Development and evaluation of ibuprofen-loaded chitosan nanoparticles for pulmonary therapy

Lung injuries are increasingly prevalent due to various diseases causing alveolar damage, potentially leading to respiratory disorders. This study employed an incubation method to develop nano-encapsulated ibuprofen within a chitosan matrix for targeted pulmonary therapy. The encapsulation was successful without altering the molecular structure of chitosan, and a 500 mg dose was identified as optimal through lung tissue cell viability and histological analysis. The controlled release mechanism of this formulation ensures targeted delivery to the lungs, reducing inflammation and promoting alveolar regeneration. This approach highlights the importance of dose optimization and presents a promising strategy to enhance the efficacy and safety of pulmonary treatments.

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Publication Details

Journal
Frontiers in Nanotechnology
Published
2024-09-12
DOI
https://doi.org/10.3389/fnano.2024.1429889
Citations
4
Primary Topic
Advanced Drug Delivery Systems
Type
article
Field-Weighted Citation Impact
0.83

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article

Development and evaluation of ibuprofen-loaded chitosan nanoparticles for pulmonary therapy

Adriana Jheny Rodríguez-Mendez, Verónica Rico Pérez, Pablo García‐Solís, Idais Rodríguez et al.
4 citations
Frontiers in Nanotechnology
Advanced Drug Delivery Systems
0.83
article

Development and evaluation of ibuprofen-loaded chitosan nanoparticles for pulmonary therapy

Adriana Jheny Rodríguez-Mendez, Verónica Rico Pérez, Pablo García‐Solís, Idais Rodríguez, José Alberto Rodríguez Morales, Carlos J. Martinez, Juan Campos‐Guillén, Angela López, Vanessa Vallejo Becerra, J. M. Mora-Muñoz, M. A. Gallegos-Reyes
article en
4 citations

Abstract

Lung injuries are increasingly prevalent due to various diseases causing alveolar damage, potentially leading to respiratory disorders. This study employed an incubation method to develop nano-encapsulated ibuprofen within a chitosan matrix for targeted pulmonary therapy. The encapsulation was successful without altering the molecular structure of chitosan, and a 500 mg dose was identified as optimal through lung tissue cell viability and histological analysis. The controlled release mechanism of this formulation ensures targeted delivery to the lungs, reducing inflammation and promoting alveolar regeneration. This approach highlights the importance of dose optimization and presents a promising strategy to enhance the efficacy and safety of pulmonary treatments.

Frontiers in NanotechnologyVol. 6
Autonomous University of Queretaro (MX)
Universidad Autónoma de Querétaro
Openalex Percentile: Top 30%
Advanced Drug Delivery Systems
0.83
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