Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe Pneumonia

Background: Dexamethasone has proven life-saving in severe acute respiratory syndrome (SARS) and COVID-19 cases. However, its systemic administration is accompanied by serious side effects. Inhalation delivery of dexamethasone (Dex) faces challenges such as low lung deposition, br...

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Main Authors: Yixiao Yang, Lizhen Yan, Han Zhang, Chuanguang Xiao, Kai Wang
Format: Article
Language:English
Published: IMR Press 2025-01-01
Series:Frontiers in Bioscience-Landmark
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Online Access:https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL26721
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author Yixiao Yang
Lizhen Yan
Han Zhang
Chuanguang Xiao
Kai Wang
author_facet Yixiao Yang
Lizhen Yan
Han Zhang
Chuanguang Xiao
Kai Wang
author_sort Yixiao Yang
collection DOAJ
description Background: Dexamethasone has proven life-saving in severe acute respiratory syndrome (SARS) and COVID-19 cases. However, its systemic administration is accompanied by serious side effects. Inhalation delivery of dexamethasone (Dex) faces challenges such as low lung deposition, brief residence in the respiratory tract, and the pulmonary mucus barrier, limiting its clinical use. Neutrophil cell membrane-derived nanovesicles, with their ability to specifically target hyper-activated immune cells and excellent mucus permeability, emerge as a promising carrier for pulmonary inhalation therapy. Methods: We designed a novel UiO66 metal-organic framework nanoparticle loaded with Dex and coated with neutrophil cell membranes (UiO66-Dex@NMP) for targeted therapy of severe pneumonia. This was achieved by loading Dex into UiO66 pores and subsequently coating with neutrophil membranes for functionalization. Results: Drug release experiments revealed UiO66-Dex@NMP to exhibit favorable sustained-release properties. Additionally, UiO66-Dex@NMP demonstrated excellent targeting capabilities both in vitro and in vivo. In a mouse model of lipopolysaccharide (LPS)-induced pneumonia, UiO66-Dex@NMP significantly reduced lung inflammation compared to both the control model and Dex administered via inhalation. Histopathological analysis further confirmed UiO66-Dex@NMP’s ability to alleviate lung tissue damage. Conclusions: UiO66-Dex@NMP represents a novel and safe inhaled delivery carrier for Dex, offering valuable insights into the clinical management of respiratory diseases, including severe pneumonia.
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spelling doaj-art-252313fe40504f4e9766c714778c131c2025-01-25T08:55:52ZengIMR PressFrontiers in Bioscience-Landmark2768-67012025-01-013012672110.31083/FBL26721S2768-6701(24)01580-6Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe PneumoniaYixiao Yang0Lizhen Yan1Han Zhang2Chuanguang Xiao3Kai Wang4Institute of Translational Medicine, Shanghai University, 200444 Shanghai, ChinaDepartment of Respiratory and Critical Care Medicine, Zibo Municipal Hospital, 255400 Zibo, Shandong, ChinaInstitute of Translational Medicine, Shanghai University, 200444 Shanghai, ChinaDepartment of Breast Thyroid Surgery, Zibo Central Hospital, 255036 Zibo, Shandong, ChinaInstitute of Translational Medicine, Shanghai University, 200444 Shanghai, ChinaBackground: Dexamethasone has proven life-saving in severe acute respiratory syndrome (SARS) and COVID-19 cases. However, its systemic administration is accompanied by serious side effects. Inhalation delivery of dexamethasone (Dex) faces challenges such as low lung deposition, brief residence in the respiratory tract, and the pulmonary mucus barrier, limiting its clinical use. Neutrophil cell membrane-derived nanovesicles, with their ability to specifically target hyper-activated immune cells and excellent mucus permeability, emerge as a promising carrier for pulmonary inhalation therapy. Methods: We designed a novel UiO66 metal-organic framework nanoparticle loaded with Dex and coated with neutrophil cell membranes (UiO66-Dex@NMP) for targeted therapy of severe pneumonia. This was achieved by loading Dex into UiO66 pores and subsequently coating with neutrophil membranes for functionalization. Results: Drug release experiments revealed UiO66-Dex@NMP to exhibit favorable sustained-release properties. Additionally, UiO66-Dex@NMP demonstrated excellent targeting capabilities both in vitro and in vivo. In a mouse model of lipopolysaccharide (LPS)-induced pneumonia, UiO66-Dex@NMP significantly reduced lung inflammation compared to both the control model and Dex administered via inhalation. Histopathological analysis further confirmed UiO66-Dex@NMP’s ability to alleviate lung tissue damage. Conclusions: UiO66-Dex@NMP represents a novel and safe inhaled delivery carrier for Dex, offering valuable insights into the clinical management of respiratory diseases, including severe pneumonia.https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL26721dexamethasonemofneutrophil cell membraneinhaled deliverysevere pneumonia
spellingShingle Yixiao Yang
Lizhen Yan
Han Zhang
Chuanguang Xiao
Kai Wang
Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe Pneumonia
Frontiers in Bioscience-Landmark
dexamethasone
mof
neutrophil cell membrane
inhaled delivery
severe pneumonia
title Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe Pneumonia
title_full Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe Pneumonia
title_fullStr Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe Pneumonia
title_full_unstemmed Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe Pneumonia
title_short Atomized Neutrophil Membrane-coated MOF Nanoparticles for Direct Delivery of Dexamethasone for Severe Pneumonia
title_sort atomized neutrophil membrane coated mof nanoparticles for direct delivery of dexamethasone for severe pneumonia
topic dexamethasone
mof
neutrophil cell membrane
inhaled delivery
severe pneumonia
url https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL26721
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