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A microneedle roller for transdermal drug delivery

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dc.contributor.authorPark, Jung-Hwan-
dc.contributor.authorChoi, Seong-O-
dc.contributor.authorSeo, Soonmin-
dc.contributor.authorBin Choy, Young-
dc.contributor.authorPrausnitz, Mark R.-
dc.date.accessioned2012-06-28T08:55:59Z-
dc.date.available2012-06-28T08:55:59Z-
dc.date.issued2010-10-
dc.identifier.citationEUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS; Vol.76 2; 282-289ko_KR
dc.identifier.issn0939-6411-
dc.identifier.urihttps://hdl.handle.net/10371/77812-
dc.description.abstractMicroneedle rollers have been used to treat large areas of skin for cosmetic purposes and to increase skin permeability for drug delivery. In this study, we introduce a polymer microneedle roller fabricated by inclined rotational UV lithography, replicated by micromolding hydrophobic polylactic acid and hydrophilic carboxy-methyl-cellulose. These microneedles created micron-scale holes in human and porcine cadaver skin that permitted entry of acetylsalicylic acid. Trypan blue and nanoparticles measuring 50 nm and 200 nm in diameter. The amount of acetylsalicylic acid delivered increased with the number of holes made in the skin and was 1-2 orders of magnitude greater than in untreated skin. Lateral diffusion in the skin between holes made by microneedles followed expected diffusional kinetics, with effective diffusivity values that were 23-160 times smaller than in water. Compared to inserting microneedles on a flat patch, the sequential insertion of microneedles row by row on a roller required less insertion force in full-thickness porcine skin. Overall, polymer microneedle rollers, prepared from replicated polymer films, offer a simple way to increase skin permeability for drug delivery. (C) 2010 Elsevier B.V. All rights reserved.ko_KR
dc.language.isoenko_KR
dc.publisherELSEVIER SCIENCE BVko_KR
dc.subjectMicroneedleko_KR
dc.subjectFabricationko_KR
dc.subjectDrug delivery propertyko_KR
dc.subjectMechanical propertyko_KR
dc.subjectPolymer filmko_KR
dc.titleA microneedle roller for transdermal drug deliveryko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor박정환-
dc.contributor.AlternativeAuthor최성오-
dc.contributor.AlternativeAuthor서순민-
dc.contributor.AlternativeAuthor조영빈-
dc.identifier.doi10.1016/j.ejpb.2010.07.001-
dc.citation.journaltitleEUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS-
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