Guimarães Diana, Noro Jennifer, Loureiro Ana, Lager Franck, Renault Gilles, Cavaco-Paulo Artur, Nogueira Eugénia
Centre of Biological Engineering, University of Minho, 4710-057 Braga, Portugal.
INSERM-Institut National de la Santé et de la Recherche Médicale, U1016, Institut Cochin, 75014 Paris, France.
Biomedicines. 2020 Dec 18;8(12):630. doi: 10.3390/biomedicines8120630.
Methotrexate (MTX) is a common drug used to treat rheumatoid arthritis. Due to the excessive side effects, encapsulation of MTX in liposomes is considered an effective delivery system, reducing drug toxicity, while maintaining its efficacy. The ethanol injection method is an interesting technique for liposome production, due to its simplicity, fast implementation, and reproducibility. However, this method occasionally requires the extrusion process, to obtain suitable size distribution, and achieve a low level of MTX encapsulation. Here, we develop a novel pre-concentration method, based on the principles of the ethanol injection, using an initial aqueous volume of 20% and 1:1 ratio of organic:aqueous phase (/). The liposomes obtained present small values of size and polydispersity index, without the extrusion process, and a higher MTX encapsulation (efficiency higher than 30%), suitable characteristics for in vivo application. The great potential of MTX to interact at the surface of the lipid bilayer was shown by nuclear magnetic resonance (NMR) studies, revealing mutual interactions between the drug and the main phospholipid via hydrogen bonding. In vivo experiments reveal that liposomes encapsulating MTX significantly increase the biological benefit in arthritic mice. This approach shows a significant advance in MTX therapeutic applications.
甲氨蝶呤(MTX)是一种用于治疗类风湿性关节炎的常用药物。由于副作用过大,将MTX包裹在脂质体中被认为是一种有效的给药系统,可降低药物毒性,同时保持其疗效。乙醇注入法是一种有趣的脂质体制备技术,因其操作简单、实施快速且可重复性强。然而,这种方法偶尔需要进行挤压过程,以获得合适的粒径分布,并实现较低水平的MTX包封率。在此,我们基于乙醇注入原理开发了一种新型预浓缩方法,使用20%的初始水相体积和1:1的有机相:水相比例(/)。所获得的脂质体在无需挤压过程的情况下,具有较小的粒径和多分散指数值,并且MTX包封率更高(效率高于30%),具有适合体内应用的特性。核磁共振(NMR)研究表明MTX在脂质双分子层表面相互作用的巨大潜力,揭示了药物与主要磷脂之间通过氢键的相互作用。体内实验表明,包裹MTX的脂质体显著提高了关节炎小鼠的生物学益处。这种方法在MTX治疗应用方面显示出显著进展。