis acellular porcine corneal matrix had better biocompatibility compared to serum acellular porcine corneal matrix (p < 0.01). This novel serum-electrophoresis decellularization method may be valuable for preparation of xenogenic corneal tissue for clinical application.
机译:介绍:本研究的目的是开发一种新型脱细胞化方法,以获得具有良好生物相容性的理想支架。方法:猪角膜分别用人血清处理5天或血清电泳。电泳(100V / cm)在含有40mm Tris碱,18mm冰醋酸的灭菌缓冲液中进行,并在4摄氏度下抗生素。通过形态学和组织学检查表征人造角膜支架的性质。通过皮下植入试验和层状静脉成形术检查了生物相容性和生物安全性。结果与结论:血清 - 电泳的透明度和外观优于血清细胞植物角膜基质。血清电泳中的DNA和α-加仑比血清细胞猪角膜基质更有效地去除(P <0.05)。皮下和角膜植入实验显示血清 - 电泳与血清细胞猪角膜基质相比具有更好的生物相容性(P <0.01)。这种新型血清电泳脱细胞化方法对于制备临床应用的肾外角膜组织可能是有价值的。

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