Department of Biomedical Engineering and Technology, Institute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, 100053, China.
J Nanobiotechnology. 2024 Sep 28;22(1):584. doi: 10.1186/s12951-024-02860-3.
Psoriasis is a chronic, relapsing, and refractory immune-mediated skin disease with the etiology and pharmaceutical targets remaining unsatisfactorily addressed. Topical herbal-derived compounds, such as tryptanthrin (Tryp), have been considered as an alternative therapy for psoriasis due to their lower costs and fewer side effects compared to other therapies. However, the effectiveness of topically administered drugs is substantially limited by the thickened pathological skin barrier and the low bioavailability of drugs in the deeper layers of the lesion. Ethosomes, being a novel phospholipid-based vesicle system with high content of ethanol, have been implicated in enhancing topical drug absorption and restoring psoriatic lesions. In this study, taking advantages of ethosomes as a soft and malleable drug carrier, we constructed the Tryp-loaded ethosome (Tryp-ES) through a one-step microfluidics-based technique. The optimal formulation of Tryp-ES was achieved by adding amino-acid-derived surfactant sodium lauroyl glutamate, and Tryp-ES exhibited homogeneous particle size and favorable stability at room temperature. In vitro evaluations showed that Tryp of Tryp-ES could be easily internalized into cells and accumulated in cell nuclei, hence inhibited the abnormally proliferated keratinocytes by inducing apoptosis. In vivo and in vitro assessment using psoritic skin of mice revealed that Tryp-ES had preferred skin retention and permeation of loaded drugs within the initial 1 h of topical administration, which could be attributed to transient disintegrations of cell membranes by ethosomes, thus improved cellular fluidity and permeability. Notably, a synergistic effect of ethosomes and Tryp was found in psoriatic mice. Tryp-ES-treated mice showed substantially ameliorated symptoms of psoriasis and reduced pathological alterations due to hyperplasia, inflammation and angiogenesis, without detectable local or systemic toxicities. Interestingly, lipidomics analysis confirmed that the supplementation of phospholipids, as in the form of ethosome vehicles, was an alterantive strategy to relieve psoriatic pathologies. Taken together, this study provides a novel impact for ethosomal topical delivery of Tryp and underlines their potential as an effective therapy for the management of psoriasis.
银屑病是一种慢性、复发性和难治性的免疫介导性皮肤病,其病因和药物靶点仍未得到满意解决。与其他疗法相比,局部草本衍生化合物,如色酮(Tryp),由于成本较低且副作用较少,被认为是治疗银屑病的一种替代疗法。然而,由于病理性皮肤屏障增厚和病变深层药物生物利用度低,局部给药药物的效果受到极大限制。醇质体作为一种新型的含有高浓度乙醇的磷脂基囊泡系统,已被证实可增强局部药物吸收并修复银屑病病变。在这项研究中,我们利用醇质体作为柔软且可塑的药物载体,通过一步微流控技术构建了负载色酮的醇质体(Tryp-ES)。通过添加氨基酸衍生表面活性剂月桂酰谷氨酸钠,优化了 Tryp-ES 的配方,Tryp-ES 表现出均匀的粒径和在室温下的良好稳定性。体外评价表明,Tryp-ES 中的 Tryp 很容易被细胞内化并积累在细胞核中,从而通过诱导细胞凋亡抑制异常增殖的角质形成细胞。使用小鼠银屑病皮肤进行的体内和体外评估表明,Tryp-ES 在局部给药最初 1 小时内具有优先的皮肤保留和负载药物的渗透能力,这可能归因于醇质体对细胞膜的瞬时崩解,从而提高了细胞的流动性和通透性。值得注意的是,在银屑病小鼠中发现了醇质体和 Tryp 的协同作用。Tryp-ES 治疗的小鼠银屑病症状明显改善,由于过度增生、炎症和血管生成导致的病理改变减少,且未检测到局部或全身毒性。有趣的是,脂质组学分析证实,补充磷脂,如以醇质体载体的形式,是缓解银屑病病理的一种替代策略。综上所述,这项研究为醇质体局部递呈 Tryp 提供了新的视角,并强调了它们作为治疗银屑病的有效疗法的潜力。