Center for Drug Delivery Systems, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
ACS Appl Mater Interfaces. 2022 Aug 31;14(34):38421-38435. doi: 10.1021/acsami.2c05220. Epub 2022 Aug 10.
Drug therapies for acute lung injury (ALI) are far from satisfactory, primarily because drugs cannot specifically target the lungs. Direct delivery of drugs to the deep alveolar regions by inhalation administration is crucial for the treatment of ALI. However, conventional inhalable carriers such as lactose and mannitol are generally inactive. Therefore, the use of a novel pharmacologically active carrier for pulmonary delivery may produce synergetic effects in treating ALI. Considering the pathophysiological environment of ALI, which typically featured excessive reactive oxygen species (ROS) and acute inflammation, we synthesized a novel kind of biodegradable and ROS-sensitive cross-linked covalent cyclodextrin frameworks (OC-COF) with uniform inhalable particle size to treat ALI. OC-COF was devised to incorporate HO-scavenging peroxalate ester linkages, which could hydrolyze and eliminate ROS generated in inflammatory sites. Ligustrazine (LIG), an antioxidant and anti-inflammatory natural compound, was loaded into OC-COF and evaluated as a dry powder inhaler (LIG@OC-COF) and , showing favorable aerodynamic properties and prominent antioxidant and anti-inflammatory capacities for the synergistic effects of OC-COF and LIG. In ALI rats, inhalation of LIG@OC-COF with a one-fifth LIG dose significantly alleviated the inflammation, oxidant stress, and lung damage. Western blot analysis demonstrated that LIG@OC-COF protected the lungs by regulating the Nrf2/NF-κB signaling pathway. In summary, this study provides a novel ROS-responsive material as an inhalable particulate carrier for the improved treatment of ALI and other medical conditions.
急性肺损伤 (ALI) 的药物治疗远未令人满意,主要是因为药物不能特异性靶向肺部。通过吸入给药将药物直接递送到深肺泡区域对于 ALI 的治疗至关重要。然而,乳糖和甘露醇等常规可吸入载体通常是无活性的。因此,使用新型药理学活性载体进行肺部给药可能会在治疗 ALI 方面产生协同作用。考虑到 ALI 的病理生理环境,其通常具有过多的活性氧 (ROS) 和急性炎症,我们合成了一种新型可生物降解且对 ROS 敏感的交联共价环糊精框架 (OC-COF),具有均匀的可吸入粒径,用于治疗 ALI。OC-COF 被设计为包含 HO 清除过氧酸盐酯键,该键可以在炎症部位水解并消除 ROS。川芎嗪 (LIG),一种抗氧化和抗炎的天然化合物,被载入 OC-COF 并作为干粉吸入剂 (LIG@OC-COF) 进行评估,表现出良好的空气动力学特性和突出的抗氧化和抗炎能力,这是 OC-COF 和 LIG 的协同作用。在 ALI 大鼠中,吸入五分之一 LIG 剂量的 LIG@OC-COF 可显著减轻炎症、氧化应激和肺损伤。Western blot 分析表明,LIG@OC-COF 通过调节 Nrf2/NF-κB 信号通路来保护肺部。总之,本研究提供了一种新型 ROS 响应性材料,作为可吸入颗粒载体,用于改善 ALI 和其他医疗条件的治疗。