|
2.2 × 10−9 (m2·s−1) (Caccavo et al.,
2015) |
Water diffusivity in the dissolved drug layer (ΩB) |
|
1.5 × 10−10 (m2·s−1) (Caccavo et al.,
2015) |
Drug diffusivity in the dissolved drug layer (ΩB) |
|
1.99 × 10−12 (m2·s−1) (from experiment) |
Water diffusivity in the polymeric film (ΩC) |
|
3.1 × 10−13 (m2·s−1) (from experiment) |
Drug diffusivity in the polymeric film (ΩC) |
|
3 × 10−9 (m2·s−1) (Holz et al.,
2000) |
Water diffusivity in the dissolution medium (ΩD) |
|
8.21 × 10−10 (m2·s−1) (Grassi et al.,
2001) |
Drug diffusivity in the dissolution medium (ΩD) |
|
0.0115 (−) (Serajuddin and Jarowski, 1985) |
Theophylline saturation mass fraction in water |
|
4.95 (−) (from experiment) |
Water equilibrium constant: relates the water mass fraction in ΩC to its equilibrium counterpart in ΩB
|
|
0.2 (−) (from experiment) |
Water equilibrium constant: relates the water mass fraction in ΩDto its equilibrium counterpart in ΩC
|
ρ10
|
1000 (kg·m−3) (Caccavo et al.,
2015) |
Pure water density |
ρ20
|
1200 (kg·m−3) (Caccavo et al.,
2015) |
Pure theophylline density |
ρ30
|
1200 (kg·m−3) (Caccavo et al.,
2015) |
Pure HPMC density |
ρ40
|
1200 (kg·m−3) |
Pure Surelease density |