Conjunctival and corneal reactions in rabbits following short- and repeated exposure to preservative-free tafluprost, commercially available latanoprost and 0.02% benzalkonium chloride
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Liang, H.
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Univ Paris 06, INSERM, Inst Vis, UMR S 592, F-75012 Paris, France
Univ Paris 05, Fac Biol & Pharmacol Sci, Dept Toxicol, Paris, FranceUniv Paris 06, INSERM, Inst Vis, UMR S 592, F-75012 Paris, France
Liang, H.
[1
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Baudouin, C.
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Pauly, A.
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Univ Paris 06, INSERM, Inst Vis, UMR S 592, F-75012 Paris, France
Univ Paris 05, Fac Biol & Pharmacol Sci, Dept Toxicol, Paris, FranceUniv Paris 06, INSERM, Inst Vis, UMR S 592, F-75012 Paris, France
Pauly, A.
[1
,2
]
Brignole-Baudouin, F.
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Univ Paris 06, INSERM, Inst Vis, UMR S 592, F-75012 Paris, France
Univ Paris 05, Fac Biol & Pharmacol Sci, Dept Toxicol, Paris, France
Quinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, Paris, FranceUniv Paris 06, INSERM, Inst Vis, UMR S 592, F-75012 Paris, France
Brignole-Baudouin, F.
[1
,2
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机构:
[1] Univ Paris 06, INSERM, Inst Vis, UMR S 592, F-75012 Paris, France
[2] Univ Paris 05, Fac Biol & Pharmacol Sci, Dept Toxicol, Paris, France
Aim: To compare the conjunctival and corneal reactions of commercially available solution of latanoprost (Xalatan) and preservative-free (PF) tafluprost in rabbits. Methods: The rabbits received 50 mu l of phosphate-buffered saline (PBS), PF-tafluprost 0.0015%, latanoprost 0.005% or benzalkonium chloride (BAK) 0.02%; all solutions were applied at 5 min intervals for a total of 15 times. The ocular surface toxicity was investigated using slit-lamp biomicroscopy examination, flow cytometry (FCM) and on imprints for CD45 and tumour necrosis factor-receptor 1 (TNFR1) conjunctival impression cytology (CIC) and corneal in vivo confocal microscopy (IVCM). Standard immunohistology also assessed inflammatory/apoptotic cells. Results: Clinical observation and IVCM images showed the highest ocular surface toxicity with latanoprost and BAK, while PF-tafluprost and PBS eyes presented almost normal corneoconjunctival aspects. FCM showed a higher expression of CD45+ and TNFR1+ in latanoprost- or BAK-instilled groups, compared with PF-tafluprost and PBS groups. Latanoprost induced fewer positive cells for inflammatory marker expressions in CIC specimens compared with BAK-alone, both of which were higher than with PF-tafluprost or PBS. Immunohistology showed the same tendency of toxic ranking. Conclusion: The authors confirm that rabbit corneoconjunctival surfaces presented a better tolerance when treated with PF-tafluprost compared with commercially available latanoprost or BAK solution.
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Quinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Brasnu, Emmanuelle
Brignole-Bauclouin, Francoise
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Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Brignole-Bauclouin, Francoise
Riancho, Luisa
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Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Riancho, Luisa
Guenoun, Jean-Marc
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Quinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Guenoun, Jean-Marc
Warnet, Jean-Michel
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Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Warnet, Jean-Michel
Baudouin, Christophe
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Quinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
机构:
Quinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Brasnu, Emmanuelle
Brignole-Bauclouin, Francoise
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Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Brignole-Bauclouin, Francoise
Riancho, Luisa
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Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Riancho, Luisa
Guenoun, Jean-Marc
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机构:
Quinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Guenoun, Jean-Marc
Warnet, Jean-Michel
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Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, France
Paris Descartes Univ, Dept Toxicol, Fac Biol & Pharmacol Sci, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Warnet, Jean-Michel
Baudouin, Christophe
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h-index: 0
机构:
Quinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France
Paris Descartes Univ, INSERM, UMR S 872, Cordeliers Biomed Insy, Paris, FranceQuinze Vingts Natl Ophthalmol Hosp, Dept Ophthalmol 3, F-75012 Paris, France