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An Insight on Microfluidic Organ-on-a-Chip Models for PM 2.5 -Induced Pulmonary Complications.

Authors :
Shah D
Dave B
Chorawala MR
Prajapati BG
Singh S
M Elossaily G
Ansari MN
Ali N
Source :
ACS omega [ACS Omega] 2024 Mar 07; Vol. 9 (12), pp. 13534-13555. Date of Electronic Publication: 2024 Mar 07 (Print Publication: 2024).
Publication Year :
2024

Abstract

Pulmonary diseases like asthma, chronic obstructive pulmonary disorder, lung fibrosis, and lung cancer pose a significant burden to global human health. Many of these complications arise as a result of exposure to particulate matter (PM), which has been examined in several preclinical and clinical trials for its effect on several respiratory diseases. Particulate matter of size less than 2.5 μm (PM <subscript>2.5</subscript> ) has been known to inflict unforeseen repercussions, although data from epidemiological studies to back this are pending. Conventionally utilized two-dimensional (2D) cell culture and preclinical animal models have provided insufficient benefits in emulating the in vivo physiological and pathological pulmonary conditions. Three-dimensional (3D) structural models, including organ-on-a-chip models, have experienced a developmental upsurge in recent times. Lung-on-a-chip models have the potential to simulate the specific features of the lungs. With the advancement of technology, an emerging and advanced technique termed microfluidic organ-on-a-chip has been developed with the aim of identifying the complexity of the respiratory cellular microenvironment of the body. In the present Review, the role of lung-on-a-chip modeling in reproducing pulmonary complications has been explored, with a specific emphasis on PM <subscript>2.5</subscript> -induced pulmonary complications.<br />Competing Interests: The authors declare no competing financial interest.<br /> (© 2024 The Authors. Published by American Chemical Society.)

Details

Language :
English
ISSN :
2470-1343
Volume :
9
Issue :
12
Database :
MEDLINE
Journal :
ACS omega
Publication Type :
Academic Journal
Accession number :
38559954
Full Text :
https://doi.org/10.1021/acsomega.3c10271