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Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model

Purpose: To evaluate effects of a novel multi-ingredient artificial tear formulation containing carboxymethylcellulose (CMC) and hyaluronic acid (HA) in a murine dry eye model. Methods: Dry eye was induced in mice (C57BL/6) using an intelligently controlled environmental system (ICES). CMC+HA (Optiv...

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Autores principales: She, Yujing, Li, Jinyang, Xiao, Bing, Lu, Huihui, Liu, Haixia, Simmons, Peter A., Vehige, Joseph G., Chen, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675178/
https://www.ncbi.nlm.nih.gov/pubmed/26322539
http://dx.doi.org/10.1089/jop.2015.0042
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author She, Yujing
Li, Jinyang
Xiao, Bing
Lu, Huihui
Liu, Haixia
Simmons, Peter A.
Vehige, Joseph G.
Chen, Wei
author_facet She, Yujing
Li, Jinyang
Xiao, Bing
Lu, Huihui
Liu, Haixia
Simmons, Peter A.
Vehige, Joseph G.
Chen, Wei
author_sort She, Yujing
collection PubMed
description Purpose: To evaluate effects of a novel multi-ingredient artificial tear formulation containing carboxymethylcellulose (CMC) and hyaluronic acid (HA) in a murine dry eye model. Methods: Dry eye was induced in mice (C57BL/6) using an intelligently controlled environmental system (ICES). CMC+HA (Optive Fusion™), CMC-only (Refresh Tears(®)), and HA-only (Hycosan(®)) artificial tears and control phosphate-buffered saline (PBS) were administered 4 times daily and compared with no treatment (n = 64 eyes per group). During regimen 1 (prevention regimen), mice were administered artificial tears or PBS for 14 days (starting day 0) while they were exposed to ICES, and assessed on days 0 and 14. During regimen 2 (treatment regimen), mice exposed to ICES for 14 days with no intervention were administered artificial tears or PBS for 14 days (starting day 14) while continuing exposure to ICES, and assessed on days 0, 14, and 28. Corneal fluorescein staining and conjunctival goblet cell density were measured. Results: Artificial tear-treated mice had significantly better outcomes than control groups on corneal staining and goblet cell density (P < 0.01). Mice administered CMC+HA also showed significantly lower corneal fluorescein staining and higher goblet cell density, compared with CMC (P < 0.01) and HA (P < 0.05) in both regimens 1 and 2. Conclusions: The artificial tear formulation containing CMC and HA was effective in preventing and treating environmentally induced dry eye. Improvements observed for corneal fluorescein staining and conjunctival goblet cell retention suggest that this combination may be a viable treatment option for dry eye disease.
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spelling pubmed-46751782015-12-15 Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model She, Yujing Li, Jinyang Xiao, Bing Lu, Huihui Liu, Haixia Simmons, Peter A. Vehige, Joseph G. Chen, Wei J Ocul Pharmacol Ther Original Articles Purpose: To evaluate effects of a novel multi-ingredient artificial tear formulation containing carboxymethylcellulose (CMC) and hyaluronic acid (HA) in a murine dry eye model. Methods: Dry eye was induced in mice (C57BL/6) using an intelligently controlled environmental system (ICES). CMC+HA (Optive Fusion™), CMC-only (Refresh Tears(®)), and HA-only (Hycosan(®)) artificial tears and control phosphate-buffered saline (PBS) were administered 4 times daily and compared with no treatment (n = 64 eyes per group). During regimen 1 (prevention regimen), mice were administered artificial tears or PBS for 14 days (starting day 0) while they were exposed to ICES, and assessed on days 0 and 14. During regimen 2 (treatment regimen), mice exposed to ICES for 14 days with no intervention were administered artificial tears or PBS for 14 days (starting day 14) while continuing exposure to ICES, and assessed on days 0, 14, and 28. Corneal fluorescein staining and conjunctival goblet cell density were measured. Results: Artificial tear-treated mice had significantly better outcomes than control groups on corneal staining and goblet cell density (P < 0.01). Mice administered CMC+HA also showed significantly lower corneal fluorescein staining and higher goblet cell density, compared with CMC (P < 0.01) and HA (P < 0.05) in both regimens 1 and 2. Conclusions: The artificial tear formulation containing CMC and HA was effective in preventing and treating environmentally induced dry eye. Improvements observed for corneal fluorescein staining and conjunctival goblet cell retention suggest that this combination may be a viable treatment option for dry eye disease. Mary Ann Liebert, Inc. 2015-11-01 /pmc/articles/PMC4675178/ /pubmed/26322539 http://dx.doi.org/10.1089/jop.2015.0042 Text en © She et al., 2015; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Articles
She, Yujing
Li, Jinyang
Xiao, Bing
Lu, Huihui
Liu, Haixia
Simmons, Peter A.
Vehige, Joseph G.
Chen, Wei
Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model
title Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model
title_full Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model
title_fullStr Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model
title_full_unstemmed Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model
title_short Evaluation of a Novel Artificial Tear in the Prevention and Treatment of Dry Eye in an Animal Model
title_sort evaluation of a novel artificial tear in the prevention and treatment of dry eye in an animal model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4675178/
https://www.ncbi.nlm.nih.gov/pubmed/26322539
http://dx.doi.org/10.1089/jop.2015.0042
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