School of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, PR China.
College of Notoginseng Medicine and Pharmacy, Wenshan University, Wenshan 663000, Yunnan, PR China.
J Control Release. 2023 Feb;354:664-679. doi: 10.1016/j.jconrel.2023.01.050. Epub 2023 Jan 25.
Deep eutectic solvents (DES) have demonstrated their ability to facilitate skin penetrability of rigid nanoparticles (NPs). Here, we reported a feasible and simple transdermal delivery strategy using mesoporous silica nanoparticles impregnated in DES hydrogels for topical management of rheumatoid arthritis (RA). To achieve this goal, nanoceria was immobilized within a silica nanoparticle matrix (MSN) and encapsulated with methotrexate (MTX). The functionalized nanoparticles were first engineered in an Arginine (Arg)-citric acid (CA) DES and then transferred to the carbomer hydrogel matrix. Due to the strong affinity of DES hydrogels to the skin, combined with solvent-driven "Drag" effects, the prepared DES-MSNs hydrogels produced dynamic mobility of MSNs through skin layers, resulting in high skin penetrability. After application to the skin, the hydrogel solvent drove the rigid NPs across the skin barrier in a nonintrusive manner, resulting in sustained penetration and accumulation of MSNs at subcutaneous inflammation sites. Subsequently, the MTX payload exerted a direct therapeutic effect, while nanoceria moderated the inflammatory microenvironment by initiating reactive oxygen species (ROS) scavenging and transformation of the macrophage phenotype. In this way, the synergistic action of the combination of immuno- and chemotherapy of the drug and its carrier on RA was achieved. Our work provides a novel strategy for multisite regulation and controlled management of RA in a noninvasive way.
深共晶溶剂 (DES) 已被证明能够促进刚性纳米颗粒 (NPs) 的皮肤穿透性。在这里,我们报告了一种使用浸渍在 DES 水凝胶中的介孔硅纳米粒子的可行且简单的透皮传递策略,用于类风湿关节炎 (RA) 的局部治疗。为了实现这一目标,纳米氧化铈被固定在二氧化硅纳米粒子基质 (MSN) 中,并封装了甲氨蝶呤 (MTX)。功能化的纳米粒子首先在精氨酸 (Arg)-柠檬酸 (CA) DES 中进行工程设计,然后转移到卡波姆水凝胶基质中。由于 DES 水凝胶对皮肤的强烈亲和力,加上溶剂驱动的“Drag”效应,所制备的 DES-MSNs 水凝胶通过皮肤层产生 MSNs 的动态迁移,从而实现高皮肤穿透性。在应用于皮肤后,水凝胶溶剂以非侵入性的方式驱动刚性 NPs 穿过皮肤屏障,导致 MSNs 持续渗透和在皮下炎症部位积累。随后,MTX 有效载荷发挥直接治疗作用,而纳米氧化铈通过引发活性氧 (ROS) 清除和巨噬细胞表型的转化来调节炎症微环境。通过这种方式,实现了药物及其载体的免疫和化学疗法对 RA 的协同作用。我们的工作为非侵入性地实现 RA 的多部位调节和控制管理提供了一种新策略。