首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Electroporation of Skin Stratum Corneum Lipid Bilayer and Molecular Mechanism of Drug Transport: A Molecular Dynamics Study
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Electroporation of Skin Stratum Corneum Lipid Bilayer and Molecular Mechanism of Drug Transport: A Molecular Dynamics Study

机译:皮肤层基层脂质化双层的电穿孔及药物运输分子机制:分子动力学研究

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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 held (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 electnc 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 :l) 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.
机译:电穿孔技术已被显着使用,以增加通过皮肤的药物渗透。该技术依赖于在皮肤上施加短时间(微秒至毫秒)电场(通常,50-300V的顺序)以产生微观孔隙。然而,孔隙形成的分子机制,导致通过皮肤增强的活性分子通量仍然不知情。在该研究中,在各种外部电场中进行了广泛的皮肤脂质的原子原子分子动力学模拟[由神经酰胺(CER),胆固醇(CHOL)和游离脂肪酸(FFA)]。我们在电穿孔期间首次表明皮肤脂质双层的孔形成。我们展示了应用的外部电气保持(0.6-1.0V / NM)对不同尺寸(154,616和2464脂质)和组合物(CER / CHOL / FFA,1: 0:0,1:0:1,1:1:0,1:1:1)。孔形成和重新密封的动力学不同,发现高度依赖于皮肤脂质双层的组成。孔形成时间随比平均尺寸的增加而降低。发现孔维持ElectNC领域为Equimolar Cer,Chol和FFA脂双层的0.20-0.25V / NM。在去除外部电场后,皮肤脂质双层(1:1:1)在20ns内密封。与被动扩散相比,我们还介绍了在外部存在的情况下提高药物渗透的分子机制。这里获得的分子水平理解可以有助于优化/设计用于有效药物递送的电穿孔实验。对于给定的皮肤组合物和药物分子的尺寸,孔形成时间和孔生长模型的组合可用于认证所需的电场和用于施加电场的时间。

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