Permeability of Dermatological Solutes through the Short Periodicity Phase of Human Stratum Corneum Lipid Bilayers

被引:1
|
作者
Zakaria, Afshin Zamani [1 ,3 ]
Malde, Alpeshkumar K. [1 ,2 ]
Gould, Tim [1 ,3 ]
机构
[1] Griffith Univ, Sch Environm & Sci, Brisbane, Qld 4111, Australia
[2] Griffith Univ, Inst Glycom, Gold Coast, Qld 4222, Australia
[3] Griffith Univ, Queensland Micro & Nanotechnol Ctr, Brisbane, Qld 4111, Australia
关键词
MOLECULAR-DYNAMICS; SKIN BARRIER; FORCE-FIELD; UNIT-CELL; CERAMIDE; SIMULATION; CHOLESTEROL; PERMEATION; TRANSPORT; BEHAVIOR;
D O I
10.1021/acs.jcim.3c01362
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Determining the permeability of drug-like solutes through the densely packed and heterogeneous stratum corneum lipid layer presents a significant challenge. In this study, we employed umbrella sampling with a periodic weighing function applied to the center of mass of the lipid bilayers. Precise umbrella sampling was conducted with an interframe distance of 0.5 angstrom, spanning from the bilayer center to the water phase, and each frame was simulated for at least 20 ns. Autocorrelation functions, potential of mean force (PMF), and diffusivity profiles were analyzed for six solutes (testosterone, benzene, caffeine, ethanol, mannitol, and histidine). The results revealed that autocorrelations were dependent solely on the medium, whether water or lipid phase. Diffusivity and PMF profiles along the reaction coordinate were influenced by the hydrophilicity of the solute rather than its size. For hydrophobic solutes, the PMF curves exhibited a minimum at the bilayer center, while for hydrophilic solutes, the PMFs peaked at the bilayer center and lipid tails (where the lipid tails are not interacting with the cholesterol). Diffusivity curves were low at the bilayer center and water phase, with peaks observed at the headgroup or the boundary between fatty acid and cholesterol (1 nm from the bilayer center). The quantitative findings presented in this work hold significance for pharmacists and drug designers.
引用
收藏
页码:276 / 288
页数:13
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