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Hydrogel-Forming Microneedles Increase in Volume During Swelling in Skin,but Skin Barrier Function Recovery is Unaffected
Institution:1. Department of Biopharmaceutics, Kyoto Pharmaceutical University, Kyoto, Japan;2. CosMED Pharmaceutical Co. Ltd., Kyoto, Japan;1. Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Guangdong Provincial Engineering and Technological Research Center for Drug Carrier Development, Department of Biomedical Engineering, Jinan University, Guangzhou 510632, China;2. Nanhai Longtime Pharmaceutical Co., Ltd, Foshan 528200, China;1. Department of Pharmaceutical Technology, Faculty of Pharmacy, Marmara University, Istanbul 34668, Turkey;2. Institute of Pharmacy, Martin Luther University Halle-Wittenberg, 06120 Halle (Saale), Germany;3. Department of Chemistry, Faculty of Arts and Sciences, Kırıkkale University, Kırıkkale 71450, Turkey;4. Department of Electrical and Electronics Engineering, Izmir Katip Celebi University, Izmir 35620, Turkey;5. Faculty of Pharmacy, The University of Sydney, Sydney, NSW 2006, Australia;1. School of Pharmacy, Queen’s University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK;2. The Wellcome-Wolfson Building, Centre for Experimental Medicine, School of Medicine, Dentistry and Biomedical Science, Queen''s University Belfast, 97 Lisburn Road, Belfast BT9 7BL, UK;3. Royal Victoria Hospital, 274 Grosvenor Road, Belfast BT12 6BA, UK
Abstract:We describe, for the first time, quantification of in-skin swelling and fluid uptake by hydrogel-forming microneedle (MN) arrays and skin barrier recovery in human volunteers. Such MN arrays, prepared from aqueous blends of hydrolyzed poly(methylvinylether/maleic anhydride) (15%, w/w) and the cross-linker poly(ethyleneglycol) 10,000 Da (7.5%, w/w), were inserted into the skin of human volunteers (n = 15) to depths of approximately 300 μm by gentle hand pressure. The MN arrays swelled in skin, taking up skin interstitial fluid, such that their mass had increased by approximately 30% after 6 h in skin. Importantly, however, skin barrier function recovered within 24 h after MN removal, regardless of how long the MN had been in skin or how much their volume had increased with swelling. Further research on closure of MN-induced micropores is required because transepidermal water loss measurements suggested micropore closure, whereas optical coherence tomography indicated that MN-induced micropores had not closed over, even 24 h after MN had been removed. There were no complaints of skin reactions, adverse events, or strong views against MN use by any of the volunteers. Only some minor erythema was noted after patch removal, although this always resolved within 48 h, and no adverse events were present on follow-up. © 2014 Wiley Periodicals, Inc. and the American Pharmacists Association.
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