Physical Science Research Area, Tata Research Development & Design Centre, TCS Innovation Labs , Pune 411013 , India.
Langmuir. 2018 May 22;34(20):5860-5870. doi: 10.1021/acs.langmuir.8b00423. Epub 2018 May 9.
The electroporation technique has been used significantly to increase drug permeation through the skin. This technique relies on the application of short-timed (microseconds to millisecond) electric fields (generally, order of 50--300 V) on the skin to create microscopic pores. However, the molecular mechanism of pore formation, resulting in an enhanced flux of active molecules through the skin, remains poorly understood. In this study, extensive atomistic molecular dynamics simulation of skin lipids [made up of ceramide (CER), cholesterol (CHOL), and free fatty acid (FFA)] has been performed at various external electric fields. We show for the first time the pore formation in the skin lipid bilayer during electroporation. We show the effect of the applied external electrical field (0.6-1.0 V/nm) on the pore formation dynamics in the lipid bilayer of different sizes (154, 616, and 2464 lipids) and compositions (CER/CHOL/FFA, 1:0:0, 1:0:1, 1:1:0, 1:1:1). The pore formation and resealing kinetics were different and were found to be highly dependent on the composition of the skin lipid bilayer. The pore formation time decreased with increase in the bilayer size. The pore sustaining electric field was found to be in the range of 0.20-0.25 V/nm for equimolar CER, CHOL, and FFA lipid bilayers. The skin lipid bilayer (1:1:1) sealed itself within 20 ns after the removal of the external electric field. We also present the molecular mechanism of enhancement of drug permeation in the presence of external field as compared to the passive diffusion. The molecular-level understanding obtained here could help in optimizing/designing the electroporation experiments for effective drug delivery. For a given skin composition and size of the drug molecule, the combination of pore formation time and pore growth model can be used to know a priori the desired electric field and time for the application of the electric field.
电穿孔技术已被广泛用于增加药物透过皮肤的渗透。该技术依赖于在皮肤上施加短时间(微秒至毫秒)的电场(通常为 50-300V),以创建微观孔。然而,导致活性分子通过皮肤通量增强的孔形成的分子机制仍知之甚少。在这项研究中,对皮肤脂质(由神经酰胺(CER)、胆固醇(CHOL)和游离脂肪酸(FFA)组成)进行了广泛的原子分子动力学模拟,在不同的外电场下进行。我们首次展示了电穿孔过程中皮肤脂质双层中的孔形成。我们展示了外加电场(0.6-1.0V/nm)对不同大小(154、616 和 2464 个脂质)和组成(CER/CHOL/FFA,1:0:0、1:0:1、1:1:0、1:1:1)的脂质双层中孔形成动力学的影响。孔形成和再封闭动力学不同,并且发现它们高度依赖于皮肤脂质双层的组成。孔形成时间随着双层尺寸的增加而减小。发现等摩尔 CER、CHOL 和 FFA 脂质双层的维持孔的电场在 0.20-0.25V/nm 的范围内。在外部电场去除后,皮肤脂质双层(1:1:1)在 20ns 内自行封闭。我们还提出了在存在外部电场的情况下增强药物渗透的分子机制,与被动扩散相比。这里获得的分子水平的理解有助于优化/设计电穿孔实验,以实现有效的药物输送。对于给定的皮肤组成和药物分子的大小,可以使用孔形成时间和孔生长模型的组合来预先知道施加电场的所需电场和时间。