Menon G K, Bommannan D B, Elias P M
Dermatology Service, Veterans Administration Medical Center, San Francisco, Calif 94121.
Skin Pharmacol. 1994;7(3):130-9. doi: 10.1159/000211287.
The mechanism of stratum corneum (SC) permeabilization by ultrasound (sonophoresis) is unknown. We studied here permeation pathways, and SC intercellular structural organization following applications of high-frequency sonophoresis to hairless mouse skin. Ruthenium tetroxide post-fixation and tracer solutions of LaNO3 and FITC-dextrans were employed to examine SC lamellar bilayers, lamellar body morphology and subcellular permeation pathways. Sonophoresis disrupted the compact organization of SC bilayers and LB-derived contents at the stratum granulosum (SG)-SC interface, leading to domain separation between 0 and 20 h, reverting by 48 h. Post-sonophoresis, tracers traversed the SC via lacunae within the lamellar bilayers, and via lamellae in sites that displayed domain separation. These studies provide insights about the penetration pathways, permeabilizing mechanisms, and kinetics of sonophoresis on the epidermis.
超声(超声透入疗法)使角质层(SC)通透性增加的机制尚不清楚。我们在此研究了对无毛小鼠皮肤应用高频超声透入疗法后的渗透途径以及SC细胞间结构组织。采用四氧化钌后固定以及硝酸镧和异硫氰酸荧光素 - 葡聚糖示踪剂溶液来检查SC板层双分子层、板层小体形态和亚细胞渗透途径。超声透入疗法破坏了颗粒层(SG)-SC界面处SC双分子层和板层小体衍生成分的紧密组织,导致0至20小时之间出现区域分离,48小时后恢复。超声透入疗法后,示踪剂通过板层双分子层内的腔隙以及显示区域分离部位的薄片穿过SC。这些研究为超声透入疗法对表皮的渗透途径、通透机制和动力学提供了见解。