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. 2014 Apr 29;2014:490595. doi: 10.1155/2014/490595

Table 3.

Effect of different viscosity modifiers on the in vitro transcorneal permeation of voriconazole from ophthalmic solution through freshly excised goat cornea.

Formulations Viscosity (cp) at 100 rpm Amount of drug permeated in 120 mins % in vitro permeation P app  × 10−6 (cm/s) Corneal hydration
None 0.98 0.317 ± 0.001†† 2.12 ± 0.003†† 30.72 ± 0.055†† 77.88 ± 0.15
PVA 1.4% 05.43 0.287 ± 0.001†† 1.918 ± 0.003†† 26.91 ± 0.051†† 77.63 ± 1.40
CS 2% 15.23 0.256 ± 0.001†† 1.71 ± 0.003†† 23.99 ± 0.050†† 77.71 ± 1.48
GG 1.5% 62.66 0.192 ± 0.001†† 1.281 ± 0.003†† 17.97 ± 0.050†† 79.36 ± 0.35
SA 2% 132.55 0.151 ± 0.001†† 1.01 ± 0.001†† 14.14 ± 0.039†† 79.93 ± 0.38
Gelrite 0.5% 147.10 0.139 ± 0.001†† 0.92 ± 0.003†† 13.03 ± 0.055†† 78.92 ± 0.47
SCMC 2.5% 167.80 0.092 ± 0.001†† 0.61 ± 0.003†† 8.75 ± 0.195†† 76.68 ± 1.82
XG 1.5% 180.28 0.071 ± 0.001 0.48 ± 0.002 6.79 ± 0.050 77.53 ± 0.47

Values are mean ± SE of 3 solutions viscosity in each group.

Statistically significant difference at P < 0.05; ††statistically significant difference at P < 0.01; †††statistically significant difference at P < 0.001 from control (voriconazole-HP-β-CD based solutions 1.5%, pH 7.0) as determined by one-way ANOVA followed by Dunnett's test.