Molecular Insights into the Penetration Enhancement Mechanism of Terpenes to Skin.

J Phys Chem B

Key Lab of Colloid and Interface Chemistry, Shandong University, Jinan, Shandong 250100, P.R. China.

Published: December 2024

AI Article Synopsis

  • Terpenes, often used in cosmetics as enhancers, help improve skin penetration through their effects on lipid membranes, but the exact mechanisms were not fully understood until this study.
  • Molecular dynamics simulations were conducted to assess how terpineol, 1,8-cineole, and limonene interacted with skin layers, revealing that they affect cholesterol and lipid structure differently.
  • The study found that limonene penetrates best due to its unique ability to create a "triple layer" membrane and that terpenes can lower energy barriers for other molecules to cross skin, providing new insights into enhancing skin penetration in cosmetic formulations.

Article Abstract

Terpenes are widely used in cosmetic formulations as chemical penetration enhancers (CPEs). However, the molecular mechanisms underlying the skin-penetration-enhancing effect have not been completely understood. In this work, molecular dynamics (MD) simulations were used to explore the influence of terpineol (TER), 1,8-cineole (CIN), and limonene (LIM) on the stratum corneum (SC) model. The results indicated that terpenes affected lipid membranes in a concentration-dependent manner and promoted skin permeation by disorganizing the cholesterol (CHOL) portion. The penetration of CPEs across the skin membrane also differed, with diffusion rates of limonene > 1,8-cineole > terpineol. The limonene molecules could penetrate the bilayer's center, forming a "triple layer" membrane structure. Furthermore, constrained simulations showed that the most favorable penetration pathway is via areas rich in CHOL. Terpineol could lower the energy barrier of the hydrophilic molecule (caffeic acid) across the cholesterol region. For the lipophilic molecule (osthole), limonene and 1,8-cineole could reduce the energy barrier across the cholesterol region. Each of the results provides novel insights into the mechanism of penetration of CPEs in the skin.

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Source
http://dx.doi.org/10.1021/acs.jpcb.4c05910DOI Listing

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