Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery

• Published in: Gels Vol. 9; no. 9; p. 707
• Main Authors: Chai, Andy, Schmidt, Keagan, Brewster, Gregory, Xiong, Lu Shi Peng, Church, Benjamin, Wahl, Timothy, Sadabadi, Hamed, Kumpaty, Subha, Zhang, Wujie
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.09.2023; MDPI
• Subjects: Antibiotics; Biocompatibility; Chemical properties; Colloids; Design of experiments; Design optimization; Dosage and administration; drug delivery; Drug delivery systems; Drugs; Electric fields; electrospray; Flow stability; Gelatin; Health aspects; hydrogel; Hydrogels; Infections; Ions; Lungs; Mannitol; Microspheres; Natural polymers; Optimization; Pectin; Pharmaceutical research; Protective coatings; Respiration; Respiratory agents; Toxicity; Vehicles; Viscosity; United States
• ISSN: 2310-2861; 2310-2861
• DOI: 10.3390/gels9090707

Pulmonary drug delivery via microspheres has gained growing interest as a noninvasive method for therapy. However, drug delivery through the lungs via inhalation faces great challenges due to the natural defense mechanisms of the respiratory tract, such as the removal or deactivation of drugs. This study aims to develop a natural polymer-based microsphere system with a diameter of around 3 μm for encapsulating pulmonary drugs and facilitating their delivery to the deep lungs. Pectin was chosen as the foundational material due to its biocompatibility and degradability in physiological environments. Electrospray was used to produce the pectin-based hydrogel microspheres, and Design-Expert software was used to optimize the production process for microsphere size and uniformity. The optimized conditions were determined to be as follows: pectin/PEO ratio of 3:1, voltage of 14.4 kV, distance of 18.2 cm, and flow rate of 0.95 mL/h. The stability and responsiveness of the pectin-based hydrogel microspheres can be altered through coatings such as gelatin. Furthermore, the potential of the microspheres for pulmonary drug delivery (i.e., their responsiveness to the deep lung environment) was investigated. Successfully coated microspheres with 0.75% gelatin in 0.3 M mannitol exhibited improved stability while retaining high responsiveness in the simulated lung fluid (Gamble’s solution). A gelatin-coated pectin-based microsphere system was developed, which could potentially be used for targeted drug delivery to reach the deep lungs and rapid release of the drug.