Nasr Ghenwa, Greige-Gerges Hélène, Elaissari Abdelhamid, Khreich Nathalie
Bioactive Molecules Research Laboratory, Faculty of Sciences, Lebanese University, Beirut, Lebanon.
ISA-UMR 5280, CNRS, Univ Lyon, Claude Bernard University Lyon-1, 69622, Villeurbanne, France.
J Membr Biol. 2021 Aug;254(4):381-395. doi: 10.1007/s00232-021-00180-3. Epub 2021 May 3.
Encapsulation in liposomes has been an efficient strategy to improve the stability of sensitive bioactive compounds such as essential oils (EOs). However, the stability of liposomal formulations remains a key parameter controlling the delivery of encapsulated ingredients. Cholesterol (Chol) modulates the membrane properties conferring stability to the lipid bilayer. Thus, the Chol content in the liposome formulations encapsulating EO components should be carefully chosen. In this work, various liposome formulations differing by Chol content (DPPC:Chol 100:10; 100:25; 100:50; 100:75; 100:100) were exposed to a series of 22 EO components at DPPC/EO 100/25. The formulations were characterized for their final composition and their permeability to the hydrophilic fluorophore, sulforhodamine B (SRB), was monitored. Results showed that the Chol content experimentally determined for the various formulations (above 10% Chol) was below the theoretical weighed Chol. Among the tested components, 13 molecules displayed a significant permeabilizing effect on 10% Chol membranes. Most of these possess a hydroxyl group. The EO induced permeability was dependent on the Chol content which affects the membrane phase: their effect was reduced upon increasing Chol content keeping five EOs components effective at 40% Chol. The EO's effect was also linked to the hydrophobicity of the molecule. Hence, the DPPC:Chol ratio of the formulation is chosen considering the structure of the compound, its hydrophobicity and its effect on the permeability at different Chol content: a formulation comprising 40% Chol is suggested for highly hydrophobic molecules whereas a formulation with higher Chol content could be selected for less hydrophobic compounds.
脂质体包封是提高精油(EOs)等敏感生物活性化合物稳定性的有效策略。然而,脂质体制剂的稳定性仍然是控制包封成分递送的关键参数。胆固醇(Chol)调节赋予脂质双层稳定性的膜特性。因此,对于包封EO成分的脂质体制剂中的Chol含量应谨慎选择。在本研究中,制备了Chol含量不同(DPPC:Chol 100:10;100:25;100:50;100:75;100:100)的各种脂质体制剂,并在DPPC/EO 100/25条件下使其接触一系列22种EO成分。对这些制剂的最终组成进行了表征,并监测了它们对亲水性荧光团磺基罗丹明B(SRB)的通透性。结果表明,通过实验测定的各种制剂中的Chol含量(Chol含量高于10%)低于理论称重的Chol含量。在测试的成分中,13种分子对含10%Chol的膜表现出显著的通透作用。其中大多数含有羟基。EO诱导的通透性取决于影响膜相的Chol含量:随着Chol含量的增加,它们的作用减弱,在40%Chol含量时仍有5种EO成分有效。EO的作用还与分子的疏水性有关。因此,考虑到化合物的结构、疏水性及其在不同Chol含量下对通透性的影响来选择制剂的DPPC:Chol比例:对于高度疏水的分子,建议使用含40%Chol的制剂,而对于疏水性较低的化合物,可以选择Chol含量较高的制剂。