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Transdermal permeation parameters of Cl-cubosomal formulae through a rabbit skin compared to the pure drug aqueous suspension.
| Experiment | J* (mg/cm2 h) | Kpa** (cm/h) × 10−2 | Enhancement factor |
|---|---|---|---|
| Pure drug | 0.554777 | 27.73885 | – |
| C13 | 3.3568 | 167.84 | 6.050719 |
| G13 | 2.347165 | 117.3582 | 4.230825 |
J* = transdermal flux value; Kpa** = the permeability coefficient.
