Esposito Elisabetta, Dzyhovski Valentyn, Santamaria Federico, Contado Catia, Brenna Cinzia, Neri Luca Maria, Secchiero Paola, Spinozzi Francesco, Pepe Alessia, Rawski Michał, Ortore Maria Grazia, Mariani Paolo, Galvan Andrea, Calderan Laura, Malatesta Manuela
Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara, I-44121 Ferrara, Italy.
Laboratory for Technologies of Advanced Therapies "LTTA"-Electron Microscopy Center, University of Ferrara, I-44121 Ferrara, Italy.
Nanomaterials (Basel). 2025 Jun 16;15(12):937. doi: 10.3390/nano15120937.
The topical administration of drugs on the skin by nanovesicular systems can represent a tool to treat skin pathologies. The study of nanovesicle biodistribution after skin administration is crucial to understanding their transdermal potential. A formative study enabled us to investigate the influence of some methods in the production of nanovesicles based on phosphatidylcholine, differing in their ethanol amount. Particularly, both liposomes and ethosomes produced by different methods, i.e., microfluidics and solvent injection, were considered. The evaluation of size distribution, shape and internal morphology was performed using photon correlation spectroscopy, cryogenic electron microscopy, hyperspectral dark-field microscopy and small-angle X-ray scattering. Transmission electron microscopy was then used to observe and compare the transdermal passage of selected liposomes and ethosomes applied to human skin explants in a bioreactor. The mean diameters of nanovesicles prepared by the ethanol injection method were smaller with respect to those obtained by microfluidics, measuring roughly 140 and 230 nm, respectively. The uni- or multilamellar ultrastructure of the vesicles was influenced by the solvent injection procedure. Ultrastructural analysis of skin penetration revealed (i) the ability of intact vesicles to cross the different skin layers, with ethosomes produced by the water injection method showing greater transdermal potential and (ii) the role of ethanol as a penetration enhancer.
通过纳米囊泡系统在皮肤上局部给药可成为治疗皮肤疾病的一种手段。研究纳米囊泡经皮肤给药后的生物分布对于了解其透皮潜力至关重要。一项基础研究使我们能够探究某些方法对基于磷脂酰胆碱的纳米囊泡生产的影响,这些方法在乙醇含量上有所不同。特别地,考虑了通过不同方法(即微流控法和溶剂注入法)制备的脂质体和醇质体。使用光子相关光谱法、低温电子显微镜、高光谱暗场显微镜和小角X射线散射对尺寸分布、形状和内部形态进行了评估。然后使用透射电子显微镜观察并比较在生物反应器中应用于人体皮肤外植体的选定脂质体和醇质体的透皮过程。通过乙醇注入法制备的纳米囊泡的平均直径比通过微流控法获得的纳米囊泡的平均直径小,分别约为140和230 nm。囊泡的单层或多层超微结构受溶剂注入过程的影响。皮肤渗透的超微结构分析表明:(i)完整囊泡穿过不同皮肤层的能力,通过水注入法制备的醇质体显示出更大的透皮潜力;(ii)乙醇作为渗透促进剂的作用。