4.8 Article

Antioxidant Biodegradable Covalent Cyclodextrin Frameworks as Particulate Carriers for Inhalation Therapy against Acute Lung Injury

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 34, Pages 38421-38435

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c05220

Keywords

reactive oxygen species-sensitive; covalent cyclodextrin frameworks; acute lung injury; pulmonary drug delivery; ligustrazine

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This study developed a novel ROS-responsive inhalable particulate carrier (OC-COF) for improved treatment of acute lung injury (ALI). The carrier can deliver drugs specifically to the deep alveolar regions of the lungs, and has antioxidant and anti-inflammatory activities. In in vivo experiments, Ligustrazine (LIG) loaded in OC-COF significantly alleviated inflammation, oxidant stress, and lung damage. This study provides a new ROS-responsive material as an inhalable particulate carrier for the treatment of ALI and other medical conditions.
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 H2O2-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) in vitro and in vivo, 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-kappa B 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.

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