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Transdermal delivery of propranolol

dc.contributor.authorKrishna R.; Pandit J.K.
dc.date.accessioned2025-05-24T09:56:11Z
dc.description.abstractThree transdermal formulations containing propranolol hydrochloride in a hydrophilic polymer matrix were prepared-one without a rate controlling membrane(H-1), one with a 20μ thick Ethylene Vinyl Acetate(EVA) rate controlling membrane (H-2) and one with a 65μ thick EVA membrane. These patches were evaluated for their in-vitro performance. Cumulative % 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 was seen with patches H-2 & H-3. Matrix diffusion profile was observed with H-1 patch. © 1994 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.
dc.identifier.doihttps://doi.org/10.3109/03639049409042650
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/20735
dc.relation.ispartofseriesDrug Development and Industrial Pharmacy
dc.titleTransdermal delivery of propranolol

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