University of Illinois at Urbana-Champaign, Beckman Institute for Advanced Science and Technology, Urbana, Illinois, United StatesbUniversity of Illinois at Urbana-Champaign, Department of Bioengineering, Urbana, Illinois, United States.
GlaxoSmithKline, King of Prussia, Pennsylvania, United States.
J Biomed Opt. 2017 Jul 1;22(7):70502. doi: 10.1117/1.JBO.22.7.070502.
Docosanol is an over-the-counter topical agent that has proved to be one of the most effective therapies for treating herpes simplex labialis. However, the mechanism by which docosanol suppresses lesion formation remains poorly understood. To elucidate its mechanism of action, we investigated the uptake of docosanol in living cells using coherent anti-Stokes Raman scattering microscopy. Based on direct visualization of the deuterated docosanol, we observed highly concentrated docosanol inside living cells 24 h after drug treatment. In addition, different spatial patterns of drug accumulation were observed in different cell lines. In keratinocytes, which are the targeted cells of docosanol, the drug molecules appeared to be docking at the periphery of the cell membrane. In contrast, the drug molecules in fibroblasts appeared to accumulate in densely packed punctate regions throughout the cytoplasm. These results suggest that this molecular imaging approach is suitable for the longitudinal tracking of drug molecules in living cells to identify cell-specific trafficking and may also have implications for elucidating the mechanism by which docosanol suppresses lesion formation.
二十二烷醇是一种非处方局部用制剂,已被证明是治疗唇疱疹的最有效疗法之一。然而,二十二烷醇抑制病变形成的机制仍不清楚。为了阐明其作用机制,我们使用相干反斯托克斯拉曼散射显微镜研究了二十二烷醇在活细胞中的摄取。基于氘代二十二烷醇的直接可视化,我们观察到在药物处理后 24 小时,活细胞内聚集了高浓度的二十二烷醇。此外,在不同的细胞系中观察到不同的药物积累空间模式。在角质形成细胞中,二十二烷醇的靶细胞,药物分子似乎停靠在细胞膜的外周。相比之下,在成纤维细胞中,药物分子似乎聚集在整个细胞质中密集的点状区域。这些结果表明,这种分子成像方法适合于在活细胞中对药物分子进行纵向跟踪,以鉴定细胞特异性转运,也可能有助于阐明二十二烷醇抑制病变形成的机制。