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Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery

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...

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Autores principales: Chai, Andy, Schmidt, Keagan, Brewster, Gregory, Xiong, Lu Shi Peng, Church, Benjamin, Wahl, Timothy, Sadabadi, Hamed, Kumpaty, Subha, Zhang, Wujie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529711/
https://www.ncbi.nlm.nih.gov/pubmed/37754388
http://dx.doi.org/10.3390/gels9090707
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author Chai, Andy
Schmidt, Keagan
Brewster, Gregory
Xiong, Lu Shi Peng
Church, Benjamin
Wahl, Timothy
Sadabadi, Hamed
Kumpaty, Subha
Zhang, Wujie
author_facet Chai, Andy
Schmidt, Keagan
Brewster, Gregory
Xiong, Lu Shi Peng
Church, Benjamin
Wahl, Timothy
Sadabadi, Hamed
Kumpaty, Subha
Zhang, Wujie
author_sort Chai, Andy
collection PubMed
description 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.
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spelling pubmed-105297112023-09-28 Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery Chai, Andy Schmidt, Keagan Brewster, Gregory Xiong, Lu Shi Peng Church, Benjamin Wahl, Timothy Sadabadi, Hamed Kumpaty, Subha Zhang, Wujie Gels Article 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. MDPI 2023-09-01 /pmc/articles/PMC10529711/ /pubmed/37754388 http://dx.doi.org/10.3390/gels9090707 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chai, Andy
Schmidt, Keagan
Brewster, Gregory
Xiong, Lu Shi Peng
Church, Benjamin
Wahl, Timothy
Sadabadi, Hamed
Kumpaty, Subha
Zhang, Wujie
Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery
title Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery
title_full Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery
title_fullStr Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery
title_full_unstemmed Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery
title_short Design of Pectin-Based Hydrogel Microspheres for Targeted Pulmonary Delivery
title_sort design of pectin-based hydrogel microspheres for targeted pulmonary delivery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529711/
https://www.ncbi.nlm.nih.gov/pubmed/37754388
http://dx.doi.org/10.3390/gels9090707
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