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The effect of microneedles on the skin permeability and antitumor activity of topical 5-fluorouracil
Topical 5-fluorouracil (5-FU) is approved for the treatment of superficial basal cell carcinoma and actinic keratosis. However, 5-FU suffers from poor skin permeation. Microneedles have been successfully applied to improve the skin permeability of small and large molecules, and even nanoparticles, b...
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Published in: | Acta pharmaceutica Sinica. B 2014-02, Vol.4 (1), p.94-99 |
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description | Topical 5-fluorouracil (5-FU) is approved for the treatment of superficial basal cell carcinoma and actinic keratosis. However, 5-FU suffers from poor skin permeation. Microneedles have been successfully applied to improve the skin permeability of small and large molecules, and even nanoparticles, by creating micron-sized pores in the stratum corneum layer of the skin. In this report, the feasibility of using microneedles to increase the skin permeability of 5-FU was tested. Using full thickness mouse skin mounted on Franz diffusion apparatus, it was shown that the flux of 5-FU through the skin was increased by up to 4.5-fold when the skin was pretreated with microneedles (500 µm in length, 50 µm in base diameter). In a mouse model with B16-F10 mouse melanoma cells implanted in the subcutaneous space, the antitumor activity of a commercially available 5-FU topical cream (5%) was significantly enhanced when the cream was applied on a skin area that was pretreated with microneedles, as compared to when the cream was simply applied on a skin area, underneath which the tumor cells were implanted, and without pretreatment of the skin with microneedles. Fluorouracil is not approved for melanoma therapy, but the clinical efficacy of topical 5-FU against tumors such as basal cell carcinoma may be improved by integrating microneedle technology into the therapy. |
doi_str_mv | 10.1016/j.apsb.2013.12.013 |
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In a mouse model with B16-F10 mouse melanoma cells implanted in the subcutaneous space, the antitumor activity of a commercially available 5-FU topical cream (5%) was significantly enhanced when the cream was applied on a skin area that was pretreated with microneedles, as compared to when the cream was simply applied on a skin area, underneath which the tumor cells were implanted, and without pretreatment of the skin with microneedles. 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B</title><addtitle>Acta Pharm Sin B</addtitle><description>Topical 5-fluorouracil (5-FU) is approved for the treatment of superficial basal cell carcinoma and actinic keratosis. However, 5-FU suffers from poor skin permeation. Microneedles have been successfully applied to improve the skin permeability of small and large molecules, and even nanoparticles, by creating micron-sized pores in the stratum corneum layer of the skin. In this report, the feasibility of using microneedles to increase the skin permeability of 5-FU was tested. Using full thickness mouse skin mounted on Franz diffusion apparatus, it was shown that the flux of 5-FU through the skin was increased by up to 4.5-fold when the skin was pretreated with microneedles (500 µm in length, 50 µm in base diameter). In a mouse model with B16-F10 mouse melanoma cells implanted in the subcutaneous space, the antitumor activity of a commercially available 5-FU topical cream (5%) was significantly enhanced when the cream was applied on a skin area that was pretreated with microneedles, as compared to when the cream was simply applied on a skin area, underneath which the tumor cells were implanted, and without pretreatment of the skin with microneedles. Fluorouracil is not approved for melanoma therapy, but the clinical efficacy of topical 5-FU against tumors such as basal cell carcinoma may be improved by integrating microneedle technology into the therapy.</description><subject>5-Fluorouracil</subject><subject>Antitumor activity</subject><subject>Cytotoxicity</subject><subject>Flux</subject><subject>Immunohistochemistry</subject><subject>Melanoma</subject><subject>Microneedles</subject><subject>Original</subject><subject>Skin permeability</subject><subject>Transdermal</subject><issn>2211-3835</issn><issn>2211-3843</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkctq3TAQhk1oSEKaF8iieNmNXY1k-bIplNBLINBNuha6jBKdypYryYG8fXR60kMjEDPMzP9p0F9V10BaINB_2rVyTaqlBFgLtC3hpLqgFKBhY8feHXPGz6urlHaknJ5QOvCz6pxyBoxxclGZ-0es0VrUuQ62np2OYUE0HlMdljqXbvrtlnrFOKNUzrv8XMvFlJtd3uYQa6mze9qXiz6H1Wnpa95Yv4UYtii18--rUyt9wqvXeFn9-vb1_uZHc_fz--3Nl7tGc9blRsPUj2VHRWHSVJrJWjUwblByY0Epyi0awhUM3GpECxb6oVMcLetVP3F2Wd0euCbInVijm2V8FkE68bcQ4oOQMTvtUVBmGXKwiAS6aeByGHEyA1VI-hEmW1ifD6x1UzMajUuO0r-Bvu0s7lE8hCfRwcQm3hXAx1dADH82TFnMLmn0Xi4YtiRgpH1PGO2GMkoPo-XzU4poj88AEXu3xU7s3RZ7twVQUUIRffh_waPkn7fsBXrlqUY</recordid><startdate>20140201</startdate><enddate>20140201</enddate><creator>Naguib, Youssef W</creator><creator>Kumar, Amit</creator><creator>Cui, Zhengrong</creator><general>Elsevier</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140201</creationdate><title>The effect of microneedles on the skin permeability and antitumor activity of topical 5-fluorouracil</title><author>Naguib, Youssef W ; Kumar, Amit ; Cui, Zhengrong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-c1968602b219c2ad9ffb735dea5df1bb25fed05b175fceef1f1674b5ef36b6953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>5-Fluorouracil</topic><topic>Antitumor activity</topic><topic>Cytotoxicity</topic><topic>Flux</topic><topic>Immunohistochemistry</topic><topic>Melanoma</topic><topic>Microneedles</topic><topic>Original</topic><topic>Skin permeability</topic><topic>Transdermal</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Naguib, Youssef W</creatorcontrib><creatorcontrib>Kumar, Amit</creatorcontrib><creatorcontrib>Cui, Zhengrong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Acta pharmaceutica Sinica. 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Microneedles have been successfully applied to improve the skin permeability of small and large molecules, and even nanoparticles, by creating micron-sized pores in the stratum corneum layer of the skin. In this report, the feasibility of using microneedles to increase the skin permeability of 5-FU was tested. Using full thickness mouse skin mounted on Franz diffusion apparatus, it was shown that the flux of 5-FU through the skin was increased by up to 4.5-fold when the skin was pretreated with microneedles (500 µm in length, 50 µm in base diameter). In a mouse model with B16-F10 mouse melanoma cells implanted in the subcutaneous space, the antitumor activity of a commercially available 5-FU topical cream (5%) was significantly enhanced when the cream was applied on a skin area that was pretreated with microneedles, as compared to when the cream was simply applied on a skin area, underneath which the tumor cells were implanted, and without pretreatment of the skin with microneedles. 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subjects | 5-Fluorouracil Antitumor activity Cytotoxicity Flux Immunohistochemistry Melanoma Microneedles Original Skin permeability Transdermal |
title | The effect of microneedles on the skin permeability and antitumor activity of topical 5-fluorouracil |
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