Maria A Amesty1, Jorge L Alio2, Alejandra E Rodriguez2. 1. Department of Ophthalmology, Nottingham University Hospitals, Nottingham, UK. 2. Vissum Corporación Oftalmológica, Alicante, Spain.
Abstract
PURPOSE: To study the tolerance and biocompatibility of micronised mineral pigments for corneal cosmetic pigmentation in an experimental animal model. METHODS: Corneal intralamellar keratopigmentation was performed in 28 New Zealand white rabbits using micronised mineral pigments. Prophylactic actions using intraoperative antibiotic prophylaxis and gamma radiation of the pigment mixtures were performed to avoid infection. Animals were examined regularly by slit lamp to detect any sign of inflammation, pigment diffusion, colour changes or neovascularisation. Histopathological examination was performed to determine the level of pigment diffusion, the level of inflammation and the presence of neovascularisation. RESULTS: No pigment diffusion or changes in colour, inflammation or neovascularisation were detected in the eyes treated. Histopathological examination corroborated clinical results regarding inflammation. Pigmented corneas showed a good cosmetic appearance without signs of ocular toxicity. CONCLUSIONS: Micronised mineral pigments could be a valid alternative treatment for cosmetic keratopigmentation. The intralamellar keratopigmentation technique presented good cosmetic appearance without adverse effects in the eyes treated. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.
PURPOSE: To study the tolerance and biocompatibility of micronised mineral pigments for corneal cosmetic pigmentation in an experimental animal model. METHODS:Corneal intralamellar keratopigmentation was performed in 28 New Zealand white rabbits using micronised mineral pigments. Prophylactic actions using intraoperative antibiotic prophylaxis and gamma radiation of the pigment mixtures were performed to avoid infection. Animals were examined regularly by slit lamp to detect any sign of inflammation, pigment diffusion, colour changes or neovascularisation. Histopathological examination was performed to determine the level of pigment diffusion, the level of inflammation and the presence of neovascularisation. RESULTS: No pigment diffusion or changes in colour, inflammation or neovascularisation were detected in the eyes treated. Histopathological examination corroborated clinical results regarding inflammation. Pigmented corneas showed a good cosmetic appearance without signs of ocular toxicity. CONCLUSIONS: Micronised mineral pigments could be a valid alternative treatment for cosmetic keratopigmentation. The intralamellar keratopigmentation technique presented good cosmetic appearance without adverse effects in the eyes treated. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.