Zhu Yongjian, Choe Chun-Sik, Ahlberg Sebastian, Meinke Martina C, Alexiev Ulrike, Lademann Juergen, Darvin Maxim E
Charité-Universitätsmedizin Berlin, Center of Experimental and Applied Cutaneous Physiology, Department of Dermatology, Venerology and Allergology, Charitéplatz 1, Berlin 10117, GermanybZhejiang University of Science and Technology, Department of Mechanic.
Charité-Universitätsmedizin Berlin, Center of Experimental and Applied Cutaneous Physiology, Department of Dermatology, Venerology and Allergology, Charitéplatz 1, Berlin 10117, GermanycKim Il Sung University, Department of Physics, Ryongnam-Dong, Taesong.
J Biomed Opt. 2015 May;20(5):051006. doi: 10.1117/1.JBO.20.5.051006.
In order to investigate the penetration depth of silver nanoparticles (Ag NPs) inside the skin, porcine ears treated with Ag NPs are measured by two-photon tomography with a fluorescence lifetime imaging microscopy (TPT-FLIM) technique, confocal Raman microscopy (CRM), and surface-enhanced Raman scattering (SERS) microscopy. Ag NPs are coated with poly-N-vinylpyrrolidone and dispersed in pure water solutions. After the application of Ag NPs, porcine ears are stored in the incubator for 24 h at a temperature of 37°C. The TPT-FLIM measurement results show a dramatic decrease of the Ag NPs' signal intensity from the skin surface to a depth of 4 μm. Below 4 μm, the Ag NPs' signal continues to decline, having completely disappeared at 12 to 14 μm depth. CRM shows that the penetration depth of Ag NPs is 11.1 ± 2.1 μm. The penetration depth measured with a highly sensitive SERS microscopy reaches 15.6 ± 8.3 μm. Several results obtained with SERS show that the penetration depth of Ag NPs can exceed the stratum corneum (SC) thickness, which can be explained by both penetration of trace amounts of Ag NPs through the SC barrier and by the measurements inside the hair follicle, which cannot be excluded in the experiment.
为了研究银纳米颗粒(Ag NPs)在皮肤内的渗透深度,采用双光子断层扫描结合荧光寿命成像显微镜(TPT-FLIM)技术、共焦拉曼显微镜(CRM)和表面增强拉曼散射(SERS)显微镜对用Ag NPs处理过的猪耳进行测量。Ag NPs用聚N-乙烯基吡咯烷酮包覆并分散在纯水溶液中。施加Ag NPs后,将猪耳在37°C的培养箱中保存24小时。TPT-FLIM测量结果显示,从皮肤表面到4μm深度,Ag NPs的信号强度急剧下降。在4μm以下,Ag NPs的信号继续下降,在12至14μm深度时完全消失。CRM显示Ag NPs的渗透深度为11.1±2.1μm。用高灵敏度SERS显微镜测量的渗透深度达到15.6±8.3μm。SERS获得的几个结果表明,Ag NPs的渗透深度可以超过角质层(SC)的厚度,这可以通过痕量Ag NPs穿过SC屏障的渗透以及毛囊内的测量来解释,而在实验中不能排除毛囊内的测量。