on the tear film and ocular surface in a mouse model of experimental dry eye (EDE). Methods: Eye drops consisting of 0.1 % HA alone or mixed with 0.1%, 0.5%, or 5.0 % MO were applied to desic-cating stress-induced murine dry eyes. Tear volume, corneal irregularity score, tear film break-up time (TBUT), and corneal fluorescein staining scores were measured at 5 and 10 days after treatment. Ten days after treatment, goblet cells in the conjunctiva were counted after Periodic acid-Schiff staining. Results: There was no significant difference in the tear volume between desiccating stress-induced groups. The corneal irregularity score was lower in the 0.5 % MO group compared with the EDE and HA groups. The 0.5 % and 5.0 % MO groups showed a sign...
Purpose: To compare the effects of topical human amniotic fluid (HAF), topical human serum (HS), and...
PubMed ID: 24566903Background: To evaluate the efficacy of autologous serum (AS) eye drops for the s...
In the current study, we used 56 female BALB/c mice with induced dry eye syndrome to evaluate the th...
Purpose: To evaluate effects of a novel multi-ingredient artificial tear formulation containing carb...
Purpose: Dry eye is often characterized by increased tear evaporation due to poor tear film quality,...
Background: Dry eye disease (DED) is a multifactorial disease where ocular surface inflammation and ...
Dry eye complaints are ranked as themost frequent symptoms of patients visiting ophthalmol-ogists. C...
Purpose: To compare the efficacy and safety of an artificial tear combining the polymers carboxymeth...
Purpose. To investigate the therapeutic effects of topical administration of antioxidant medicinal p...
Purpose: Hydroxypropyl guar (HPG) and hyaluronic acid (HA) have been individually shown to improve d...
[Purpose]: To evaluate the effect of tear supplementation with preservative free 0.15% zinc-hyaluron...
AIM: To study the effect of uncrosslinked and crosslinked hyaluronic acid combined with other artifi...
Purpose: To assess the six-month therapeutic profiles of lipid and non-lipid-based artificial tear s...
Background: The mainstay of dry eye treatment is artificial tear solutions. Contralateral eye compar...
PURPOSE: We compared the efficacy and safety of sodium hyaluronate (SH) and carboxymethylcellulose (...
Purpose: To compare the effects of topical human amniotic fluid (HAF), topical human serum (HS), and...
PubMed ID: 24566903Background: To evaluate the efficacy of autologous serum (AS) eye drops for the s...
In the current study, we used 56 female BALB/c mice with induced dry eye syndrome to evaluate the th...
Purpose: To evaluate effects of a novel multi-ingredient artificial tear formulation containing carb...
Purpose: Dry eye is often characterized by increased tear evaporation due to poor tear film quality,...
Background: Dry eye disease (DED) is a multifactorial disease where ocular surface inflammation and ...
Dry eye complaints are ranked as themost frequent symptoms of patients visiting ophthalmol-ogists. C...
Purpose: To compare the efficacy and safety of an artificial tear combining the polymers carboxymeth...
Purpose. To investigate the therapeutic effects of topical administration of antioxidant medicinal p...
Purpose: Hydroxypropyl guar (HPG) and hyaluronic acid (HA) have been individually shown to improve d...
[Purpose]: To evaluate the effect of tear supplementation with preservative free 0.15% zinc-hyaluron...
AIM: To study the effect of uncrosslinked and crosslinked hyaluronic acid combined with other artifi...
Purpose: To assess the six-month therapeutic profiles of lipid and non-lipid-based artificial tear s...
Background: The mainstay of dry eye treatment is artificial tear solutions. Contralateral eye compar...
PURPOSE: We compared the efficacy and safety of sodium hyaluronate (SH) and carboxymethylcellulose (...
Purpose: To compare the effects of topical human amniotic fluid (HAF), topical human serum (HS), and...
PubMed ID: 24566903Background: To evaluate the efficacy of autologous serum (AS) eye drops for the s...
In the current study, we used 56 female BALB/c mice with induced dry eye syndrome to evaluate the th...