Department of Biomolecular Sciences, University of Urbino Carlo Bo, Piazza del Rinascimento, 6, 61029 Urbino, PU, Italy.
Department of Biomolecular Sciences, University of Urbino Carlo Bo, Piazza del Rinascimento, 6, 61029 Urbino, PU, Italy; Department of Life Sciences, School of Sciences, European University Cyprus, Nicosia, Cyprus.
Int J Pharm. 2020 Jun 30;584:119436. doi: 10.1016/j.ijpharm.2020.119436. Epub 2020 May 21.
18-α-Glycyrrhetinic acid (GA) is a bioactive compound extracted from licorice that exhibits many biological and pharmacological effects such as anti-inflammatory and antioxidant activities on the skin. However, its lipophilic nature results in poor bioavailability that limits clinical applications. Liposomes, presenting the ability to carry both hydrophobic and hydrophilic payloads and a good cytocompatibility, are effective to overcome this barrier. Furthermore, the addition of permeation enhancers such as ethanol into liposomal formulations helps the diffusion of these systems through the skin barrier. Here, we aimed to formulate GA-loaded ethanolic liposomes, using a natural soybean lecithin via a microfluidic approach. Using a fused deposition modeling (FDM) 3D printer we customized a microfluidic chip, and manufactured vesicles that presented spherical shape with a size of 202 ± 5.2 nm, a narrow size distribution and a good stability over a period of 30 days. After reaching a drug encapsulation efficiency of 63.15 ± 2.2%, liposomes were evaluated for their cytocompatibility and skin permeation potentiality after hydrogelation using xanthan gum. The in vitro release and permeation studies were performed using Franz diffusion cells comparing two different media and three synthetic membranes including a polymeric skin-mimicking membrane. The selected formulation presented no cytotoxicity and an increased permeation compared to GA saturated hydrogel. It could perform therapeutically better effects than conventional formulations containing free GA, as prolonged and controlled release topical dosage forms, which may lead to improved efficiency and better patient compliance.
18-α-甘草次酸(GA)是从甘草中提取的一种具有生物活性的化合物,具有抗炎和抗氧化等多种生物学和药理学作用。然而,其亲脂性导致生物利用度差,限制了临床应用。脂质体具有携带亲脂性和亲水性有效载荷的能力,且细胞相容性良好,是克服这一障碍的有效方法。此外,在脂质体制剂中添加乙醇等渗透增强剂有助于这些系统通过皮肤屏障扩散。在这里,我们旨在通过微流控方法使用天然大豆卵磷脂来制备 GA 负载的乙醇脂质体。我们使用熔丝制造(FDM)3D 打印机定制了一个微流控芯片,并制造了具有球形的囊泡,其粒径为 202±5.2nm,粒径分布较窄,在 30 天内具有良好的稳定性。达到 63.15±2.2%的药物包封效率后,用黄原胶水凝胶化后评估了脂质体的细胞相容性和皮肤渗透潜力。使用 Franz 扩散池进行了体外释放和渗透研究,比较了两种不同的介质和三种合成膜,包括聚合物模拟皮肤的膜。所选配方无细胞毒性,与 GA 饱和水凝胶相比,渗透能力增强。与含有游离 GA 的常规制剂相比,它可以发挥更好的治疗效果,因为它是一种延长和控制释放的局部剂型,可能会提高效率并提高患者的顺应性。