Yakobi Arancibia Ravit, Bentov-Arava Einav, Morshin Anna, Elia Jhonathan, Natsheh Hiba, Levi-Kalisman Yael, Ushki Rotem, Elia Anna, Touitou Elka, Margulis Katherine
The Institute for Drug Research, the School of Pharmacy Faculty of Medicine The Center for Nanoscience and Nanotechnology The Hebrew University of Jerusalem Jerusalem 9112001 Israel.
Department of Plastic Surgery The Hadassah Medical Center Hebrew University School of Medicine POB 12000 Jerusalem il-91120 Israel.
Small Sci. 2025 Jun 1;5(8):2500061. doi: 10.1002/smsc.202500061. eCollection 2025 Aug.
A novel mass spectrometry imaging (MSI)-based concept that enables rapid visualization and evaluation of active pharmaceutical ingredient (API) distribution across skin layers following dermal delivery is presented. This approach integrates desorption electrospray ionization MSI with a newly developed automated computational tool (access provided) that efficiently processes MSI data, isolates skin tissue signals from background interference, and segments the tissue into precise layers. The tool facilitates detailed and rapid assessment of API localization within skin strata in under 10 min per skin specimen. To validate this method, three nanoscale dermal drug delivery systems (DDSs) for the antifungal terbinafine that target distinct skin strata-ethosomes, transethosomes, and microemulsion-are designed and characterized. API permeation in human and porcine skin is evaluated using both manual and automated workflows. The integrated approach demonstrates superior accuracy in skin distribution analysis, a substantial reduction in processing time, and improved efficiency in signal-tissue overlay. Comparative analysis of the DDSs reveals marked differences in drug permeation depth and localization, with transethosomes showing the highest potential for deeper dermal delivery. This method not only provides a powerful tool for DDS evaluation but also enables detailed kinetic studies, offering insights into drug permeation dynamics.
本文提出了一种基于新型质谱成像(MSI)的概念,该概念能够在经皮给药后快速可视化并评估活性药物成分(API)在皮肤各层中的分布情况。这种方法将解吸电喷雾电离MSI与新开发的自动化计算工具(已提供访问权限)相结合,该工具能有效处理MSI数据,从背景干扰中分离出皮肤组织信号,并将组织精确分割成不同的层。该工具能够在每份皮肤样本10分钟内完成对API在皮肤各层中定位的详细快速评估。为验证该方法,设计并表征了三种用于抗真菌药特比萘芬的纳米级经皮给药系统(DDS)——乙醇脂质体、转乙醇脂质体和微乳剂,它们靶向不同的皮肤层。使用手动和自动化工作流程评估了API在人和猪皮肤中的渗透情况。这种综合方法在皮肤分布分析中显示出更高的准确性,显著缩短了处理时间,并提高了信号与组织叠加的效率。对这些DDS的比较分析揭示了药物渗透深度和定位的显著差异,其中转乙醇脂质体在更深层经皮给药方面显示出最高潜力。该方法不仅为DDS评估提供了一个强大的工具,还能进行详细的动力学研究,深入了解药物渗透动力学。