Three transdermal formulations containing propranolol hydrochloride in
a hydrophilic polymer matrix were prepared - one without a rate contr
olling membrane(H-1), one with a 20 mu thick Ethylene Vinyl Acetate(EV
A) rate controlling membrane (H-2) and one with a 65 mu thick EVA memb
rane. These patches were evaluated for their in-vitro performance. Cum
ulative % permeated across excised hairfree rat skin were 79.2% from H
-1, 65.53% from H-2 and 53.44% from H-3. Increase in thickness of EVA
lead to greater retention of drug in device and a zero order profile w
as seen with patches H-2 and H-3. Matrix diffusion profile was observe
d with H-1 patch.