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Improvement of pneumonia by curcumin-loaded bionanosystems based on platycodon grandiflorum polysaccharides via calming cytokine storm.

Authors :
Li, Yi
Guo, Chunjing
Chen, Qiang
Su, Yanguo
Guo, Huimin
Liu, Ruoyang
Sun, Changgang
Mi, Shuqi
Wang, Jinqiu
Chen, Daquan
Source :
International Journal of Biological Macromolecules. Mar2022, Vol. 202, p691-706. 16p.
Publication Year :
2022

Abstract

Pneumonia can lead to high morbidity and mortality secondary to uncontrolled inflammation of the lung tissue. Blocking cytokine storm storms may be the key to saving the life of patients with severe pneumonia. According to the medicinal guide theory of Traditional Chinese Medicine (TCM) and the inherent affinity with macrophages for the site of inflammation, we constructed the drug delivery platform (MNPs) derived from macrophage-membrane encapsulated reaction oxygen species (ROS)-responsive Platycodon grandiflorum polysaccharides (PGP) nanoparticles (PNPs) to calm the cytokine storm and improve lung inflammation. By loading the anti-inflammatory agent Curcumin (Cur), we demonstrated that MNPs@Cur significantly attenuated inflammation and cytokine storm syndrome in acute lung injury (ALI) mice by suppressing pro-inflammatory factor production and inflammatory cell infiltration. Interestingly, we observed that the PNPs also have potent pulmonary targeting ability compared to other polysaccharide carriers, which is in line with the medicinal guide theory of TCM. Our study revealed the rational design of drug delivery platforms to improve the treatment of lung injury, which inherits and develops the important theories of TCM through the perfect combination of guide theory and biomimetic nanotechnology and provides the experimental scientific basis for the clinical application of channel ushering drugs. • The novel drug delivery platform draws on the medicinal guide theory of TCM. • MNPs could efficiently target pneumonia tissue. • MNPs@Cur could effectively calm down cytokine storm in the lung. • ROS-responsive MNPs enable precise drug release while reducing side effects. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01418130
Volume :
202
Database :
Academic Search Index
Journal :
International Journal of Biological Macromolecules
Publication Type :
Academic Journal
Accession number :
155427533
Full Text :
https://doi.org/10.1016/j.ijbiomac.2022.01.194