Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery

Author:

Chai Andy1,Schmidt Keagan2,Brewster Gregory2,Xiong Lu Shi Peng2,Church Benjamin34ORCID,Wahl Timothy5,Sadabadi Hamed3,Kumpaty Subha6,Zhang Wujie2ORCID

Affiliation:

1. Department of Chemistry, Rhodes College, Memphis, TN 38112, USA

2. Chemical and Biomolecular Engineering Program, Department of Physics and Chemistry, Milwaukee School of Engineering, Milwaukee, WI 53202, USA

3. Advanced Analysis Facility, College of Engineering & Applied Science, University of Wisconsin—Milwaukee, Milwaukee, WI 53211, USA

4. Materials Science & Engineering Department, University of Wisconsin—Milwaukee, Milwaukee, WI 53211, USA

5. School of Freshwater Sciences, University of Wisconsin—Milwaukee, Milwaukee, WI 53204, USA

6. Department of Mechanical Engineering, Milwaukee School of Engineering, Milwaukee, WI 53211, USA

Abstract

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.

Funder

National Science Foundation

Publisher

MDPI AG

Subject

Polymers and Plastics,Organic Chemistry,Biomaterials,Bioengineering

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