皮肤模型对涂覆佐米曲坦的皮肤贴敷微阵列体外性能的影响。

Journal of Pharmaceutics Pub Date : 2018-06-03 eCollection Date: 2018-01-01 DOI:10.1155/2018/7459124
Mahmoud Ameri, Hayley Lewis, Paul Lehman
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引用次数: 9

摘要

利用不同的人体皮肤和人造膜进行Franz细胞研究,评估皮肤模型对涂覆在钛微投影阵列上的唑米曲坦渗透的影响。评估全层和离体皮肤,以及合成疏水膜(Strat-M®)。结果表明,模型的选择对唑米曲坦的渗透具有不同的吸收动力学。对于合成膜,只有11%的唑米曲坦包被剂量渗透到受体介质中,而对于皮肤化的皮肤,85%渗透到受体中。佐米曲坦通过全层皮肤的吸收曲线和达到最大通量的时间与人造皮肤和皮肤模型有显著不同。在这些结果的基础上,皮肤可以更好地估计药物包覆金属微投影的体内性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of Skin Model on <i>In Vitro</i> Performance of an Adhesive Dermally Applied Microarray Coated with Zolmitriptan.

Effect of Skin Model on <i>In Vitro</i> Performance of an Adhesive Dermally Applied Microarray Coated with Zolmitriptan.

Effect of Skin Model on In Vitro Performance of an Adhesive Dermally Applied Microarray Coated with Zolmitriptan.

Franz cell studies, utilizing different human skin and an artificial membrane, evaluating the influence of skin model on permeation of zolmitriptan coated on an array of titanium microprojections, were evaluated. Full thickness and dermatomed ex vivo human skin, as well as a synthetic hydrophobic membrane (Strat-M®), were assessed. It was found that the choice of model demonstrated different absorption kinetics for the permeation of zolmitriptan. For the synthetic membrane only 11% of the zolmitriptan coated dose permeated into the receptor media, whilst for the dermatomed skin 85% permeated into the receptor. The permeation of zolmitriptan through full thickness skin had a significantly different absorption profile and time to maximum flux in comparison to the dermatomed skin and synthetic model. On the basis of these results dermatomed skin may be a better estimate of in vivo performance of drug-coated metallic microprojections.

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来源期刊
Journal of Pharmaceutics
Journal of Pharmaceutics PHARMACOLOGY & PHARMACY-
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