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Modeling of Drug Diffusion Based on Concentration Profiles in Healthy and Damaged Human Skin

机译:基于浓度曲线在健康和受损人体皮肤中的药物扩散建模

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摘要

Based on experimental drug concentration profiles in healthy as well as tape-stripped ex vivo human skin, we model the penetration of the antiinflammatory drug dexamethasone into the skin layers by the one-dimensional generalized diffusion equation. We estimate the position-dependent free-energy and diffusivity profiles by solving the conjugated minimization problem, in which the only inputs are concentration profiles of dexamethasone in skin at three consecutive penetration times. The resulting free-energy profiles for damaged and healthy skin show only minor differences. In contrast, the drug diffusivity in the first 10 μm of the upper skin layer of damaged skin is 200-fold increased compared to healthy skin, which reflects the corrupted barrier function of tape-stripped skin. For the case of healthy skin, we examine the robustness of our method by analyzing the behavior of the extracted skin parameters when the number of input and output parameters are reduced. We also discuss techniques for the regularization of our parameter extraction method.
机译:基于健康的实验药物浓度曲线以及带卷剥离的离体皮肤,我们通过一维广义扩散方程模拟抗炎药物地塞米松的渗透到皮肤层中。通过解决共轭的最小化问题,估计依赖于依赖性的自由能和扩散性分布,其中唯一的输入是在连续三次渗透时间的皮肤中的地塞米松的浓度谱。受损和健康皮肤的产生的自由能曲线仅显示微小的差异。相反,与健康的皮肤相比,受损皮肤的上皮层的前10μm的前10μm的药物扩散率增加了200倍,这反映了剥离皮肤的腐蚀功能损坏的障碍功能。对于健康皮肤的情况,我们通过分析输入和输出参数的数量时,通过分析提取的皮肤参数的行为来检查方法的稳健性。我们还讨论了我们参数提取方法的正则化的技术。

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