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Nanoengineered Neutrophil as 19 F-MRI Tracer for Alert Diagnosis and Severity A of Acute Lung Injury.

Authors :
Li S
Zhang L
Xu Q
Sui M
Xiao L
Chen D
Jiang ZX
Zhou X
Chen S
Source :
Advanced materials (Deerfield Beach, Fla.) [Adv Mater] 2024 Oct 03, pp. e2401513. Date of Electronic Publication: 2024 Oct 03.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Acute lung injury (ALI) is a severe complication in clinical settings. Alert diagnosis and severity assessment of ALI is pivotal to ensure curative treatment and increase survival rates. However, the development of a precise ALI diagnostic strategy remains a pending task. Here, leveraging neutrophil's inflammation-homing and physiological barrier-navigating capability, a facile strategy is proposed for achieving targeted <superscript>19</superscript> F-MRI detection of ALI based on the nanoengineered neutrophil internalized with perfluorocarbon nanoemulsion (Neu@PFC). The remodeling process poses a negligible impact on the neutrophil's inherent activation and transmigration functions. The migratory behavior of Neu@PFC toward pneumonia is confirmed in vivo using an LPS-induced ALI murine model. Direct intratracheal (i.t.) administration contributes to a vast deposition of Neu@PFC within the lung, allowing for real-time <superscript>19</superscript> F-MRI visualization and the potential to predict progressive pneumonia. Furthermore, intravenous (i.v.) administration of Neu@PFC enables quantitative assessment of the extent of ALI due to the chemokine-guided neutrophil migration. This study not only provides a pathway to diagnose ALI, but also sheds light on the neutrophil recruitment and activation cues in different tissues and inflammatory conditions, which is a prerequisite for developing potential therapeutic approaches.<br /> (© 2024 Wiley‐VCH GmbH.)

Details

Language :
English
ISSN :
1521-4095
Database :
MEDLINE
Journal :
Advanced materials (Deerfield Beach, Fla.)
Publication Type :
Academic Journal
Accession number :
39361266
Full Text :
https://doi.org/10.1002/adma.202401513