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. 2014 Mar 18;3(2):91–98. doi: 10.1016/j.imr.2014.03.002

Table 5.

Postcompression parameters of orodispersible tablets of valsartan

Formulation code Parameters
In vitro disintegration time (s) a Wetting time
(s) a
Water absorption ratio a Drug content b
F1 60.27 ± 0.62 46.73 ± 0.39 110.88 ± 0.24 100.00 ± 002
F2 57.29 ± 0.62 42.39 ± 0.35 119.04 ± 0.33 99.86 ± 0.1
F3 47.68 ± 0.53 37.05 ± 0.56 126.80 ± 1.02 99.81 ± 0.18
F4 32.34 ± 0.78 26.2 ± 0.25 133.55 ± 0.28 98.36 ± 0.43
F5 70.56 ± 1.82 54.17 ± 0.48 99.67 ± 0.49 98.54 ± 0.85
F6 61.32 ± 0.58 50.46 ± 0.76 99.24 ± 0.24 99.5 ± 0.77
F7 55.16 ± 1.44 47.90 ± 0.44 104.66 ± 0.70 99.84 ± 0.33
F8 46.96 ± 0.70 39.18 ± 0.43 109.52 ± 0.99 100.04 ± 0.20

All values are presented as mean ± SD, n = 6 a/10 b.