Implantation of Hydroxyapatite–Titanium Corneal Implants in Rat Cornea

PURPOSE:To evaluate the biocompatibility of hydroxyapatite-coated titanium (HA/Ti) corneal implants at the molecular levels with histopathology. METHODS:Eighty Sprague-Dawley rats were divided into 2 equal groups. In the study group, HA/Ti prosthetics were implanted into the right corneal stroma. Th...

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Veröffentlicht in:Cornea 2011-01, Vol.30 (1), p.67-72
Hauptverfasser: Fang, Yin Dong, Xiao, Ma, Fei, Huang Yi
Format: Artikel
Sprache:eng
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Zusammenfassung:PURPOSE:To evaluate the biocompatibility of hydroxyapatite-coated titanium (HA/Ti) corneal implants at the molecular levels with histopathology. METHODS:Eighty Sprague-Dawley rats were divided into 2 equal groups. In the study group, HA/Ti prosthetics were implanted into the right corneal stroma. The control group received a sham incision. Corneas were collected and studied with histopathological examination (HE), immunohistochemical, and other stains, including scanned electron microscopy and reverse transcription-polymerase chain reaction, to evaluate inflammatory reactions, tissue repair, and expression of various biological factors during healing. RESULTS:In the control group, corneal neovascularization occurred 7 days after surgery, and the corneas recovered 28 days after surgery. In the study group, corneal vascularization increased substantially on day 7 and stabilized on day 28. For both groups, reverse transcription-polymerase chain reaction detected expressions of 6 primers at all time points. The amplified sequences were consistent with the designed sequences. The expression of matrix metalloproteinase-2, matrix metalloproteinase-9, bFGF, vascular endothelial growth factor, and type III collagen were delayed in the study group compared with the control group. Histological analyses showed a tight attachment of the corneal tissue to the HA/Ti implant on day 28. CONCLUSIONS:The HA/Ti corneal implants can remain stable in corneal tissue for a long time, induce corneal neovascularization, and stimulate inflammatory cells and keratocytes to synthesize or activate matrix metalloproteinases. Artificial cornea made from this material show enhanced stability and biocompatibility in vivo.
ISSN:0277-3740
1536-4798
DOI:10.1097/ICO.0b013e3181d92817