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应用单分子荧光显微镜表征一种大型两亲性分子在人皮肤角质层中的渗透情况。

Application of single molecule fluorescence microscopy to characterize the penetration of a large amphiphilic molecule in the stratum corneum of human skin.

作者信息

Volz Pierre, Boreham Alexander, Wolf Alexander, Kim Tai-Yang, Balke Jens, Frombach Janna, Hadam Sabrina, Afraz Zahra, Rancan Fiorenza, Blume-Peytavi Ulrike, Vogt Annika, Alexiev Ulrike

机构信息

Department of Physics, Institute of Experimental Physics, Freie Universität Berlin, Arnimallee 14, 14195 Berlin, Germany.

Clinical Research Center for Hair and Skin Science, Department of Dermatology, Charité-Universitaetsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany.

出版信息

Int J Mol Sci. 2015 Mar 27;16(4):6960-77. doi: 10.3390/ijms16046960.

Abstract

We report here on the application of laser-based single molecule total internal reflection fluorescence microscopy (TIRFM) to study the penetration of molecules through the skin. Penetration of topically applied drug molecules is often observed to be limited by the size of the respective drug. However, the molecular mechanisms which govern the penetration of molecules through the outermost layer of the skin are still largely unknown. As a model compound we have chosen a larger amphiphilic molecule (fluorescent dye ATTO-Oxa12) with a molecular weight >700 Da that was applied to excised human skin. ATTO-Oxa12 penetrated through the stratum corneum (SC) into the viable epidermis as revealed by TIRFM of cryosections. Single particle tracking of ATTO-Oxa12 within SC sheets obtained by tape stripping allowed us to gain information on the localization as well as the lateral diffusion dynamics of these molecules. ATTO-Oxa12 appeared to be highly confined in the SC lipid region between (intercellular space) or close to the envelope of the corneocytes. Three main distinct confinement sizes of 52 ± 6, 118 ± 4, and 205 ± 5 nm were determined. We conclude that for this amphiphilic model compound several pathways through the skin exist.

摘要

我们在此报告基于激光的单分子全内反射荧光显微镜(TIRFM)在研究分子透过皮肤渗透方面的应用。通常观察到局部应用的药物分子的渗透受到各自药物大小的限制。然而,控制分子透过皮肤最外层渗透的分子机制在很大程度上仍然未知。作为模型化合物,我们选择了一种分子量>700 Da的较大两亲性分子(荧光染料ATTO - Oxa12),并将其应用于切除的人体皮肤。冷冻切片的TIRFM显示,ATTO - Oxa12透过角质层(SC)进入有活力的表皮。通过胶带剥离获得的SC薄片内ATTO - Oxa12的单粒子追踪使我们能够获取这些分子的定位以及横向扩散动力学信息。ATTO - Oxa12似乎高度局限于角质形成细胞之间(细胞间空间)或靠近其包膜的SC脂质区域。确定了52±6、118±4和205±5 nm三种主要不同的局限尺寸。我们得出结论,对于这种两亲性模型化合物,存在几种透过皮肤的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc12/4424999/ab06c63ce304/ijms-16-06960-g001.jpg

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