Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.ejpb.2006.12.010
DC FieldValue
dc.titleReversible effects of permeation enhancers on human skin
dc.contributor.authorKang, L.
dc.contributor.authorPoh, A.L.
dc.contributor.authorFan, S.K.
dc.contributor.authorHo, P.C.
dc.contributor.authorChan, Y.W.
dc.contributor.authorChan, S.Y.
dc.date.accessioned2014-05-19T02:54:40Z
dc.date.available2014-05-19T02:54:40Z
dc.date.issued2007-08
dc.identifier.citationKang, L., Poh, A.L., Fan, S.K., Ho, P.C., Chan, Y.W., Chan, S.Y. (2007-08). Reversible effects of permeation enhancers on human skin. European Journal of Pharmaceutics and Biopharmaceutics 67 (1) : 149-155. ScholarBank@NUS Repository. https://doi.org/10.1016/j.ejpb.2006.12.010
dc.identifier.issn09396411
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/53135
dc.description.abstractThis study outlines a systematic approach for investigating a desired characteristic of chemicals used to facilitate the permeation of drugs across the skin that is, the reversibility of the permeation enhancement effect. This implies that the vital skin barrier function is restored and not permanently impaired after the application of these enhancers. The reversible effects of two terpene enhancers, (R)-(-)-carvone and eucarvone, on excised human skin were evaluated by in vitro permeation and extraction studies on normal (untreated) and enhancer-pretreated epidermis, respectively. For the permeation studies on normal epidermis, the donor solutions were the model drug, haloperidol (HP, 3 mg/ml), in propylene glycol (PG) with or without 5% (w/v) enhancer and for the extraction studies using epidermis pretreated with enhancer, a solution of HP (3 mg/ml) in PG was used. The solubilities of the enhancers in 0.03% lactic acid (receptor solution) and of HP in PG (donor solution) were determined to demonstrate that the sink and saturated conditions were maintained in the respective compartments of the flow-through cells throughout the in vitro experiments. (R)-(-)-Carvone cleared out of the skin faster than eucarvone. This could be due to the 4-fold higher skin permeability of (R)-(-)-carvone compared to that of eucarvone. The amount of HP deposited in the epidermis was much lower in the eucarvone-pretreated epidermis than that pretreated with (R)-(-)-carvone. The permeation profile of HP across the enhancer-pretreated skin was 4-fold greater than in the vehicle alone (control), but similar to that across untreated skin with enhancer present in the donor solution, indicating that permeation across the enhancer-pretreated skin did not change. The enhancing effects of both terpenes on the skin were found to be reversible and the permeability of the skin was left intact after the passage of the drug in the vehicle with these enhancers. © 2007 Elsevier B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.ejpb.2006.12.010
dc.sourceScopus
dc.subjectChemical enhancer
dc.subjectHaloperidol
dc.subjectReversibility
dc.subjectSkin permeation
dc.subjectTerpene
dc.subjectTransdermal drug delivery
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.contributor.departmentSTATISTICS & APPLIED PROBABILITY
dc.description.doi10.1016/j.ejpb.2006.12.010
dc.description.sourcetitleEuropean Journal of Pharmaceutics and Biopharmaceutics
dc.description.volume67
dc.description.issue1
dc.description.page149-155
dc.description.codenEJPBE
dc.identifier.isiut000248560900017
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.