A new variety of hydroxyapatite: The Chinese implant

Citation
Dr. Jordan et al., A new variety of hydroxyapatite: The Chinese implant, OPHTHAL PL, 15(6), 1999, pp. 420-424
Citations number
9
Categorie Soggetti
Optalmology
Journal title
OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY
ISSN journal
07409303 → ACNP
Volume
15
Issue
6
Year of publication
1999
Pages
420 - 424
Database
ISI
SICI code
0740-9303(199911)15:6<420:ANVOHT>2.0.ZU;2-#
Abstract
Purpose: This study was designed to evaluate a new type of hydroxyapatite ( HA) implant (produced in China) in a rabbit model. Methods: Three New Zealand white rabbits underwent enucleation of one eye f ollowed by implantation of a 12-mm Chinese HA implant wrapped in Vicryl mes h (polyglactin 910). Magnetic resonance imaging was performed to assess hos t fibrovascularization of the implant 4, 8, and 12 weeks after implantation . One animal was sacrificed at each of these times for histopathologic exam ination. The Chinese implant was also examined chemically and by scanning e lectron microscopy. It was compared to the original BioEye and the third ge neration synthetic HA implant produced in France by FCI (FCI3). Results: This new variety of HA implant from China is heavier than the FCI, implant but lighter than the original BioEye. The Chinese implant was easy to work with and not fragile. The pore size was more uniform than the FCI, implant and similar to the BioEye implant clinically and by scanning elect ron microscopy. The pores in this implant are unidirectional. Analysis for impurities revealed a calcium oxide (CaO) content of 4.4%. Histopathologica lly, central vascularization occurred by 4 weeks and was similar in extent to the vascularization seen with the FCI, implant and the BioEye. Conclusions: The Chinese implant is less expensive then the BioEye and the FCI, implants, and appears to be a viable alternative to the BioEye. Furthe r refinements are in progress to eliminate the CaO contaminant.